[{"type":"journal_article","status":"public","_id":"715","article_number":"aao4218","publist_id":"6968","author":[{"first_name":"Gaia","id":"3E57A680-F248-11E8-B48F-1D18A9856A87","last_name":"Novarino","full_name":"Novarino, Gaia","orcid":"0000-0002-7673-7178"}],"title":"More excitation for Rett syndrome","department":[{"_id":"GaNo"}],"date_updated":"2021-01-12T08:12:04Z","citation":{"mla":"Novarino, Gaia. “More Excitation for Rett Syndrome.” Science Translational Medicine, vol. 9, no. 405, aao4218, American Association for the Advancement of Science, 2017, doi:10.1126/scitranslmed.aao4218.","ama":"Novarino G. More excitation for Rett syndrome. Science Translational Medicine. 2017;9(405). doi:10.1126/scitranslmed.aao4218","apa":"Novarino, G. (2017). More excitation for Rett syndrome. Science Translational Medicine. American Association for the Advancement of Science. https://doi.org/10.1126/scitranslmed.aao4218","ieee":"G. Novarino, “More excitation for Rett syndrome,” Science Translational Medicine, vol. 9, no. 405. American Association for the Advancement of Science, 2017.","short":"G. Novarino, Science Translational Medicine 9 (2017).","chicago":"Novarino, Gaia. “More Excitation for Rett Syndrome.” Science Translational Medicine. American Association for the Advancement of Science, 2017. https://doi.org/10.1126/scitranslmed.aao4218.","ista":"Novarino G. 2017. More excitation for Rett syndrome. Science Translational Medicine. 9(405), aao4218."},"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","quality_controlled":"1","publisher":"American Association for the Advancement of Science","scopus_import":1,"month":"08","intvolume":" 9","abstract":[{"text":"D-cycloserine ameliorates breathing abnormalities and survival rate in a mouse model of Rett syndrome.","lang":"eng"}],"oa_version":"None","volume":9,"issue":"405","doi":"10.1126/scitranslmed.aao4218","date_published":"2017-08-30T00:00:00Z","date_created":"2018-12-11T11:48:06Z","publication_identifier":{"issn":["19466234"]},"year":"2017","publication_status":"published","day":"30","publication":"Science Translational Medicine","language":[{"iso":"eng"}]},{"scopus_import":1,"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1201.2829"}],"month":"09","intvolume":" 64","abstract":[{"text":"Two-player games on graphs are central in many problems in formal verification and program analysis, such as synthesis and verification of open systems. In this work, we consider solving recursive game graphs (or pushdown game graphs) that model the control flow of sequential programs with recursion.While pushdown games have been studied before with qualitative objectives-such as reachability and ?-regular objectives- in this work, we study for the first time such games with the most well-studied quantitative objective, the mean-payoff objective. In pushdown games, two types of strategies are relevant: (1) global strategies, which depend on the entire global history; and (2) modular strategies, which have only local memory and thus do not depend on the context of invocation but rather only on the history of the current invocation of the module. Our main results are as follows: (1) One-player pushdown games with mean-payoff objectives under global strategies are decidable in polynomial time. (2) Two-player pushdown games with mean-payoff objectives under global strategies are undecidable. (3) One-player pushdown games with mean-payoff objectives under modular strategies are NP-hard. (4) Two-player pushdown games with mean-payoff objectives under modular strategies can be solved in NP (i.e., both one-player and two-player pushdown games with mean-payoff objectives under modular strategies are NP-complete). We also establish the optimal strategy complexity by showing that global strategies for mean-payoff objectives require infinite memory even in one-player pushdown games and memoryless modular strategies are sufficient in two-player pushdown games. Finally, we also show that all the problems have the same complexity if the stack boundedness condition is added, where along with the mean-payoff objective the player must also ensure that the stack height is bounded.","lang":"eng"}],"oa_version":"Preprint","issue":"5","volume":64,"ec_funded":1,"publication_identifier":{"issn":["00045411"]},"publication_status":"published","language":[{"iso":"eng"}],"article_type":"original","type":"journal_article","status":"public","_id":"716","department":[{"_id":"KrCh"}],"date_updated":"2021-01-12T08:12:08Z","publisher":"ACM","quality_controlled":"1","oa":1,"page":"34","date_published":"2017-09-01T00:00:00Z","doi":"10.1145/3121408","date_created":"2018-12-11T11:48:06Z","year":"2017","day":"01","publication":"Journal of the ACM","project":[{"name":"Modern Graph Algorithmic Techniques in Formal Verification","grant_number":"P 23499-N23","call_identifier":"FWF","_id":"2584A770-B435-11E9-9278-68D0E5697425"},{"grant_number":"S11407","name":"Game Theory","call_identifier":"FWF","_id":"25863FF4-B435-11E9-9278-68D0E5697425"},{"grant_number":"279307","name":"Quantitative Graph Games: Theory and Applications","_id":"2581B60A-B435-11E9-9278-68D0E5697425","call_identifier":"FP7"}],"publist_id":"6964","author":[{"full_name":"Chatterjee, Krishnendu","orcid":"0000-0002-4561-241X","last_name":"Chatterjee","first_name":"Krishnendu","id":"2E5DCA20-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Yaron","full_name":"Velner, Yaron","last_name":"Velner"}],"external_id":{"arxiv":["1201.2829"]},"title":"The complexity of mean-payoff pushdown games","citation":{"ista":"Chatterjee K, Velner Y. 2017. The complexity of mean-payoff pushdown games. Journal of the ACM. 64(5), 34.","chicago":"Chatterjee, Krishnendu, and Yaron Velner. “The Complexity of Mean-Payoff Pushdown Games.” Journal of the ACM. ACM, 2017. https://doi.org/10.1145/3121408.","ieee":"K. Chatterjee and Y. Velner, “The complexity of mean-payoff pushdown games,” Journal of the ACM, vol. 64, no. 5. ACM, p. 34, 2017.","short":"K. Chatterjee, Y. Velner, Journal of the ACM 64 (2017) 34.","ama":"Chatterjee K, Velner Y. The complexity of mean-payoff pushdown games. Journal of the ACM. 2017;64(5):34. doi:10.1145/3121408","apa":"Chatterjee, K., & Velner, Y. (2017). The complexity of mean-payoff pushdown games. Journal of the ACM. ACM. https://doi.org/10.1145/3121408","mla":"Chatterjee, Krishnendu, and Yaron Velner. “The Complexity of Mean-Payoff Pushdown Games.” Journal of the ACM, vol. 64, no. 5, ACM, 2017, p. 34, doi:10.1145/3121408."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"page":"236 - 259","date_created":"2018-12-11T11:48:07Z","date_published":"2017-09-01T00:00:00Z","doi":"10.1016/j.jcss.2017.04.005","year":"2017","publication":"Journal of Computer and System Sciences","day":"01","oa":1,"publisher":"Academic Press","quality_controlled":"1","acknowledgement":"The research was supported by Austrian Science Fund (FWF) Grant No. P 23499-N23, FWF NFN Grant No. S11407-N23 (RiSE), ERC Start grant (279307: Graph Games), Microsoft faculty fellows award, the RICH Model Toolkit (ICT COST Action IC0901), and was carried out in partial fulfillment of the requirements for the Ph.D. degree of the second author.","author":[{"full_name":"Chatterjee, Krishnendu","orcid":"0000-0002-4561-241X","last_name":"Chatterjee","id":"2E5DCA20-F248-11E8-B48F-1D18A9856A87","first_name":"Krishnendu"},{"first_name":"Yaron","last_name":"Velner","full_name":"Velner, Yaron"}],"publist_id":"6963","title":"Hyperplane separation technique for multidimensional mean-payoff games","citation":{"short":"K. Chatterjee, Y. Velner, Journal of Computer and System Sciences 88 (2017) 236–259.","ieee":"K. Chatterjee and Y. Velner, “Hyperplane separation technique for multidimensional mean-payoff games,” Journal of Computer and System Sciences, vol. 88. Academic Press, pp. 236–259, 2017.","ama":"Chatterjee K, Velner Y. Hyperplane separation technique for multidimensional mean-payoff games. Journal of Computer and System Sciences. 2017;88:236-259. doi:10.1016/j.jcss.2017.04.005","apa":"Chatterjee, K., & Velner, Y. (2017). Hyperplane separation technique for multidimensional mean-payoff games. Journal of Computer and System Sciences. Academic Press. https://doi.org/10.1016/j.jcss.2017.04.005","mla":"Chatterjee, Krishnendu, and Yaron Velner. “Hyperplane Separation Technique for Multidimensional Mean-Payoff Games.” Journal of Computer and System Sciences, vol. 88, Academic Press, 2017, pp. 236–59, doi:10.1016/j.jcss.2017.04.005.","ista":"Chatterjee K, Velner Y. 2017. Hyperplane separation technique for multidimensional mean-payoff games. Journal of Computer and System Sciences. 88, 236–259.","chicago":"Chatterjee, Krishnendu, and Yaron Velner. “Hyperplane Separation Technique for Multidimensional Mean-Payoff Games.” Journal of Computer and System Sciences. Academic Press, 2017. https://doi.org/10.1016/j.jcss.2017.04.005."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","project":[{"name":"Modern Graph Algorithmic Techniques in Formal Verification","grant_number":"P 23499-N23","call_identifier":"FWF","_id":"2584A770-B435-11E9-9278-68D0E5697425"},{"name":"Game Theory","grant_number":"S11407","_id":"25863FF4-B435-11E9-9278-68D0E5697425","call_identifier":"FWF"},{"call_identifier":"FP7","_id":"2581B60A-B435-11E9-9278-68D0E5697425","grant_number":"279307","name":"Quantitative Graph Games: Theory and Applications"},{"name":"Microsoft Research Faculty Fellowship","_id":"2587B514-B435-11E9-9278-68D0E5697425"}],"ec_funded":1,"volume":88,"related_material":{"record":[{"relation":"earlier_version","status":"public","id":"2329"}]},"publication_status":"published","language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1210.3141"}],"scopus_import":1,"intvolume":" 88","month":"09","abstract":[{"lang":"eng","text":"We consider finite-state and recursive game graphs with multidimensional mean-payoff objectives. In recursive games two types of strategies are relevant: global strategies and modular strategies. Our contributions are: (1) We show that finite-state multidimensional mean-payoff games can be solved in polynomial time if the number of dimensions and the maximal absolute value of weights are fixed; whereas for arbitrary dimensions the problem is coNP-complete. (2) We show that one-player recursive games with multidimensional mean-payoff objectives can be solved in polynomial time. Both above algorithms are based on hyperplane separation technique. (3) For recursive games we show that under modular strategies the multidimensional problem is undecidable. We show that if the number of modules, exits, and the maximal absolute value of the weights are fixed, then one-dimensional recursive mean-payoff games under modular strategies can be solved in polynomial time, whereas for unbounded number of exits or modules the problem is NP-hard."}],"oa_version":"Preprint","department":[{"_id":"KrCh"}],"date_updated":"2023-02-23T10:38:15Z","type":"journal_article","status":"public","_id":"717"},{"day":"01","language":[{"iso":"eng"}],"publication":"Acta Informatica","publication_identifier":{"issn":["00015903"]},"publication_status":"published","year":"2017","date_published":"2017-09-01T00:00:00Z","issue":"6","doi":"10.1007/s00236-017-0299-0","volume":54,"date_created":"2018-12-11T11:48:07Z","page":"543 - 544","oa_version":"None","abstract":[{"text":"The ubiquity of computation in modern machines and devices imposes a need to assert the correctness of their behavior. Especially in the case of safety-critical systems, their designers need to take measures that enforce their safe operation. Formal methods has emerged as a research field that addresses this challenge: by rigorously proving that all system executions adhere to their specifications, the correctness of an implementation under concern can be assured. To achieve this goal, a plethora of techniques are nowadays available, all of which are optimized for different system types and application domains.","lang":"eng"}],"month":"09","intvolume":" 54","publisher":"Springer","quality_controlled":"1","scopus_import":1,"user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","date_updated":"2021-01-12T08:12:18Z","citation":{"mla":"Chatterjee, Krishnendu, and Rüdiger Ehlers. “Special Issue: Synthesis and SYNT 2014.” Acta Informatica, vol. 54, no. 6, Springer, 2017, pp. 543–44, doi:10.1007/s00236-017-0299-0.","ama":"Chatterjee K, Ehlers R. Special issue: Synthesis and SYNT 2014. Acta Informatica. 2017;54(6):543-544. doi:10.1007/s00236-017-0299-0","apa":"Chatterjee, K., & Ehlers, R. (2017). Special issue: Synthesis and SYNT 2014. Acta Informatica. Springer. https://doi.org/10.1007/s00236-017-0299-0","ieee":"K. Chatterjee and R. Ehlers, “Special issue: Synthesis and SYNT 2014,” Acta Informatica, vol. 54, no. 6. Springer, pp. 543–544, 2017.","short":"K. Chatterjee, R. Ehlers, Acta Informatica 54 (2017) 543–544.","chicago":"Chatterjee, Krishnendu, and Rüdiger Ehlers. “Special Issue: Synthesis and SYNT 2014.” Acta Informatica. Springer, 2017. https://doi.org/10.1007/s00236-017-0299-0.","ista":"Chatterjee K, Ehlers R. 2017. Special issue: Synthesis and SYNT 2014. Acta Informatica. 54(6), 543–544."},"title":"Special issue: Synthesis and SYNT 2014","department":[{"_id":"KrCh"}],"author":[{"last_name":"Chatterjee","full_name":"Chatterjee, Krishnendu","orcid":"0000-0002-4561-241X","first_name":"Krishnendu","id":"2E5DCA20-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Rüdiger","full_name":"Ehlers, Rüdiger","last_name":"Ehlers"}],"publist_id":"6961","_id":"719","status":"public","type":"journal_article"},{"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Humplik, Jan, and Gašper Tkačik. “Probabilistic Models for Neural Populations That Naturally Capture Global Coupling and Criticality.” PLoS Computational Biology. Public Library of Science, 2017. https://doi.org/10.1371/journal.pcbi.1005763.","ista":"Humplik J, Tkačik G. 2017. Probabilistic models for neural populations that naturally capture global coupling and criticality. PLoS Computational Biology. 13(9), e1005763.","mla":"Humplik, Jan, and Gašper Tkačik. “Probabilistic Models for Neural Populations That Naturally Capture Global Coupling and Criticality.” PLoS Computational Biology, vol. 13, no. 9, e1005763, Public Library of Science, 2017, doi:10.1371/journal.pcbi.1005763.","apa":"Humplik, J., & Tkačik, G. (2017). Probabilistic models for neural populations that naturally capture global coupling and criticality. PLoS Computational Biology. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1005763","ama":"Humplik J, Tkačik G. Probabilistic models for neural populations that naturally capture global coupling and criticality. PLoS Computational Biology. 2017;13(9). doi:10.1371/journal.pcbi.1005763","ieee":"J. Humplik and G. Tkačik, “Probabilistic models for neural populations that naturally capture global coupling and criticality,” PLoS Computational Biology, vol. 13, no. 9. Public Library of Science, 2017.","short":"J. Humplik, G. Tkačik, PLoS Computational Biology 13 (2017)."},"title":"Probabilistic models for neural populations that naturally capture global coupling and criticality","article_processing_charge":"Yes","publist_id":"6960","author":[{"first_name":"Jan","id":"2E9627A8-F248-11E8-B48F-1D18A9856A87","full_name":"Humplik, Jan","last_name":"Humplik"},{"id":"3D494DCA-F248-11E8-B48F-1D18A9856A87","first_name":"Gasper","full_name":"Tkacik, Gasper","orcid":"0000-0002-6699-1455","last_name":"Tkacik"}],"article_number":"e1005763","project":[{"_id":"255008E4-B435-11E9-9278-68D0E5697425","name":"Information processing and computation in fish groups","grant_number":"RGP0065/2012"},{"grant_number":"P 25651-N26","name":"Sensitivity to higher-order statistics in natural scenes","_id":"254D1A94-B435-11E9-9278-68D0E5697425","call_identifier":"FWF"}],"publication":"PLoS Computational Biology","day":"19","year":"2017","has_accepted_license":"1","date_created":"2018-12-11T11:48:08Z","date_published":"2017-09-19T00:00:00Z","doi":"10.1371/journal.pcbi.1005763","oa":1,"publisher":"Public Library of Science","quality_controlled":"1","ddc":["530","571"],"date_updated":"2021-01-12T08:12:21Z","department":[{"_id":"GaTk"}],"file_date_updated":"2020-07-14T12:47:53Z","_id":"720","pubrep_id":"884","status":"public","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"type":"journal_article","language":[{"iso":"eng"}],"file":[{"content_type":"application/pdf","access_level":"open_access","relation":"main_file","file_id":"5352","checksum":"81107096c19771c36ddbe6f0282a3acb","date_updated":"2020-07-14T12:47:53Z","file_size":14167050,"creator":"system","date_created":"2018-12-12T10:18:30Z","file_name":"IST-2017-884-v1+1_journal.pcbi.1005763.pdf"}],"publication_status":"published","publication_identifier":{"issn":["1553734X"]},"volume":13,"issue":"9","oa_version":"Published Version","abstract":[{"text":"Advances in multi-unit recordings pave the way for statistical modeling of activity patterns in large neural populations. Recent studies have shown that the summed activity of all neurons strongly shapes the population response. A separate recent finding has been that neural populations also exhibit criticality, an anomalously large dynamic range for the probabilities of different population activity patterns. Motivated by these two observations, we introduce a class of probabilistic models which takes into account the prior knowledge that the neural population could be globally coupled and close to critical. These models consist of an energy function which parametrizes interactions between small groups of neurons, and an arbitrary positive, strictly increasing, and twice differentiable function which maps the energy of a population pattern to its probability. We show that: 1) augmenting a pairwise Ising model with a nonlinearity yields an accurate description of the activity of retinal ganglion cells which outperforms previous models based on the summed activity of neurons; 2) prior knowledge that the population is critical translates to prior expectations about the shape of the nonlinearity; 3) the nonlinearity admits an interpretation in terms of a continuous latent variable globally coupling the system whose distribution we can infer from data. Our method is independent of the underlying system’s state space; hence, it can be applied to other systems such as natural scenes or amino acid sequences of proteins which are also known to exhibit criticality.","lang":"eng"}],"intvolume":" 13","month":"09","scopus_import":1},{"title":"Singularities of solutions to quadratic vector equations on the complex upper half plane","publist_id":"6959","author":[{"first_name":"Oskari H","id":"36F2FB7E-F248-11E8-B48F-1D18A9856A87","last_name":"Ajanki","full_name":"Ajanki, Oskari H"},{"first_name":"Torben H","id":"3020C786-F248-11E8-B48F-1D18A9856A87","full_name":"Krüger, Torben H","orcid":"0000-0002-4821-3297","last_name":"Krüger"},{"first_name":"László","id":"4DBD5372-F248-11E8-B48F-1D18A9856A87","last_name":"Erdös","orcid":"0000-0001-5366-9603","full_name":"Erdös, László"}],"user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Ajanki OH, Krüger TH, Erdös L. 2017. Singularities of solutions to quadratic vector equations on the complex upper half plane. Communications on Pure and Applied Mathematics. 70(9), 1672–1705.","chicago":"Ajanki, Oskari H, Torben H Krüger, and László Erdös. “Singularities of Solutions to Quadratic Vector Equations on the Complex Upper Half Plane.” Communications on Pure and Applied Mathematics. Wiley-Blackwell, 2017. https://doi.org/10.1002/cpa.21639.","apa":"Ajanki, O. H., Krüger, T. H., & Erdös, L. (2017). Singularities of solutions to quadratic vector equations on the complex upper half plane. Communications on Pure and Applied Mathematics. Wiley-Blackwell. https://doi.org/10.1002/cpa.21639","ama":"Ajanki OH, Krüger TH, Erdös L. Singularities of solutions to quadratic vector equations on the complex upper half plane. Communications on Pure and Applied Mathematics. 2017;70(9):1672-1705. doi:10.1002/cpa.21639","ieee":"O. H. Ajanki, T. H. Krüger, and L. Erdös, “Singularities of solutions to quadratic vector equations on the complex upper half plane,” Communications on Pure and Applied Mathematics, vol. 70, no. 9. Wiley-Blackwell, pp. 1672–1705, 2017.","short":"O.H. Ajanki, T.H. Krüger, L. Erdös, Communications on Pure and Applied Mathematics 70 (2017) 1672–1705.","mla":"Ajanki, Oskari H., et al. “Singularities of Solutions to Quadratic Vector Equations on the Complex Upper Half Plane.” Communications on Pure and Applied Mathematics, vol. 70, no. 9, Wiley-Blackwell, 2017, pp. 1672–705, doi:10.1002/cpa.21639."},"project":[{"_id":"258DCDE6-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","grant_number":"338804","name":"Random matrices, universality and disordered quantum systems"}],"doi":"10.1002/cpa.21639","date_published":"2017-09-01T00:00:00Z","date_created":"2018-12-11T11:48:08Z","page":"1672 - 1705","day":"01","publication":"Communications on Pure and Applied Mathematics","year":"2017","quality_controlled":"1","publisher":"Wiley-Blackwell","oa":1,"department":[{"_id":"LaEr"}],"date_updated":"2021-01-12T08:12:24Z","status":"public","type":"journal_article","_id":"721","issue":"9","volume":70,"ec_funded":1,"language":[{"iso":"eng"}],"publication_identifier":{"issn":["00103640"]},"publication_status":"published","month":"09","intvolume":" 70","scopus_import":1,"main_file_link":[{"url":"https://arxiv.org/abs/1512.03703","open_access":"1"}],"oa_version":"Submitted Version","abstract":[{"lang":"eng","text":"Let S be a positivity-preserving symmetric linear operator acting on bounded functions. The nonlinear equation -1/m=z+Sm with a parameter z in the complex upper half-plane ℍ has a unique solution m with values in ℍ. We show that the z-dependence of this solution can be represented as the Stieltjes transforms of a family of probability measures v on ℝ. Under suitable conditions on S, we show that v has a real analytic density apart from finitely many algebraic singularities of degree at most 3. Our motivation comes from large random matrices. The solution m determines the density of eigenvalues of two prominent matrix ensembles: (i) matrices with centered independent entries whose variances are given by S and (ii) matrices with correlated entries with a translation-invariant correlation structure. Our analysis shows that the limiting eigenvalue density has only square root singularities or cubic root cusps; no other singularities occur."}]},{"publisher":"Cell Press","quality_controlled":"1","oa":1,"day":"11","publication":"Current Biology","has_accepted_license":"1","year":"2017","date_published":"2017-09-11T00:00:00Z","doi":"10.1016/j.cub.2017.06.043","date_created":"2018-12-11T11:48:08Z","page":"R919 - R930","project":[{"grant_number":"291734","name":"International IST Postdoc Fellowship Programme","_id":"25681D80-B435-11E9-9278-68D0E5697425","call_identifier":"FP7"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ama":"Morris E, Griffiths M, Golebiowska A, et al. Shaping 3D root system architecture. Current Biology. 2017;27(17):R919-R930. doi:10.1016/j.cub.2017.06.043","apa":"Morris, E., Griffiths, M., Golebiowska, A., Mairhofer, S., Burr Hersey, J., Goh, T., … Bennett, M. (2017). Shaping 3D root system architecture. Current Biology. Cell Press. https://doi.org/10.1016/j.cub.2017.06.043","ieee":"E. Morris et al., “Shaping 3D root system architecture,” Current Biology, vol. 27, no. 17. Cell Press, pp. R919–R930, 2017.","short":"E. Morris, M. Griffiths, A. Golebiowska, S. Mairhofer, J. Burr Hersey, T. Goh, D. von Wangenheim, B. Atkinson, C. Sturrock, J. Lynch, K. Vissenberg, K. Ritz, D. Wells, S. Mooney, M. Bennett, Current Biology 27 (2017) R919–R930.","mla":"Morris, Emily, et al. “Shaping 3D Root System Architecture.” Current Biology, vol. 27, no. 17, Cell Press, 2017, pp. R919–30, doi:10.1016/j.cub.2017.06.043.","ista":"Morris E, Griffiths M, Golebiowska A, Mairhofer S, Burr Hersey J, Goh T, von Wangenheim D, Atkinson B, Sturrock C, Lynch J, Vissenberg K, Ritz K, Wells D, Mooney S, Bennett M. 2017. Shaping 3D root system architecture. Current Biology. 27(17), R919–R930.","chicago":"Morris, Emily, Marcus Griffiths, Agata Golebiowska, Stefan Mairhofer, Jasmine Burr Hersey, Tatsuaki Goh, Daniel von Wangenheim, et al. “Shaping 3D Root System Architecture.” Current Biology. Cell Press, 2017. https://doi.org/10.1016/j.cub.2017.06.043."},"title":"Shaping 3D root system architecture","publist_id":"6956","author":[{"last_name":"Morris","full_name":"Morris, Emily","first_name":"Emily"},{"first_name":"Marcus","last_name":"Griffiths","full_name":"Griffiths, Marcus"},{"first_name":"Agata","last_name":"Golebiowska","full_name":"Golebiowska, Agata"},{"last_name":"Mairhofer","full_name":"Mairhofer, Stefan","first_name":"Stefan"},{"full_name":"Burr Hersey, Jasmine","last_name":"Burr Hersey","first_name":"Jasmine"},{"last_name":"Goh","full_name":"Goh, Tatsuaki","first_name":"Tatsuaki"},{"orcid":"0000-0002-6862-1247","full_name":"Von Wangenheim, Daniel","last_name":"Von Wangenheim","first_name":"Daniel","id":"49E91952-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Atkinson, Brian","last_name":"Atkinson","first_name":"Brian"},{"last_name":"Sturrock","full_name":"Sturrock, Craig","first_name":"Craig"},{"first_name":"Jonathan","last_name":"Lynch","full_name":"Lynch, Jonathan"},{"first_name":"Kris","full_name":"Vissenberg, Kris","last_name":"Vissenberg"},{"first_name":"Karl","last_name":"Ritz","full_name":"Ritz, Karl"},{"full_name":"Wells, Darren","last_name":"Wells","first_name":"Darren"},{"last_name":"Mooney","full_name":"Mooney, Sacha","first_name":"Sacha"},{"first_name":"Malcolm","last_name":"Bennett","full_name":"Bennett, Malcolm"}],"external_id":{"pmid":["28898665"]},"oa_version":"Submitted Version","pmid":1,"abstract":[{"text":"Plants are sessile organisms rooted in one place. The soil resources that plants require are often distributed in a highly heterogeneous pattern. To aid foraging, plants have evolved roots whose growth and development are highly responsive to soil signals. As a result, 3D root architecture is shaped by myriad environmental signals to ensure resource capture is optimised and unfavourable environments are avoided. The first signals sensed by newly germinating seeds — gravity and light — direct root growth into the soil to aid seedling establishment. Heterogeneous soil resources, such as water, nitrogen and phosphate, also act as signals that shape 3D root growth to optimise uptake. Root architecture is also modified through biotic interactions that include soil fungi and neighbouring plants. This developmental plasticity results in a ‘custom-made’ 3D root system that is best adapted to forage for resources in each soil environment that a plant colonises.","lang":"eng"}],"month":"09","intvolume":" 27","scopus_import":1,"file":[{"relation":"main_file","access_level":"open_access","content_type":"application/pdf","checksum":"e45588b21097b408da6276a3e5eedb2e","file_id":"6332","creator":"dernst","file_size":1576593,"date_updated":"2020-07-14T12:47:54Z","file_name":"2017_CurrentBiology_Morris.pdf","date_created":"2019-04-17T07:46:40Z"}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["09609822"]},"publication_status":"published","issue":"17","volume":27,"ec_funded":1,"_id":"722","status":"public","pubrep_id":"982","type":"journal_article","tmp":{"short":"CC BY-NC-ND (4.0)","name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","image":"/images/cc_by_nc_nd.png"},"ddc":["581"],"date_updated":"2021-01-12T08:12:29Z","department":[{"_id":"JiFr"}],"file_date_updated":"2020-07-14T12:47:54Z"},{"date_created":"2018-12-11T11:48:10Z","doi":"10.1073/pnas.1703817114","date_published":"2017-09-19T00:00:00Z","page":"10149 - 10154","publication":"PNAS","day":"19","year":"2017","oa":1,"quality_controlled":"1","publisher":"National Academy of Sciences","title":"Discrete modes of social information processing predict individual behavior of fish in a group","external_id":{"pmid":["28874581"]},"author":[{"last_name":"Harpaz","full_name":"Harpaz, Roy","first_name":"Roy"},{"id":"3D494DCA-F248-11E8-B48F-1D18A9856A87","first_name":"Gasper","last_name":"Tkacik","orcid":"0000-0002-6699-1455","full_name":"Tkacik, Gasper"},{"full_name":"Schneidman, Elad","last_name":"Schneidman","first_name":"Elad"}],"publist_id":"6953","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ieee":"R. Harpaz, G. Tkačik, and E. Schneidman, “Discrete modes of social information processing predict individual behavior of fish in a group,” PNAS, vol. 114, no. 38. National Academy of Sciences, pp. 10149–10154, 2017.","short":"R. Harpaz, G. Tkačik, E. Schneidman, PNAS 114 (2017) 10149–10154.","apa":"Harpaz, R., Tkačik, G., & Schneidman, E. (2017). Discrete modes of social information processing predict individual behavior of fish in a group. PNAS. National Academy of Sciences. https://doi.org/10.1073/pnas.1703817114","ama":"Harpaz R, Tkačik G, Schneidman E. Discrete modes of social information processing predict individual behavior of fish in a group. PNAS. 2017;114(38):10149-10154. doi:10.1073/pnas.1703817114","mla":"Harpaz, Roy, et al. “Discrete Modes of Social Information Processing Predict Individual Behavior of Fish in a Group.” PNAS, vol. 114, no. 38, National Academy of Sciences, 2017, pp. 10149–54, doi:10.1073/pnas.1703817114.","ista":"Harpaz R, Tkačik G, Schneidman E. 2017. Discrete modes of social information processing predict individual behavior of fish in a group. PNAS. 114(38), 10149–10154.","chicago":"Harpaz, Roy, Gašper Tkačik, and Elad Schneidman. “Discrete Modes of Social Information Processing Predict Individual Behavior of Fish in a Group.” PNAS. National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1703817114."},"volume":114,"issue":"38","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["00278424"]},"intvolume":" 114","month":"09","main_file_link":[{"open_access":"1","url":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617265/"}],"scopus_import":1,"pmid":1,"oa_version":"Submitted Version","abstract":[{"lang":"eng","text":"Individual computations and social interactions underlying collective behavior in groups of animals are of great ethological, behavioral, and theoretical interest. While complex individual behaviors have successfully been parsed into small dictionaries of stereotyped behavioral modes, studies of collective behavior largely ignored these findings; instead, their focus was on inferring single, mode-independent social interaction rules that reproduced macroscopic and often qualitative features of group behavior. Here, we bring these two approaches together to predict individual swimming patterns of adult zebrafish in a group. We show that fish alternate between an “active” mode, in which they are sensitive to the swimming patterns of conspecifics, and a “passive” mode, where they ignore them. Using a model that accounts for these two modes explicitly, we predict behaviors of individual fish with high accuracy, outperforming previous approaches that assumed a single continuous computation by individuals and simple metric or topological weighing of neighbors’ behavior. At the group level, switching between active and passive modes is uncorrelated among fish, but correlated directional swimming behavior still emerges. Our quantitative approach for studying complex, multi-modal individual behavior jointly with emergent group behavior is readily extensible to additional behavioral modes and their neural correlates as well as to other species."}],"department":[{"_id":"GaTk"}],"date_updated":"2021-01-12T08:12:36Z","status":"public","type":"journal_article","_id":"725"},{"citation":{"ieee":"D. Hetterich, M. Serbyn, F. Domínguez, F. Pollmann, and B. Trauzettel, “Noninteracting central site model localization and logarithmic entanglement growth,” Physical Review B, vol. 96, no. 10. American Physical Society, 2017.","short":"D. Hetterich, M. Serbyn, F. Domínguez, F. Pollmann, B. Trauzettel, Physical Review B 96 (2017).","ama":"Hetterich D, Serbyn M, Domínguez F, Pollmann F, Trauzettel B. Noninteracting central site model localization and logarithmic entanglement growth. Physical Review B. 2017;96(10). doi:10.1103/PhysRevB.96.104203","apa":"Hetterich, D., Serbyn, M., Domínguez, F., Pollmann, F., & Trauzettel, B. (2017). Noninteracting central site model localization and logarithmic entanglement growth. Physical Review B. American Physical Society. https://doi.org/10.1103/PhysRevB.96.104203","mla":"Hetterich, Daniel, et al. “Noninteracting Central Site Model Localization and Logarithmic Entanglement Growth.” Physical Review B, vol. 96, no. 10, 104203, American Physical Society, 2017, doi:10.1103/PhysRevB.96.104203.","ista":"Hetterich D, Serbyn M, Domínguez F, Pollmann F, Trauzettel B. 2017. Noninteracting central site model localization and logarithmic entanglement growth. Physical Review B. 96(10), 104203.","chicago":"Hetterich, Daniel, Maksym Serbyn, Fernando Domínguez, Frank Pollmann, and Björn Trauzettel. “Noninteracting Central Site Model Localization and Logarithmic Entanglement Growth.” Physical Review B. American Physical Society, 2017. https://doi.org/10.1103/PhysRevB.96.104203."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publist_id":"6955","author":[{"last_name":"Hetterich","full_name":"Hetterich, Daniel","first_name":"Daniel"},{"last_name":"Serbyn","orcid":"0000-0002-2399-5827","full_name":"Serbyn, Maksym","id":"47809E7E-F248-11E8-B48F-1D18A9856A87","first_name":"Maksym"},{"first_name":"Fernando","full_name":"Domínguez, Fernando","last_name":"Domínguez"},{"first_name":"Frank","last_name":"Pollmann","full_name":"Pollmann, Frank"},{"first_name":"Björn","full_name":"Trauzettel, Björn","last_name":"Trauzettel"}],"title":"Noninteracting central site model localization and logarithmic entanglement growth","article_number":"104203","year":"2017","day":"13","publication":"Physical Review B","doi":"10.1103/PhysRevB.96.104203","date_published":"2017-09-13T00:00:00Z","date_created":"2018-12-11T11:48:09Z","acknowledgement":"We would like to thank Dmitry Abanin, Christophe De\r\nBeule, Joel Moore, Romain Vasseur, and Norman Yao for\r\nmany stimulating discussions. Financial support has been\r\nprovided by the Deutsche Forschungsgemeinschaft (DFG)\r\nvia Grant No. TR950/8-1, SFB 1170 “ToCoTronics” and the\r\nENB Graduate School on Topological Insulators. M.S. was\r\nsupported by Gordon and Betty Moore Foundation’s EPiQS\r\nInitiative through Grant No. GBMF4307. F.P. acknowledges\r\nsupport from the DFG Research Unit FOR 1807 through Grant\r\nNo. PO 1370/2-1.","publisher":"American Physical Society","quality_controlled":"1","oa":1,"date_updated":"2021-01-12T08:12:35Z","department":[{"_id":"MaSe"}],"_id":"724","type":"journal_article","status":"public","publication_identifier":{"issn":["24699950"]},"publication_status":"published","language":[{"iso":"eng"}],"volume":96,"issue":"10","abstract":[{"text":"We investigate the stationary and dynamical behavior of an Anderson localized chain coupled to a single central bound state. Although this coupling partially dilutes the Anderson localized peaks towards nearly resonant sites, the most weight of the original peaks remains unchanged. This leads to multifractal wave functions with a frozen spectrum of fractal dimensions, which is characteristic for localized phases in models with power-law hopping. Using a perturbative approach we identify two different dynamical regimes. At weak couplings to the central site, the transport of particles and information is logarithmic in time, a feature usually attributed to many-body localization. We connect such transport to the persistence of the Poisson statistics of level spacings in parts of the spectrum. In contrast, at stronger couplings the level repulsion is established in the entire spectrum, the problem can be mapped to the Fano resonance, and the transport is ballistic.","lang":"eng"}],"oa_version":"Submitted Version","scopus_import":1,"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1701.02744"}],"month":"09","intvolume":" 96"},{"publication":"Angewandte Chemie International Edition","day":"04","year":"2017","has_accepted_license":"1","date_created":"2020-01-15T12:15:05Z","doi":"10.1002/anie.201709351","date_published":"2017-12-04T00:00:00Z","page":"15728-15732","oa":1,"quality_controlled":"1","publisher":"Wiley","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Schafzahl, Lukas, Nika Mahne, Bettina Schafzahl, Martin Wilkening, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” Angewandte Chemie International Edition. Wiley, 2017. https://doi.org/10.1002/anie.201709351.","ista":"Schafzahl L, Mahne N, Schafzahl B, Wilkening M, Slugovc C, Borisov SM, Freunberger SA. 2017. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. 56(49), 15728–15732.","mla":"Schafzahl, Lukas, et al. “Singlet Oxygen during Cycling of the Aprotic Sodium-O2 Battery.” Angewandte Chemie International Edition, vol. 56, no. 49, Wiley, 2017, pp. 15728–32, doi:10.1002/anie.201709351.","ieee":"L. Schafzahl et al., “Singlet oxygen during cycling of the aprotic sodium-O2 battery,” Angewandte Chemie International Edition, vol. 56, no. 49. Wiley, pp. 15728–15732, 2017.","short":"L. Schafzahl, N. Mahne, B. Schafzahl, M. Wilkening, C. Slugovc, S.M. Borisov, S.A. Freunberger, Angewandte Chemie International Edition 56 (2017) 15728–15732.","ama":"Schafzahl L, Mahne N, Schafzahl B, et al. Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. 2017;56(49):15728-15732. doi:10.1002/anie.201709351","apa":"Schafzahl, L., Mahne, N., Schafzahl, B., Wilkening, M., Slugovc, C., Borisov, S. M., & Freunberger, S. A. (2017). Singlet oxygen during cycling of the aprotic sodium-O2 battery. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201709351"},"title":"Singlet oxygen during cycling of the aprotic sodium-O2 battery","article_processing_charge":"No","author":[{"last_name":"Schafzahl","full_name":"Schafzahl, Lukas","first_name":"Lukas"},{"first_name":"Nika","last_name":"Mahne","full_name":"Mahne, Nika"},{"full_name":"Schafzahl, Bettina","last_name":"Schafzahl","first_name":"Bettina"},{"last_name":"Wilkening","full_name":"Wilkening, Martin","first_name":"Martin"},{"first_name":"Christian","last_name":"Slugovc","full_name":"Slugovc, Christian"},{"first_name":"Sergey M.","last_name":"Borisov","full_name":"Borisov, Sergey M."},{"last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"}],"language":[{"iso":"eng"}],"file":[{"date_created":"2020-01-26T14:58:07Z","file_name":"2017_AngChemieInternat_Schafzahl.pdf","creator":"dernst","date_updated":"2020-07-14T12:47:55Z","file_size":1013492,"checksum":"3c5b1e51954554dffb13c7d58f69836c","file_id":"7362","access_level":"open_access","relation":"main_file","content_type":"application/pdf"}],"publication_status":"published","publication_identifier":{"issn":["1433-7851"]},"volume":56,"issue":"49","oa_version":"Published Version","abstract":[{"lang":"eng","text":"Aprotic sodium–O2 batteries require the reversible formation/dissolution of sodium superoxide (NaO2) on cycling. Poor cycle life has been associated with parasitic chemistry caused by the reactivity of electrolyte and electrode with NaO2, a strong nucleophile and base. Its reactivity can, however, not consistently explain the side reactions and irreversibility. Herein we show that singlet oxygen (1O2) forms at all stages of cycling and that it is a main driver for parasitic chemistry. It was detected in‐ and ex‐situ via a 1O2 trap that selectively and rapidly forms a stable adduct with 1O2. The 1O2 formation mechanism involves proton‐mediated superoxide disproportionation on discharge, rest, and charge below ca. 3.3 V, and direct electrochemical 1O2 evolution above ca. 3.3 V. Trace water, which is needed for high capacities also drives parasitic chemistry. Controlling the highly reactive singlet oxygen is thus crucial for achieving highly reversible cell operation."}],"intvolume":" 56","month":"12","ddc":["540"],"extern":"1","date_updated":"2021-01-12T08:12:47Z","file_date_updated":"2020-07-14T12:47:55Z","_id":"7289","status":"public","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode","image":"/images/cc_by_nc.png","name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","short":"CC BY-NC (4.0)"},"article_type":"original","type":"journal_article"},{"author":[{"last_name":"Bodin","full_name":"Bodin, C.","first_name":"C."},{"first_name":"E.","full_name":"Mourad, E.","last_name":"Mourad"},{"first_name":"D.","full_name":"Zigah, D.","last_name":"Zigah"},{"first_name":"S.","full_name":"Le Vot, S.","last_name":"Le Vot"},{"last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"},{"first_name":"F.","full_name":"Favier, F.","last_name":"Favier"},{"full_name":"Fontaine, O.","last_name":"Fontaine","first_name":"O."}],"article_processing_charge":"No","title":"Biredox ionic liquids: New opportunities toward high performance supercapacitors","citation":{"ista":"Bodin C, Mourad E, Zigah D, Le Vot S, Freunberger SA, Favier F, Fontaine O. 2017. Biredox ionic liquids: New opportunities toward high performance supercapacitors. Faraday Discussions. 206, 393–404.","chicago":"Bodin, C., E. Mourad, D. Zigah, S. Le Vot, Stefan Alexander Freunberger, F. Favier, and O. Fontaine. “Biredox Ionic Liquids: New Opportunities toward High Performance Supercapacitors.” Faraday Discussions. Royal Society of Chemistry, 2017. https://doi.org/10.1039/c7fd00174f.","ieee":"C. Bodin et al., “Biredox ionic liquids: New opportunities toward high performance supercapacitors,” Faraday Discussions, vol. 206. Royal Society of Chemistry, pp. 393–404, 2017.","short":"C. Bodin, E. Mourad, D. Zigah, S. Le Vot, S.A. Freunberger, F. Favier, O. Fontaine, Faraday Discussions 206 (2017) 393–404.","ama":"Bodin C, Mourad E, Zigah D, et al. Biredox ionic liquids: New opportunities toward high performance supercapacitors. Faraday Discussions. 2017;206:393-404. doi:10.1039/c7fd00174f","apa":"Bodin, C., Mourad, E., Zigah, D., Le Vot, S., Freunberger, S. A., Favier, F., & Fontaine, O. (2017). Biredox ionic liquids: New opportunities toward high performance supercapacitors. Faraday Discussions. Royal Society of Chemistry. https://doi.org/10.1039/c7fd00174f","mla":"Bodin, C., et al. “Biredox Ionic Liquids: New Opportunities toward High Performance Supercapacitors.” Faraday Discussions, vol. 206, Royal Society of Chemistry, 2017, pp. 393–404, doi:10.1039/c7fd00174f."},"date_updated":"2021-06-10T06:17:17Z","extern":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","article_type":"original","type":"journal_article","status":"public","_id":"7288","page":"393-404","date_published":"2017-06-29T00:00:00Z","doi":"10.1039/c7fd00174f","volume":206,"date_created":"2020-01-15T12:14:04Z","publication_identifier":{"issn":["1359-6640","1364-5498"]},"year":"2017","publication_status":"published","day":"29","language":[{"iso":"eng"}],"publication":"Faraday Discussions","publisher":"Royal Society of Chemistry","quality_controlled":"1","month":"06","intvolume":" 206","abstract":[{"lang":"eng","text":"Nowadays commercial supercapacitors are based on purely capacitive storage at the porous carbons that are used for the electrodes. However, the limits that capacitive storage imposes on energy density calls to investigate new materials to improve the capacitance of the device. This new type of electrodes (e.g., RuO2, MnO2…) involves pseudo-capacitive faradaic redox processes with the solid material. Ion exchange with solid materials is, however, much slower than the adsorption process in capacitive storage and inevitably leads to significant loss of power. Faradaic process in the liquid state, in contrast can be similarly fast as capacitive processes due to the fast ion transport. Designing new devices with liquid like dynamics and improved specific capacitance is challenging. We present a new approach to increase the specific capacitance using biredox ionic liquids, where redox moieties are tethered to the electrolyte ions, allowing high redox concentrations and significant pseudo-capacitive storage in the liquid state. Anions and cations are functionalized with anthraquinone (AQ) and 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) moieties, respectively. Glassy carbon, carbon-onion, and commercial activated carbon electrodes that exhibit different double layer structures and thus different diffusion dynamics were used to simultaneously study the electrochemical response of biredox ionic liquids at the positive and negative electrode."}],"oa_version":"None"},{"oa":1,"quality_controlled":"1","publisher":"ACS","publication":"ACS Applied Materials & Interfaces","day":"10","year":"2017","has_accepted_license":"1","date_created":"2020-01-15T12:15:16Z","date_published":"2017-10-10T00:00:00Z","doi":"10.1021/acsami.7b10669","page":"38008-38023","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ieee":"P. W. Zach, S. A. Freunberger, I. Klimant, and S. M. Borisov, “Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter,” ACS Applied Materials & Interfaces, vol. 9, no. 43. ACS, pp. 38008–38023, 2017.","short":"P.W. Zach, S.A. Freunberger, I. Klimant, S.M. Borisov, ACS Applied Materials & Interfaces 9 (2017) 38008–38023.","ama":"Zach PW, Freunberger SA, Klimant I, Borisov SM. Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter. ACS Applied Materials & Interfaces. 2017;9(43):38008-38023. doi:10.1021/acsami.7b10669","apa":"Zach, P. W., Freunberger, S. A., Klimant, I., & Borisov, S. M. (2017). Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter. ACS Applied Materials & Interfaces. ACS. https://doi.org/10.1021/acsami.7b10669","mla":"Zach, Peter W., et al. “Electron-Deficient near-Infrared Pt(II) and Pd(II) Benzoporphyrins with Dual Phosphorescence and Unusually Efficient Thermally Activated Delayed Fluorescence: First Demonstration of Simultaneous Oxygen and Temperature Sensing with a Single Emitter.” ACS Applied Materials & Interfaces, vol. 9, no. 43, ACS, 2017, pp. 38008–23, doi:10.1021/acsami.7b10669.","ista":"Zach PW, Freunberger SA, Klimant I, Borisov SM. 2017. Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter. ACS Applied Materials & Interfaces. 9(43), 38008–38023.","chicago":"Zach, Peter W., Stefan Alexander Freunberger, Ingo Klimant, and Sergey M. Borisov. “Electron-Deficient near-Infrared Pt(II) and Pd(II) Benzoporphyrins with Dual Phosphorescence and Unusually Efficient Thermally Activated Delayed Fluorescence: First Demonstration of Simultaneous Oxygen and Temperature Sensing with a Single Emitter.” ACS Applied Materials & Interfaces. ACS, 2017. https://doi.org/10.1021/acsami.7b10669."},"title":"Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter","article_processing_charge":"No","author":[{"last_name":"Zach","full_name":"Zach, Peter W.","first_name":"Peter W."},{"last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","first_name":"Stefan Alexander"},{"full_name":"Klimant, Ingo","last_name":"Klimant","first_name":"Ingo"},{"first_name":"Sergey M.","full_name":"Borisov, Sergey M.","last_name":"Borisov"}],"oa_version":"Submitted Version","abstract":[{"lang":"eng","text":"We report a family of Pt and Pd benzoporphyrin dyes with versatile photophysical properties and easy access from cheap and abundant chemicals. Attaching 4 or 8 alkylsulfone groups onto a meso-tetraphenyltetrabenzoporphyrin (TPTBP) macrocylcle renders the dyes highly soluble in organic solvents, photostable, and electron-deficient with the redox potential raised up to 0.65 V versus the parent porphyrin. The new dyes intensively absorb in the blue (Soret band, 440–480 nm) and in the red (Q-band, 620–650 nm) parts of the electromagnetic spectrum and show bright phosphorescence at room-temperature in the NIR with quantum yields up to 30% in solution. The small singlet–triplet energy gap yields unusually efficient thermally activated delayed fluorescence (TADF) at elevated temperatures in solution and in polymeric matrices with quantum yields as high as 27% at 120 °C, which is remarkable for benzoporphyrins. Apart from oxygen sensing, these properties enable unprecedented simultaneous, self-referenced oxygen and temperature sensing with a single indicator dye: whereas oxygen can be determined either via the decay time of phosphorescence or TADF, the temperature is accessed via the ratio of the two emissions. Moreover, the dyes are efficient sensitizers for triplet–triplet annihilation (TTA)-based upconversion making possible longer sensitization wavelength than the conventional benzoporphyrin complexes. The Pt-octa-sulfone dye also features interesting semireversible transformation in basic media, which generates new NIR absorbing species."}],"intvolume":" 9","month":"10","language":[{"iso":"eng"}],"file":[{"file_name":"Paper_Manuscript_submitted.pdf","date_created":"2020-06-29T14:49:32Z","creator":"sfreunbe","file_size":2072792,"date_updated":"2020-07-14T12:47:55Z","file_id":"8051","checksum":"0461c990eb910f19a70c6e5349ec35ed","relation":"main_file","access_level":"open_access","content_type":"application/pdf"}],"publication_status":"published","publication_identifier":{"issn":["1944-8244"],"eissn":["1944-8252"]},"volume":9,"issue":"43","_id":"7290","status":"public","type":"journal_article","article_type":"original","ddc":["540","543"],"extern":"1","date_updated":"2021-01-12T08:12:48Z","file_date_updated":"2020-07-14T12:47:55Z"},{"quality_controlled":"1","publisher":"RSC","oa":1,"has_accepted_license":"1","year":"2017","day":"31","publication":"Chemical Science","page":"6716-6729","doi":"10.1039/c7sc02519j","date_published":"2017-07-31T00:00:00Z","date_created":"2020-01-15T12:15:42Z","citation":{"apa":"Mahne, N., Fontaine, O., Thotiyl, M. O., Wilkening, M., & Freunberger, S. A. (2017). Mechanism and performance of lithium–oxygen batteries – a perspective. Chemical Science. RSC. https://doi.org/10.1039/c7sc02519j","ama":"Mahne N, Fontaine O, Thotiyl MO, Wilkening M, Freunberger SA. Mechanism and performance of lithium–oxygen batteries – a perspective. Chemical Science. 2017;8(10):6716-6729. doi:10.1039/c7sc02519j","short":"N. Mahne, O. Fontaine, M.O. Thotiyl, M. Wilkening, S.A. Freunberger, Chemical Science 8 (2017) 6716–6729.","ieee":"N. Mahne, O. Fontaine, M. O. Thotiyl, M. Wilkening, and S. A. Freunberger, “Mechanism and performance of lithium–oxygen batteries – a perspective,” Chemical Science, vol. 8, no. 10. RSC, pp. 6716–6729, 2017.","mla":"Mahne, Nika, et al. “Mechanism and Performance of Lithium–Oxygen Batteries – a Perspective.” Chemical Science, vol. 8, no. 10, RSC, 2017, pp. 6716–29, doi:10.1039/c7sc02519j.","ista":"Mahne N, Fontaine O, Thotiyl MO, Wilkening M, Freunberger SA. 2017. Mechanism and performance of lithium–oxygen batteries – a perspective. Chemical Science. 8(10), 6716–6729.","chicago":"Mahne, Nika, Olivier Fontaine, Musthafa Ottakam Thotiyl, Martin Wilkening, and Stefan Alexander Freunberger. “Mechanism and Performance of Lithium–Oxygen Batteries – a Perspective.” Chemical Science. RSC, 2017. https://doi.org/10.1039/c7sc02519j."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Nika","last_name":"Mahne","full_name":"Mahne, Nika"},{"full_name":"Fontaine, Olivier","last_name":"Fontaine","first_name":"Olivier"},{"last_name":"Thotiyl","full_name":"Thotiyl, Musthafa Ottakam","first_name":"Musthafa Ottakam"},{"first_name":"Martin","full_name":"Wilkening, Martin","last_name":"Wilkening"},{"first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319"}],"article_processing_charge":"No","title":"Mechanism and performance of lithium–oxygen batteries – a perspective","abstract":[{"text":"Rechargeable Li–O2 batteries have amongst the highest formal energy and could store significantly more energy than other rechargeable batteries in practice if at least a large part of their promise could be realized. Realization, however, still faces many challenges than can only be overcome by fundamental understanding of the processes taking place. Here, we review recent advances in understanding the chemistry of the Li–O2 cathode and provide a perspective on dominant research needs. We put particular emphasis on issues that are often grossly misunderstood: realistic performance metrics and their reporting as well as identifying reversibility and quantitative measures to do so. Parasitic reactions are the prime obstacle for reversible cell operation and have recently been identified to be predominantly caused by singlet oxygen and not by reduced oxygen species as thought before. We discuss the far reaching implications of this finding on electrolyte and cathode stability, electrocatalysis, and future research needs.","lang":"eng"}],"oa_version":"Published Version","month":"07","intvolume":" 8","publication_identifier":{"issn":["2041-6520"],"eissn":["2041-6539"]},"publication_status":"published","file":[{"date_created":"2020-01-26T15:04:44Z","file_name":"2017_ChemicalScience_Mahne.pdf","date_updated":"2020-07-14T12:47:55Z","file_size":992106,"creator":"dernst","file_id":"7363","checksum":"70c7c2ce5430b6e8605ccbf0275f1e80","content_type":"application/pdf","access_level":"open_access","relation":"main_file"}],"language":[{"iso":"eng"}],"volume":8,"issue":"10","_id":"7292","type":"journal_article","article_type":"original","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public","date_updated":"2021-01-12T08:12:49Z","extern":"1","ddc":["540"],"file_date_updated":"2020-07-14T12:47:55Z"},{"status":"public","type":"journal_article","article_type":"original","_id":"7291","title":"An electrolyte for reversible cycling of sodium metal and intercalation compounds","article_processing_charge":"No","author":[{"first_name":"Lukas","full_name":"Schafzahl, Lukas","last_name":"Schafzahl"},{"first_name":"Ilie","last_name":"Hanzu","full_name":"Hanzu, Ilie"},{"full_name":"Wilkening, Martin","last_name":"Wilkening","first_name":"Martin"},{"orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","first_name":"Stefan Alexander"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:12:48Z","citation":{"ista":"Schafzahl L, Hanzu I, Wilkening M, Freunberger SA. 2017. An electrolyte for reversible cycling of sodium metal and intercalation compounds. ChemSusChem. 10(2), 401–408.","chicago":"Schafzahl, Lukas, Ilie Hanzu, Martin Wilkening, and Stefan Alexander Freunberger. “An Electrolyte for Reversible Cycling of Sodium Metal and Intercalation Compounds.” ChemSusChem. Wiley, 2017. https://doi.org/10.1002/cssc.201601222.","ieee":"L. Schafzahl, I. Hanzu, M. Wilkening, and S. A. Freunberger, “An electrolyte for reversible cycling of sodium metal and intercalation compounds,” ChemSusChem, vol. 10, no. 2. Wiley, pp. 401–408, 2017.","short":"L. Schafzahl, I. Hanzu, M. Wilkening, S.A. Freunberger, ChemSusChem 10 (2017) 401–408.","apa":"Schafzahl, L., Hanzu, I., Wilkening, M., & Freunberger, S. A. (2017). An electrolyte for reversible cycling of sodium metal and intercalation compounds. ChemSusChem. Wiley. https://doi.org/10.1002/cssc.201601222","ama":"Schafzahl L, Hanzu I, Wilkening M, Freunberger SA. An electrolyte for reversible cycling of sodium metal and intercalation compounds. ChemSusChem. 2017;10(2):401-408. doi:10.1002/cssc.201601222","mla":"Schafzahl, Lukas, et al. “An Electrolyte for Reversible Cycling of Sodium Metal and Intercalation Compounds.” ChemSusChem, vol. 10, no. 2, Wiley, 2017, pp. 401–08, doi:10.1002/cssc.201601222."},"intvolume":" 10","month":"01","quality_controlled":"1","publisher":"Wiley","oa_version":"None","abstract":[{"lang":"eng","text":"Na battery chemistries show poor passivation behavior of low voltage Na storage compounds and Na metal with organic carbonate‐based electrolytes adopted from Li‐ion batteries. Therefore, a suitable electrolyte remains a major challenge for establishing Na batteries. Here we report highly concentrated sodium bis(fluorosulfonyl)imide (NaFSI) in dimethoxyethane (DME) electrolytes and investigate them for Na metal and hard carbon anodes and intercalation cathodes. For a DME/NaFSI ratio of 2, a stable passivation of anode materials was found owing to the formation of a stable solid electrolyte interface, which was characterized spectroscopically. This permitted non‐dentritic Na metal cycling with approximately 98 % coulombic efficiency as shown for up to 300 cycles. The NaFSI/DME electrolyte may enable Na‐metal anodes and allows for more reliable assessment of electrode materials in Na‐ion half‐cells, as is demonstrated by comparing half‐cell cycling of hard carbon anodes and Na3V2(PO4)3 cathodes with a widely used carbonate and the NaFSI/DME electrolyte."}],"date_created":"2020-01-15T12:15:29Z","doi":"10.1002/cssc.201601222","issue":"2","volume":10,"date_published":"2017-01-20T00:00:00Z","page":"401-408","language":[{"iso":"eng"}],"publication":"ChemSusChem","day":"20","year":"2017","publication_status":"published","publication_identifier":{"issn":["1864-5631"]}},{"article_number":"eaap8168","_id":"731","status":"public","type":"journal_article","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Novarino G. 2017. The science of love in ASD and ADHD. Science Translational Medicine. 9(411), eaap8168.","chicago":"Novarino, Gaia. “The Science of Love in ASD and ADHD.” Science Translational Medicine. American Association for the Advancement of Science, 2017. https://doi.org/10.1126/scitranslmed.aap8168.","ieee":"G. Novarino, “The science of love in ASD and ADHD,” Science Translational Medicine, vol. 9, no. 411. American Association for the Advancement of Science, 2017.","short":"G. Novarino, Science Translational Medicine 9 (2017).","apa":"Novarino, G. (2017). The science of love in ASD and ADHD. Science Translational Medicine. American Association for the Advancement of Science. https://doi.org/10.1126/scitranslmed.aap8168","ama":"Novarino G. The science of love in ASD and ADHD. Science Translational Medicine. 2017;9(411). doi:10.1126/scitranslmed.aap8168","mla":"Novarino, Gaia. “The Science of Love in ASD and ADHD.” Science Translational Medicine, vol. 9, no. 411, eaap8168, American Association for the Advancement of Science, 2017, doi:10.1126/scitranslmed.aap8168."},"date_updated":"2021-01-12T08:12:57Z","department":[{"_id":"GaNo"}],"title":"The science of love in ASD and ADHD","author":[{"id":"3E57A680-F248-11E8-B48F-1D18A9856A87","first_name":"Gaia","orcid":"0000-0002-7673-7178","full_name":"Novarino, Gaia","last_name":"Novarino"}],"publist_id":"6938","oa_version":"None","abstract":[{"lang":"eng","text":"Genetic variations in the oxytocin receptor gene affect patients with ASD and ADHD differently."}],"intvolume":" 9","month":"10","quality_controlled":"1","publisher":"American Association for the Advancement of Science","scopus_import":1,"language":[{"iso":"eng"}],"publication":"Science Translational Medicine","day":"11","year":"2017","publication_status":"published","publication_identifier":{"issn":["19466234"]},"date_created":"2018-12-11T11:48:12Z","issue":"411","doi":"10.1126/scitranslmed.aap8168","date_published":"2017-10-11T00:00:00Z","volume":9},{"ddc":["570"],"date_updated":"2021-01-12T08:13:14Z","department":[{"_id":"MaLo"}],"file_date_updated":"2020-07-14T12:47:56Z","_id":"7360","status":"public","tmp":{"short":"CC BY-NC-ND (4.0)","name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","image":"/images/cc_by_nc_nd.png"},"article_type":"original","type":"journal_article","language":[{"iso":"eng"}],"file":[{"checksum":"ea8b1b28606dd1edab7379ba4fa3641f","file_id":"7561","relation":"main_file","access_level":"open_access","content_type":"application/pdf","file_name":"2017_MolecularTherapy_Smole.pdf","date_created":"2020-03-03T10:55:13Z","creator":"dernst","file_size":3404806,"date_updated":"2020-07-14T12:47:56Z"}],"publication_status":"published","publication_identifier":{"issn":["1525-0016"]},"issue":"1","volume":25,"pmid":1,"oa_version":"Published Version","abstract":[{"text":"Inflammation, which is a highly regulated host response against danger signals, may be harmful if it is excessive and deregulated. Ideally, anti-inflammatory therapy should autonomously commence as soon as possible after the onset of inflammation, should be controllable by a physician, and should not systemically block beneficial immune response in the long term. We describe a genetically encoded anti-inflammatory mammalian cell device based on a modular engineered genetic circuit comprising a sensor, an amplifier, a “thresholder” to restrict activation of a positive-feedback loop, a combination of advanced clinically used biopharmaceutical proteins, and orthogonal regulatory elements that linked modules into the functional device. This genetic circuit was autonomously activated by inflammatory signals, including endogenous cecal ligation and puncture (CLP)-induced inflammation in mice and serum from a systemic juvenile idiopathic arthritis (sIJA) patient, and could be reset externally by a chemical signal. The microencapsulated anti-inflammatory device significantly reduced the pathology in dextran sodium sulfate (DSS)-induced acute murine colitis, demonstrating a synthetic immunological approach for autonomous anti-inflammatory therapy.","lang":"eng"}],"intvolume":" 25","month":"01","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Smole A, Lainšček D, Bezeljak U, Horvat S, Jerala R. 2017. A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation. Molecular Therapy. 25(1), 102–119.","chicago":"Smole, Anže, Duško Lainšček, Urban Bezeljak, Simon Horvat, and Roman Jerala. “A Synthetic Mammalian Therapeutic Gene Circuit for Sensing and Suppressing Inflammation.” Molecular Therapy. Elsevier, 2017. https://doi.org/10.1016/j.ymthe.2016.10.005.","ieee":"A. Smole, D. Lainšček, U. Bezeljak, S. Horvat, and R. Jerala, “A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation,” Molecular Therapy, vol. 25, no. 1. Elsevier, pp. 102–119, 2017.","short":"A. Smole, D. Lainšček, U. Bezeljak, S. Horvat, R. Jerala, Molecular Therapy 25 (2017) 102–119.","ama":"Smole A, Lainšček D, Bezeljak U, Horvat S, Jerala R. A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation. Molecular Therapy. 2017;25(1):102-119. doi:10.1016/j.ymthe.2016.10.005","apa":"Smole, A., Lainšček, D., Bezeljak, U., Horvat, S., & Jerala, R. (2017). A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation. Molecular Therapy. Elsevier. https://doi.org/10.1016/j.ymthe.2016.10.005","mla":"Smole, Anže, et al. “A Synthetic Mammalian Therapeutic Gene Circuit for Sensing and Suppressing Inflammation.” Molecular Therapy, vol. 25, no. 1, Elsevier, 2017, pp. 102–19, doi:10.1016/j.ymthe.2016.10.005."},"title":"A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation","article_processing_charge":"No","external_id":{"pmid":["28129106"]},"author":[{"full_name":"Smole, Anže","last_name":"Smole","first_name":"Anže"},{"full_name":"Lainšček, Duško","last_name":"Lainšček","first_name":"Duško"},{"id":"2A58201A-F248-11E8-B48F-1D18A9856A87","first_name":"Urban","orcid":"0000-0003-1365-5631","full_name":"Bezeljak, Urban","last_name":"Bezeljak"},{"first_name":"Simon","last_name":"Horvat","full_name":"Horvat, Simon"},{"first_name":"Roman","last_name":"Jerala","full_name":"Jerala, Roman"}],"publication":"Molecular Therapy","day":"01","year":"2017","has_accepted_license":"1","date_created":"2020-01-25T15:55:39Z","date_published":"2017-01-01T00:00:00Z","doi":"10.1016/j.ymthe.2016.10.005","page":"102-119","oa":1,"publisher":"Elsevier","quality_controlled":"1"},{"_id":"748","type":"book_chapter","status":"public","date_updated":"2021-01-12T08:13:49Z","citation":{"ista":"Wenzl B. 2017.‘...beyond the invisible barrier at Portage and Main’: Liminality in John Marlyn’s Under the Ribs of Death. In: In-Between - Liminal Spaces in Canadian Literature and Culture. Canadiana, , 91–100.","chicago":"Wenzl, Bernhard. “‘...Beyond the Invisible Barrier at Portage and Main’: Liminality in John Marlyn’s Under the Ribs of Death.” In In-Between - Liminal Spaces in Canadian Literature and Culture, edited by Stefan Brandt, 91–100. Peter Lang GmbH, 2017. https://doi.org/10.3726/b11899.","ama":"Wenzl B. “...beyond the invisible barrier at Portage and Main”: Liminality in John Marlyn’s Under the Ribs of Death. In: Brandt S, ed. In-Between - Liminal Spaces in Canadian Literature and Culture. Peter Lang GmbH; 2017:91-100. doi:10.3726/b11899","apa":"Wenzl, B. (2017). “...beyond the invisible barrier at Portage and Main”: Liminality in John Marlyn’s Under the Ribs of Death. In S. Brandt (Ed.), In-Between - Liminal Spaces in Canadian Literature and Culture (pp. 91–100). Peter Lang GmbH. https://doi.org/10.3726/b11899","short":"B. Wenzl, in:, S. Brandt (Ed.), In-Between - Liminal Spaces in Canadian Literature and Culture, Peter Lang GmbH, 2017, pp. 91–100.","ieee":"B. Wenzl, “‘...beyond the invisible barrier at Portage and Main’: Liminality in John Marlyn’s Under the Ribs of Death,” in In-Between - Liminal Spaces in Canadian Literature and Culture, S. Brandt, Ed. Peter Lang GmbH, 2017, pp. 91–100.","mla":"Wenzl, Bernhard. “‘...Beyond the Invisible Barrier at Portage and Main’: Liminality in John Marlyn’s Under the Ribs of Death.” In-Between - Liminal Spaces in Canadian Literature and Culture, edited by Stefan Brandt, Peter Lang GmbH, 2017, pp. 91–100, doi:10.3726/b11899."},"extern":1,"author":[{"last_name":"Wenzl","full_name":"Bernhard Wenzl","first_name":"Bernhard","id":"479E9046-F248-11E8-B48F-1D18A9856A87"}],"publist_id":"6909","editor":[{"first_name":"Stefan","last_name":"Brandt","full_name":"Brandt, Stefan L."}],"title":"'...beyond the invisible barrier at Portage and Main': Liminality in John Marlyn's Under the Ribs of Death","abstract":[{"text":"The essay focuses on individual and collective forms of liminality in John Marlyn’s Under the Ribs of Death. Set in early twentieth-century Winnipeg, the 1957 immigrant novel explores liminal experiences related to ethnic identity, male sexuality, social class, urban spaces and turbulent economic times. As the son of a poor working-class family from Hungary, Sandor Hunyadi makes every effort to become a true Canadian and a successful businessman, but, no matter how hard he tries to overcome contemporary ethnic prejudices and economic hardships, his personal and professional life remains in liminality. In other words, the protagonist undergoes separation, fails at incorporation, and becomes stuck in transition.","lang":"eng"}],"publisher":"Peter Lang GmbH","alternative_title":["Canadiana"],"quality_controlled":0,"month":"12","year":"2017","publication_status":"published","publication":"In-Between - Liminal Spaces in Canadian Literature and Culture","day":"01","page":"91 - 100","date_created":"2018-12-11T11:48:18Z","doi":"10.3726/b11899","date_published":"2017-12-01T00:00:00Z"},{"quality_controlled":"1","scopus_import":1,"publisher":"IEEE","month":"12","abstract":[{"lang":"eng","text":"Modern communication technologies allow first responders to contact thousands of potential volunteers simultaneously for support during a crisis or disaster event. However, such volunteer efforts must be well coordinated and monitored, in order to offer an effective relief to the professionals. In this paper we extend earlier work on optimally assigning volunteers to selected landmark locations. In particular, we emphasize the aspect that obtaining good assignments requires not only advanced computational tools, but also a realistic measure of distance between volunteers and landmarks. Specifically, we propose the use of the Open Street Map (OSM) driving distance instead of he previously used flight distance. We find the OSM driving distance to be better aligned with the interests of volunteers and first responders. Furthermore, we show that relying on the flying distance leads to a substantial underestimation of the number of required volunteers, causing negative side effects in case of an actual crisis situation."}],"oa_version":"None","page":"3760 - 3763","date_published":"2017-12-01T00:00:00Z","doi":"10.1109/BigData.2017.8258375","date_created":"2018-12-11T11:48:18Z","publication_identifier":{"isbn":["978-153862714-3"]},"publication_status":"published","year":"2017","day":"01","language":[{"iso":"eng"}],"publication":"2017 IEEE International Conference on Big Data","type":"conference","conference":{"location":"Boston, MA, United States","end_date":"2017-12-14","start_date":"2017-12-11","name":"Big Data"},"status":"public","_id":"750","author":[{"first_name":"Jasmin","id":"49BC895A-F248-11E8-B48F-1D18A9856A87","last_name":"Pielorz","full_name":"Pielorz, Jasmin"},{"last_name":"Prandtstetter","full_name":"Prandtstetter, Matthias","first_name":"Matthias"},{"first_name":"Markus","full_name":"Straub, Markus","last_name":"Straub"},{"full_name":"Lampert, Christoph","orcid":"0000-0001-8622-7887","last_name":"Lampert","id":"40C20FD2-F248-11E8-B48F-1D18A9856A87","first_name":"Christoph"}],"publist_id":"6906","title":"Optimal geospatial volunteer allocation needs realistic distances","department":[{"_id":"ChLa"}],"citation":{"short":"J. Pielorz, M. Prandtstetter, M. Straub, C. Lampert, in:, 2017 IEEE International Conference on Big Data, IEEE, 2017, pp. 3760–3763.","ieee":"J. Pielorz, M. Prandtstetter, M. Straub, and C. Lampert, “Optimal geospatial volunteer allocation needs realistic distances,” in 2017 IEEE International Conference on Big Data, Boston, MA, United States, 2017, pp. 3760–3763.","apa":"Pielorz, J., Prandtstetter, M., Straub, M., & Lampert, C. (2017). Optimal geospatial volunteer allocation needs realistic distances. In 2017 IEEE International Conference on Big Data (pp. 3760–3763). Boston, MA, United States: IEEE. https://doi.org/10.1109/BigData.2017.8258375","ama":"Pielorz J, Prandtstetter M, Straub M, Lampert C. Optimal geospatial volunteer allocation needs realistic distances. In: 2017 IEEE International Conference on Big Data. IEEE; 2017:3760-3763. doi:10.1109/BigData.2017.8258375","mla":"Pielorz, Jasmin, et al. “Optimal Geospatial Volunteer Allocation Needs Realistic Distances.” 2017 IEEE International Conference on Big Data, IEEE, 2017, pp. 3760–63, doi:10.1109/BigData.2017.8258375.","ista":"Pielorz J, Prandtstetter M, Straub M, Lampert C. 2017. Optimal geospatial volunteer allocation needs realistic distances. 2017 IEEE International Conference on Big Data. Big Data, 3760–3763.","chicago":"Pielorz, Jasmin, Matthias Prandtstetter, Markus Straub, and Christoph Lampert. “Optimal Geospatial Volunteer Allocation Needs Realistic Distances.” In 2017 IEEE International Conference on Big Data, 3760–63. IEEE, 2017. https://doi.org/10.1109/BigData.2017.8258375."},"date_updated":"2021-01-12T08:13:55Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"publisher":"Springer Nature","quality_controlled":"1","intvolume":" 1","month":"09","abstract":[{"text":"Meta-analyses of genome-wide association studies, which dominate genetic discovery, are based on data from diverse historical time periods and populations. Genetic scores derived from genome-wide association studies explain only a fraction of the heritability estimates obtained from whole-genome studies on single populations, known as the ‘hidden heritability’ puzzle. Using seven sampling populations (n = 35,062), we test whether hidden heritability is attributed to heterogeneity across sampling populations and time, showing that estimates are substantially smaller across populations compared with within populations. We show that the hidden heritability varies substantially: from zero for height to 20% for body mass index, 37% for education, 40% for age at first birth and up to 75% for number of children. Simulations demonstrate that our results are more likely to reflect heterogeneity in phenotypic measurement or gene–environment interactions than genetic heterogeneity. These findings have substantial implications for genetic discovery, suggesting that large homogenous datasets are required for behavioural phenotypes and that gene–environment interaction may be a central challenge for genetic discovery.","lang":"eng"}],"oa_version":"None","page":"757-765","date_created":"2020-04-30T10:47:02Z","issue":"10","date_published":"2017-09-11T00:00:00Z","volume":1,"doi":"10.1038/s41562-017-0195-1","publication_status":"published","year":"2017","publication_identifier":{"issn":["2397-3374"]},"publication":"Nature Human Behaviour","language":[{"iso":"eng"}],"day":"11","article_type":"original","type":"journal_article","status":"public","_id":"7728","article_processing_charge":"No","author":[{"first_name":"Felix C.","full_name":"Tropf, Felix C.","last_name":"Tropf"},{"full_name":"Lee, S. Hong","last_name":"Lee","first_name":"S. Hong"},{"full_name":"Verweij, Renske M.","last_name":"Verweij","first_name":"Renske M."},{"first_name":"Gert","full_name":"Stulp, Gert","last_name":"Stulp"},{"first_name":"Peter J.","last_name":"van der Most","full_name":"van der Most, Peter J."},{"full_name":"de Vlaming, Ronald","last_name":"de Vlaming","first_name":"Ronald"},{"first_name":"Andrew","last_name":"Bakshi","full_name":"Bakshi, Andrew"},{"first_name":"Daniel A.","full_name":"Briley, Daniel A.","last_name":"Briley"},{"first_name":"Charles","last_name":"Rahal","full_name":"Rahal, Charles"},{"first_name":"Robert","full_name":"Hellpap, Robert","last_name":"Hellpap"},{"last_name":"Iliadou","full_name":"Iliadou, Anastasia N.","first_name":"Anastasia N."},{"full_name":"Esko, Tõnu","last_name":"Esko","first_name":"Tõnu"},{"full_name":"Metspalu, Andres","last_name":"Metspalu","first_name":"Andres"},{"last_name":"Medland","full_name":"Medland, Sarah E.","first_name":"Sarah E."},{"full_name":"Martin, Nicholas G.","last_name":"Martin","first_name":"Nicholas G."},{"first_name":"Nicola","last_name":"Barban","full_name":"Barban, Nicola"},{"full_name":"Snieder, Harold","last_name":"Snieder","first_name":"Harold"},{"last_name":"Robinson","orcid":"0000-0001-8982-8813","full_name":"Robinson, Matthew Richard","id":"E5D42276-F5DA-11E9-8E24-6303E6697425","first_name":"Matthew Richard"},{"full_name":"Mills, Melinda C.","last_name":"Mills","first_name":"Melinda C."}],"title":"Hidden heritability due to heterogeneity across seven populations","citation":{"ama":"Tropf FC, Lee SH, Verweij RM, et al. Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour. 2017;1(10):757-765. doi:10.1038/s41562-017-0195-1","apa":"Tropf, F. C., Lee, S. H., Verweij, R. M., Stulp, G., van der Most, P. J., de Vlaming, R., … Mills, M. C. (2017). Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour. Springer Nature. https://doi.org/10.1038/s41562-017-0195-1","ieee":"F. C. Tropf et al., “Hidden heritability due to heterogeneity across seven populations,” Nature Human Behaviour, vol. 1, no. 10. Springer Nature, pp. 757–765, 2017.","short":"F.C. Tropf, S.H. Lee, R.M. Verweij, G. Stulp, P.J. van der Most, R. de Vlaming, A. Bakshi, D.A. Briley, C. Rahal, R. Hellpap, A.N. Iliadou, T. Esko, A. Metspalu, S.E. Medland, N.G. Martin, N. Barban, H. Snieder, M.R. Robinson, M.C. Mills, Nature Human Behaviour 1 (2017) 757–765.","mla":"Tropf, Felix C., et al. “Hidden Heritability Due to Heterogeneity across Seven Populations.” Nature Human Behaviour, vol. 1, no. 10, Springer Nature, 2017, pp. 757–65, doi:10.1038/s41562-017-0195-1.","ista":"Tropf FC, Lee SH, Verweij RM, Stulp G, van der Most PJ, de Vlaming R, Bakshi A, Briley DA, Rahal C, Hellpap R, Iliadou AN, Esko T, Metspalu A, Medland SE, Martin NG, Barban N, Snieder H, Robinson MR, Mills MC. 2017. Hidden heritability due to heterogeneity across seven populations. Nature Human Behaviour. 1(10), 757–765.","chicago":"Tropf, Felix C., S. Hong Lee, Renske M. Verweij, Gert Stulp, Peter J. van der Most, Ronald de Vlaming, Andrew Bakshi, et al. “Hidden Heritability Due to Heterogeneity across Seven Populations.” Nature Human Behaviour. Springer Nature, 2017. https://doi.org/10.1038/s41562-017-0195-1."},"date_updated":"2021-01-12T08:15:08Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1"},{"author":[{"first_name":"D.","last_name":"Burger","full_name":"Burger, D."},{"last_name":"Thomas","full_name":"Thomas, S.","first_name":"S."},{"full_name":"Aepli, H.","last_name":"Aepli","first_name":"H."},{"full_name":"Dreyer, M.","last_name":"Dreyer","first_name":"M."},{"last_name":"Fabre","full_name":"Fabre, G.","first_name":"G."},{"full_name":"Marti, E.","last_name":"Marti","first_name":"E."},{"last_name":"Sieme","full_name":"Sieme, H.","first_name":"H."},{"full_name":"Robinson, Matthew Richard","orcid":"0000-0001-8982-8813","last_name":"Robinson","id":"E5D42276-F5DA-11E9-8E24-6303E6697425","first_name":"Matthew Richard"},{"first_name":"C.","full_name":"Wedekind, C.","last_name":"Wedekind"}],"external_id":{"pmid":["29212724"]},"article_processing_charge":"No","title":"Major histocompatibility complex-linked social signalling affects female fertility","citation":{"ista":"Burger D, Thomas S, Aepli H, Dreyer M, Fabre G, Marti E, Sieme H, Robinson MR, Wedekind C. 2017. Major histocompatibility complex-linked social signalling affects female fertility. Proceedings of the Royal Society B: Biological Sciences. 284(1868), 20171824.","chicago":"Burger, D., S. Thomas, H. Aepli, M. Dreyer, G. Fabre, E. Marti, H. Sieme, Matthew Richard Robinson, and C. Wedekind. “Major Histocompatibility Complex-Linked Social Signalling Affects Female Fertility.” Proceedings of the Royal Society B: Biological Sciences. The Royal Society, 2017. https://doi.org/10.1098/rspb.2017.1824.","ama":"Burger D, Thomas S, Aepli H, et al. Major histocompatibility complex-linked social signalling affects female fertility. Proceedings of the Royal Society B: Biological Sciences. 2017;284(1868). doi:10.1098/rspb.2017.1824","apa":"Burger, D., Thomas, S., Aepli, H., Dreyer, M., Fabre, G., Marti, E., … Wedekind, C. (2017). Major histocompatibility complex-linked social signalling affects female fertility. Proceedings of the Royal Society B: Biological Sciences. The Royal Society. https://doi.org/10.1098/rspb.2017.1824","short":"D. Burger, S. Thomas, H. Aepli, M. Dreyer, G. Fabre, E. Marti, H. Sieme, M.R. Robinson, C. Wedekind, Proceedings of the Royal Society B: Biological Sciences 284 (2017).","ieee":"D. Burger et al., “Major histocompatibility complex-linked social signalling affects female fertility,” Proceedings of the Royal Society B: Biological Sciences, vol. 284, no. 1868. The Royal Society, 2017.","mla":"Burger, D., et al. “Major Histocompatibility Complex-Linked Social Signalling Affects Female Fertility.” Proceedings of the Royal Society B: Biological Sciences, vol. 284, no. 1868, 20171824, The Royal Society, 2017, doi:10.1098/rspb.2017.1824."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_number":"20171824","date_published":"2017-12-06T00:00:00Z","doi":"10.1098/rspb.2017.1824","date_created":"2020-04-30T10:46:43Z","year":"2017","day":"06","publication":"Proceedings of the Royal Society B: Biological Sciences","publisher":"The Royal Society","quality_controlled":"1","date_updated":"2021-01-12T08:15:08Z","extern":"1","type":"journal_article","article_type":"original","status":"public","_id":"7727","volume":284,"issue":"1868","publication_identifier":{"issn":["0962-8452","1471-2954"]},"publication_status":"published","language":[{"iso":"eng"}],"month":"12","intvolume":" 284","abstract":[{"lang":"eng","text":"Genes of the major histocompatibility complex (MHC) have been shown to influence social signalling and mate preferences in many species, including humans. First observations suggest that MHC signalling may also affect female fertility. To test this hypothesis, we exposed 191 female horses (Equus caballus) to either an MHC-similar or an MHC-dissimilar stimulus male around the time of ovulation and conception. A within-subject experimental design controlled for non-MHC-linked male characteristics, and instrumental insemination with semen of other males (n = 106) controlled for potential confounding effects of semen or embryo characteristics. We found that females were more likely to become pregnant if exposed to an MHC-dissimilar than to an MHC-similar male, while overall genetic distance to the stimulus males (based on microsatellite markers on 20 chromosomes) had no effect. Our results demonstrate that early pregnancy failures can be due to maternal life-history decisions (cryptic female choice) influenced by MHC-linked social signalling."}],"pmid":1,"oa_version":"None"},{"abstract":[{"lang":"eng","text":"Quantifying the effects of inbreeding is critical to characterizing the genetic architecture of complex traits. This study highlights through theory and simulations the strengths and shortcomings of three SNP-based inbreeding measures commonly used to estimate inbreeding depression (ID). We demonstrate that heterogeneity in linkage disequilibrium (LD) between causal variants and SNPs biases ID estimates, and we develop an approach to correct this bias using LD and minor allele frequency stratified inference (LDMS). We quantified ID in 25 traits measured in ∼140,000 participants of the UK Biobank, using LDMS, and confirmed previously published ID for 4 traits. We find unique evidence of ID for handgrip strength, waist/hip ratio, and visual and auditory acuity (ID between −2.3 and −5.2 phenotypic SDs for complete inbreeding; P<0.001). Our results illustrate that a careful choice of the measure of inbreeding combined with LDMS stratification improves both detection and quantification of ID using SNP data."}],"oa_version":"None","quality_controlled":"1","publisher":"Proceedings of the National Academy of Sciences","month":"08","intvolume":" 114","publication_identifier":{"issn":["0027-8424","1091-6490"]},"year":"2017","publication_status":"published","day":"08","publication":"Proceedings of the National Academy of Sciences","language":[{"iso":"eng"}],"page":"8602-8607","date_published":"2017-08-08T00:00:00Z","volume":114,"doi":"10.1073/pnas.1621096114","related_material":{"link":[{"url":"https://doi.org/10.1073/pnas.1718598115","relation":"other"}]},"issue":"32","date_created":"2020-04-30T10:47:19Z","_id":"7729","article_type":"original","type":"journal_article","status":"public","citation":{"chicago":"Yengo, Loic, Zhihong Zhu, Naomi R. Wray, Bruce S. Weir, Jian Yang, Matthew Richard Robinson, and Peter M. Visscher. “Detection and Quantification of Inbreeding Depression for Complex Traits from SNP Data.” Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1621096114.","ista":"Yengo L, Zhu Z, Wray NR, Weir BS, Yang J, Robinson MR, Visscher PM. 2017. Detection and quantification of inbreeding depression for complex traits from SNP data. Proceedings of the National Academy of Sciences. 114(32), 8602–8607.","mla":"Yengo, Loic, et al. “Detection and Quantification of Inbreeding Depression for Complex Traits from SNP Data.” Proceedings of the National Academy of Sciences, vol. 114, no. 32, Proceedings of the National Academy of Sciences, 2017, pp. 8602–07, doi:10.1073/pnas.1621096114.","short":"L. Yengo, Z. Zhu, N.R. Wray, B.S. Weir, J. Yang, M.R. Robinson, P.M. Visscher, Proceedings of the National Academy of Sciences 114 (2017) 8602–8607.","ieee":"L. Yengo et al., “Detection and quantification of inbreeding depression for complex traits from SNP data,” Proceedings of the National Academy of Sciences, vol. 114, no. 32. Proceedings of the National Academy of Sciences, pp. 8602–8607, 2017.","apa":"Yengo, L., Zhu, Z., Wray, N. R., Weir, B. S., Yang, J., Robinson, M. R., & Visscher, P. M. (2017). Detection and quantification of inbreeding depression for complex traits from SNP data. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1621096114","ama":"Yengo L, Zhu Z, Wray NR, et al. Detection and quantification of inbreeding depression for complex traits from SNP data. Proceedings of the National Academy of Sciences. 2017;114(32):8602-8607. doi:10.1073/pnas.1621096114"},"date_updated":"2021-01-12T08:15:09Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Loic","last_name":"Yengo","full_name":"Yengo, Loic"},{"first_name":"Zhihong","full_name":"Zhu, Zhihong","last_name":"Zhu"},{"full_name":"Wray, Naomi R.","last_name":"Wray","first_name":"Naomi R."},{"full_name":"Weir, Bruce S.","last_name":"Weir","first_name":"Bruce S."},{"first_name":"Jian","full_name":"Yang, Jian","last_name":"Yang"},{"first_name":"Matthew Richard","id":"E5D42276-F5DA-11E9-8E24-6303E6697425","orcid":"0000-0001-8982-8813","full_name":"Robinson, Matthew Richard","last_name":"Robinson"},{"first_name":"Peter M.","last_name":"Visscher","full_name":"Visscher, Peter M."}],"article_processing_charge":"No","title":"Detection and quantification of inbreeding depression for complex traits from SNP data"},{"abstract":[{"text":"Phenotypic plasticity is the ability of an individual genotype to alter aspects of its phenotype depending on the current environment. It is central to the persistence, resistance and resilience of populations facing variation in physical or biological factors. Genetic variation in plasticity is pervasive, which suggests its local adaptation is plausible. Existing studies on the adaptation of plasticity typically focus on single traits and a few populations, while theory about interactions among genes (for example, pleiotropy) suggests that a multi-trait, landscape scale (for example, multiple populations) perspective is required. We present data from a landscape scale, replicated, multi-trait experiment using a classic predator–prey system centred on the water flea Daphnia pulex. We find predator regime-driven differences in genetic variation of multivariate plasticity. These differences are associated with strong divergent selection linked to a predation regime. Our findings are evidence for local adaptation of plasticity, suggesting that responses of populations to environmental variation depend on the conditions in which they evolved in the past.","lang":"eng"}],"oa_version":"None","publisher":"Springer Nature","quality_controlled":"1","intvolume":" 2","month":"11","publication_status":"published","year":"2017","publication_identifier":{"issn":["2397-334X"]},"publication":"Nature Ecology & Evolution","language":[{"iso":"eng"}],"day":"27","page":"100-107","date_created":"2020-04-30T10:46:02Z","doi":"10.1038/s41559-017-0373-6","volume":2,"date_published":"2017-11-27T00:00:00Z","_id":"7725","article_type":"original","type":"journal_article","status":"public","date_updated":"2021-01-12T08:15:07Z","citation":{"chicago":"Reger, Julia, Martin I. Lind, Matthew Richard Robinson, and Andrew P. Beckerman. “Predation Drives Local Adaptation of Phenotypic Plasticity.” Nature Ecology & Evolution. Springer Nature, 2017. https://doi.org/10.1038/s41559-017-0373-6.","ista":"Reger J, Lind MI, Robinson MR, Beckerman AP. 2017. Predation drives local adaptation of phenotypic plasticity. Nature Ecology & Evolution. 2, 100–107.","mla":"Reger, Julia, et al. “Predation Drives Local Adaptation of Phenotypic Plasticity.” Nature Ecology & Evolution, vol. 2, Springer Nature, 2017, pp. 100–07, doi:10.1038/s41559-017-0373-6.","ieee":"J. Reger, M. I. Lind, M. R. Robinson, and A. P. Beckerman, “Predation drives local adaptation of phenotypic plasticity,” Nature Ecology & Evolution, vol. 2. Springer Nature, pp. 100–107, 2017.","short":"J. Reger, M.I. Lind, M.R. Robinson, A.P. Beckerman, Nature Ecology & Evolution 2 (2017) 100–107.","apa":"Reger, J., Lind, M. I., Robinson, M. R., & Beckerman, A. P. (2017). Predation drives local adaptation of phenotypic plasticity. Nature Ecology & Evolution. Springer Nature. https://doi.org/10.1038/s41559-017-0373-6","ama":"Reger J, Lind MI, Robinson MR, Beckerman AP. Predation drives local adaptation of phenotypic plasticity. Nature Ecology & Evolution. 2017;2:100-107. doi:10.1038/s41559-017-0373-6"},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","article_processing_charge":"No","author":[{"first_name":"Julia","last_name":"Reger","full_name":"Reger, Julia"},{"first_name":"Martin I.","last_name":"Lind","full_name":"Lind, Martin I."},{"last_name":"Robinson","orcid":"0000-0001-8982-8813","full_name":"Robinson, Matthew Richard","first_name":"Matthew Richard","id":"E5D42276-F5DA-11E9-8E24-6303E6697425"},{"full_name":"Beckerman, Andrew P.","last_name":"Beckerman","first_name":"Andrew P."}],"title":"Predation drives local adaptation of phenotypic plasticity"},{"article_processing_charge":"No","author":[{"full_name":"Garton, Fleur C.","last_name":"Garton","first_name":"Fleur C."},{"full_name":"Benyamin, Beben","last_name":"Benyamin","first_name":"Beben"},{"last_name":"Zhao","full_name":"Zhao, Qiongyi","first_name":"Qiongyi"},{"full_name":"Liu, Zhijun","last_name":"Liu","first_name":"Zhijun"},{"last_name":"Gratten","full_name":"Gratten, Jacob","first_name":"Jacob"},{"first_name":"Anjali K.","full_name":"Henders, Anjali K.","last_name":"Henders"},{"first_name":"Zong-Hong","last_name":"Zhang","full_name":"Zhang, Zong-Hong"},{"first_name":"Janette","last_name":"Edson","full_name":"Edson, Janette"},{"full_name":"Furlong, Sarah","last_name":"Furlong","first_name":"Sarah"},{"first_name":"Sarah","last_name":"Morgan","full_name":"Morgan, Sarah"},{"last_name":"Heggie","full_name":"Heggie, Susan","first_name":"Susan"},{"first_name":"Kathryn","last_name":"Thorpe","full_name":"Thorpe, Kathryn"},{"last_name":"Pfluger","full_name":"Pfluger, Casey","first_name":"Casey"},{"full_name":"Mather, Karen A.","last_name":"Mather","first_name":"Karen A."},{"last_name":"Sachdev","full_name":"Sachdev, Perminder S.","first_name":"Perminder S."},{"full_name":"McRae, Allan F.","last_name":"McRae","first_name":"Allan F."},{"orcid":"0000-0001-8982-8813","full_name":"Robinson, Matthew Richard","last_name":"Robinson","first_name":"Matthew Richard","id":"E5D42276-F5DA-11E9-8E24-6303E6697425"},{"last_name":"Shah","full_name":"Shah, Sonia","first_name":"Sonia"},{"first_name":"Peter M.","full_name":"Visscher, Peter M.","last_name":"Visscher"},{"last_name":"Mangelsdorf","full_name":"Mangelsdorf, Marie","first_name":"Marie"},{"first_name":"Robert D.","full_name":"Henderson, Robert D.","last_name":"Henderson"},{"last_name":"Wray","full_name":"Wray, Naomi R.","first_name":"Naomi R."},{"last_name":"McCombe","full_name":"McCombe, Pamela A.","first_name":"Pamela A."}],"title":"Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort","citation":{"mla":"Garton, Fleur C., et al. “Whole Exome Sequencing and DNA Methylation Analysis in a Clinical Amyotrophic Lateral Sclerosis Cohort.” Molecular Genetics & Genomic Medicine, vol. 5, no. 4, Wiley, 2017, pp. 418–28, doi:10.1002/mgg3.302.","ieee":"F. C. Garton et al., “Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort,” Molecular Genetics & Genomic Medicine, vol. 5, no. 4. Wiley, pp. 418–428, 2017.","short":"F.C. Garton, B. Benyamin, Q. Zhao, Z. Liu, J. Gratten, A.K. Henders, Z.-H. Zhang, J. Edson, S. Furlong, S. Morgan, S. Heggie, K. Thorpe, C. Pfluger, K.A. Mather, P.S. Sachdev, A.F. McRae, M.R. Robinson, S. Shah, P.M. Visscher, M. Mangelsdorf, R.D. Henderson, N.R. Wray, P.A. McCombe, Molecular Genetics & Genomic Medicine 5 (2017) 418–428.","apa":"Garton, F. C., Benyamin, B., Zhao, Q., Liu, Z., Gratten, J., Henders, A. K., … McCombe, P. A. (2017). Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics & Genomic Medicine. Wiley. https://doi.org/10.1002/mgg3.302","ama":"Garton FC, Benyamin B, Zhao Q, et al. Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics & Genomic Medicine. 2017;5(4):418-428. doi:10.1002/mgg3.302","chicago":"Garton, Fleur C., Beben Benyamin, Qiongyi Zhao, Zhijun Liu, Jacob Gratten, Anjali K. Henders, Zong-Hong Zhang, et al. “Whole Exome Sequencing and DNA Methylation Analysis in a Clinical Amyotrophic Lateral Sclerosis Cohort.” Molecular Genetics & Genomic Medicine. Wiley, 2017. https://doi.org/10.1002/mgg3.302.","ista":"Garton FC, Benyamin B, Zhao Q, Liu Z, Gratten J, Henders AK, Zhang Z-H, Edson J, Furlong S, Morgan S, Heggie S, Thorpe K, Pfluger C, Mather KA, Sachdev PS, McRae AF, Robinson MR, Shah S, Visscher PM, Mangelsdorf M, Henderson RD, Wray NR, McCombe PA. 2017. Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort. Molecular Genetics & Genomic Medicine. 5(4), 418–428."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","page":"418-428","date_created":"2020-04-30T10:48:25Z","doi":"10.1002/mgg3.302","date_published":"2017-07-01T00:00:00Z","year":"2017","publication":"Molecular Genetics & Genomic Medicine","day":"01","oa":1,"quality_controlled":"1","publisher":"Wiley","date_updated":"2021-01-12T08:15:10Z","extern":"1","article_type":"original","type":"journal_article","status":"public","_id":"7733","issue":"4","volume":5,"publication_status":"published","publication_identifier":{"issn":["2324-9269"]},"language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1002/mgg3.302","open_access":"1"}],"intvolume":" 5","month":"07","abstract":[{"text":"Sections\r\nPDFPDF\r\nTools\r\nShare\r\nAbstract\r\nBackground: Gene discovery has provided remarkable biological insights into amyotrophic lateral sclerosis (ALS). One challenge for clinical application of genetic testing is critical evaluation of the significance of reported variants.\r\nMethods: We use whole exome sequencing (WES) to develop a clinically relevant approach to identify a subset of ALS patients harboring likely pathogenic mutations. In parallel, we assess if DNA methylation can be used to screen for pathogenicity of novel variants since a methylation signature has been shown to associate with the pathogenic C9orf72 expansion, but has not been explored for other ALS mutations. Australian patients identified with ALS‐relevant variants were cross‐checked with population databases and case reports to critically assess whether they were “likely causal,” “uncertain significance,” or “unlikely causal.”\r\nResults: Published ALS variants were identified in >10% of patients; however, in only 3% of patients (4/120) could these be confidently considered pathogenic (in SOD1 and TARDBP). We found no evidence for a differential DNA methylation signature in these mutation carriers.\r\nConclusions: The use of WES in a typical ALS clinic demonstrates a critical approach to variant assessment with the capability to combine cohorts to enhance the largely unknown genetic basis of ALS.","lang":"eng"}],"oa_version":"Published Version"},{"abstract":[{"text":"Genetic association studies in admixed populations are underrepresented in the genomics literature, with a key concern for researchers being the adequate control of spurious associations due to population structure. Linear mixed models (LMMs) are well suited for genome-wide association studies (GWAS) because they account for both population stratification and cryptic relatedness and achieve increased statistical power by jointly modeling all genotyped markers. Additionally, Bayesian LMMs allow for more flexible assumptions about the underlying distribution of genetic effects, and can concurrently estimate the proportion of phenotypic variance explained by genetic markers. Using three recently published Bayesian LMMs, Bayes R, BSLMM, and BOLT-LMM, we investigate an existing data set on eye (n = 625) and skin (n = 684) color from Cape Verde, an island nation off West Africa that is home to individuals with a broad range of phenotypic values for eye and skin color due to the mix of West African and European ancestry. We use simulations to demonstrate the utility of Bayesian LMMs for mapping loci and studying the genetic architecture of quantitative traits in admixed populations. The Bayesian LMMs provide evidence for two new pigmentation loci: one for eye color (AHRR) and one for skin color (DDB1).","lang":"eng"}],"oa_version":"None","quality_controlled":"1","publisher":"Genetics Society of America","month":"06","intvolume":" 206","publication_identifier":{"issn":["0016-6731","1943-2631"]},"publication_status":"published","year":"2017","day":"01","language":[{"iso":"eng"}],"publication":"Genetics","page":"1113-1126","date_published":"2017-06-01T00:00:00Z","volume":206,"issue":"2","doi":"10.1534/genetics.116.193383","date_created":"2020-04-30T10:47:50Z","_id":"7731","type":"journal_article","article_type":"original","status":"public","citation":{"short":"L.R. Lloyd-Jones, M.R. Robinson, G. Moser, J. Zeng, S. Beleza, G.S. Barsh, H. Tang, P.M. Visscher, Genetics 206 (2017) 1113–1126.","ieee":"L. R. Lloyd-Jones et al., “Inference on the genetic basis of eye and skin color in an admixed population via Bayesian linear mixed models,” Genetics, vol. 206, no. 2. Genetics Society of America, pp. 1113–1126, 2017.","apa":"Lloyd-Jones, L. R., Robinson, M. R., Moser, G., Zeng, J., Beleza, S., Barsh, G. S., … Visscher, P. M. (2017). Inference on the genetic basis of eye and skin color in an admixed population via Bayesian linear mixed models. Genetics. Genetics Society of America. https://doi.org/10.1534/genetics.116.193383","ama":"Lloyd-Jones LR, Robinson MR, Moser G, et al. Inference on the genetic basis of eye and skin color in an admixed population via Bayesian linear mixed models. Genetics. 2017;206(2):1113-1126. doi:10.1534/genetics.116.193383","mla":"Lloyd-Jones, Luke R., et al. “Inference on the Genetic Basis of Eye and Skin Color in an Admixed Population via Bayesian Linear Mixed Models.” Genetics, vol. 206, no. 2, Genetics Society of America, 2017, pp. 1113–26, doi:10.1534/genetics.116.193383.","ista":"Lloyd-Jones LR, Robinson MR, Moser G, Zeng J, Beleza S, Barsh GS, Tang H, Visscher PM. 2017. Inference on the genetic basis of eye and skin color in an admixed population via Bayesian linear mixed models. Genetics. 206(2), 1113–1126.","chicago":"Lloyd-Jones, Luke R., Matthew Richard Robinson, Gerhard Moser, Jian Zeng, Sandra Beleza, Gregory S. Barsh, Hua Tang, and Peter M. Visscher. “Inference on the Genetic Basis of Eye and Skin Color in an Admixed Population via Bayesian Linear Mixed Models.” Genetics. Genetics Society of America, 2017. https://doi.org/10.1534/genetics.116.193383."},"date_updated":"2021-01-12T08:15:10Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"full_name":"Lloyd-Jones, Luke R.","last_name":"Lloyd-Jones","first_name":"Luke R."},{"first_name":"Matthew Richard","id":"E5D42276-F5DA-11E9-8E24-6303E6697425","full_name":"Robinson, Matthew Richard","orcid":"0000-0001-8982-8813","last_name":"Robinson"},{"first_name":"Gerhard","last_name":"Moser","full_name":"Moser, Gerhard"},{"full_name":"Zeng, Jian","last_name":"Zeng","first_name":"Jian"},{"last_name":"Beleza","full_name":"Beleza, Sandra","first_name":"Sandra"},{"full_name":"Barsh, Gregory S.","last_name":"Barsh","first_name":"Gregory S."},{"full_name":"Tang, Hua","last_name":"Tang","first_name":"Hua"},{"last_name":"Visscher","full_name":"Visscher, Peter M.","first_name":"Peter M."}],"article_processing_charge":"No","title":"Inference on the genetic basis of eye and skin color in an admixed population via Bayesian linear mixed models"},{"author":[{"last_name":"Sethna","full_name":"Sethna, James P.","first_name":"James P."},{"last_name":"Bierbaum","full_name":"Bierbaum, Matthew K.","first_name":"Matthew K."},{"full_name":"Dahmen, Karin A.","last_name":"Dahmen","first_name":"Karin A."},{"first_name":"Carl Peter","id":"EB352CD2-F68A-11E9-89C5-A432E6697425","full_name":"Goodrich, Carl Peter","orcid":"0000-0002-1307-5074","last_name":"Goodrich"},{"full_name":"Greer, Julia R.","last_name":"Greer","first_name":"Julia R."},{"full_name":"Hayden, Lorien X.","last_name":"Hayden","first_name":"Lorien X."},{"first_name":"Jaron P.","full_name":"Kent-Dobias, Jaron P.","last_name":"Kent-Dobias"},{"first_name":"Edward D.","last_name":"Lee","full_name":"Lee, Edward D."},{"last_name":"Liarte","full_name":"Liarte, Danilo B.","first_name":"Danilo B."},{"full_name":"Ni, Xiaoyue","last_name":"Ni","first_name":"Xiaoyue"},{"first_name":"Katherine N.","last_name":"Quinn","full_name":"Quinn, Katherine N."},{"first_name":"Archishman","last_name":"Raju","full_name":"Raju, Archishman"},{"first_name":"D. Zeb","full_name":"Rocklin, D. Zeb","last_name":"Rocklin"},{"first_name":"Ashivni","full_name":"Shekhawat, Ashivni","last_name":"Shekhawat"},{"full_name":"Zapperi, Stefano","last_name":"Zapperi","first_name":"Stefano"}],"article_processing_charge":"No","title":"Deformation of crystals: Connections with statistical physics","citation":{"ama":"Sethna JP, Bierbaum MK, Dahmen KA, et al. Deformation of crystals: Connections with statistical physics. Annual Review of Materials Research. 2017;47:217-246. doi:10.1146/annurev-matsci-070115-032036","apa":"Sethna, J. P., Bierbaum, M. K., Dahmen, K. A., Goodrich, C. P., Greer, J. R., Hayden, L. X., … Zapperi, S. (2017). Deformation of crystals: Connections with statistical physics. Annual Review of Materials Research. Annual Reviews. https://doi.org/10.1146/annurev-matsci-070115-032036","short":"J.P. Sethna, M.K. Bierbaum, K.A. Dahmen, C.P. Goodrich, J.R. Greer, L.X. Hayden, J.P. Kent-Dobias, E.D. Lee, D.B. Liarte, X. Ni, K.N. Quinn, A. Raju, D.Z. Rocklin, A. Shekhawat, S. Zapperi, Annual Review of Materials Research 47 (2017) 217–246.","ieee":"J. P. Sethna et al., “Deformation of crystals: Connections with statistical physics,” Annual Review of Materials Research, vol. 47. Annual Reviews, pp. 217–246, 2017.","mla":"Sethna, James P., et al. “Deformation of Crystals: Connections with Statistical Physics.” Annual Review of Materials Research, vol. 47, Annual Reviews, 2017, pp. 217–46, doi:10.1146/annurev-matsci-070115-032036.","ista":"Sethna JP, Bierbaum MK, Dahmen KA, Goodrich CP, Greer JR, Hayden LX, Kent-Dobias JP, Lee ED, Liarte DB, Ni X, Quinn KN, Raju A, Rocklin DZ, Shekhawat A, Zapperi S. 2017. Deformation of crystals: Connections with statistical physics. Annual Review of Materials Research. 47, 217–246.","chicago":"Sethna, James P., Matthew K. Bierbaum, Karin A. Dahmen, Carl Peter Goodrich, Julia R. Greer, Lorien X. Hayden, Jaron P. Kent-Dobias, et al. “Deformation of Crystals: Connections with Statistical Physics.” Annual Review of Materials Research. Annual Reviews, 2017. https://doi.org/10.1146/annurev-matsci-070115-032036."},"date_updated":"2021-01-12T08:15:18Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_type":"original","type":"journal_article","status":"public","_id":"7755","page":"217-246","doi":"10.1146/annurev-matsci-070115-032036","volume":47,"date_published":"2017-07-01T00:00:00Z","date_created":"2020-04-30T11:38:24Z","publication_identifier":{"issn":["1531-7331","1545-4118"]},"publication_status":"published","year":"2017","day":"01","publication":"Annual Review of Materials Research","language":[{"iso":"eng"}],"publisher":"Annual Reviews","quality_controlled":"1","main_file_link":[{"url":"https://doi.org/10.1146/annurev-matsci-070115-032036","open_access":"1"}],"oa":1,"month":"07","intvolume":" 47","abstract":[{"text":"We give a bird's-eye view of the plastic deformation of crystals aimed at the statistical physics community, as well as a broad introduction to the statistical theories of forced rigid systems aimed at the plasticity community. Memory effects in magnets, spin glasses, charge density waves, and dilute colloidal suspensions are discussed in relation to the onset of plastic yielding in crystals. Dislocation avalanches and complex dislocation tangles are discussed via a brief introduction to the renormalization group and scaling. Analogies to emergent scale invariance in fracture, jamming, coarsening, and a variety of depinning transitions are explored. Dislocation dynamics in crystals challenge nonequilibrium statistical physics. Statistical physics provides both cautionary tales of subtle memory effects in nonequilibrium systems and systematic tools designed to address complex scale-invariant behavior on multiple length scales and timescales.","lang":"eng"}],"oa_version":"Published Version"},{"publication_status":"published","year":"2017","publication_identifier":{"issn":["0027-8424","1091-6490"]},"publication":"Proceedings of the National Academy of Sciences","language":[{"iso":"eng"}],"day":"07","page":"2520-2525","date_created":"2020-04-30T11:38:53Z","volume":114,"doi":"10.1073/pnas.1612139114","issue":"10","date_published":"2017-03-07T00:00:00Z","abstract":[{"lang":"eng","text":"Recent advances in designing metamaterials have demonstrated that global mechanical properties of disordered spring networks can be tuned by selectively modifying only a small subset of bonds. Here, using a computationally efficient approach, we extend this idea to tune more general properties of networks. With nearly complete success, we are able to produce a strain between any two target nodes in a network in response to an applied source strain on any other pair of nodes by removing only ∼1% of the bonds. We are also able to control multiple pairs of target nodes, each with a different individual response, from a single source, and to tune multiple independent source/target responses simultaneously into a network. We have fabricated physical networks in macroscopic 2D and 3D systems that exhibit these responses. This work is inspired by the long-range coupled conformational changes that constitute allosteric function in proteins. The fact that allostery is a common means for regulation in biological molecules suggests that it is a relatively easy property to develop through evolution. In analogy, our results show that long-range coupled mechanical responses are similarly easy to achieve in disordered networks."}],"oa_version":"None","publisher":"Proceedings of the National Academy of Sciences","quality_controlled":"1","intvolume":" 114","month":"03","citation":{"ista":"Rocks JW, Pashine N, Bischofberger I, Goodrich CP, Liu AJ, Nagel SR. 2017. Designing allostery-inspired response in mechanical networks. Proceedings of the National Academy of Sciences. 114(10), 2520–2525.","chicago":"Rocks, Jason W., Nidhi Pashine, Irmgard Bischofberger, Carl Peter Goodrich, Andrea J. Liu, and Sidney R. Nagel. “Designing Allostery-Inspired Response in Mechanical Networks.” Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1612139114.","apa":"Rocks, J. W., Pashine, N., Bischofberger, I., Goodrich, C. P., Liu, A. J., & Nagel, S. R. (2017). Designing allostery-inspired response in mechanical networks. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1612139114","ama":"Rocks JW, Pashine N, Bischofberger I, Goodrich CP, Liu AJ, Nagel SR. Designing allostery-inspired response in mechanical networks. Proceedings of the National Academy of Sciences. 2017;114(10):2520-2525. doi:10.1073/pnas.1612139114","ieee":"J. W. Rocks, N. Pashine, I. Bischofberger, C. P. Goodrich, A. J. Liu, and S. R. Nagel, “Designing allostery-inspired response in mechanical networks,” Proceedings of the National Academy of Sciences, vol. 114, no. 10. Proceedings of the National Academy of Sciences, pp. 2520–2525, 2017.","short":"J.W. Rocks, N. Pashine, I. Bischofberger, C.P. Goodrich, A.J. Liu, S.R. Nagel, Proceedings of the National Academy of Sciences 114 (2017) 2520–2525.","mla":"Rocks, Jason W., et al. “Designing Allostery-Inspired Response in Mechanical Networks.” Proceedings of the National Academy of Sciences, vol. 114, no. 10, Proceedings of the National Academy of Sciences, 2017, pp. 2520–25, doi:10.1073/pnas.1612139114."},"date_updated":"2021-01-12T08:15:19Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","article_processing_charge":"No","author":[{"last_name":"Rocks","full_name":"Rocks, Jason W.","first_name":"Jason W."},{"full_name":"Pashine, Nidhi","last_name":"Pashine","first_name":"Nidhi"},{"first_name":"Irmgard","full_name":"Bischofberger, Irmgard","last_name":"Bischofberger"},{"first_name":"Carl Peter","id":"EB352CD2-F68A-11E9-89C5-A432E6697425","full_name":"Goodrich, Carl Peter","orcid":"0000-0002-1307-5074","last_name":"Goodrich"},{"first_name":"Andrea J.","last_name":"Liu","full_name":"Liu, Andrea J."},{"first_name":"Sidney R.","full_name":"Nagel, Sidney R.","last_name":"Nagel"}],"title":"Designing allostery-inspired response in mechanical networks","_id":"7757","type":"journal_article","article_type":"original","status":"public"},{"oa_version":"None","abstract":[{"text":"Controlling motion at the microscopic scale is a fundamental goal in the development of biologically inspired systems. We show that the motion of active, self-propelled colloids can be sufficiently controlled for use as a tool to assemble complex structures such as braids and weaves out of microscopic filaments. Unlike typical self-assembly paradigms, these structures are held together by geometric constraints rather than adhesive bonds. The out-of-equilibrium assembly that we propose involves precisely controlling the 2D motion of active colloids so that their path has a nontrivial topology. We demonstrate with proof-of-principle Brownian dynamics simulations that, when the colloids are attached to long semiflexible filaments, this motion causes the filaments to braid. The ability of the active particles to provide sufficient force necessary to bend the filaments into a braid depends on a number of factors, including the self-propulsion mechanism, the properties of the filament, and the maximum curvature in the braid. Our work demonstrates that nonequilibrium assembly pathways can be designed using active particles.","lang":"eng"}],"month":"01","intvolume":" 114","quality_controlled":"1","publisher":"Proceedings of the National Academy of Sciences","day":"10","language":[{"iso":"eng"}],"publication":"Proceedings of the National Academy of Sciences","publication_identifier":{"issn":["0027-8424","1091-6490"]},"year":"2017","publication_status":"published","doi":"10.1073/pnas.1608838114","date_published":"2017-01-10T00:00:00Z","issue":"2","volume":114,"date_created":"2020-04-30T11:39:09Z","page":"257-262","_id":"7758","status":"public","article_type":"original","type":"journal_article","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ama":"Goodrich CP, Brenner MP. Using active colloids as machines to weave and braid on the micrometer scale. Proceedings of the National Academy of Sciences. 2017;114(2):257-262. doi:10.1073/pnas.1608838114","apa":"Goodrich, C. P., & Brenner, M. P. (2017). Using active colloids as machines to weave and braid on the micrometer scale. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1608838114","short":"C.P. Goodrich, M.P. Brenner, Proceedings of the National Academy of Sciences 114 (2017) 257–262.","ieee":"C. P. Goodrich and M. P. Brenner, “Using active colloids as machines to weave and braid on the micrometer scale,” Proceedings of the National Academy of Sciences, vol. 114, no. 2. Proceedings of the National Academy of Sciences, pp. 257–262, 2017.","mla":"Goodrich, Carl Peter, and Michael P. Brenner. “Using Active Colloids as Machines to Weave and Braid on the Micrometer Scale.” Proceedings of the National Academy of Sciences, vol. 114, no. 2, Proceedings of the National Academy of Sciences, 2017, pp. 257–62, doi:10.1073/pnas.1608838114.","ista":"Goodrich CP, Brenner MP. 2017. Using active colloids as machines to weave and braid on the micrometer scale. Proceedings of the National Academy of Sciences. 114(2), 257–262.","chicago":"Goodrich, Carl Peter, and Michael P. Brenner. “Using Active Colloids as Machines to Weave and Braid on the Micrometer Scale.” Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1608838114."},"date_updated":"2021-01-12T08:15:20Z","title":"Using active colloids as machines to weave and braid on the micrometer scale","author":[{"full_name":"Goodrich, Carl Peter","orcid":"0000-0002-1307-5074","last_name":"Goodrich","first_name":"Carl Peter","id":"EB352CD2-F68A-11E9-89C5-A432E6697425"},{"full_name":"Brenner, Michael P.","last_name":"Brenner","first_name":"Michael P."}],"article_processing_charge":"No"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:15:19Z","citation":{"chicago":"Baity-Jesi, Marco, Carl Peter Goodrich, Andrea J. Liu, Sidney R. Nagel, and James P. Sethna. “Emergent SO(3) Symmetry of the Frictionless Shear Jamming Transition.” Journal of Statistical Physics. Springer Nature, 2017. https://doi.org/10.1007/s10955-016-1703-9.","ista":"Baity-Jesi M, Goodrich CP, Liu AJ, Nagel SR, Sethna JP. 2017. Emergent SO(3) symmetry of the frictionless shear jamming transition. Journal of Statistical Physics. 167(3–4), 735–748.","mla":"Baity-Jesi, Marco, et al. “Emergent SO(3) Symmetry of the Frictionless Shear Jamming Transition.” Journal of Statistical Physics, vol. 167, no. 3–4, Springer Nature, 2017, pp. 735–48, doi:10.1007/s10955-016-1703-9.","ieee":"M. Baity-Jesi, C. P. Goodrich, A. J. Liu, S. R. Nagel, and J. P. Sethna, “Emergent SO(3) symmetry of the frictionless shear jamming transition,” Journal of Statistical Physics, vol. 167, no. 3–4. Springer Nature, pp. 735–748, 2017.","short":"M. Baity-Jesi, C.P. Goodrich, A.J. Liu, S.R. Nagel, J.P. Sethna, Journal of Statistical Physics 167 (2017) 735–748.","apa":"Baity-Jesi, M., Goodrich, C. P., Liu, A. J., Nagel, S. R., & Sethna, J. P. (2017). Emergent SO(3) symmetry of the frictionless shear jamming transition. Journal of Statistical Physics. Springer Nature. https://doi.org/10.1007/s10955-016-1703-9","ama":"Baity-Jesi M, Goodrich CP, Liu AJ, Nagel SR, Sethna JP. Emergent SO(3) symmetry of the frictionless shear jamming transition. Journal of Statistical Physics. 2017;167(3-4):735-748. doi:10.1007/s10955-016-1703-9"},"title":"Emergent SO(3) symmetry of the frictionless shear jamming transition","article_processing_charge":"No","author":[{"full_name":"Baity-Jesi, Marco","last_name":"Baity-Jesi","first_name":"Marco"},{"last_name":"Goodrich","full_name":"Goodrich, Carl Peter","orcid":"0000-0002-1307-5074","id":"EB352CD2-F68A-11E9-89C5-A432E6697425","first_name":"Carl Peter"},{"first_name":"Andrea J.","last_name":"Liu","full_name":"Liu, Andrea J."},{"first_name":"Sidney R.","full_name":"Nagel, Sidney R.","last_name":"Nagel"},{"full_name":"Sethna, James P.","last_name":"Sethna","first_name":"James P."}],"_id":"7756","status":"public","type":"journal_article","article_type":"original","publication":"Journal of Statistical Physics","language":[{"iso":"eng"}],"day":"03","year":"2017","publication_status":"published","publication_identifier":{"issn":["0022-4715","1572-9613"]},"date_created":"2020-04-30T11:38:38Z","doi":"10.1007/s10955-016-1703-9","date_published":"2017-01-03T00:00:00Z","issue":"3-4","volume":167,"page":"735-748","oa_version":"None","abstract":[{"text":"We study the shear jamming of athermal frictionless soft spheres, and find that in the thermodynamic limit, a shear-jammed state exists with different elastic properties from the isotropically-jammed state. For example, shear-jammed states can have a non-zero residual shear stress in the thermodynamic limit that arises from long-range stress-stress correlations. As a result, the ratio of the shear and bulk moduli, which in isotropically-jammed systems vanishes as the jamming transition is approached from above, instead approaches a constant. Despite these striking differences, we argue that in a deeper sense, the shear jamming and isotropic jamming transitions actually have the same symmetry, and that the differences can be fully understood by rotating the six-dimensional basis of the elastic modulus tensor.","lang":"eng"}],"intvolume":" 167","month":"01","publisher":"Springer Nature","quality_controlled":"1"},{"type":"conference","conference":{"name":"DNA Computing and Molecular Programming"},"status":"public","_id":"788","date_updated":"2022-03-18T12:48:02Z","extern":"1","alternative_title":["LNCS"],"scopus_import":"1","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1706.09937"}],"month":"01","abstract":[{"lang":"eng","text":"In contrast to electronic computation, chemical computation is noisy and susceptible to a variety of sources of error, which has prevented the construction of robust complex systems. To be effective, chemical algorithms must be designed with an appropriate error model in mind. Here we consider the model of chemical reaction networks that preserve molecular count (population protocols), and ask whether computation can be made robust to a natural model of unintended “leak” reactions. Our definition of leak is motivated by both the particular spurious behavior seen when implementing chemical reaction networks with DNA strand displacement cascades, as well as the unavoidable side reactions in any implementation due to the basic laws of chemistry. We develop a new “Robust Detection” algorithm for the problem of fast (logarithmic time) single molecule detection, and prove that it is robust to this general model of leaks. Besides potential applications in single molecule detection, the error-correction ideas developed here might enable a new class of robust-by-design chemical algorithms. Our analysis is based on a non-standard hybrid argument, combining ideas from discrete analysis of population protocols with classic Markov chain techniques."}],"oa_version":"None","volume":"10467 LNCS","publication_status":"published","language":[{"iso":"eng"}],"publist_id":"6868","author":[{"last_name":"Alistarh","orcid":"0000-0003-3650-940X","full_name":"Alistarh, Dan-Adrian","id":"4A899BFC-F248-11E8-B48F-1D18A9856A87","first_name":"Dan-Adrian"},{"first_name":"Bartłomiej","full_name":"Dudek, Bartłomiej","last_name":"Dudek"},{"full_name":"Kosowski, Adrian","last_name":"Kosowski","first_name":"Adrian"},{"first_name":"David","last_name":"Soloveichik","full_name":"Soloveichik, David"},{"last_name":"Uznański","full_name":"Uznański, Przemysław","first_name":"Przemysław"}],"article_processing_charge":"No","external_id":{"arxiv":["1706.09937"]},"title":"Robust detection in leak-prone population protocols","citation":{"mla":"Alistarh, Dan-Adrian, et al. Robust Detection in Leak-Prone Population Protocols. Vol. 10467 LNCS, Springer, 2017, pp. 155–71, doi:10.1007/978-3-319-66799-7_11.","ieee":"D.-A. Alistarh, B. Dudek, A. Kosowski, D. Soloveichik, and P. Uznański, “Robust detection in leak-prone population protocols,” presented at the DNA Computing and Molecular Programming, 2017, vol. 10467 LNCS, pp. 155–171.","short":"D.-A. Alistarh, B. Dudek, A. Kosowski, D. Soloveichik, P. Uznański, in:, Springer, 2017, pp. 155–171.","ama":"Alistarh D-A, Dudek B, Kosowski A, Soloveichik D, Uznański P. Robust detection in leak-prone population protocols. In: Vol 10467 LNCS. Springer; 2017:155-171. doi:10.1007/978-3-319-66799-7_11","apa":"Alistarh, D.-A., Dudek, B., Kosowski, A., Soloveichik, D., & Uznański, P. (2017). Robust detection in leak-prone population protocols (Vol. 10467 LNCS, pp. 155–171). Presented at the DNA Computing and Molecular Programming, Springer. https://doi.org/10.1007/978-3-319-66799-7_11","chicago":"Alistarh, Dan-Adrian, Bartłomiej Dudek, Adrian Kosowski, David Soloveichik, and Przemysław Uznański. “Robust Detection in Leak-Prone Population Protocols,” 10467 LNCS:155–71. Springer, 2017. https://doi.org/10.1007/978-3-319-66799-7_11.","ista":"Alistarh D-A, Dudek B, Kosowski A, Soloveichik D, Uznański P. 2017. Robust detection in leak-prone population protocols. DNA Computing and Molecular Programming, LNCS, vol. 10467 LNCS, 155–171."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","quality_controlled":"1","publisher":"Springer","oa":1,"acknowledgement":"D. Alistarh - Supported by an SNF Ambizione Fellowship. A. Kosowski — Supported by Inria project GANG, ANR project DESCARTES, and\r\nNCN grant 2015/17/B/ST6/01897. D. Soloveichik — Supported by NSF grants CCF-1618895 and CCF-1652824.\r\n\r\n","page":"155 - 171","doi":"10.1007/978-3-319-66799-7_11","date_published":"2017-01-01T00:00:00Z","date_created":"2018-12-11T11:48:30Z","year":"2017","day":"01"},{"oa_version":"None","acknowledgement":"Dan Alistarh was supported by a Swiss National Science\r\nFoundation Ambizione Fellowship. James Aspnes was supported by the National Science Foundation under grants\r\nCCF-1637385 and CCF-1650596. Rati Gelashvili was supported by the National Science Foundation under grants\r\nCCF-1217921, CCF-1301926, and IIS-1447786, the Department of Energy under grant ER26116/DE-SC0008923, and\r\nOracle and Intel corporations.\r\nThe authors would like to thank David Doty, David\r\nSoloveichik, and Milan Vojnovic for insightful discussions\r\nand feedback during the development of this work.","abstract":[{"text":"Population protocols are a popular model of distributed computing, in which randomly-interacting agents with little computational power cooperate to jointly perform computational tasks. Inspired by developments in molecular computation, and in particular DNA computing, recent algorithmic work has focused on the complexity of solving simple yet fundamental tasks in the population model, such as leader election (which requires convergence to a single agent in a special "leader" state), and majority (in which agents must converge to a decision as to which of two possible initial states had higher initial count). Known results point towards an inherent trade-off between the time complexity of such algorithms, and the space complexity, i.e. size of the memory available to each agent. In this paper, we explore this trade-off and provide new upper and lower bounds for majority and leader election. First, we prove a unified lower bound, which relates the space available per node with the time complexity achievable by a protocol: for instance, our result implies that any protocol solving either of these tasks for n agents using O(log log n) states must take (n=polylogn) expected time. This is the first result to characterize time complexity for protocols which employ super-constant number of states per node, and proves that fast, poly-logarithmic running times require protocols to have relatively large space costs. On the positive side, we give algorithms showing that fast, poly-logarithmic convergence time can be achieved using O(log2 n) space per node, in the case of both tasks. Overall, our results highlight a time complexity separation between O(log log n) and (log2 n) state space size for both majority and leader election in population protocols, and introduce new techniques, which should be applicable more broadly.","lang":"eng"}],"month":"01","publisher":"SIAM","main_file_link":[{"url":"https://arxiv.org/abs/1602.08032","open_access":"1"}],"oa":1,"day":"01","language":[{"iso":"eng"}],"publication_status":"published","year":"2017","doi":"doi.org/10.1137/1.9781611974782.169","date_published":"2017-01-01T00:00:00Z","date_created":"2018-12-11T11:48:30Z","page":"2560 - 2579","_id":"787","status":"public","type":"conference","conference":{"name":"SODA: Symposium on Discrete Algorithms"},"extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Alistarh D-A, Aspnes J, Eisenstat D, Rivest R, Gelashvili R. 2017. Time-space trade-offs in population protocols. SODA: Symposium on Discrete Algorithms, 2560–2579.","chicago":"Alistarh, Dan-Adrian, James Aspnes, David Eisenstat, Ronald Rivest, and Rati Gelashvili. “Time-Space Trade-Offs in Population Protocols,” 2560–79. SIAM, 2017. https://doi.org/doi.org/10.1137/1.9781611974782.169.","ieee":"D.-A. Alistarh, J. Aspnes, D. Eisenstat, R. Rivest, and R. Gelashvili, “Time-space trade-offs in population protocols,” presented at the SODA: Symposium on Discrete Algorithms, 2017, pp. 2560–2579.","short":"D.-A. Alistarh, J. Aspnes, D. Eisenstat, R. Rivest, R. Gelashvili, in:, SIAM, 2017, pp. 2560–2579.","apa":"Alistarh, D.-A., Aspnes, J., Eisenstat, D., Rivest, R., & Gelashvili, R. (2017). Time-space trade-offs in population protocols (pp. 2560–2579). Presented at the SODA: Symposium on Discrete Algorithms, SIAM. https://doi.org/doi.org/10.1137/1.9781611974782.169","ama":"Alistarh D-A, Aspnes J, Eisenstat D, Rivest R, Gelashvili R. Time-space trade-offs in population protocols. In: SIAM; 2017:2560-2579. doi:doi.org/10.1137/1.9781611974782.169","mla":"Alistarh, Dan-Adrian, et al. Time-Space Trade-Offs in Population Protocols. SIAM, 2017, pp. 2560–79, doi:doi.org/10.1137/1.9781611974782.169."},"date_updated":"2023-02-23T13:19:13Z","title":"Time-space trade-offs in population protocols","publist_id":"6869","author":[{"full_name":"Alistarh, Dan-Adrian","orcid":"0000-0003-3650-940X","last_name":"Alistarh","first_name":"Dan-Adrian","id":"4A899BFC-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Aspnes, James","last_name":"Aspnes","first_name":"James"},{"last_name":"Eisenstat","full_name":"Eisenstat, David","first_name":"David"},{"full_name":"Rivest, Ronald","last_name":"Rivest","first_name":"Ronald"},{"first_name":"Rati","full_name":"Gelashvili, Rati","last_name":"Gelashvili"}]},{"oa_version":"None","acknowledgement":"William Leiserson, Alexander Matveev, and Nir Shavit were supported by the NSF under grants IIS-1447786 and CCF-1563880, and Dan Alistarh was supported by a Swiss National Fund Ambizione Fellowship.","abstract":[{"lang":"eng","text":"The problem of efficient concurrent memory reclamation in unmanaged languages such as C or C++ is one of the major challenges facing the parallelization of billions of lines of legacy code. Garbage collectors for C/C++ can be inefficient; thus, programmers are often forced to use finely-crafted concurrent memory reclamation techniques. These techniques can provide good performance, but require considerable programming effort to deploy, and have strict requirements, allowing the programmer very little room for error. In this work, we present Forkscan, a new conservative concurrent memory reclamation scheme which is fully automatic and surprisingly scalable. Forkscan's semantics place it between automatic garbage collectors (it requires the programmer to explicitly retire nodes before they can be reclaimed), and concurrent memory reclamation techniques (as it does not assume that nodes are completely unlinked from the data structure for correctness). Forkscan's implementation exploits these new semantics for efficiency: we leverage parallelism and optimized implementations of signaling and copy-on-write in modern operating systems to efficiently obtain and process consistent snapshots of memory that can be scanned concurrently with the normal program operation. Empirical evaluation on a range of classical concurrent data structure microbenchmarks shows that Forkscan can preserve the scalability of the original code, while maintaining an order of magnitude lower latency than automatic garbage collection, and demonstrating competitive performance with finely crafted memory reclamation techniques."}],"month":"01","publisher":"ACM","day":"01","language":[{"iso":"eng"}],"publication_status":"published","year":"2017","date_published":"2017-01-01T00:00:00Z","doi":"10.1145/3064176.3064214","date_created":"2018-12-11T11:48:30Z","page":"483 - 498","_id":"789","status":"public","type":"conference","conference":{"name":"EuroSys: European Conference on Computer Systems"},"extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_updated":"2023-02-23T13:19:44Z","citation":{"chicago":"Alistarh, Dan-Adrian, William Leiserson, Alexander Matveev, and Nir Shavit. “Forkscan: Conservative Memory Reclamation for Modern Operating Systems,” 483–98. ACM, 2017. https://doi.org/10.1145/3064176.3064214.","ista":"Alistarh D-A, Leiserson W, Matveev A, Shavit N. 2017. Forkscan: Conservative memory reclamation for modern operating systems. EuroSys: European Conference on Computer Systems, 483–498.","mla":"Alistarh, Dan-Adrian, et al. Forkscan: Conservative Memory Reclamation for Modern Operating Systems. ACM, 2017, pp. 483–98, doi:10.1145/3064176.3064214.","ama":"Alistarh D-A, Leiserson W, Matveev A, Shavit N. Forkscan: Conservative memory reclamation for modern operating systems. In: ACM; 2017:483-498. doi:10.1145/3064176.3064214","apa":"Alistarh, D.-A., Leiserson, W., Matveev, A., & Shavit, N. (2017). Forkscan: Conservative memory reclamation for modern operating systems (pp. 483–498). Presented at the EuroSys: European Conference on Computer Systems, ACM. https://doi.org/10.1145/3064176.3064214","short":"D.-A. Alistarh, W. Leiserson, A. Matveev, N. Shavit, in:, ACM, 2017, pp. 483–498.","ieee":"D.-A. Alistarh, W. Leiserson, A. Matveev, and N. Shavit, “Forkscan: Conservative memory reclamation for modern operating systems,” presented at the EuroSys: European Conference on Computer Systems, 2017, pp. 483–498."},"title":"Forkscan: Conservative memory reclamation for modern operating systems","publist_id":"6867","author":[{"id":"4A899BFC-F248-11E8-B48F-1D18A9856A87","first_name":"Dan-Adrian","orcid":"0000-0003-3650-940X","full_name":"Alistarh, Dan-Adrian","last_name":"Alistarh"},{"first_name":"William","full_name":"Leiserson, William","last_name":"Leiserson"},{"last_name":"Matveev","full_name":"Matveev, Alexander","first_name":"Alexander"},{"full_name":"Shavit, Nir","last_name":"Shavit","first_name":"Nir"}],"article_processing_charge":"No"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2023-02-23T13:19:52Z","citation":{"ieee":"K. Kara, D.-A. Alistarh, G. Alonso, O. Mutlu, and C. Zhang, “FPGA-accelerated dense linear machine learning: A precision-convergence trade-off,” presented at the FCCM: Field-Programmable Custom Computing Machines, 2017, pp. 160–167.","short":"K. Kara, D.-A. Alistarh, G. Alonso, O. Mutlu, C. Zhang, in:, IEEE, 2017, pp. 160–167.","apa":"Kara, K., Alistarh, D.-A., Alonso, G., Mutlu, O., & Zhang, C. (2017). FPGA-accelerated dense linear machine learning: A precision-convergence trade-off (pp. 160–167). Presented at the FCCM: Field-Programmable Custom Computing Machines, IEEE. https://doi.org/10.1109/FCCM.2017.39","ama":"Kara K, Alistarh D-A, Alonso G, Mutlu O, Zhang C. FPGA-accelerated dense linear machine learning: A precision-convergence trade-off. In: IEEE; 2017:160-167. doi:10.1109/FCCM.2017.39","mla":"Kara, Kaan, et al. FPGA-Accelerated Dense Linear Machine Learning: A Precision-Convergence Trade-Off. IEEE, 2017, pp. 160–67, doi:10.1109/FCCM.2017.39.","ista":"Kara K, Alistarh D-A, Alonso G, Mutlu O, Zhang C. 2017. FPGA-accelerated dense linear machine learning: A precision-convergence trade-off. FCCM: Field-Programmable Custom Computing Machines, 160–167.","chicago":"Kara, Kaan, Dan-Adrian Alistarh, Gustavo Alonso, Onur Mutlu, and Ce Zhang. “FPGA-Accelerated Dense Linear Machine Learning: A Precision-Convergence Trade-Off,” 160–67. IEEE, 2017. https://doi.org/10.1109/FCCM.2017.39."},"title":"FPGA-accelerated dense linear machine learning: A precision-convergence trade-off","article_processing_charge":"No","author":[{"first_name":"Kaan","last_name":"Kara","full_name":"Kara, Kaan"},{"last_name":"Alistarh","full_name":"Alistarh, Dan-Adrian","orcid":"0000-0003-3650-940X","id":"4A899BFC-F248-11E8-B48F-1D18A9856A87","first_name":"Dan-Adrian"},{"first_name":"Gustavo","full_name":"Alonso, Gustavo","last_name":"Alonso"},{"full_name":"Mutlu, Onur","last_name":"Mutlu","first_name":"Onur"},{"full_name":"Zhang, Ce","last_name":"Zhang","first_name":"Ce"}],"publist_id":"6865","_id":"790","status":"public","conference":{"name":"FCCM: Field-Programmable Custom Computing Machines"},"type":"conference","language":[{"iso":"eng"}],"day":"30","publication_status":"published","year":"2017","date_created":"2018-12-11T11:48:31Z","doi":"10.1109/FCCM.2017.39","date_published":"2017-06-30T00:00:00Z","page":"160 - 167","oa_version":"None","abstract":[{"lang":"eng","text":"Stochastic gradient descent (SGD) is a commonly used algorithm for training linear machine learning models. Based on vector algebra, it benefits from the inherent parallelism available in an FPGA. In this paper, we first present a single-precision floating-point SGD implementation on an FPGA that provides similar performance as a 10-core CPU. We then adapt the design to make it capable of processing low-precision data. The low-precision data is obtained from a novel compression scheme - called stochastic quantization, specifically designed for machine learning applications. We test both full-precision and low-precision designs on various regression and classification data sets. We achieve up to an order of magnitude training speedup when using low-precision data compared to a full-precision SGD on the same FPGA and a state-of-the-art multi-core solution, while maintaining the quality of training. We open source the designs presented in this paper."}],"month":"06","publisher":"IEEE"},{"file_date_updated":"2020-07-14T12:48:06Z","department":[{"_id":"UlWa"}],"date_updated":"2022-03-18T12:58:53Z","ddc":["000"],"article_type":"original","type":"journal_article","status":"public","_id":"795","issue":"3","volume":24,"ec_funded":1,"publication_identifier":{"issn":["10778926"]},"publication_status":"published","file":[{"file_id":"5853","checksum":"ef320cff0f062051e858f929be6a3581","access_level":"open_access","relation":"main_file","content_type":"application/pdf","date_created":"2019-01-18T14:04:08Z","file_name":"2017_ElectrCombi_Fulek.pdf","creator":"dernst","date_updated":"2020-07-14T12:48:06Z","file_size":236944}],"language":[{"iso":"eng"}],"scopus_import":"1","month":"07","intvolume":" 24","abstract":[{"lang":"eng","text":"We introduce a common generalization of the strong Hanani–Tutte theorem and the weak Hanani–Tutte theorem: if a graph G has a drawing D in the plane where every pair of independent edges crosses an even number of times, then G has a planar drawing preserving the rotation of each vertex whose incident edges cross each other evenly in D. The theorem is implicit in the proof of the strong Hanani–Tutte theorem by Pelsmajer, Schaefer and Štefankovič. We give a new, somewhat simpler proof."}],"oa_version":"Published Version","author":[{"id":"39F3FFE4-F248-11E8-B48F-1D18A9856A87","first_name":"Radoslav","orcid":"0000-0001-8485-1774","full_name":"Fulek, Radoslav","last_name":"Fulek"},{"full_name":"Kynčl, Jan","last_name":"Kynčl","first_name":"Jan"},{"first_name":"Dömötör","full_name":"Pálvölgyi, Dömötör","last_name":"Pálvölgyi"}],"publist_id":"6859","article_processing_charge":"No","title":"Unified Hanani Tutte theorem","citation":{"chicago":"Fulek, Radoslav, Jan Kynčl, and Dömötör Pálvölgyi. “Unified Hanani Tutte Theorem.” Electronic Journal of Combinatorics. International Press, 2017. https://doi.org/10.37236/6663.","ista":"Fulek R, Kynčl J, Pálvölgyi D. 2017. Unified Hanani Tutte theorem. Electronic Journal of Combinatorics. 24(3), P3.18.","mla":"Fulek, Radoslav, et al. “Unified Hanani Tutte Theorem.” Electronic Journal of Combinatorics, vol. 24, no. 3, P3.18, International Press, 2017, doi:10.37236/6663.","ieee":"R. Fulek, J. Kynčl, and D. Pálvölgyi, “Unified Hanani Tutte theorem,” Electronic Journal of Combinatorics, vol. 24, no. 3. International Press, 2017.","short":"R. Fulek, J. Kynčl, D. Pálvölgyi, Electronic Journal of Combinatorics 24 (2017).","apa":"Fulek, R., Kynčl, J., & Pálvölgyi, D. (2017). Unified Hanani Tutte theorem. Electronic Journal of Combinatorics. International Press. https://doi.org/10.37236/6663","ama":"Fulek R, Kynčl J, Pálvölgyi D. Unified Hanani Tutte theorem. Electronic Journal of Combinatorics. 2017;24(3). doi:10.37236/6663"},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","project":[{"_id":"25681D80-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","grant_number":"291734","name":"International IST Postdoc Fellowship Programme"}],"article_number":"P3.18","date_published":"2017-07-28T00:00:00Z","doi":"10.37236/6663","date_created":"2018-12-11T11:48:32Z","has_accepted_license":"1","year":"2017","day":"28","publication":"Electronic Journal of Combinatorics","publisher":"International Press","quality_controlled":"1","oa":1},{"month":"12","intvolume":" 129","oa_version":"Published Version","abstract":[{"lang":"ger","text":"Aprotische Natrium‐O2‐Batterien basieren auf der reversiblen Bildung und Auflösung von Natriumsuperoxid (NaO2) während des Zellbetriebs. Nebenreaktionen des Elektrolyten und der Elektrode mit dem stark nukleophilen und basischen NaO2 führen zu mangelhafter Zyklenstabilität. Seine Reaktivität allein kann die Nebenreaktionen und schlechte Reversibilität jedoch nicht schlüssig erklären. Hier wird gezeigt, dass Singulett‐Sauerstoff (1O2) in allen Phasen des Betriebs entsteht und eine Hauptursache für Nebenreaktionen ist. 1O2 wurde in situ und ex situ mit einem 1O2‐Fänger detektiert, der schnell und selektiv ein Addukt mit 1O2 bildet. Mechanistisch betrachtet entsteht 1O2 entweder durch protonenunterstützte Disproportionierung von Superoxid während des Entladens, Lagerns und Ladens unter ca. 3.3 V oder durch direkte elektrochemische 1O2‐Entwicklung über ca. 3.3 V. Spuren von Wasser ermöglichen hohe Kapazitäten, beschleunigen aber auch Nebenreaktionen. Daher muss das hochreaktive 1O2 unbedingt kontrolliert werden, um die Zelle reversibel zu betreiben."}],"volume":129,"issue":"49","file":[{"file_id":"7987","checksum":"38f2c2383bc9573f6770c1dba72d7a9a","content_type":"application/pdf","access_level":"open_access","relation":"main_file","date_created":"2020-06-19T11:39:09Z","file_name":"2017_AngChemieDT_Schafzahl.pdf","date_updated":"2020-07-14T12:48:06Z","file_size":988125,"creator":"dernst"}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["0044-8249"]},"publication_status":"published","status":"public","article_type":"original","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by-nc/4.0/legalcode","image":"/images/cc_by_nc.png","name":"Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)","short":"CC BY-NC (4.0)"},"_id":"7981","file_date_updated":"2020-07-14T12:48:06Z","extern":"1","ddc":["540"],"date_updated":"2021-01-12T08:16:20Z","quality_controlled":"1","publisher":"Wiley","oa":1,"doi":"10.1002/ange.201709351","date_published":"2017-12-04T00:00:00Z","date_created":"2020-06-19T08:22:06Z","page":"15934-15938","day":"04","publication":"Angewandte Chemie","has_accepted_license":"1","year":"2017","title":"Singulett-Sauerstoff in der aprotischen Natrium-O2-Batterie","author":[{"last_name":"Schafzahl","full_name":"Schafzahl, Lukas","first_name":"Lukas"},{"full_name":"Mahne, Nika","last_name":"Mahne","first_name":"Nika"},{"full_name":"Schafzahl, Bettina","last_name":"Schafzahl","first_name":"Bettina"},{"full_name":"Wilkening, Martin","last_name":"Wilkening","first_name":"Martin"},{"first_name":"Christian","full_name":"Slugovc, Christian","last_name":"Slugovc"},{"full_name":"Borisov, Sergey M.","last_name":"Borisov","first_name":"Sergey M."},{"id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","first_name":"Stefan Alexander","orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger"}],"article_processing_charge":"No","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"apa":"Schafzahl, L., Mahne, N., Schafzahl, B., Wilkening, M., Slugovc, C., Borisov, S. M., & Freunberger, S. A. (2017). Singulett-Sauerstoff in der aprotischen Natrium-O2-Batterie. Angewandte Chemie. Wiley. https://doi.org/10.1002/ange.201709351","ama":"Schafzahl L, Mahne N, Schafzahl B, et al. Singulett-Sauerstoff in der aprotischen Natrium-O2-Batterie. Angewandte Chemie. 2017;129(49):15934-15938. doi:10.1002/ange.201709351","ieee":"L. Schafzahl et al., “Singulett-Sauerstoff in der aprotischen Natrium-O2-Batterie,” Angewandte Chemie, vol. 129, no. 49. Wiley, pp. 15934–15938, 2017.","short":"L. Schafzahl, N. Mahne, B. Schafzahl, M. Wilkening, C. Slugovc, S.M. Borisov, S.A. Freunberger, Angewandte Chemie 129 (2017) 15934–15938.","mla":"Schafzahl, Lukas, et al. “Singulett-Sauerstoff in Der Aprotischen Natrium-O2-Batterie.” Angewandte Chemie, vol. 129, no. 49, Wiley, 2017, pp. 15934–38, doi:10.1002/ange.201709351.","ista":"Schafzahl L, Mahne N, Schafzahl B, Wilkening M, Slugovc C, Borisov SM, Freunberger SA. 2017. Singulett-Sauerstoff in der aprotischen Natrium-O2-Batterie. Angewandte Chemie. 129(49), 15934–15938.","chicago":"Schafzahl, Lukas, Nika Mahne, Bettina Schafzahl, Martin Wilkening, Christian Slugovc, Sergey M. Borisov, and Stefan Alexander Freunberger. “Singulett-Sauerstoff in Der Aprotischen Natrium-O2-Batterie.” Angewandte Chemie. Wiley, 2017. https://doi.org/10.1002/ange.201709351."}},{"status":"public","type":"book_chapter","_id":"7980","file_date_updated":"2020-07-14T12:48:06Z","ddc":["540","541"],"extern":"1","date_updated":"2021-01-12T08:16:19Z","month":"03","alternative_title":["SpringerBriefs in Molecular Science"],"oa_version":"Submitted Version","abstract":[{"lang":"eng","text":"In this part, the use of polysaccharides, either directly through composite approaches, or by carbonization will be described. In many cases, materials are obtained which are competitive in terms of capacitance and cycle lifetime. In this part, the use of polysaccharides, either directly through composite approaches, or by carbonization will be described. In many cases, materials are obtained which are competitive in terms of capacitance and cycle lifetime. The following part will focus mainly on cellulosic composites with conductive polymers since cellulose is most abundant and therefore has attracted much more research interest in this field whereas in the second part also other polysaccharides, such as chitin, xylans, alginates, pectins, dextrans and caragenaans have been used in carbonization experiments."}],"language":[{"iso":"eng"}],"file":[{"file_id":"8048","checksum":"4182aeee32c9263a626a7e522f1934f5","content_type":"application/pdf","relation":"main_file","access_level":"open_access","file_name":"Final_EPNOE.pdf","date_created":"2020-06-29T14:13:44Z","file_size":3339826,"date_updated":"2020-07-14T12:48:06Z","creator":"sfreunbe"}],"publication_status":"published","publication_identifier":{"issn":["2191-5407","2191-5415"],"isbn":["9783319507538","9783319507545"]},"title":"Polysaccharides in supercapacitors","editor":[{"first_name":"Soon","last_name":"Yee Liew","full_name":"Yee Liew, Soon"},{"first_name":"Wim","full_name":"Thielemans, Wim","last_name":"Thielemans"},{"id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425","first_name":"Stefan Alexander","last_name":"Freunberger","full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319"},{"full_name":"Spirk, Stefan","last_name":"Spirk","first_name":"Stefan"}],"article_processing_charge":"No","author":[{"first_name":"Soon","full_name":"Yee Liew, Soon","last_name":"Yee Liew"},{"full_name":"Thielemans, Wim","last_name":"Thielemans","first_name":"Wim"},{"full_name":"Freunberger, Stefan Alexander","orcid":"0000-0003-2902-5319","last_name":"Freunberger","first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"},{"first_name":"Stefan","full_name":"Spirk, Stefan","last_name":"Spirk"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Yee Liew S, Thielemans W, Freunberger SA, Spirk S. 2017.Polysaccharides in supercapacitors. In: Polysaccharide Based Supercapacitors. SpringerBriefs in Molecular Science, , 15–53.","chicago":"Yee Liew, Soon, Wim Thielemans, Stefan Alexander Freunberger, and Stefan Spirk. “Polysaccharides in Supercapacitors.” In Polysaccharide Based Supercapacitors, edited by Soon Yee Liew, Wim Thielemans, Stefan Alexander Freunberger, and Stefan Spirk, 15–53. Springer Nature, 2017. https://doi.org/10.1007/978-3-319-50754-5_2.","short":"S. Yee Liew, W. Thielemans, S.A. Freunberger, S. Spirk, in:, S. Yee Liew, W. Thielemans, S.A. Freunberger, S. Spirk (Eds.), Polysaccharide Based Supercapacitors, Springer Nature, 2017, pp. 15–53.","ieee":"S. Yee Liew, W. Thielemans, S. A. Freunberger, and S. Spirk, “Polysaccharides in supercapacitors,” in Polysaccharide Based Supercapacitors, S. Yee Liew, W. Thielemans, S. A. Freunberger, and S. Spirk, Eds. Springer Nature, 2017, pp. 15–53.","apa":"Yee Liew, S., Thielemans, W., Freunberger, S. A., & Spirk, S. (2017). Polysaccharides in supercapacitors. In S. Yee Liew, W. Thielemans, S. A. Freunberger, & S. Spirk (Eds.), Polysaccharide Based Supercapacitors (pp. 15–53). Springer Nature. https://doi.org/10.1007/978-3-319-50754-5_2","ama":"Yee Liew S, Thielemans W, Freunberger SA, Spirk S. Polysaccharides in supercapacitors. In: Yee Liew S, Thielemans W, Freunberger SA, Spirk S, eds. Polysaccharide Based Supercapacitors. Springer Nature; 2017:15-53. doi:10.1007/978-3-319-50754-5_2","mla":"Yee Liew, Soon, et al. “Polysaccharides in Supercapacitors.” Polysaccharide Based Supercapacitors, edited by Soon Yee Liew et al., Springer Nature, 2017, pp. 15–53, doi:10.1007/978-3-319-50754-5_2."},"oa":1,"quality_controlled":"1","publisher":"Springer Nature","date_created":"2020-06-19T08:11:08Z","doi":"10.1007/978-3-319-50754-5_2","date_published":"2017-03-26T00:00:00Z","page":"15-53","publication":"Polysaccharide Based Supercapacitors","day":"26","year":"2017","has_accepted_license":"1"},{"file_date_updated":"2020-07-14T12:48:06Z","date_updated":"2021-01-12T08:16:20Z","ddc":["540","546","541"],"extern":"1","article_type":"original","type":"journal_article","status":"public","_id":"7982","volume":2,"issue":"7","publication_status":"published","publication_identifier":{"issn":["2058-7546"]},"language":[{"iso":"eng"}],"file":[{"relation":"main_file","access_level":"open_access","content_type":"application/pdf","checksum":"2564255b76f5346a32e764dbfd17fa2f","file_id":"8046","creator":"sfreunbe","file_size":817665,"date_updated":"2020-07-14T12:48:06Z","file_name":"NEnergy_Comment_final.pdf","date_created":"2020-06-29T13:26:55Z"}],"main_file_link":[{"url":"https://arxiv.org/abs/2002.00712","open_access":"1"}],"intvolume":" 2","month":"06","abstract":[{"text":"Beyond-intercalation batteries promise a step-change in energy storage compared to intercalation-based lithium-ion and sodium-ion batteries. However, only performance metrics that include all cell components and operation parameters can tell whether a true advance over intercalation batteries has been achieved.","lang":"eng"}],"oa_version":"Submitted Version","article_processing_charge":"No","external_id":{"arxiv":["2002.00712"]},"author":[{"orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger","first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"}],"title":"True performance metrics in beyond-intercalation batteries","citation":{"mla":"Freunberger, Stefan Alexander. “True Performance Metrics in Beyond-Intercalation Batteries.” Nature Energy, vol. 2, no. 7, 17091, Springer Nature, 2017, doi:10.1038/nenergy.2017.91.","apa":"Freunberger, S. A. (2017). True performance metrics in beyond-intercalation batteries. Nature Energy. Springer Nature. https://doi.org/10.1038/nenergy.2017.91","ama":"Freunberger SA. True performance metrics in beyond-intercalation batteries. Nature Energy. 2017;2(7). doi:10.1038/nenergy.2017.91","ieee":"S. A. Freunberger, “True performance metrics in beyond-intercalation batteries,” Nature Energy, vol. 2, no. 7. Springer Nature, 2017.","short":"S.A. Freunberger, Nature Energy 2 (2017).","chicago":"Freunberger, Stefan Alexander. “True Performance Metrics in Beyond-Intercalation Batteries.” Nature Energy. Springer Nature, 2017. https://doi.org/10.1038/nenergy.2017.91.","ista":"Freunberger SA. 2017. True performance metrics in beyond-intercalation batteries. Nature Energy. 2(7), 17091."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_number":"17091","date_created":"2020-06-19T08:23:47Z","doi":"10.1038/nenergy.2017.91","date_published":"2017-06-05T00:00:00Z","year":"2017","has_accepted_license":"1","publication":"Nature Energy","day":"05","oa":1,"quality_controlled":"1","publisher":"Springer Nature"},{"year":"2017","day":"20","publication":"Nature Energy","doi":"10.1038/nenergy.2017.36","date_published":"2017-03-20T00:00:00Z","date_created":"2020-06-19T10:42:33Z","quality_controlled":"1","publisher":"Springer Nature","oa":1,"citation":{"ama":"Mahne N, Schafzahl B, Leypold C, et al. Singlet oxygen generation as a major cause for parasitic reactions during cycling of aprotic lithium–oxygen batteries. Nature Energy. 2017;2(5). doi:10.1038/nenergy.2017.36","apa":"Mahne, N., Schafzahl, B., Leypold, C., Leypold, M., Grumm, S., Leitgeb, A., … Freunberger, S. A. (2017). Singlet oxygen generation as a major cause for parasitic reactions during cycling of aprotic lithium–oxygen batteries. Nature Energy. Springer Nature. https://doi.org/10.1038/nenergy.2017.36","ieee":"N. Mahne et al., “Singlet oxygen generation as a major cause for parasitic reactions during cycling of aprotic lithium–oxygen batteries,” Nature Energy, vol. 2, no. 5. Springer Nature, 2017.","short":"N. Mahne, B. Schafzahl, C. Leypold, M. Leypold, S. Grumm, A. Leitgeb, G.A. Strohmeier, M. Wilkening, O. Fontaine, D. Kramer, C. Slugovc, S.M. Borisov, S.A. Freunberger, Nature Energy 2 (2017).","mla":"Mahne, Nika, et al. “Singlet Oxygen Generation as a Major Cause for Parasitic Reactions during Cycling of Aprotic Lithium–Oxygen Batteries.” Nature Energy, vol. 2, no. 5, 17036, Springer Nature, 2017, doi:10.1038/nenergy.2017.36.","ista":"Mahne N, Schafzahl B, Leypold C, Leypold M, Grumm S, Leitgeb A, Strohmeier GA, Wilkening M, Fontaine O, Kramer D, Slugovc C, Borisov SM, Freunberger SA. 2017. Singlet oxygen generation as a major cause for parasitic reactions during cycling of aprotic lithium–oxygen batteries. Nature Energy. 2(5), 17036.","chicago":"Mahne, Nika, Bettina Schafzahl, Christian Leypold, Mario Leypold, Sandra Grumm, Anita Leitgeb, Gernot A. Strohmeier, et al. “Singlet Oxygen Generation as a Major Cause for Parasitic Reactions during Cycling of Aprotic Lithium–Oxygen Batteries.” Nature Energy. Springer Nature, 2017. https://doi.org/10.1038/nenergy.2017.36."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"last_name":"Mahne","full_name":"Mahne, Nika","first_name":"Nika"},{"first_name":"Bettina","last_name":"Schafzahl","full_name":"Schafzahl, Bettina"},{"full_name":"Leypold, Christian","last_name":"Leypold","first_name":"Christian"},{"first_name":"Mario","full_name":"Leypold, Mario","last_name":"Leypold"},{"first_name":"Sandra","full_name":"Grumm, Sandra","last_name":"Grumm"},{"first_name":"Anita","full_name":"Leitgeb, Anita","last_name":"Leitgeb"},{"full_name":"Strohmeier, Gernot A.","last_name":"Strohmeier","first_name":"Gernot A."},{"first_name":"Martin","full_name":"Wilkening, Martin","last_name":"Wilkening"},{"first_name":"Olivier","full_name":"Fontaine, Olivier","last_name":"Fontaine"},{"last_name":"Kramer","full_name":"Kramer, Denis","first_name":"Denis"},{"last_name":"Slugovc","full_name":"Slugovc, Christian","first_name":"Christian"},{"first_name":"Sergey M.","last_name":"Borisov","full_name":"Borisov, Sergey M."},{"orcid":"0000-0003-2902-5319","full_name":"Freunberger, Stefan Alexander","last_name":"Freunberger","first_name":"Stefan Alexander","id":"A8CA28E6-CE23-11E9-AD2D-EC27E6697425"}],"article_processing_charge":"No","external_id":{"arxiv":["1711.10340"]},"title":"Singlet oxygen generation as a major cause for parasitic reactions during cycling of aprotic lithium–oxygen batteries","article_number":"17036 ","publication_identifier":{"issn":["2058-7546"]},"publication_status":"published","language":[{"iso":"eng"}],"volume":2,"issue":"5","oa_version":"Preprint","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1711.10340"}],"month":"03","intvolume":" 2","date_updated":"2021-01-12T08:16:21Z","extern":"1","_id":"7986","type":"journal_article","article_type":"original","status":"public"},{"publication_status":"published","year":"2017","language":[{"iso":"eng"}],"publication":"Physik in unserer Zeit","day":"01","page":"111 - 113","date_created":"2018-12-11T11:48:33Z","issue":"3","doi":"10.1002/piuz.201770305","volume":48,"date_published":"2017-05-01T00:00:00Z","abstract":[{"text":"Phasenübergänge helfen beim Verständnis von Vielteilchensystemen in der Festkörperphysik und Fluiddynamik bis hin zur Teilchenphysik. Unserer internationalen Kollaboration ist es gelungen, einen neuartigen Phasenübergang in einem Quantensystem zu beobachten [1]. In einem Mikrowellenresonator konnte erstmals die spontane Zustandsänderung von undurchsichtig zu transparent nachgewiesen werden.","lang":"ger"}],"oa_version":"None","quality_controlled":"1","publisher":"Wiley","intvolume":" 48","month":"05","citation":{"ista":"Fink JM. 2017. Photonenblockade aufgelöst. Physik in unserer Zeit. 48(3), 111–113.","chicago":"Fink, Johannes M. “Photonenblockade Aufgelöst.” Physik in Unserer Zeit. Wiley, 2017. https://doi.org/10.1002/piuz.201770305.","apa":"Fink, J. M. (2017). Photonenblockade aufgelöst. Physik in Unserer Zeit. Wiley. https://doi.org/10.1002/piuz.201770305","ama":"Fink JM. Photonenblockade aufgelöst. Physik in unserer Zeit. 2017;48(3):111-113. doi:10.1002/piuz.201770305","short":"J.M. Fink, Physik in Unserer Zeit 48 (2017) 111–113.","ieee":"J. M. Fink, “Photonenblockade aufgelöst,” Physik in unserer Zeit, vol. 48, no. 3. Wiley, pp. 111–113, 2017.","mla":"Fink, Johannes M. “Photonenblockade Aufgelöst.” Physik in Unserer Zeit, vol. 48, no. 3, Wiley, 2017, pp. 111–13, doi:10.1002/piuz.201770305."},"date_updated":"2022-03-24T09:16:20Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_processing_charge":"No","publist_id":"6856","author":[{"last_name":"Fink","orcid":"0000-0001-8112-028X","full_name":"Fink, Johannes M","id":"4B591CBA-F248-11E8-B48F-1D18A9856A87","first_name":"Johannes M"}],"department":[{"_id":"JoFi"}],"title":"Photonenblockade aufgelöst","_id":"797","type":"journal_article","article_type":"original","status":"public"},{"tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"type":"journal_article","article_type":"original","status":"public","_id":"8016","file_date_updated":"2020-07-14T12:48:08Z","date_updated":"2021-01-12T08:16:32Z","ddc":["570"],"extern":"1","intvolume":" 96","month":"09","abstract":[{"lang":"eng","text":"Long-term modifications of neuronal connections are critical for reliable memory storage in the brain. However, their locus of expression—pre- or postsynaptic—is highly variable. Here we introduce a theoretical framework in which long-term plasticity performs an optimization of the postsynaptic response statistics toward a given mean with minimal variance. Consequently, the state of the synapse at the time of plasticity induction determines the ratio of pre- and postsynaptic modifications. Our theory explains the experimentally observed expression loci of the hippocampal and neocortical synaptic potentiation studies we examined. Moreover, the theory predicts presynaptic expression of long-term depression, consistent with experimental observations. At inhibitory synapses, the theory suggests a statistically efficient excitatory-inhibitory balance in which changes in inhibitory postsynaptic response statistics specifically target the mean excitation. Our results provide a unifying theory for understanding the expression mechanisms and functions of long-term synaptic transmission plasticity."}],"oa_version":"Published Version","pmid":1,"issue":"1","volume":96,"publication_status":"published","publication_identifier":{"issn":["0896-6273"]},"language":[{"iso":"eng"}],"file":[{"checksum":"49fbca2821066c0965bd5678b32b6b48","file_id":"8103","content_type":"application/pdf","relation":"main_file","access_level":"open_access","file_name":"2017_Neuron_Costa.pdf","date_created":"2020-07-09T09:42:49Z","file_size":7140149,"date_updated":"2020-07-14T12:48:08Z","creator":"cziletti"}],"article_processing_charge":"No","external_id":{"pmid":["28957667"]},"author":[{"last_name":"Costa","full_name":"Costa, Rui Ponte","first_name":"Rui Ponte"},{"first_name":"Zahid","last_name":"Padamsey","full_name":"Padamsey, Zahid"},{"first_name":"James A.","last_name":"D’Amour","full_name":"D’Amour, James A."},{"full_name":"Emptage, Nigel J.","last_name":"Emptage","first_name":"Nigel J."},{"full_name":"Froemke, Robert C.","last_name":"Froemke","first_name":"Robert C."},{"full_name":"Vogels, Tim P","orcid":"0000-0003-3295-6181","last_name":"Vogels","first_name":"Tim P","id":"CB6FF8D2-008F-11EA-8E08-2637E6697425"}],"title":"Synaptic transmission optimization predicts expression loci of long-term plasticity","citation":{"chicago":"Costa, Rui Ponte, Zahid Padamsey, James A. D’Amour, Nigel J. Emptage, Robert C. Froemke, and Tim P Vogels. “Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity.” Neuron. Elsevier, 2017. https://doi.org/10.1016/j.neuron.2017.09.021.","ista":"Costa RP, Padamsey Z, D’Amour JA, Emptage NJ, Froemke RC, Vogels TP. 2017. Synaptic transmission optimization predicts expression loci of long-term plasticity. Neuron. 96(1), 177–189.e7.","mla":"Costa, Rui Ponte, et al. “Synaptic Transmission Optimization Predicts Expression Loci of Long-Term Plasticity.” Neuron, vol. 96, no. 1, Elsevier, 2017, p. 177–189.e7, doi:10.1016/j.neuron.2017.09.021.","short":"R.P. Costa, Z. Padamsey, J.A. D’Amour, N.J. Emptage, R.C. Froemke, T.P. Vogels, Neuron 96 (2017) 177–189.e7.","ieee":"R. P. Costa, Z. Padamsey, J. A. D’Amour, N. J. Emptage, R. C. Froemke, and T. P. Vogels, “Synaptic transmission optimization predicts expression loci of long-term plasticity,” Neuron, vol. 96, no. 1. Elsevier, p. 177–189.e7, 2017.","apa":"Costa, R. P., Padamsey, Z., D’Amour, J. A., Emptage, N. J., Froemke, R. C., & Vogels, T. P. (2017). Synaptic transmission optimization predicts expression loci of long-term plasticity. Neuron. Elsevier. https://doi.org/10.1016/j.neuron.2017.09.021","ama":"Costa RP, Padamsey Z, D’Amour JA, Emptage NJ, Froemke RC, Vogels TP. Synaptic transmission optimization predicts expression loci of long-term plasticity. Neuron. 2017;96(1):177-189.e7. doi:10.1016/j.neuron.2017.09.021"},"user_id":"D865714E-FA4E-11E9-B85B-F5C5E5697425","oa":1,"quality_controlled":"1","publisher":"Elsevier","page":"177-189.e7","date_created":"2020-06-25T12:54:46Z","date_published":"2017-09-27T00:00:00Z","doi":"10.1016/j.neuron.2017.09.021","year":"2017","has_accepted_license":"1","publication":"Neuron","day":"27"},{"author":[{"last_name":"Barron","full_name":"Barron, Helen C.","first_name":"Helen C."},{"id":"CB6FF8D2-008F-11EA-8E08-2637E6697425","first_name":"Tim P","last_name":"Vogels","full_name":"Vogels, Tim P","orcid":"0000-0003-3295-6181"},{"first_name":"Timothy E.","full_name":"Behrens, Timothy E.","last_name":"Behrens"},{"first_name":"Mani","full_name":"Ramaswami, Mani","last_name":"Ramaswami"}],"article_processing_charge":"No","external_id":{"pmid":["28611219"]},"title":"Inhibitory engrams in perception and memory","citation":{"ista":"Barron HC, Vogels TP, Behrens TE, Ramaswami M. 2017. Inhibitory engrams in perception and memory. Proceedings of the National Academy of Sciences. 114(26), 6666–6674.","chicago":"Barron, Helen C., Tim P Vogels, Timothy E. Behrens, and Mani Ramaswami. “Inhibitory Engrams in Perception and Memory.” Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1701812114.","short":"H.C. Barron, T.P. Vogels, T.E. Behrens, M. Ramaswami, Proceedings of the National Academy of Sciences 114 (2017) 6666–6674.","ieee":"H. C. Barron, T. P. Vogels, T. E. Behrens, and M. Ramaswami, “Inhibitory engrams in perception and memory,” Proceedings of the National Academy of Sciences, vol. 114, no. 26. Proceedings of the National Academy of Sciences, pp. 6666–6674, 2017.","ama":"Barron HC, Vogels TP, Behrens TE, Ramaswami M. Inhibitory engrams in perception and memory. Proceedings of the National Academy of Sciences. 2017;114(26):6666-6674. doi:10.1073/pnas.1701812114","apa":"Barron, H. C., Vogels, T. P., Behrens, T. E., & Ramaswami, M. (2017). Inhibitory engrams in perception and memory. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1701812114","mla":"Barron, Helen C., et al. “Inhibitory Engrams in Perception and Memory.” Proceedings of the National Academy of Sciences, vol. 114, no. 26, Proceedings of the National Academy of Sciences, 2017, pp. 6666–74, doi:10.1073/pnas.1701812114."},"user_id":"D865714E-FA4E-11E9-B85B-F5C5E5697425","quality_controlled":"1","publisher":"Proceedings of the National Academy of Sciences","oa":1,"page":"6666-6674","date_published":"2017-06-27T00:00:00Z","doi":"10.1073/pnas.1701812114","date_created":"2020-06-25T12:56:58Z","year":"2017","day":"27","publication":"Proceedings of the National Academy of Sciences","article_type":"original","type":"journal_article","status":"public","_id":"8018","date_updated":"2021-01-12T08:16:33Z","extern":"1","main_file_link":[{"url":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5495250/","open_access":"1"}],"month":"06","intvolume":" 114","abstract":[{"lang":"eng","text":"Nervous systems use excitatory cell assemblies to encode and represent sensory percepts. Similarly, synaptically connected cell assemblies or \"engrams\" are thought to represent memories of past experience. Multiple lines of recent evidence indicate that brain systems create and use inhibitory replicas of excitatory representations for important cognitive functions. Such matched \"inhibitory engrams\" can form through homeostatic potentiation of inhibition onto postsynaptic cells that show increased levels of excitation. Inhibitory engrams can reduce behavioral responses to familiar stimuli, thereby resulting in behavioral habituation. In addition, by preventing inappropriate activation of excitatory memory engrams, inhibitory engrams can make memories quiescent, stored in a latent form that is available for context-relevant activation. In neural networks with balanced excitatory and inhibitory engrams, the release of innate responses and recall of associative memories can occur through focused disinhibition. Understanding mechanisms that regulate the formation and expression of inhibitory engrams in vivo may help not only to explain key features of cognition but also to provide insight into transdiagnostic traits associated with psychiatric conditions such as autism, schizophrenia, and posttraumatic stress disorder. "}],"pmid":1,"oa_version":"Published Version","volume":114,"issue":"26","publication_identifier":{"issn":["0027-8424"],"eissn":["1091-6490"]},"publication_status":"published","language":[{"iso":"eng"}]},{"citation":{"short":"T.P. Vogels, L.C. Griffith, Current Opinion in Neurobiology 43 (2017) A1–A5.","ieee":"T. P. Vogels and L. C. Griffith, “Editorial overview: Neurobiology of learning and plasticity 2017,” Current Opinion in Neurobiology, vol. 43. Elsevier, pp. A1–A5, 2017.","ama":"Vogels TP, Griffith LC. Editorial overview: Neurobiology of learning and plasticity 2017. Current Opinion in Neurobiology. 2017;43:A1-A5. doi:10.1016/j.conb.2017.04.002","apa":"Vogels, T. P., & Griffith, L. C. (2017). Editorial overview: Neurobiology of learning and plasticity 2017. Current Opinion in Neurobiology. Elsevier. https://doi.org/10.1016/j.conb.2017.04.002","mla":"Vogels, Tim P., and Leslie C. Griffith. “Editorial Overview: Neurobiology of Learning and Plasticity 2017.” Current Opinion in Neurobiology, vol. 43, Elsevier, 2017, pp. A1–5, doi:10.1016/j.conb.2017.04.002.","ista":"Vogels TP, Griffith LC. 2017. Editorial overview: Neurobiology of learning and plasticity 2017. Current Opinion in Neurobiology. 43, A1–A5.","chicago":"Vogels, Tim P, and Leslie C Griffith. “Editorial Overview: Neurobiology of Learning and Plasticity 2017.” Current Opinion in Neurobiology. Elsevier, 2017. https://doi.org/10.1016/j.conb.2017.04.002."},"date_updated":"2021-01-12T08:16:33Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","external_id":{"pmid":["28427877"]},"article_processing_charge":"No","author":[{"id":"CB6FF8D2-008F-11EA-8E08-2637E6697425","first_name":"Tim P","last_name":"Vogels","full_name":"Vogels, Tim P","orcid":"0000-0003-3295-6181"},{"last_name":"Griffith","full_name":"Griffith, Leslie C","first_name":"Leslie C"}],"title":"Editorial overview: Neurobiology of learning and plasticity 2017","_id":"8019","type":"journal_article","article_type":"letter_note","status":"public","publication_status":"published","year":"2017","publication_identifier":{"issn":["0959-4388"]},"language":[{"iso":"eng"}],"publication":"Current Opinion in Neurobiology","day":"17","page":"A1-A5","date_created":"2020-06-25T13:03:30Z","date_published":"2017-04-17T00:00:00Z","doi":"10.1016/j.conb.2017.04.002","volume":43,"abstract":[{"text":"Synaptic plasticity is essential for the function of neural systems. It sets up initial circuitry and adjusts connection strengths according to the maintenance requirements of its host networks. Like all things biological, synaptic plasticity must rely on genetic programs to provide the molecular components of its machinery to integrate ongoing, often multi-sensory experience without destabilising effects. Because of its fundamental importance to healthy behaviour, understanding plasticity is thought to hold the key to understanding the brain. There are innumerable ways to approach this topic and a complete review of its status quo would be impossible. In the current issue we dig into some of the finer points of synaptic plasticity, starting small, at the level of genes, and slowly zooming out to synapses, populations of synapses, and finally entire systems and brain regions. At each level, we tried to represent different perspectives, different systems, and approaches to the same questions to give a broad sampling of how synaptic plasticity is being studied.","lang":"eng"}],"pmid":1,"oa_version":"None","quality_controlled":"1","publisher":"Elsevier","intvolume":" 43","month":"04"},{"status":"public","type":"journal_article","article_type":"original","_id":"8017","extern":"1","date_updated":"2021-01-12T08:16:32Z","intvolume":" 40","month":"07","oa_version":"None","pmid":1,"abstract":[{"lang":"eng","text":"nhibitory neurons, although relatively few in number, exert powerful control over brain circuits. They stabilize network activity in the face of strong feedback excitation and actively engage in computations. Recent studies reveal the importance of a precise balance of excitation and inhibition in neural circuits, which often requires exquisite fine-tuning of inhibitory connections. We review inhibitory synaptic plasticity and its roles in shaping both feedforward and feedback control. We discuss the necessity of complex, codependent plasticity mechanisms to build nontrivial, functioning networks, and we end by summarizing experimental evidence of such interactions."}],"issue":"1","volume":40,"language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["0147-006X","1545-4126"]},"title":"Inhibitory plasticity: Balance, control, and codependence","external_id":{"pmid":["28598717"]},"article_processing_charge":"No","author":[{"last_name":"Hennequin","full_name":"Hennequin, Guillaume","first_name":"Guillaume"},{"first_name":"Everton J.","last_name":"Agnes","full_name":"Agnes, Everton J."},{"first_name":"Tim P","id":"CB6FF8D2-008F-11EA-8E08-2637E6697425","orcid":"0000-0003-3295-6181","full_name":"Vogels, Tim P","last_name":"Vogels"}],"user_id":"D865714E-FA4E-11E9-B85B-F5C5E5697425","citation":{"mla":"Hennequin, Guillaume, et al. “Inhibitory Plasticity: Balance, Control, and Codependence.” Annual Review of Neuroscience, vol. 40, no. 1, Annual Reviews, 2017, pp. 557–79, doi:10.1146/annurev-neuro-072116-031005.","apa":"Hennequin, G., Agnes, E. J., & Vogels, T. P. (2017). Inhibitory plasticity: Balance, control, and codependence. Annual Review of Neuroscience. Annual Reviews. https://doi.org/10.1146/annurev-neuro-072116-031005","ama":"Hennequin G, Agnes EJ, Vogels TP. Inhibitory plasticity: Balance, control, and codependence. Annual Review of Neuroscience. 2017;40(1):557-579. doi:10.1146/annurev-neuro-072116-031005","ieee":"G. Hennequin, E. J. Agnes, and T. P. Vogels, “Inhibitory plasticity: Balance, control, and codependence,” Annual Review of Neuroscience, vol. 40, no. 1. Annual Reviews, pp. 557–579, 2017.","short":"G. Hennequin, E.J. Agnes, T.P. Vogels, Annual Review of Neuroscience 40 (2017) 557–579.","chicago":"Hennequin, Guillaume, Everton J. Agnes, and Tim P Vogels. “Inhibitory Plasticity: Balance, Control, and Codependence.” Annual Review of Neuroscience. Annual Reviews, 2017. https://doi.org/10.1146/annurev-neuro-072116-031005.","ista":"Hennequin G, Agnes EJ, Vogels TP. 2017. Inhibitory plasticity: Balance, control, and codependence. Annual Review of Neuroscience. 40(1), 557–579."},"publisher":"Annual Reviews","quality_controlled":"1","date_created":"2020-06-25T12:55:53Z","doi":"10.1146/annurev-neuro-072116-031005","date_published":"2017-07-01T00:00:00Z","page":"557-579","publication":"Annual Review of Neuroscience","day":"01","year":"2017"},{"article_number":"e22152","user_id":"D865714E-FA4E-11E9-B85B-F5C5E5697425","citation":{"mla":"Podlaski, William F., et al. “Mapping the Function of Neuronal Ion Channels in Model and Experiment.” ELife, vol. 6, e22152, eLife Sciences Publications, Ltd, 2017, doi:10.7554/elife.22152.","ama":"Podlaski WF, Seeholzer A, Groschner LN, Miesenböck G, Ranjan R, Vogels TP. Mapping the function of neuronal ion channels in model and experiment. eLife. 2017;6. doi:10.7554/elife.22152","apa":"Podlaski, W. F., Seeholzer, A., Groschner, L. N., Miesenböck, G., Ranjan, R., & Vogels, T. P. (2017). Mapping the function of neuronal ion channels in model and experiment. ELife. eLife Sciences Publications, Ltd. https://doi.org/10.7554/elife.22152","ieee":"W. F. Podlaski, A. Seeholzer, L. N. Groschner, G. Miesenböck, R. Ranjan, and T. P. Vogels, “Mapping the function of neuronal ion channels in model and experiment,” eLife, vol. 6. eLife Sciences Publications, Ltd, 2017.","short":"W.F. Podlaski, A. Seeholzer, L.N. Groschner, G. Miesenböck, R. Ranjan, T.P. Vogels, ELife 6 (2017).","chicago":"Podlaski, William F, Alexander Seeholzer, Lukas N Groschner, Gero Miesenböck, Rajnish Ranjan, and Tim P Vogels. “Mapping the Function of Neuronal Ion Channels in Model and Experiment.” ELife. eLife Sciences Publications, Ltd, 2017. https://doi.org/10.7554/elife.22152.","ista":"Podlaski WF, Seeholzer A, Groschner LN, Miesenböck G, Ranjan R, Vogels TP. 2017. Mapping the function of neuronal ion channels in model and experiment. eLife. 6, e22152."},"title":"Mapping the function of neuronal ion channels in model and experiment","author":[{"first_name":"William F","full_name":"Podlaski, William F","last_name":"Podlaski"},{"first_name":"Alexander","last_name":"Seeholzer","full_name":"Seeholzer, Alexander"},{"first_name":"Lukas N","full_name":"Groschner, Lukas N","last_name":"Groschner"},{"first_name":"Gero","full_name":"Miesenböck, Gero","last_name":"Miesenböck"},{"first_name":"Rajnish","last_name":"Ranjan","full_name":"Ranjan, Rajnish"},{"first_name":"Tim P","id":"CB6FF8D2-008F-11EA-8E08-2637E6697425","orcid":"0000-0003-3295-6181","full_name":"Vogels, Tim P","last_name":"Vogels"}],"article_processing_charge":"No","external_id":{"pmid":["28267430"]},"quality_controlled":"1","publisher":"eLife Sciences Publications, Ltd","oa":1,"day":"06","publication":"eLife","has_accepted_license":"1","year":"2017","date_published":"2017-03-06T00:00:00Z","doi":"10.7554/elife.22152","date_created":"2020-06-30T13:32:18Z","_id":"8075","status":"public","article_type":"original","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"extern":"1","ddc":["570"],"date_updated":"2021-01-12T08:16:46Z","file_date_updated":"2020-07-16T12:08:40Z","oa_version":"Published Version","pmid":1,"abstract":[{"lang":"eng","text":"Ion channel models are the building blocks of computational neuron models. Their biological fidelity is therefore crucial for the interpretation of simulations. However, the number of published models, and the lack of standardization, make the comparison of ion channel models with one another and with experimental data difficult. Here, we present a framework for the automated large-scale classification of ion channel models. Using annotated metadata and responses to a set of voltage-clamp protocols, we assigned 2378 models of voltage- and calcium-gated ion channels coded in NEURON to 211 clusters. The IonChannelGenealogy (ICGenealogy) web interface provides an interactive resource for the categorization of new and existing models and experimental recordings. It enables quantitative comparisons of simulated and/or measured ion channel kinetics, and facilitates field-wide standardization of experimentally-constrained modeling."}],"month":"03","intvolume":" 6","file":[{"relation":"main_file","access_level":"open_access","content_type":"application/pdf","success":1,"file_id":"8124","checksum":"e5c5a33bcb3ac38ad62df1010ab29040","creator":"cziletti","file_size":16034505,"date_updated":"2020-07-16T12:08:40Z","file_name":"2017_elife_Podlaski.pdf","date_created":"2020-07-16T12:08:40Z"}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["2050-084X"]},"publication_status":"published","volume":6},{"department":[{"_id":"E-Lib"}],"file_date_updated":"2020-07-14T12:48:09Z","ddc":["020"],"date_updated":"2021-01-12T08:16:45Z","status":"public","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"type":"journal_article","_id":"807","issue":"2","volume":70,"language":[{"iso":"eng"}],"file":[{"checksum":"558c18bcf5580d87dd371ec626d52075","file_id":"5851","content_type":"application/pdf","relation":"main_file","access_level":"open_access","file_name":"2017_VOEB_Andrae.pdf","date_created":"2019-01-18T13:39:26Z","file_size":125065,"date_updated":"2020-07-14T12:48:09Z","creator":"dernst"}],"publication_status":"published","publication_identifier":{"issn":["10222588"]},"intvolume":" 70","month":"08","scopus_import":1,"oa_version":"Published Version","abstract":[{"lang":"eng","text":"On January the 1st, 2016 a new agreement between 32 Austrian scientific libraries and the publisher Springer took its effect: this deal covers accessing the licensed content on the one hand, and publishing open access on the other hand. More than 1000 papers by Austrian authors were published open access at Springer in the first year alone. The working group "Springer Compact Evaluierung" made the data for these articles available via the platform OpenAPC and would like to use this opportunity to give a short account of what this publishing agreement actually entails and the working group intends to do."}],"title":"Der Springer Compact-Deal – Ein erster Einblick in die Evaluierung einer Offsetting-Vereinbarung","author":[{"first_name":"Magdalena","last_name":"Andrae","full_name":"Andrae, Magdalena"},{"orcid":"0000-0001-8126-0426","full_name":"Villányi, Márton","last_name":"Villányi","id":"3FFCCD3A-F248-11E8-B48F-1D18A9856A87","first_name":"Márton"}],"publist_id":"6843","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"ieee":"M. Andrae and M. Villányi, “Der Springer Compact-Deal – Ein erster Einblick in die Evaluierung einer Offsetting-Vereinbarung,” Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen und Bibliothekare, vol. 70, no. 2. VÖB, pp. 274–280, 2017.","short":"M. Andrae, M. Villányi, Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen Und Bibliothekare 70 (2017) 274–280.","apa":"Andrae, M., & Villányi, M. (2017). Der Springer Compact-Deal – Ein erster Einblick in die Evaluierung einer Offsetting-Vereinbarung. Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen Und Bibliothekare. VÖB. https://doi.org/10.31263/voebm.v70i2.1898","ama":"Andrae M, Villányi M. Der Springer Compact-Deal – Ein erster Einblick in die Evaluierung einer Offsetting-Vereinbarung. Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen und Bibliothekare. 2017;70(2):274-280. doi:10.31263/voebm.v70i2.1898","mla":"Andrae, Magdalena, and Márton Villányi. “Der Springer Compact-Deal – Ein Erster Einblick in Die Evaluierung Einer Offsetting-Vereinbarung.” Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen Und Bibliothekare, vol. 70, no. 2, VÖB, 2017, pp. 274–80, doi:10.31263/voebm.v70i2.1898.","ista":"Andrae M, Villányi M. 2017. Der Springer Compact-Deal – Ein erster Einblick in die Evaluierung einer Offsetting-Vereinbarung. Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen und Bibliothekare. 70(2), 274–280.","chicago":"Andrae, Magdalena, and Márton Villányi. “Der Springer Compact-Deal – Ein Erster Einblick in Die Evaluierung Einer Offsetting-Vereinbarung.” Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen Und Bibliothekare. VÖB, 2017. https://doi.org/10.31263/voebm.v70i2.1898."},"date_created":"2018-12-11T11:48:36Z","doi":"10.31263/voebm.v70i2.1898","date_published":"2017-08-01T00:00:00Z","page":"274 - 280","publication":"Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen und Bibliothekare","day":"01","year":"2017","popular_science":"1","has_accepted_license":"1","oa":1,"publisher":"VÖB"},{"month":"12","intvolume":" 30","publisher":"Neural Information Processing Systems Foundation","quality_controlled":"1","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1711.02448"}],"oa":1,"oa_version":"Preprint","abstract":[{"lang":"eng","text":"Cortical circuits exhibit intricate recurrent architectures that are remarkably similar across different brain areas. Such stereotyped structure suggests the existence of common computational principles. However, such principles have remained largely elusive. Inspired by gated-memory networks, namely long short-term memory networks (LSTMs), we introduce a recurrent neural network in which information is gated through inhibitory cells that are subtractive (subLSTM). We propose a natural mapping of subLSTMs onto known canonical excitatory-inhibitory cortical microcircuits. Our empirical evaluation across sequential image classification and language modelling tasks shows that subLSTM units can achieve similar performance to LSTM units. These results suggest that cortical circuits can be optimised to solve complex contextual problems and proposes a novel view on their computational function.\r\nOverall our work provides a step towards unifying recurrent networks as used in machine learning with their biological counterparts."}],"volume":30,"date_published":"2017-12-01T00:00:00Z","date_created":"2020-07-16T19:13:10Z","page":"272-283","day":"01","publication":"Advances in Neural Information Processing Systems","language":[{"iso":"eng"}],"publication_identifier":{"issn":["10495258"]},"publication_status":"published","year":"2017","status":"public","type":"conference","conference":{"name":"NIPS: Neural Information Processing System","start_date":"2017-12-04","location":"Long Beach, CA, United States","end_date":"2017-12-09"},"_id":"8129","title":"Cortical microcircuits as gated-recurrent neural networks","author":[{"first_name":"Rui Ponte","last_name":"Costa","full_name":"Costa, Rui Ponte"},{"last_name":"Assael","full_name":"Assael, Yannis M.","first_name":"Yannis M."},{"last_name":"Shillingford","full_name":"Shillingford, Brendan","first_name":"Brendan"},{"first_name":"Nando de","full_name":"Freitas, Nando de","last_name":"Freitas"},{"last_name":"Vogels","full_name":"Vogels, Tim P","orcid":"0000-0003-3295-6181","first_name":"Tim P","id":"CB6FF8D2-008F-11EA-8E08-2637E6697425"}],"article_processing_charge":"No","external_id":{"arxiv":["1711.02448"]},"extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_updated":"2021-01-12T08:17:03Z","citation":{"ista":"Costa RP, Assael YM, Shillingford B, Freitas N de, Vogels TP. 2017. Cortical microcircuits as gated-recurrent neural networks. Advances in Neural Information Processing Systems. NIPS: Neural Information Processing System vol. 30, 272–283.","chicago":"Costa, Rui Ponte, Yannis M. Assael, Brendan Shillingford, Nando de Freitas, and Tim P Vogels. “Cortical Microcircuits as Gated-Recurrent Neural Networks.” In Advances in Neural Information Processing Systems, 30:272–83. Neural Information Processing Systems Foundation, 2017.","ama":"Costa RP, Assael YM, Shillingford B, Freitas N de, Vogels TP. Cortical microcircuits as gated-recurrent neural networks. In: Advances in Neural Information Processing Systems. Vol 30. Neural Information Processing Systems Foundation; 2017:272-283.","apa":"Costa, R. P., Assael, Y. M., Shillingford, B., Freitas, N. de, & Vogels, T. P. (2017). Cortical microcircuits as gated-recurrent neural networks. In Advances in Neural Information Processing Systems (Vol. 30, pp. 272–283). Long Beach, CA, United States: Neural Information Processing Systems Foundation.","short":"R.P. Costa, Y.M. Assael, B. Shillingford, N. de Freitas, T.P. Vogels, in:, Advances in Neural Information Processing Systems, Neural Information Processing Systems Foundation, 2017, pp. 272–283.","ieee":"R. P. Costa, Y. M. Assael, B. Shillingford, N. de Freitas, and T. P. Vogels, “Cortical microcircuits as gated-recurrent neural networks,” in Advances in Neural Information Processing Systems, Long Beach, CA, United States, 2017, vol. 30, pp. 272–283.","mla":"Costa, Rui Ponte, et al. “Cortical Microcircuits as Gated-Recurrent Neural Networks.” Advances in Neural Information Processing Systems, vol. 30, Neural Information Processing Systems Foundation, 2017, pp. 272–83."}},{"tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"type":"journal_article","status":"public","_id":"817","file_date_updated":"2020-07-14T12:48:09Z","date_updated":"2021-01-12T08:17:16Z","ddc":["570"],"extern":"1","intvolume":" 199","month":"09","abstract":[{"text":"Cryo-electron tomography (cryo-ET) allows cellular ultrastructures and macromolecular complexes to be imaged in three-dimensions in their native environments. Cryo-electron tomograms are reconstructed from projection images taken at defined tilt-angles. In order to recover high-resolution information from cryo-electron tomograms, it is necessary to measure and correct for the contrast transfer function (CTF) of the microscope. Most commonly, this is performed using protocols that approximate the sample as a two-dimensional (2D) plane. This approximation accounts for differences in defocus and therefore CTF across the tilted sample. It does not account for differences in defocus of objects at different heights within the sample; instead, a 3D approach is required. Currently available approaches for 3D-CTF correction are computationally expensive and have not been widely implemented. Here we simulate the benefits of 3D-CTF correction for high-resolution subtomogram averaging, and present a user-friendly, computationally-efficient 3D-CTF correction tool, NovaCTF, that is compatible with standard tomogram reconstruction workflows in IMOD. We validate the approach on synthetic data and test it using subtomogram averaging of real data. Consistent with our simulations, we find that 3D-CTF correction allows high-resolution structures to be obtained with much smaller subtomogram averaging datasets than are required using 2D-CTF. We also show that using equivalent dataset sizes, 3D-CTF correction can be used to obtain higher-resolution structures. We present a 3.4. Å resolution structure determined by subtomogram averaging.","lang":"eng"}],"oa_version":"Published Version","volume":199,"issue":"3","publication_status":"published","language":[{"iso":"eng"}],"file":[{"file_name":"2017_Elsevier_Turonova.pdf","date_created":"2019-03-22T09:29:44Z","creator":"kschuh","file_size":1310009,"date_updated":"2020-07-14T12:48:09Z","checksum":"7f2d4bbac767f9acc254d1a4114d181a","file_id":"6168","relation":"main_file","access_level":"open_access","content_type":"application/pdf"}],"author":[{"first_name":"Beata","full_name":"Turoňová, Beata","last_name":"Turoňová"},{"last_name":"Schur","orcid":"0000-0003-4790-8078","full_name":"Schur, Florian","first_name":"Florian","id":"48AD8942-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Wan","full_name":"Wan, William","first_name":"William"},{"first_name":"John","last_name":"Briggs","full_name":"Briggs, John"}],"publist_id":"6832","title":"Efficient 3D-CTF correction for cryo-electron tomography using NovaCTF improves subtomogram averaging resolution to 3.4Å","citation":{"apa":"Turoňová, B., Schur, F. K., Wan, W., & Briggs, J. (2017). Efficient 3D-CTF correction for cryo-electron tomography using NovaCTF improves subtomogram averaging resolution to 3.4Å. Journal of Structural Biology. Academic Press. https://doi.org/10.1016/j.jsb.2017.07.007","ama":"Turoňová B, Schur FK, Wan W, Briggs J. Efficient 3D-CTF correction for cryo-electron tomography using NovaCTF improves subtomogram averaging resolution to 3.4Å. Journal of Structural Biology. 2017;199(3):187-195. doi:10.1016/j.jsb.2017.07.007","short":"B. Turoňová, F.K. Schur, W. Wan, J. Briggs, Journal of Structural Biology 199 (2017) 187–195.","ieee":"B. Turoňová, F. K. Schur, W. Wan, and J. Briggs, “Efficient 3D-CTF correction for cryo-electron tomography using NovaCTF improves subtomogram averaging resolution to 3.4Å,” Journal of Structural Biology, vol. 199, no. 3. Academic Press, pp. 187–195, 2017.","mla":"Turoňová, Beata, et al. “Efficient 3D-CTF Correction for Cryo-Electron Tomography Using NovaCTF Improves Subtomogram Averaging Resolution to 3.4Å.” Journal of Structural Biology, vol. 199, no. 3, Academic Press, 2017, pp. 187–95, doi:10.1016/j.jsb.2017.07.007.","ista":"Turoňová B, Schur FK, Wan W, Briggs J. 2017. Efficient 3D-CTF correction for cryo-electron tomography using NovaCTF improves subtomogram averaging resolution to 3.4Å. Journal of Structural Biology. 199(3), 187–195.","chicago":"Turoňová, Beata, Florian KM Schur, William Wan, and John Briggs. “Efficient 3D-CTF Correction for Cryo-Electron Tomography Using NovaCTF Improves Subtomogram Averaging Resolution to 3.4Å.” Journal of Structural Biology. Academic Press, 2017. https://doi.org/10.1016/j.jsb.2017.07.007."},"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","oa":1,"quality_controlled":"1","publisher":"Academic Press","page":"187-195","date_created":"2018-12-11T11:48:40Z","date_published":"2017-09-01T00:00:00Z","doi":"10.1016/j.jsb.2017.07.007","year":"2017","has_accepted_license":"1","publication":"Journal of Structural Biology","day":"01"},{"_id":"8237","article_number":"1112","article_type":"original","type":"journal_article","status":"public","citation":{"chicago":"Ilieva, Kristina M., Judit Singer, Daniela Y. Achkova, Tihomir S. Dodev, Silvia Mele, Silvia Crescioli, Heather J. Bax, et al. “Functionally Active Fc Mutant Antibodies Recognizing Cancer Antigens Generated Rapidly at High Yields.” Frontiers in Immunology. Frontiers, 2017. https://doi.org/10.3389/fimmu.2017.01112.","ista":"Ilieva KM, Singer J, Achkova DY, Dodev TS, Mele S, Crescioli S, Bax HJ, Cheung A, Karagiannis P, Correa I, Figini M, Marlow R, Josephs DH, Beavil AJ, Maher J, Spicer JF, Jensen-Jarolim E, Tutt AN, Karagiannis SN. 2017. Functionally active Fc mutant antibodies recognizing cancer antigens generated rapidly at high yields. Frontiers in Immunology. 8, 1112.","mla":"Ilieva, Kristina M., et al. “Functionally Active Fc Mutant Antibodies Recognizing Cancer Antigens Generated Rapidly at High Yields.” Frontiers in Immunology, vol. 8, 1112, Frontiers, 2017, doi:10.3389/fimmu.2017.01112.","ieee":"K. M. Ilieva et al., “Functionally active Fc mutant antibodies recognizing cancer antigens generated rapidly at high yields,” Frontiers in Immunology, vol. 8. Frontiers, 2017.","short":"K.M. Ilieva, J. Singer, D.Y. Achkova, T.S. Dodev, S. Mele, S. Crescioli, H.J. Bax, A. Cheung, P. Karagiannis, I. Correa, M. Figini, R. Marlow, D.H. Josephs, A.J. Beavil, J. Maher, J.F. Spicer, E. Jensen-Jarolim, A.N. Tutt, S.N. Karagiannis, Frontiers in Immunology 8 (2017).","apa":"Ilieva, K. M., Singer, J., Achkova, D. Y., Dodev, T. S., Mele, S., Crescioli, S., … Karagiannis, S. N. (2017). Functionally active Fc mutant antibodies recognizing cancer antigens generated rapidly at high yields. Frontiers in Immunology. Frontiers. https://doi.org/10.3389/fimmu.2017.01112","ama":"Ilieva KM, Singer J, Achkova DY, et al. Functionally active Fc mutant antibodies recognizing cancer antigens generated rapidly at high yields. Frontiers in Immunology. 2017;8. doi:10.3389/fimmu.2017.01112"},"date_updated":"2021-01-12T08:17:39Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"full_name":"Ilieva, Kristina M.","last_name":"Ilieva","first_name":"Kristina M."},{"full_name":"Fazekas-Singer, Judit","orcid":"0000-0002-8777-3502","last_name":"Fazekas-Singer","first_name":"Judit","id":"36432834-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Achkova","full_name":"Achkova, Daniela Y.","first_name":"Daniela Y."},{"first_name":"Tihomir S.","full_name":"Dodev, Tihomir S.","last_name":"Dodev"},{"last_name":"Mele","full_name":"Mele, Silvia","first_name":"Silvia"},{"first_name":"Silvia","full_name":"Crescioli, Silvia","last_name":"Crescioli"},{"first_name":"Heather J.","full_name":"Bax, Heather J.","last_name":"Bax"},{"full_name":"Cheung, Anthony","last_name":"Cheung","first_name":"Anthony"},{"first_name":"Panagiotis","full_name":"Karagiannis, Panagiotis","last_name":"Karagiannis"},{"full_name":"Correa, Isabel","last_name":"Correa","first_name":"Isabel"},{"first_name":"Mariangela","last_name":"Figini","full_name":"Figini, Mariangela"},{"full_name":"Marlow, Rebecca","last_name":"Marlow","first_name":"Rebecca"},{"last_name":"Josephs","full_name":"Josephs, Debra H.","first_name":"Debra H."},{"last_name":"Beavil","full_name":"Beavil, Andrew J.","first_name":"Andrew J."},{"full_name":"Maher, John","last_name":"Maher","first_name":"John"},{"full_name":"Spicer, James F.","last_name":"Spicer","first_name":"James F."},{"full_name":"Jensen-Jarolim, Erika","last_name":"Jensen-Jarolim","first_name":"Erika"},{"full_name":"Tutt, Andrew N.","last_name":"Tutt","first_name":"Andrew N."},{"first_name":"Sophia N.","full_name":"Karagiannis, Sophia N.","last_name":"Karagiannis"}],"article_processing_charge":"No","title":"Functionally active Fc mutant antibodies recognizing cancer antigens generated rapidly at high yields","abstract":[{"lang":"eng","text":"Monoclonal antibodies find broad application as therapy for various types of cancer by employing multiple mechanisms of action against tumors. Manipulating the Fc-mediated functions of antibodies that engage immune effector cells, such as NK cells, represents a strategy to influence effector cell activation and to enhance antibody potency and potentially efficacy. We developed a novel approach to generate and ascertain the functional attributes of Fc mutant monoclonal antibodies. This entailed coupling single expression vector (pVitro1) antibody cloning, using polymerase incomplete primer extension (PIPE) polymerase chain reaction, together with simultaneous Fc region point mutagenesis and high yield transient expression in human mammalian cells. Employing this, we engineered wild type, low (N297Q, NQ), and high (S239D/I332E, DE) FcR-binding Fc mutant monoclonal antibody panels recognizing two cancer antigens, HER2/neu and chondroitin sulfate proteoglycan 4. Antibodies were generated with universal mutagenic primers applicable to any IgG1 pVitro1 constructs, with high mutagenesis and transfection efficiency, in small culture volumes, at high yields and within 12 days from design to purified material. Antibody variants conserved their Fab-mediated recognition of target antigens and their direct anti-proliferative effects against cancer cells. Fc mutations had a significant impact on antibody interactions with Fc receptors (FcRs) on human NK cells, and consequently on the potency of NK cell activation, quantified by immune complex-mediated calcium mobilization and by antibody-dependent cellular cytotoxicity (ADCC) of tumor cells. This strategy for manipulation and testing of Fc region engagement with cognate FcRs can facilitate the design of antibodies with defined effector functions and potentially enhanced efficacy against tumor cells."}],"oa_version":"Published Version","quality_controlled":"1","publisher":"Frontiers","main_file_link":[{"url":"https://doi.org/10.3389/fimmu.2017.01112","open_access":"1"}],"oa":1,"month":"09","intvolume":" 8","publication_identifier":{"issn":["1664-3224"]},"publication_status":"published","year":"2017","day":"11","language":[{"iso":"eng"}],"publication":"Frontiers in Immunology","date_published":"2017-09-11T00:00:00Z","volume":8,"doi":"10.3389/fimmu.2017.01112","date_created":"2020-08-10T11:53:32Z"},{"volume":72,"issue":"6","publication_status":"published","publication_identifier":{"issn":["0105-4538"]},"language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1111/all.13119","open_access":"1"}],"intvolume":" 72","month":"06","abstract":[{"text":"Th2 immunity and allergic immune surveillance play critical roles in host responses to pathogens, parasites and allergens. Numerous studies have reported significant links between Th2 responses and cancer, including insights into the functions of IgE antibodies and associated effector cells in both antitumour immune surveillance and therapy. The interdisciplinary field of AllergoOncology was given Task Force status by the European Academy of Allergy and Clinical Immunology in 2014. Affiliated expert groups focus on the interface between allergic responses and cancer, applied to immune surveillance, immunomodulation and the functions of IgE‐mediated immune responses against cancer, to derive novel insights into more effective treatments. Coincident with rapid expansion in clinical application of cancer immunotherapies, here we review the current state‐of‐the‐art and future translational opportunities, as well as challenges in this relatively new field. Recent developments include improved understanding of Th2 antibodies, intratumoral innate allergy effector cells and mediators, IgE‐mediated tumour antigen cross‐presentation by dendritic cells, as well as immunotherapeutic strategies such as vaccines and recombinant antibodies, and finally, the management of allergy in daily clinical oncology. Shedding light on the crosstalk between allergic response and cancer is paving the way for new avenues of treatment.","lang":"eng"}],"oa_version":"Published Version","date_updated":"2021-01-12T08:17:39Z","extern":"1","type":"journal_article","article_type":"original","status":"public","_id":"8236","page":"866-887","date_created":"2020-08-10T11:53:26Z","doi":"10.1111/all.13119","date_published":"2017-06-01T00:00:00Z","year":"2017","publication":"Allergy","day":"01","oa":1,"quality_controlled":"1","publisher":"Wiley","article_processing_charge":"No","author":[{"first_name":"E.","last_name":"Jensen-Jarolim","orcid":"0000-0003-4019-5765","full_name":"Jensen-Jarolim, E."},{"last_name":"Bax","full_name":"Bax, H. J.","first_name":"H. J."},{"first_name":"R.","full_name":"Bianchini, R.","last_name":"Bianchini"},{"first_name":"M.","last_name":"Capron","full_name":"Capron, M."},{"last_name":"Corrigan","full_name":"Corrigan, C.","first_name":"C."},{"full_name":"Castells, M.","last_name":"Castells","first_name":"M."},{"full_name":"Dombrowicz, D.","last_name":"Dombrowicz","first_name":"D."},{"first_name":"T. R.","last_name":"Daniels-Wells","full_name":"Daniels-Wells, T. R."},{"orcid":"0000-0002-8777-3502","full_name":"Fazekas, Judit","last_name":"Fazekas","id":"36432834-F248-11E8-B48F-1D18A9856A87","first_name":"Judit"},{"last_name":"Fiebiger","full_name":"Fiebiger, E.","first_name":"E."},{"first_name":"S.","last_name":"Gatault","full_name":"Gatault, S."},{"last_name":"Gould","full_name":"Gould, H. J.","first_name":"H. J."},{"full_name":"Janda, J.","last_name":"Janda","first_name":"J."},{"first_name":"D. H.","full_name":"Josephs, D. H.","last_name":"Josephs"},{"first_name":"P.","last_name":"Karagiannis","full_name":"Karagiannis, P."},{"first_name":"F.","last_name":"Levi-Schaffer","full_name":"Levi-Schaffer, F."},{"full_name":"Meshcheryakova, A.","last_name":"Meshcheryakova","first_name":"A."},{"last_name":"Mechtcheriakova","full_name":"Mechtcheriakova, D.","first_name":"D."},{"full_name":"Mekori, Y.","last_name":"Mekori","first_name":"Y."},{"first_name":"F.","full_name":"Mungenast, F.","last_name":"Mungenast"},{"first_name":"E. A.","last_name":"Nigro","full_name":"Nigro, E. A."},{"last_name":"Penichet","full_name":"Penichet, M. L.","first_name":"M. L."},{"first_name":"F.","full_name":"Redegeld, F.","last_name":"Redegeld"},{"full_name":"Saul, L.","last_name":"Saul","first_name":"L."},{"first_name":"J.","full_name":"Singer, J.","last_name":"Singer"},{"first_name":"J. F.","full_name":"Spicer, J. F.","last_name":"Spicer"},{"first_name":"A. G.","full_name":"Siccardi, A. G.","last_name":"Siccardi"},{"first_name":"E.","full_name":"Spillner, E.","last_name":"Spillner"},{"last_name":"Turner","full_name":"Turner, M. C.","first_name":"M. C."},{"full_name":"Untersmayr, E.","last_name":"Untersmayr","first_name":"E."},{"first_name":"L.","full_name":"Vangelista, L.","last_name":"Vangelista"},{"first_name":"S. N.","full_name":"Karagiannis, S. N.","last_name":"Karagiannis"}],"title":"AllergoOncology - the impact of allergy in oncology: EAACI position paper","citation":{"mla":"Jensen-Jarolim, E., et al. “AllergoOncology - the Impact of Allergy in Oncology: EAACI Position Paper.” Allergy, vol. 72, no. 6, Wiley, 2017, pp. 866–87, doi:10.1111/all.13119.","ama":"Jensen-Jarolim E, Bax HJ, Bianchini R, et al. AllergoOncology - the impact of allergy in oncology: EAACI position paper. Allergy. 2017;72(6):866-887. doi:10.1111/all.13119","apa":"Jensen-Jarolim, E., Bax, H. J., Bianchini, R., Capron, M., Corrigan, C., Castells, M., … Karagiannis, S. N. (2017). AllergoOncology - the impact of allergy in oncology: EAACI position paper. Allergy. Wiley. https://doi.org/10.1111/all.13119","ieee":"E. Jensen-Jarolim et al., “AllergoOncology - the impact of allergy in oncology: EAACI position paper,” Allergy, vol. 72, no. 6. Wiley, pp. 866–887, 2017.","short":"E. Jensen-Jarolim, H.J. Bax, R. Bianchini, M. Capron, C. Corrigan, M. Castells, D. Dombrowicz, T.R. Daniels-Wells, J. Singer, E. Fiebiger, S. Gatault, H.J. Gould, J. Janda, D.H. Josephs, P. Karagiannis, F. Levi-Schaffer, A. Meshcheryakova, D. Mechtcheriakova, Y. Mekori, F. Mungenast, E.A. Nigro, M.L. Penichet, F. Redegeld, L. Saul, J. Singer, J.F. Spicer, A.G. Siccardi, E. Spillner, M.C. Turner, E. Untersmayr, L. Vangelista, S.N. Karagiannis, Allergy 72 (2017) 866–887.","chicago":"Jensen-Jarolim, E., H. J. Bax, R. Bianchini, M. Capron, C. Corrigan, M. Castells, D. Dombrowicz, et al. “AllergoOncology - the Impact of Allergy in Oncology: EAACI Position Paper.” Allergy. Wiley, 2017. https://doi.org/10.1111/all.13119.","ista":"Jensen-Jarolim E, Bax HJ, Bianchini R, Capron M, Corrigan C, Castells M, Dombrowicz D, Daniels-Wells TR, Singer J, Fiebiger E, Gatault S, Gould HJ, Janda J, Josephs DH, Karagiannis P, Levi-Schaffer F, Meshcheryakova A, Mechtcheriakova D, Mekori Y, Mungenast F, Nigro EA, Penichet ML, Redegeld F, Saul L, Singer J, Spicer JF, Siccardi AG, Spillner E, Turner MC, Untersmayr E, Vangelista L, Karagiannis SN. 2017. AllergoOncology - the impact of allergy in oncology: EAACI position paper. Allergy. 72(6), 866–887."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"date_published":"2017-03-23T00:00:00Z","doi":"10.1038/srep45067","volume":7,"date_created":"2020-08-10T11:53:46Z","day":"23","publication":"Scientific Reports","language":[{"iso":"eng"}],"publication_identifier":{"issn":["2045-2322"]},"year":"2017","publication_status":"published","month":"03","intvolume":" 7","publisher":"Springer Nature","quality_controlled":"1","oa":1,"main_file_link":[{"url":"https://doi.org/10.1038/srep45067","open_access":"1"}],"oa_version":"Published Version","abstract":[{"text":"Acrolein, a highly reactive unsaturated aldehyde, is generated in large amounts during smoking and is best known for its genotoxic capacity. Here, we aimed to assess whether acrolein at concentrations relevant for smokers may also exert immunomodulatory effects that could be relevant in allergy or cancer. In a BALB/c allergy model repeated nasal exposure to acrolein abrogated allergen-specific antibody and cytokine formation, and led to a relative accumulation of regulatory T cells in the lungs. Only the acrolein-treated mice were protected from bronchial hyperreactivity as well as from anaphylactic reactions upon challenge with the specific allergen. Moreover, grafted D2F2 tumor cells grew faster and intratumoral Foxp3+ cell accumulation was observed in these mice compared to sham-treated controls. Results from reporter cell lines suggested that acrolein acts via the aryl-hydrocarbon receptor which could be inhibited by resveratrol and 3′-methoxy-4′-nitroflavone Acrolein- stimulation of human PBMCs increased Foxp3+ expression by T cells which could be antagonized by resveratrol. Our mouse and human data thus revealed that acrolein exerts systemic immunosuppression by promoting Foxp3+ regulatory cells. This provides a novel explanation why smokers have a lower allergy, but higher cancer risk.","lang":"eng"}],"title":"Janus-faced Acrolein prevents allergy but accelerates tumor growth by promoting immunoregulatory Foxp3+ cells: Mouse model for passive respiratory exposure","author":[{"first_name":"Franziska","full_name":"Roth-Walter, Franziska","last_name":"Roth-Walter"},{"first_name":"Cornelia","last_name":"Bergmayr","full_name":"Bergmayr, Cornelia"},{"first_name":"Sarah","last_name":"Meitz","full_name":"Meitz, Sarah"},{"last_name":"Buchleitner","full_name":"Buchleitner, Stefan","first_name":"Stefan"},{"full_name":"Stremnitzer, Caroline","last_name":"Stremnitzer","first_name":"Caroline"},{"first_name":"Judit","id":"36432834-F248-11E8-B48F-1D18A9856A87","last_name":"Fazekas","orcid":"0000-0002-8777-3502","full_name":"Fazekas, Judit"},{"full_name":"Moskovskich, Anna","last_name":"Moskovskich","first_name":"Anna"},{"first_name":"Mario A.","last_name":"Müller","full_name":"Müller, Mario A."},{"full_name":"Roth, Georg A.","last_name":"Roth","first_name":"Georg A."},{"last_name":"Manzano-Szalai","full_name":"Manzano-Szalai, Krisztina","first_name":"Krisztina"},{"last_name":"Dvorak","full_name":"Dvorak, Zdenek","first_name":"Zdenek"},{"first_name":"Alina","full_name":"Neunkirchner, Alina","last_name":"Neunkirchner"},{"full_name":"Jensen-Jarolim, Erika","last_name":"Jensen-Jarolim","first_name":"Erika"}],"article_processing_charge":"No","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Roth-Walter, Franziska, Cornelia Bergmayr, Sarah Meitz, Stefan Buchleitner, Caroline Stremnitzer, Judit Singer, Anna Moskovskich, et al. “Janus-Faced Acrolein Prevents Allergy but Accelerates Tumor Growth by Promoting Immunoregulatory Foxp3+ Cells: Mouse Model for Passive Respiratory Exposure.” Scientific Reports. Springer Nature, 2017. https://doi.org/10.1038/srep45067.","ista":"Roth-Walter F, Bergmayr C, Meitz S, Buchleitner S, Stremnitzer C, Singer J, Moskovskich A, Müller MA, Roth GA, Manzano-Szalai K, Dvorak Z, Neunkirchner A, Jensen-Jarolim E. 2017. Janus-faced Acrolein prevents allergy but accelerates tumor growth by promoting immunoregulatory Foxp3+ cells: Mouse model for passive respiratory exposure. Scientific Reports. 7, 45067.","mla":"Roth-Walter, Franziska, et al. “Janus-Faced Acrolein Prevents Allergy but Accelerates Tumor Growth by Promoting Immunoregulatory Foxp3+ Cells: Mouse Model for Passive Respiratory Exposure.” Scientific Reports, vol. 7, 45067, Springer Nature, 2017, doi:10.1038/srep45067.","ieee":"F. Roth-Walter et al., “Janus-faced Acrolein prevents allergy but accelerates tumor growth by promoting immunoregulatory Foxp3+ cells: Mouse model for passive respiratory exposure,” Scientific Reports, vol. 7. Springer Nature, 2017.","short":"F. Roth-Walter, C. Bergmayr, S. Meitz, S. Buchleitner, C. Stremnitzer, J. Singer, A. Moskovskich, M.A. Müller, G.A. Roth, K. Manzano-Szalai, Z. Dvorak, A. Neunkirchner, E. Jensen-Jarolim, Scientific Reports 7 (2017).","apa":"Roth-Walter, F., Bergmayr, C., Meitz, S., Buchleitner, S., Stremnitzer, C., Singer, J., … Jensen-Jarolim, E. (2017). Janus-faced Acrolein prevents allergy but accelerates tumor growth by promoting immunoregulatory Foxp3+ cells: Mouse model for passive respiratory exposure. Scientific Reports. Springer Nature. https://doi.org/10.1038/srep45067","ama":"Roth-Walter F, Bergmayr C, Meitz S, et al. Janus-faced Acrolein prevents allergy but accelerates tumor growth by promoting immunoregulatory Foxp3+ cells: Mouse model for passive respiratory exposure. Scientific Reports. 2017;7. doi:10.1038/srep45067"},"date_updated":"2021-01-12T08:17:40Z","status":"public","article_type":"original","type":"journal_article","article_number":"45067","_id":"8239"},{"abstract":[{"lang":"eng","text":"Background/Aim: Cancer cell lines are indispensible surrogate models in cancer research, as they can be used off-the-shelf, expanded to the desired extent, easily modified and exchanged between research groups for affirmation, reproduction or follow-up experiments.\r\nAs malignant cells are prone to genomic instability, phenotypical changes may occur after certain passages in culture. Thus, cell lines have to be regularly authenticated to ensure data quality. In between experiments these cell lines are often stored in liquid nitrogen for extended time periods.\r\nAlthough freezing of cells is a necessary evil, little research is performed on how long-term storage affects cancer cell lines. Therefore, this study investigated the effects of a 28-year long liquid nitrogen storage period on BT474 cells with regard to phenotypical changes, differences in cell-surface receptor expression as well as cytokine and gene expressional variations.\r\nMethods: Two batches of BT474 cells, one frozen in 1986, the other directly purchased from ATCC were investigated by light microscopy, cell growth analysis, flow cytometry and cytokine as well as whole-transcriptome expression profiling.\r\nResults: The cell lines were morphologically indifferent and showed similar growth rates and similar cell-surface receptor expression. Transcriptome analysis revealed significant differences in only 26 of 40,716 investigated RefSeq transcripts with 4 of them being up-regulated and 22 down-regulated.\r\nConclusion: This study demonstrates that even after very long periods of storage in liquid nitrogen, cancer cell lines display only minimal changes in their gene expression profiles. However, also such minor changes should be carefully assessed before continuation of experiments, especially if phenotypic alterations can be additionally observed."}],"oa_version":"Published Version","oa":1,"main_file_link":[{"open_access":"1","url":"https://doi.org/10.18632/oncotarget.16623"}],"publisher":"Impact Journals","quality_controlled":"1","intvolume":" 8","month":"03","year":"2017","publication_status":"published","publication_identifier":{"issn":["1949-2553"]},"language":[{"iso":"eng"}],"publication":"Oncotarget","day":"28","page":"35076-35087","date_created":"2020-08-10T11:53:53Z","date_published":"2017-03-28T00:00:00Z","volume":8,"doi":"10.18632/oncotarget.16623","_id":"8240","article_type":"original","type":"journal_article","status":"public","citation":{"apa":"Singer, J., Grunt, T. W., Jensen-Jarolim, E., & Singer, J. (2017). Long term storage in liquid nitrogen leads to only minor phenotypic and gene expression changes in the mammary carcinoma model cell line BT474. Oncotarget. Impact Journals. https://doi.org/10.18632/oncotarget.16623","ama":"Singer J, Grunt TW, Jensen-Jarolim E, Singer J. Long term storage in liquid nitrogen leads to only minor phenotypic and gene expression changes in the mammary carcinoma model cell line BT474. Oncotarget. 2017;8:35076-35087. doi:10.18632/oncotarget.16623","ieee":"J. Singer, T. W. Grunt, E. Jensen-Jarolim, and J. Singer, “Long term storage in liquid nitrogen leads to only minor phenotypic and gene expression changes in the mammary carcinoma model cell line BT474,” Oncotarget, vol. 8. Impact Journals, pp. 35076–35087, 2017.","short":"J. Singer, T.W. Grunt, E. Jensen-Jarolim, J. Singer, Oncotarget 8 (2017) 35076–35087.","mla":"Singer, Judit, et al. “Long Term Storage in Liquid Nitrogen Leads to Only Minor Phenotypic and Gene Expression Changes in the Mammary Carcinoma Model Cell Line BT474.” Oncotarget, vol. 8, Impact Journals, 2017, pp. 35076–87, doi:10.18632/oncotarget.16623.","ista":"Singer J, Grunt TW, Jensen-Jarolim E, Singer J. 2017. Long term storage in liquid nitrogen leads to only minor phenotypic and gene expression changes in the mammary carcinoma model cell line BT474. Oncotarget. 8, 35076–35087.","chicago":"Singer, Judit, Thomas W. Grunt, Erika Jensen-Jarolim, and Josef Singer. “Long Term Storage in Liquid Nitrogen Leads to Only Minor Phenotypic and Gene Expression Changes in the Mammary Carcinoma Model Cell Line BT474.” Oncotarget. Impact Journals, 2017. https://doi.org/10.18632/oncotarget.16623."},"date_updated":"2021-01-12T08:17:41Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","article_processing_charge":"No","author":[{"orcid":"0000-0002-8777-3502","full_name":"Fazekas, Judit","last_name":"Fazekas","first_name":"Judit","id":"36432834-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Thomas W.","full_name":"Grunt, Thomas W.","last_name":"Grunt"},{"first_name":"Erika","full_name":"Jensen-Jarolim, Erika","last_name":"Jensen-Jarolim"},{"full_name":"Singer, Josef","last_name":"Singer","first_name":"Josef"}],"title":"Long term storage in liquid nitrogen leads to only minor phenotypic and gene expression changes in the mammary carcinoma model cell line BT474"},{"status":"public","article_type":"original","type":"journal_article","_id":"8235","title":"Development of a radiolabeled caninized anti-EGFR antibody for comparative oncology trials","author":[{"full_name":"Fazekas-Singer, Judit","orcid":"0000-0002-8777-3502","last_name":"Fazekas-Singer","id":"36432834-F248-11E8-B48F-1D18A9856A87","first_name":"Judit"},{"last_name":"Berroterán-Infante","full_name":"Berroterán-Infante, Neydher","first_name":"Neydher"},{"first_name":"Christina","last_name":"Rami-Mark","full_name":"Rami-Mark, Christina"},{"first_name":"Monika","full_name":"Dumanic, Monika","last_name":"Dumanic"},{"last_name":"Matz","full_name":"Matz, Miroslawa","first_name":"Miroslawa"},{"full_name":"Willmann, Michael","last_name":"Willmann","first_name":"Michael"},{"first_name":"Fritz","full_name":"Andreae, Fritz","last_name":"Andreae"},{"full_name":"Singer, Josef","last_name":"Singer","first_name":"Josef"},{"first_name":"Wolfgang","full_name":"Wadsak, Wolfgang","last_name":"Wadsak"},{"first_name":"Markus","full_name":"Mitterhauser, Markus","last_name":"Mitterhauser"},{"last_name":"Jensen-Jarolim","full_name":"Jensen-Jarolim, Erika","first_name":"Erika"}],"article_processing_charge":"No","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Singer, Judit, Neydher Berroterán-Infante, Christina Rami-Mark, Monika Dumanic, Miroslawa Matz, Michael Willmann, Fritz Andreae, et al. “Development of a Radiolabeled Caninized Anti-EGFR Antibody for Comparative Oncology Trials.” Oncotarget. Impact Journals, 2017. https://doi.org/10.18632/oncotarget.20914.","ista":"Singer J, Berroterán-Infante N, Rami-Mark C, Dumanic M, Matz M, Willmann M, Andreae F, Singer J, Wadsak W, Mitterhauser M, Jensen-Jarolim E. 2017. Development of a radiolabeled caninized anti-EGFR antibody for comparative oncology trials. Oncotarget. 8, 83128–83141.","mla":"Singer, Judit, et al. “Development of a Radiolabeled Caninized Anti-EGFR Antibody for Comparative Oncology Trials.” Oncotarget, vol. 8, Impact Journals, 2017, pp. 83128–41, doi:10.18632/oncotarget.20914.","short":"J. Singer, N. Berroterán-Infante, C. Rami-Mark, M. Dumanic, M. Matz, M. Willmann, F. Andreae, J. Singer, W. Wadsak, M. Mitterhauser, E. Jensen-Jarolim, Oncotarget 8 (2017) 83128–83141.","ieee":"J. Singer et al., “Development of a radiolabeled caninized anti-EGFR antibody for comparative oncology trials,” Oncotarget, vol. 8. Impact Journals, pp. 83128–83141, 2017.","ama":"Singer J, Berroterán-Infante N, Rami-Mark C, et al. Development of a radiolabeled caninized anti-EGFR antibody for comparative oncology trials. Oncotarget. 2017;8:83128-83141. doi:10.18632/oncotarget.20914","apa":"Singer, J., Berroterán-Infante, N., Rami-Mark, C., Dumanic, M., Matz, M., Willmann, M., … Jensen-Jarolim, E. (2017). Development of a radiolabeled caninized anti-EGFR antibody for comparative oncology trials. Oncotarget. Impact Journals. https://doi.org/10.18632/oncotarget.20914"},"date_updated":"2021-01-12T08:17:39Z","month":"09","intvolume":" 8","publisher":"Impact Journals","quality_controlled":"1","oa":1,"main_file_link":[{"url":"https://doi.org/10.18632/oncotarget.20914","open_access":"1"}],"oa_version":"Published Version","abstract":[{"lang":"eng","text":"Due to large homology of human and canine EGFR, dogs suffering from spontaneous EGFR+ cancer can be considered as ideal translational models. Thereby, novel immunotherapeutic compounds can be developed for both human and veterinary patients. This study describes the radiolabeling of a canine anti-EGFR IgG antibody (can225IgG) with potential diagnostic and therapeutic value in comparative clinical settings. Can225IgG was functionalized with DTPA for subsequent chelation with the radionuclide 99mTc. Successful coupling of 10 DTPA molecules per antibody on average was proven by significant mass increase in MALDI-TOF spectroscopy, gel electrophoresis and immunoblots. Following functionalization and radiolabeling, 99mTc-DTPA-can225IgG fully retained its binding capacity towards human and canine EGFR in flow cytometry, immuno- and radioblots, and autoradiography. The affinity of radiolabeled can225IgG was determined to KD 0.8 ±0.0031 nM in a real-time kinetics assay on canine carcinoma cells by a competition binding technique. Stability tests of the radiolabeled compound identified TRIS buffered saline as the ideal formulation for short-term storage with 87.11 ±6.04% intact compound being still detected 60 minutes post radiolabeling. High stability, specificity and EGFR binding affinity pinpoint towards 99mTc-radiolabeled can225IgG antibody as an ideal lead compound for the first proof-of-concept diagnostic and therapeutic applications in canine cancer patients."}],"volume":8,"doi":"10.18632/oncotarget.20914","date_published":"2017-09-15T00:00:00Z","date_created":"2020-08-10T11:53:18Z","page":"83128-83141","day":"15","language":[{"iso":"eng"}],"publication":"Oncotarget","publication_identifier":{"issn":["1949-2553"]},"publication_status":"published","year":"2017"},{"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Petritsch, Barbara. “Metadata for Research Data in Practice.” Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. VÖB, 2017. https://doi.org/10.31263/voebm.v70i2.1678.","ista":"Petritsch B. 2017. Metadata for research data in practice. Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. 70(2), 200–207.","mla":"Petritsch, Barbara. “Metadata for Research Data in Practice.” Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare, vol. 70, no. 2, VÖB, 2017, pp. 200–07, doi:10.31263/voebm.v70i2.1678.","short":"B. Petritsch, Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare 70 (2017) 200–207.","ieee":"B. Petritsch, “Metadata for research data in practice,” Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare, vol. 70, no. 2. VÖB, pp. 200–207, 2017.","apa":"Petritsch, B. (2017). Metadata for research data in practice. Mitteilungen Der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. VÖB. https://doi.org/10.31263/voebm.v70i2.1678","ama":"Petritsch B. Metadata for research data in practice. Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare. 2017;70(2):200-207. doi:10.31263/voebm.v70i2.1678"},"title":"Metadata for research data in practice","author":[{"id":"406048EC-F248-11E8-B48F-1D18A9856A87","first_name":"Barbara","full_name":"Petritsch, Barbara","orcid":"0000-0003-2724-4614","last_name":"Petritsch"}],"publist_id":"6823","publisher":"VÖB","oa":1,"day":"01","publication":"Mitteilungen der Vereinigung Österreichischer Bibliothekarinnen & Bibliothekare","has_accepted_license":"1","year":"2017","doi":"10.31263/voebm.v70i2.1678","date_published":"2017-08-01T00:00:00Z","date_created":"2018-12-11T11:48:42Z","page":"200 - 207","_id":"825","status":"public","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"ddc":["020"],"date_updated":"2021-01-12T08:17:44Z","department":[{"_id":"E-Lib"}],"file_date_updated":"2020-07-14T12:48:11Z","oa_version":"Published Version","abstract":[{"text":"What data is needed about data? Describing the process to answer this question for the institutional data repository IST DataRep.","lang":"eng"}],"month":"08","intvolume":" 70","scopus_import":1,"file":[{"file_name":"2017_VOEB_Petritsch.pdf","date_created":"2019-01-18T13:32:17Z","file_size":7843975,"date_updated":"2020-07-14T12:48:11Z","creator":"dernst","checksum":"7c4544d07efa2c2add8612b489abb4e2","file_id":"5850","content_type":"application/pdf","relation":"main_file","access_level":"open_access"}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["10222588"]},"publication_status":"published","volume":70,"issue":"2"},{"doi":"10.1109/eurospw.2017.46","date_published":"2017-06-30T00:00:00Z","date_created":"2020-08-26T11:48:11Z","day":"30","language":[{"iso":"eng"}],"publication":"2017 IEEE European Symposium on Security and Privacy Workshops","publication_identifier":{"eisbn":["9781538622445"]},"publication_status":"published","year":"2017","month":"06","quality_controlled":"1","publisher":"IEEE","oa_version":"None","abstract":[{"text":"Permissionless blockchain-based cryptocurrencies commonly use proof-of-work (PoW) or proof-of-stake (PoS) to ensure their security, e.g. to prevent double spending attacks. However, both approaches have disadvantages: PoW leads to massive amounts of wasted electricity and re-centralization, whereas major stakeholders in PoS might be able to create a monopoly. In this work, we propose proof-of-personhood (PoP), a mechanism that binds physical entities to virtual identities in a way that enables accountability while preserving anonymity. Afterwards we introduce PoPCoin, a new cryptocurrency, whose consensus mechanism leverages PoP to eliminate the dis-advantages of PoW and PoS while ensuring security. PoPCoin leads to a continuously fair and democratic wealth creation process which paves the way for an experimental basic income infrastructure.","lang":"eng"}],"title":"Proof-of-personhood: Redemocratizing permissionless cryptocurrencies","author":[{"first_name":"Maria","last_name":"Borge","full_name":"Borge, Maria"},{"id":"f5983044-d7ef-11ea-ac6d-fd1430a26d30","first_name":"Eleftherios","last_name":"Kokoris Kogias","full_name":"Kokoris Kogias, Eleftherios"},{"first_name":"Philipp","full_name":"Jovanovic, Philipp","last_name":"Jovanovic"},{"first_name":"Linus","full_name":"Gasser, Linus","last_name":"Gasser"},{"full_name":"Gailly, Nicolas","last_name":"Gailly","first_name":"Nicolas"},{"first_name":"Bryan","full_name":"Ford, Bryan","last_name":"Ford"}],"article_processing_charge":"No","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Borge, Maria, Eleftherios Kokoris Kogias, Philipp Jovanovic, Linus Gasser, Nicolas Gailly, and Bryan Ford. “Proof-of-Personhood: Redemocratizing Permissionless Cryptocurrencies.” In 2017 IEEE European Symposium on Security and Privacy Workshops. IEEE, 2017. https://doi.org/10.1109/eurospw.2017.46.","ista":"Borge M, Kokoris Kogias E, Jovanovic P, Gasser L, Gailly N, Ford B. 2017. Proof-of-personhood: Redemocratizing permissionless cryptocurrencies. 2017 IEEE European Symposium on Security and Privacy Workshops. EuroS&PW: European Symposium on Security and Privacy Workshops, 7966966.","mla":"Borge, Maria, et al. “Proof-of-Personhood: Redemocratizing Permissionless Cryptocurrencies.” 2017 IEEE European Symposium on Security and Privacy Workshops, 7966966, IEEE, 2017, doi:10.1109/eurospw.2017.46.","ieee":"M. Borge, E. Kokoris Kogias, P. Jovanovic, L. Gasser, N. Gailly, and B. Ford, “Proof-of-personhood: Redemocratizing permissionless cryptocurrencies,” in 2017 IEEE European Symposium on Security and Privacy Workshops, Paris, France, 2017.","short":"M. Borge, E. Kokoris Kogias, P. Jovanovic, L. Gasser, N. Gailly, B. Ford, in:, 2017 IEEE European Symposium on Security and Privacy Workshops, IEEE, 2017.","apa":"Borge, M., Kokoris Kogias, E., Jovanovic, P., Gasser, L., Gailly, N., & Ford, B. (2017). Proof-of-personhood: Redemocratizing permissionless cryptocurrencies. In 2017 IEEE European Symposium on Security and Privacy Workshops. Paris, France: IEEE. https://doi.org/10.1109/eurospw.2017.46","ama":"Borge M, Kokoris Kogias E, Jovanovic P, Gasser L, Gailly N, Ford B. Proof-of-personhood: Redemocratizing permissionless cryptocurrencies. In: 2017 IEEE European Symposium on Security and Privacy Workshops. IEEE; 2017. doi:10.1109/eurospw.2017.46"},"date_updated":"2021-01-12T08:17:57Z","status":"public","type":"conference","conference":{"name":"EuroS&PW: European Symposium on Security and Privacy Workshops","location":"Paris, France","end_date":"2017-04-28","start_date":"2017-04-26"},"article_number":"7966966","_id":"8299"},{"oa_version":"Preprint","abstract":[{"text":"Bias-resistant public randomness is a critical component in many (distributed) protocols. Generating public randomness is hard, however, because active adversaries may behave dishonestly to bias public random choices toward their advantage. Existing solutions do not scale to hundreds or thousands of participants, as is needed in many decentralized systems. We propose two large-scale distributed protocols, RandHound and RandHerd, which provide publicly-verifiable, unpredictable, and unbiasable randomness against Byzantine adversaries. RandHound relies on an untrusted client to divide a set of randomness servers into groups for scalability, and it depends on the pigeonhole principle to ensure output integrity, even for non-random, adversarial group choices. RandHerd implements an efficient, decentralized randomness beacon. RandHerd is structurally similar to a BFT protocol, but uses RandHound in a one-time setup to arrange participants into verifiably unbiased random secret-sharing groups, which then repeatedly produce random output at predefined intervals. Our prototype demonstrates that RandHound and RandHerd achieve good performance across hundreds of participants while retaining a low failure probability by properly selecting protocol parameters, such as a group size and secret-sharing threshold. For example, when sharding 512 nodes into groups of 32, our experiments show that RandHound can produce fresh random output after 240 seconds. RandHerd, after a setup phase of 260 seconds, is able to generate fresh random output in intervals of approximately 6 seconds. For this configuration, both protocols operate at a failure probability of at most 0.08% against a Byzantine adversary.","lang":"eng"}],"month":"06","main_file_link":[{"url":"https://eprint.iacr.org/2016/1067","open_access":"1"}],"oa":1,"publisher":"IEEE","quality_controlled":"1","language":[{"iso":"eng"}],"publication":"2017 IEEE Symposium on Security and Privacy","day":"01","publication_status":"published","year":"2017","publication_identifier":{"issn":["2375-1207"],"isbn":["9781509055340"]},"date_created":"2020-08-26T12:26:08Z","doi":"10.1109/SP.2017.45","date_published":"2017-06-01T00:00:00Z","page":"444-460","_id":"8306","status":"public","conference":{"name":"SP: Symposium on Security and Privacy","location":"San Jose, CA, United States","end_date":"2017-05-26","start_date":"2017-05-22"},"type":"conference","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","citation":{"mla":"Syta, E., et al. “Scalable Bias-Resistant Distributed Randomness.” 2017 IEEE Symposium on Security and Privacy, IEEE, 2017, pp. 444–60, doi:10.1109/SP.2017.45.","ieee":"E. Syta et al., “Scalable bias-resistant distributed randomness,” in 2017 IEEE Symposium on Security and Privacy, San Jose, CA, United States, 2017, pp. 444–460.","short":"E. Syta, P. Jovanovic, E. Kokoris Kogias, N. Gailly, L. Gasser, I. Khoffi, M.J. Fischer, B. Ford, in:, 2017 IEEE Symposium on Security and Privacy, IEEE, 2017, pp. 444–460.","ama":"Syta E, Jovanovic P, Kokoris Kogias E, et al. Scalable bias-resistant distributed randomness. In: 2017 IEEE Symposium on Security and Privacy. IEEE; 2017:444-460. doi:10.1109/SP.2017.45","apa":"Syta, E., Jovanovic, P., Kokoris Kogias, E., Gailly, N., Gasser, L., Khoffi, I., … Ford, B. (2017). Scalable bias-resistant distributed randomness. In 2017 IEEE Symposium on Security and Privacy (pp. 444–460). San Jose, CA, United States: IEEE. https://doi.org/10.1109/SP.2017.45","chicago":"Syta, E., P. Jovanovic, Eleftherios Kokoris Kogias, N. Gailly, L. Gasser, I. Khoffi, M. J. Fischer, and B. Ford. “Scalable Bias-Resistant Distributed Randomness.” In 2017 IEEE Symposium on Security and Privacy, 444–60. IEEE, 2017. https://doi.org/10.1109/SP.2017.45.","ista":"Syta E, Jovanovic P, Kokoris Kogias E, Gailly N, Gasser L, Khoffi I, Fischer MJ, Ford B. 2017. Scalable bias-resistant distributed randomness. 2017 IEEE Symposium on Security and Privacy. SP: Symposium on Security and Privacy, 444–460."},"date_updated":"2021-01-12T08:18:02Z","title":"Scalable bias-resistant distributed randomness","article_processing_charge":"No","author":[{"first_name":"E.","full_name":"Syta, E.","last_name":"Syta"},{"first_name":"P.","full_name":"Jovanovic, P.","last_name":"Jovanovic"},{"id":"f5983044-d7ef-11ea-ac6d-fd1430a26d30","first_name":"Eleftherios","last_name":"Kokoris Kogias","full_name":"Kokoris Kogias, Eleftherios"},{"first_name":"N.","last_name":"Gailly","full_name":"Gailly, N."},{"full_name":"Gasser, L.","last_name":"Gasser","first_name":"L."},{"full_name":"Khoffi, I.","last_name":"Khoffi","first_name":"I."},{"last_name":"Fischer","full_name":"Fischer, M. J.","first_name":"M. J."},{"last_name":"Ford","full_name":"Ford, B.","first_name":"B."}]},{"page":"1271–1287","date_published":"2017-09-01T00:00:00Z","date_created":"2020-08-26T12:04:44Z","publication_identifier":{"isbn":["9781931971409"]},"year":"2017","publication_status":"published","day":"01","language":[{"iso":"eng"}],"publication":"Proceedings of the 26th USENIX Conference on Security Symposium","quality_controlled":"1","publisher":"USENIX Association","main_file_link":[{"url":"https://www.usenix.org/system/files/conference/usenixsecurity17/sec17-nikitin.pdf","open_access":"1"}],"oa":1,"month":"09","abstract":[{"text":"Software-update mechanisms are critical to the security of modern systems, but their typically centralized design presents a lucrative and frequently attacked target. In this work, we propose CHAINIAC, a decentralized software-update framework that eliminates single points of failure, enforces transparency, and provides efficient verifiability of integrity and authenticity for software-release processes. Independent witness servers collectively verify conformance of software updates to release policies, build verifiers validate the source-to-binary correspondence, and a tamper-proof release log stores collectively signed updates, thus ensuring that no release is accepted by clients before being widely disclosed and validated. The release log embodies a skipchain, a novel data structure, enabling arbitrarily out-of-date clients to efficiently validate updates and signing keys. Evaluation of our CHAINIAC prototype on reproducible Debian packages shows that the automated update process takes the average of 5 minutes per release for individual packages, and only 20 seconds for the aggregate timeline. We further evaluate the framework using real-world data from the PyPI package repository and show that it offers clients security comparable to verifying every single update themselves while consuming only one-fifth of the bandwidth and having a minimal computational overhead.","lang":"eng"}],"oa_version":"Published Version","author":[{"first_name":"Kirill","last_name":"Nikitin","full_name":"Nikitin, Kirill"},{"full_name":"Kokoris Kogias, Eleftherios","last_name":"Kokoris Kogias","id":"f5983044-d7ef-11ea-ac6d-fd1430a26d30","first_name":"Eleftherios"},{"last_name":"Jovanovic","full_name":"Jovanovic, Philipp","first_name":"Philipp"},{"full_name":"Gasser, Linus","last_name":"Gasser","first_name":"Linus"},{"full_name":"Gailly, Nicolas","last_name":"Gailly","first_name":"Nicolas"},{"last_name":"Khoffi","full_name":"Khoffi, Ismail","first_name":"Ismail"},{"full_name":"Cappos, Justin","last_name":"Cappos","first_name":"Justin"},{"last_name":"Ford","full_name":"Ford, Bryan","first_name":"Bryan"}],"article_processing_charge":"No","title":"CHAINIAC: Proactive software-update transparency via collectively signed skipchains and verified builds","citation":{"chicago":"Nikitin, Kirill, Eleftherios Kokoris Kogias, Philipp Jovanovic, Linus Gasser, Nicolas Gailly, Ismail Khoffi, Justin Cappos, and Bryan Ford. “CHAINIAC: Proactive Software-Update Transparency via Collectively Signed Skipchains and Verified Builds.” In Proceedings of the 26th USENIX Conference on Security Symposium, 1271–1287. USENIX Association, 2017.","ista":"Nikitin K, Kokoris Kogias E, Jovanovic P, Gasser L, Gailly N, Khoffi I, Cappos J, Ford B. 2017. CHAINIAC: Proactive software-update transparency via collectively signed skipchains and verified builds. Proceedings of the 26th USENIX Conference on Security Symposium. SEC: Security Symposium, 1271–1287.","mla":"Nikitin, Kirill, et al. “CHAINIAC: Proactive Software-Update Transparency via Collectively Signed Skipchains and Verified Builds.” Proceedings of the 26th USENIX Conference on Security Symposium, USENIX Association, 2017, pp. 1271–1287.","ama":"Nikitin K, Kokoris Kogias E, Jovanovic P, et al. CHAINIAC: Proactive software-update transparency via collectively signed skipchains and verified builds. In: Proceedings of the 26th USENIX Conference on Security Symposium. USENIX Association; 2017:1271–1287.","apa":"Nikitin, K., Kokoris Kogias, E., Jovanovic, P., Gasser, L., Gailly, N., Khoffi, I., … Ford, B. (2017). CHAINIAC: Proactive software-update transparency via collectively signed skipchains and verified builds. In Proceedings of the 26th USENIX Conference on Security Symposium (pp. 1271–1287). Vancouver, Canada: USENIX Association.","ieee":"K. Nikitin et al., “CHAINIAC: Proactive software-update transparency via collectively signed skipchains and verified builds,” in Proceedings of the 26th USENIX Conference on Security Symposium, Vancouver, Canada, 2017, pp. 1271–1287.","short":"K. Nikitin, E. Kokoris Kogias, P. Jovanovic, L. Gasser, N. Gailly, I. Khoffi, J. Cappos, B. Ford, in:, Proceedings of the 26th USENIX Conference on Security Symposium, USENIX Association, 2017, pp. 1271–1287."},"date_updated":"2021-01-12T08:18:00Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","type":"conference","conference":{"name":"SEC: Security Symposium","start_date":"2017-08-16","end_date":"2017-08-18","location":"Vancouver, Canada"},"status":"public","_id":"8301"},{"citation":{"mla":"Fraga, Hugo, et al. “Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D Correlation Experiments for Resonance Assignment of Large Proteins.” ChemPhysChem, vol. 18, no. 19, Wiley, 2017, pp. 2697–703, doi:10.1002/cphc.201700572.","short":"H. Fraga, C. Arnaud, D.F. Gauto, M. Audin, V. Kurauskas, P. Macek, C. Krichel, J. Guan, J. Boisbouvier, R. Sprangers, C. Breyton, P. Schanda, ChemPhysChem 18 (2017) 2697–2703.","ieee":"H. Fraga et al., “Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D correlation experiments for resonance assignment of large proteins,” ChemPhysChem, vol. 18, no. 19. Wiley, pp. 2697–2703, 2017.","apa":"Fraga, H., Arnaud, C., Gauto, D. F., Audin, M., Kurauskas, V., Macek, P., … Schanda, P. (2017). Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D correlation experiments for resonance assignment of large proteins. ChemPhysChem. Wiley. https://doi.org/10.1002/cphc.201700572","ama":"Fraga H, Arnaud C, Gauto DF, et al. Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D correlation experiments for resonance assignment of large proteins. ChemPhysChem. 2017;18(19):2697-2703. doi:10.1002/cphc.201700572","chicago":"Fraga, Hugo, Charles‐Adrien Arnaud, Diego F. Gauto, Maxime Audin, Vilius Kurauskas, Pavel Macek, Carsten Krichel, et al. “Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D Correlation Experiments for Resonance Assignment of Large Proteins.” ChemPhysChem. Wiley, 2017. https://doi.org/10.1002/cphc.201700572.","ista":"Fraga H, Arnaud C, Gauto DF, Audin M, Kurauskas V, Macek P, Krichel C, Guan J, Boisbouvier J, Sprangers R, Breyton C, Schanda P. 2017. Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D correlation experiments for resonance assignment of large proteins. ChemPhysChem. 18(19), 2697–2703."},"date_updated":"2021-01-12T08:19:19Z","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"last_name":"Fraga","full_name":"Fraga, Hugo","first_name":"Hugo"},{"last_name":"Arnaud","full_name":"Arnaud, Charles‐Adrien","first_name":"Charles‐Adrien"},{"first_name":"Diego F.","last_name":"Gauto","full_name":"Gauto, Diego F."},{"full_name":"Audin, Maxime","last_name":"Audin","first_name":"Maxime"},{"first_name":"Vilius","full_name":"Kurauskas, Vilius","last_name":"Kurauskas"},{"full_name":"Macek, Pavel","last_name":"Macek","first_name":"Pavel"},{"full_name":"Krichel, Carsten","last_name":"Krichel","first_name":"Carsten"},{"last_name":"Guan","full_name":"Guan, Jia‐Ying","first_name":"Jia‐Ying"},{"first_name":"Jerome","last_name":"Boisbouvier","full_name":"Boisbouvier, Jerome"},{"full_name":"Sprangers, Remco","last_name":"Sprangers","first_name":"Remco"},{"first_name":"Cécile","full_name":"Breyton, Cécile","last_name":"Breyton"},{"last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","first_name":"Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425"}],"article_processing_charge":"No","title":"Solid‐state NMR H–N–(C)–H and H–N–C–C 3D/4D correlation experiments for resonance assignment of large proteins","_id":"8446","article_type":"original","type":"journal_article","status":"public","keyword":["Physical and Theoretical Chemistry","Atomic and Molecular Physics","and Optics"],"publication_identifier":{"issn":["1439-4235","1439-7641"]},"publication_status":"published","year":"2017","day":"09","publication":"ChemPhysChem","language":[{"iso":"eng"}],"page":"2697-2703","date_published":"2017-08-09T00:00:00Z","doi":"10.1002/cphc.201700572","volume":18,"issue":"19","date_created":"2020-09-18T10:06:09Z","abstract":[{"lang":"eng","text":"Solid‐state NMR spectroscopy can provide insight into protein structure and dynamics at the atomic level without inherent protein size limitations. However, a major hurdle to studying large proteins by solid‐state NMR spectroscopy is related to spectral complexity and resonance overlap, which increase with molecular weight and severely hamper the assignment process. Here the use of two sets of experiments is shown to expand the tool kit of 1H‐detected assignment approaches, which correlate a given amide pair either to the two adjacent CO–CA pairs (4D hCOCANH/hCOCAcoNH), or to the amide 1H of the neighboring residue (3D HcocaNH/HcacoNH, which can be extended to 5D). The experiments are based on efficient coherence transfers between backbone atoms using INEPT transfers between carbons and cross‐polarization for heteronuclear transfers. The utility of these experiments is exemplified with application to assemblies of deuterated, fully amide‐protonated proteins from approximately 20 to 60 kDa monomer, at magic‐angle spinning (MAS) frequencies from approximately 40 to 55 kHz. These experiments will also be applicable to protonated proteins at higher MAS frequencies. The resonance assignment of a domain within the 50.4 kDa bacteriophage T5 tube protein pb6 is reported, and this is compared to NMR assignments of the isolated domain in solution. This comparison reveals contacts of this domain to the core of the polymeric tail tube assembly."}],"oa_version":"None","quality_controlled":"1","publisher":"Wiley","month":"08","intvolume":" 18"},{"article_number":"145","_id":"8445","status":"public","article_type":"original","type":"journal_article","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:19:19Z","citation":{"apa":"Kurauskas, V., Izmailov, S. A., Rogacheva, O. N., Hessel, A., Ayala, I., Woodhouse, J., … Schanda, P. (2017). Slow conformational exchange and overall rocking motion in ubiquitin protein crystals. Nature Communications. Springer Nature. https://doi.org/10.1038/s41467-017-00165-8","ama":"Kurauskas V, Izmailov SA, Rogacheva ON, et al. Slow conformational exchange and overall rocking motion in ubiquitin protein crystals. Nature Communications. 2017;8. doi:10.1038/s41467-017-00165-8","short":"V. Kurauskas, S.A. Izmailov, O.N. Rogacheva, A. Hessel, I. Ayala, J. Woodhouse, A. Shilova, Y. Xue, T. Yuwen, N. Coquelle, J.-P. Colletier, N.R. Skrynnikov, P. Schanda, Nature Communications 8 (2017).","ieee":"V. Kurauskas et al., “Slow conformational exchange and overall rocking motion in ubiquitin protein crystals,” Nature Communications, vol. 8. Springer Nature, 2017.","mla":"Kurauskas, Vilius, et al. “Slow Conformational Exchange and Overall Rocking Motion in Ubiquitin Protein Crystals.” Nature Communications, vol. 8, 145, Springer Nature, 2017, doi:10.1038/s41467-017-00165-8.","ista":"Kurauskas V, Izmailov SA, Rogacheva ON, Hessel A, Ayala I, Woodhouse J, Shilova A, Xue Y, Yuwen T, Coquelle N, Colletier J-P, Skrynnikov NR, Schanda P. 2017. Slow conformational exchange and overall rocking motion in ubiquitin protein crystals. Nature Communications. 8, 145.","chicago":"Kurauskas, Vilius, Sergei A. Izmailov, Olga N. Rogacheva, Audrey Hessel, Isabel Ayala, Joyce Woodhouse, Anastasya Shilova, et al. “Slow Conformational Exchange and Overall Rocking Motion in Ubiquitin Protein Crystals.” Nature Communications. Springer Nature, 2017. https://doi.org/10.1038/s41467-017-00165-8."},"title":"Slow conformational exchange and overall rocking motion in ubiquitin protein crystals","article_processing_charge":"No","author":[{"full_name":"Kurauskas, Vilius","last_name":"Kurauskas","first_name":"Vilius"},{"last_name":"Izmailov","full_name":"Izmailov, Sergei A.","first_name":"Sergei A."},{"full_name":"Rogacheva, Olga N.","last_name":"Rogacheva","first_name":"Olga N."},{"full_name":"Hessel, Audrey","last_name":"Hessel","first_name":"Audrey"},{"last_name":"Ayala","full_name":"Ayala, Isabel","first_name":"Isabel"},{"first_name":"Joyce","last_name":"Woodhouse","full_name":"Woodhouse, Joyce"},{"first_name":"Anastasya","last_name":"Shilova","full_name":"Shilova, Anastasya"},{"last_name":"Xue","full_name":"Xue, Yi","first_name":"Yi"},{"last_name":"Yuwen","full_name":"Yuwen, Tairan","first_name":"Tairan"},{"full_name":"Coquelle, Nicolas","last_name":"Coquelle","first_name":"Nicolas"},{"last_name":"Colletier","full_name":"Colletier, Jacques-Philippe","first_name":"Jacques-Philippe"},{"first_name":"Nikolai R.","full_name":"Skrynnikov, Nikolai R.","last_name":"Skrynnikov"},{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","last_name":"Schanda"}],"oa_version":"Published Version","abstract":[{"text":"Proteins perform their functions in solution but their structures are most frequently studied inside crystals. Here we probe how the crystal packing alters microsecond dynamics, using solid-state NMR measurements and multi-microsecond MD simulations of different crystal forms of ubiquitin. In particular, near-rotary-resonance relaxation dispersion (NERRD) experiments probe angular backbone motion, while Bloch–McConnell relaxation dispersion data report on fluctuations of the local electronic environment. These experiments and simulations reveal that the packing of the protein can significantly alter the thermodynamics and kinetics of local conformational exchange. Moreover, we report small-amplitude reorientational motion of protein molecules in the crystal lattice with an ~3–5° amplitude on a tens-of-microseconds time scale in one of the crystals, but not in others. An intriguing possibility arises that overall motion is to some extent coupled to local dynamics. Our study highlights the importance of considering the packing when analyzing dynamics of crystalline proteins.","lang":"eng"}],"intvolume":" 8","month":"07","quality_controlled":"1","publisher":"Springer Nature","publication":"Nature Communications","language":[{"iso":"eng"}],"day":"27","publication_status":"published","year":"2017","publication_identifier":{"issn":["2041-1723"]},"date_created":"2020-09-18T10:06:01Z","volume":8,"date_published":"2017-07-27T00:00:00Z","doi":"10.1038/s41467-017-00165-8"},{"oa_version":"None","abstract":[{"lang":"eng","text":"Biophysical investigation of membrane proteins generally requires their extraction from native sources using detergents, a step that can lead, possibly irreversibly, to protein denaturation. The propensity of dodecylphosphocholine (DPC), a detergent widely utilized in NMR studies of membrane proteins, to distort their structure has been the subject of much controversy. It has been recently proposed that the binding specificity of the yeast mitochondrial ADP/ATP carrier (yAAC3) toward cardiolipins is preserved in DPC, thereby suggesting that DPC is a suitable environment in which to study membrane proteins. In this communication, we used all-atom molecular dynamics simulations to investigate the specific binding of cardiolipins to yAAC3. Our data demonstrate that the interaction interface observed in a native-like environment differs markedly from that inferred from an NMR investigation in DPC, implying that in this detergent, the protein structure is distorted. We further investigated yAAC3 solubilized in DPC and in the milder dodecylmaltoside with thermal-shift assays. The loss of thermal transition observed in DPC confirms that the protein is no longer properly folded in this environment."}],"intvolume":" 113","month":"12","quality_controlled":"1","publisher":"Elsevier","publication":"Biophysical Journal","language":[{"iso":"eng"}],"day":"05","year":"2017","publication_status":"published","publication_identifier":{"issn":["0006-3495"]},"date_created":"2020-09-18T10:05:54Z","date_published":"2017-12-05T00:00:00Z","doi":"10.1016/j.bpj.2017.09.019","volume":113,"issue":"11","page":"2311-2315","_id":"8444","keyword":["Biophysics"],"status":"public","type":"journal_article","article_type":"original","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:19:18Z","citation":{"mla":"Dehez, François, et al. “Mitochondrial ADP/ATP Carrier in Dodecylphosphocholine Binds Cardiolipins with Non-Native Affinity.” Biophysical Journal, vol. 113, no. 11, Elsevier, 2017, pp. 2311–15, doi:10.1016/j.bpj.2017.09.019.","ama":"Dehez F, Schanda P, King MS, Kunji ERS, Chipot C. Mitochondrial ADP/ATP carrier in dodecylphosphocholine binds cardiolipins with non-native affinity. Biophysical Journal. 2017;113(11):2311-2315. doi:10.1016/j.bpj.2017.09.019","apa":"Dehez, F., Schanda, P., King, M. S., Kunji, E. R. S., & Chipot, C. (2017). Mitochondrial ADP/ATP carrier in dodecylphosphocholine binds cardiolipins with non-native affinity. Biophysical Journal. Elsevier. https://doi.org/10.1016/j.bpj.2017.09.019","ieee":"F. Dehez, P. Schanda, M. S. King, E. R. S. Kunji, and C. Chipot, “Mitochondrial ADP/ATP carrier in dodecylphosphocholine binds cardiolipins with non-native affinity,” Biophysical Journal, vol. 113, no. 11. Elsevier, pp. 2311–2315, 2017.","short":"F. Dehez, P. Schanda, M.S. King, E.R.S. Kunji, C. Chipot, Biophysical Journal 113 (2017) 2311–2315.","chicago":"Dehez, François, Paul Schanda, Martin S. King, Edmund R.S. Kunji, and Christophe Chipot. “Mitochondrial ADP/ATP Carrier in Dodecylphosphocholine Binds Cardiolipins with Non-Native Affinity.” Biophysical Journal. Elsevier, 2017. https://doi.org/10.1016/j.bpj.2017.09.019.","ista":"Dehez F, Schanda P, King MS, Kunji ERS, Chipot C. 2017. Mitochondrial ADP/ATP carrier in dodecylphosphocholine binds cardiolipins with non-native affinity. Biophysical Journal. 113(11), 2311–2315."},"title":"Mitochondrial ADP/ATP carrier in dodecylphosphocholine binds cardiolipins with non-native affinity","article_processing_charge":"No","author":[{"first_name":"François","full_name":"Dehez, François","last_name":"Dehez"},{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul","last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul"},{"full_name":"King, Martin S.","last_name":"King","first_name":"Martin S."},{"first_name":"Edmund R.S.","last_name":"Kunji","full_name":"Kunji, Edmund R.S."},{"last_name":"Chipot","full_name":"Chipot, Christophe","first_name":"Christophe"}]},{"date_created":"2021-02-02T15:49:21Z","date_published":"2017-10-01T00:00:00Z","issue":"15","volume":96,"doi":"10.1103/physrevb.96.155102","publication":"Physical Review B","language":[{"iso":"eng"}],"day":"01","year":"2017","publication_status":"published","publication_identifier":{"issn":["2469-9950","2469-9969"]},"intvolume":" 96","month":"10","publisher":"American Physical Society","quality_controlled":"1","oa_version":"None","abstract":[{"text":"Magnetic anisotropy in strontium iridate (Sr2IrO4) is found to be large because of the strong spin-orbit interactions. In our work, we studied the in-plane magnetic anisotropy of Sr2IrO4 and traced the anisotropic exchange interactions between the isospins in the crystal. The magnetic-field-dependent torque τ(H) showed a prominent transition from the canted antiferromagnetic state to the weak ferromagnetic (WFM) state. A comprehensive analysis was conducted to examine the isotropic and anisotropic regimes and probe the easy magnetization axis along the a b plane. The angle-dependent torque τ(θ) revealed a deviation from the sinusoidal behavior, and small differences in hysteresis were observed around 0° and 90° in the low-magnetic-field regime. This indicates that the orientation of the easy axis of the FM component is along the b axis, where the antiferromagnetic to WFM spin-flop transition occurs. We compared the coefficients of the magnetic susceptibility tensors and captured the anisotropy of the material. The in-plane τ(θ) revealed a tendency toward isotropic behavior for fields with values above the field value of the WFM transition.","lang":"eng"}],"title":"In-plane magnetic anisotropy in strontium iridate Sr2IrO4","article_processing_charge":"No","author":[{"full_name":"Nauman, Muhammad","orcid":"0000-0002-2111-4846","last_name":"Nauman","first_name":"Muhammad","id":"32c21954-2022-11eb-9d5f-af9f93c24e71"},{"first_name":"Yunjeong","last_name":"Hong","full_name":"Hong, Yunjeong"},{"full_name":"Hussain, Tayyaba","last_name":"Hussain","first_name":"Tayyaba"},{"full_name":"Seo, M. S.","last_name":"Seo","first_name":"M. S."},{"full_name":"Park, S. Y.","last_name":"Park","first_name":"S. Y."},{"first_name":"N.","last_name":"Lee","full_name":"Lee, N."},{"last_name":"Choi","full_name":"Choi, Y. J.","first_name":"Y. J."},{"full_name":"Kang, Woun","last_name":"Kang","first_name":"Woun"},{"full_name":"Jo, Younjung","last_name":"Jo","first_name":"Younjung"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","citation":{"chicago":"Nauman, Muhammad, Yunjeong Hong, Tayyaba Hussain, M. S. Seo, S. Y. Park, N. Lee, Y. J. Choi, Woun Kang, and Younjung Jo. “In-Plane Magnetic Anisotropy in Strontium Iridate Sr2IrO4.” Physical Review B. American Physical Society, 2017. https://doi.org/10.1103/physrevb.96.155102.","ista":"Nauman M, Hong Y, Hussain T, Seo MS, Park SY, Lee N, Choi YJ, Kang W, Jo Y. 2017. In-plane magnetic anisotropy in strontium iridate Sr2IrO4. Physical Review B. 96(15), 155102.","mla":"Nauman, Muhammad, et al. “In-Plane Magnetic Anisotropy in Strontium Iridate Sr2IrO4.” Physical Review B, vol. 96, no. 15, 155102, American Physical Society, 2017, doi:10.1103/physrevb.96.155102.","apa":"Nauman, M., Hong, Y., Hussain, T., Seo, M. S., Park, S. Y., Lee, N., … Jo, Y. (2017). In-plane magnetic anisotropy in strontium iridate Sr2IrO4. Physical Review B. American Physical Society. https://doi.org/10.1103/physrevb.96.155102","ama":"Nauman M, Hong Y, Hussain T, et al. In-plane magnetic anisotropy in strontium iridate Sr2IrO4. Physical Review B. 2017;96(15). doi:10.1103/physrevb.96.155102","ieee":"M. Nauman et al., “In-plane magnetic anisotropy in strontium iridate Sr2IrO4,” Physical Review B, vol. 96, no. 15. American Physical Society, 2017.","short":"M. Nauman, Y. Hong, T. Hussain, M.S. Seo, S.Y. Park, N. Lee, Y.J. Choi, W. Kang, Y. Jo, Physical Review B 96 (2017)."},"date_updated":"2021-02-03T12:53:00Z","status":"public","article_type":"original","type":"journal_article","article_number":"155102","_id":"9065"},{"citation":{"mla":"Aubret, A., et al. “Eppur Si Muove, and yet It Moves: Patchy (Phoretic) Swimmers.” Current Opinion in Colloid & Interface Science, vol. 30, Elsevier, 2017, pp. 81–89, doi:10.1016/j.cocis.2017.05.007.","ama":"Aubret A, Ramananarivo S, Palacci JA. Eppur si muove, and yet it moves: Patchy (phoretic) swimmers. Current Opinion in Colloid & Interface Science. 2017;30:81-89. doi:10.1016/j.cocis.2017.05.007","apa":"Aubret, A., Ramananarivo, S., & Palacci, J. A. (2017). Eppur si muove, and yet it moves: Patchy (phoretic) swimmers. Current Opinion in Colloid & Interface Science. Elsevier. https://doi.org/10.1016/j.cocis.2017.05.007","short":"A. Aubret, S. Ramananarivo, J.A. Palacci, Current Opinion in Colloid & Interface Science 30 (2017) 81–89.","ieee":"A. Aubret, S. Ramananarivo, and J. A. Palacci, “Eppur si muove, and yet it moves: Patchy (phoretic) swimmers,” Current Opinion in Colloid & Interface Science, vol. 30. Elsevier, pp. 81–89, 2017.","chicago":"Aubret, A., S. Ramananarivo, and Jérémie A Palacci. “Eppur Si Muove, and yet It Moves: Patchy (Phoretic) Swimmers.” Current Opinion in Colloid & Interface Science. Elsevier, 2017. https://doi.org/10.1016/j.cocis.2017.05.007.","ista":"Aubret A, Ramananarivo S, Palacci JA. 2017. Eppur si muove, and yet it moves: Patchy (phoretic) swimmers. Current Opinion in Colloid & Interface Science. 30, 81–89."},"date_updated":"2021-02-22T09:32:11Z","user_id":"D865714E-FA4E-11E9-B85B-F5C5E5697425","extern":"1","article_processing_charge":"No","author":[{"first_name":"A.","full_name":"Aubret, A.","last_name":"Aubret"},{"first_name":"S.","last_name":"Ramananarivo","full_name":"Ramananarivo, S."},{"first_name":"Jérémie A","id":"8fb92548-2b22-11eb-b7c1-a3f0d08d7c7d","orcid":"0000-0002-7253-9465","full_name":"Palacci, Jérémie A","last_name":"Palacci"}],"title":"Eppur si muove, and yet it moves: Patchy (phoretic) swimmers","_id":"9165","article_type":"original","type":"journal_article","status":"public","year":"2017","publication_status":"published","publication_identifier":{"issn":["1359-0294"]},"language":[{"iso":"eng"}],"publication":"Current Opinion in Colloid & Interface Science","day":"01","page":"81-89","date_created":"2021-02-18T14:29:42Z","date_published":"2017-07-01T00:00:00Z","doi":"10.1016/j.cocis.2017.05.007","volume":30,"abstract":[{"lang":"eng","text":"Advances in colloidal synthesis allow for the design of particles with controlled patches. This article reviews routes towards colloidal locomotion, where energy is consumed and converted into motion, and its implementation with active patchy particles. A special emphasis is given to phoretic swimmers, where the self-propulsion originates from an interfacial phenomenon, raising experimental challenges and opening up opportunities for particles with controlled anisotropic surface chemistry and novel behaviors."}],"oa_version":"None","scopus_import":"1","publisher":"Elsevier","quality_controlled":"1","intvolume":" 30","month":"07"},{"month":"10","intvolume":" 6","abstract":[{"lang":"eng","text":"Plant meristems carry pools of continuously active stem cells, whose activity is controlled by developmental and environmental signals. After stem cell division, daughter cells that exit the stem cell domain acquire transit amplifying cell identity before they are incorporated into organs and differentiate. In this study, we used an integrated approach to elucidate the role of HECATE (HEC) genes in regulating developmental trajectories of shoot stem cells in Arabidopsis thaliana. Our work reveals that HEC function stabilizes cell fate in distinct zones of the shoot meristem thereby controlling the spatio-temporal dynamics of stem cell differentiation. Importantly, this activity is concomitant with the local modulation of cellular responses to cytokinin and auxin, two key phytohormones regulating cell behaviour. Mechanistically, we show that HEC factors transcriptionally control and physically interact with MONOPTEROS (MP), a key regulator of auxin signalling, and modulate the autocatalytic stabilization of auxin signalling output."}],"oa_version":"Published Version","pmid":1,"volume":6,"publication_identifier":{"issn":["2050-084X"]},"publication_status":"published","file":[{"date_created":"2021-03-02T09:29:56Z","file_name":"2017_eLife_Gaillochet.pdf","creator":"dernst","date_updated":"2021-03-02T09:29:56Z","file_size":11669407,"checksum":"51c8968a845df5077643c3e3e139d34f","file_id":"9214","success":1,"access_level":"open_access","relation":"main_file","content_type":"application/pdf"}],"language":[{"iso":"eng"}],"article_type":"original","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public","_id":"9190","file_date_updated":"2021-03-02T09:29:56Z","date_updated":"2021-03-02T09:33:54Z","extern":"1","ddc":["580"],"publisher":"eLife Sciences Publications","quality_controlled":"1","oa":1,"date_published":"2017-10-23T00:00:00Z","doi":"10.7554/elife.30135","date_created":"2021-02-24T17:06:13Z","has_accepted_license":"1","year":"2017","day":"23","publication":"eLife","article_number":"e30135","author":[{"last_name":"Gaillochet","full_name":"Gaillochet, Christophe","first_name":"Christophe"},{"full_name":"Stiehl, Thomas","last_name":"Stiehl","first_name":"Thomas"},{"first_name":"Christian","last_name":"Wenzl","full_name":"Wenzl, Christian"},{"first_name":"Juan-José","full_name":"Ripoll, Juan-José","last_name":"Ripoll"},{"first_name":"Lindsay J","full_name":"Bailey-Steinitz, Lindsay J","last_name":"Bailey-Steinitz"},{"id":"367EF8FA-F248-11E8-B48F-1D18A9856A87","first_name":"Lanxin","last_name":"Li","orcid":"0000-0002-5607-272X","full_name":"Li, Lanxin"},{"first_name":"Anne","last_name":"Pfeiffer","full_name":"Pfeiffer, Anne"},{"first_name":"Andrej","last_name":"Miotk","full_name":"Miotk, Andrej"},{"first_name":"Jana P","full_name":"Hakenjos, Jana P","last_name":"Hakenjos"},{"first_name":"Joachim","full_name":"Forner, Joachim","last_name":"Forner"},{"first_name":"Martin F","full_name":"Yanofsky, Martin F","last_name":"Yanofsky"},{"first_name":"Anna","full_name":"Marciniak-Czochra, Anna","last_name":"Marciniak-Czochra"},{"first_name":"Jan U","full_name":"Lohmann, Jan U","last_name":"Lohmann"}],"external_id":{"pmid":["29058667"]},"article_processing_charge":"No","title":"Control of plant cell fate transitions by transcriptional and hormonal signals","citation":{"ista":"Gaillochet C, Stiehl T, Wenzl C, Ripoll J-J, Bailey-Steinitz LJ, Li L, Pfeiffer A, Miotk A, Hakenjos JP, Forner J, Yanofsky MF, Marciniak-Czochra A, Lohmann JU. 2017. Control of plant cell fate transitions by transcriptional and hormonal signals. eLife. 6, e30135.","chicago":"Gaillochet, Christophe, Thomas Stiehl, Christian Wenzl, Juan-José Ripoll, Lindsay J Bailey-Steinitz, Lanxin Li, Anne Pfeiffer, et al. “Control of Plant Cell Fate Transitions by Transcriptional and Hormonal Signals.” ELife. eLife Sciences Publications, 2017. https://doi.org/10.7554/elife.30135.","ama":"Gaillochet C, Stiehl T, Wenzl C, et al. Control of plant cell fate transitions by transcriptional and hormonal signals. eLife. 2017;6. doi:10.7554/elife.30135","apa":"Gaillochet, C., Stiehl, T., Wenzl, C., Ripoll, J.-J., Bailey-Steinitz, L. J., Li, L., … Lohmann, J. U. (2017). Control of plant cell fate transitions by transcriptional and hormonal signals. ELife. eLife Sciences Publications. https://doi.org/10.7554/elife.30135","short":"C. Gaillochet, T. Stiehl, C. Wenzl, J.-J. Ripoll, L.J. Bailey-Steinitz, L. Li, A. Pfeiffer, A. Miotk, J.P. Hakenjos, J. Forner, M.F. Yanofsky, A. Marciniak-Czochra, J.U. Lohmann, ELife 6 (2017).","ieee":"C. Gaillochet et al., “Control of plant cell fate transitions by transcriptional and hormonal signals,” eLife, vol. 6. eLife Sciences Publications, 2017.","mla":"Gaillochet, Christophe, et al. “Control of Plant Cell Fate Transitions by Transcriptional and Hormonal Signals.” ELife, vol. 6, e30135, eLife Sciences Publications, 2017, doi:10.7554/elife.30135."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87"},{"extern":"1","date_updated":"2021-01-12T08:21:59Z","_id":"93","status":"public","type":"journal_article","language":[{"iso":"eng"}],"publication_status":"published","volume":88,"issue":"9","oa_version":"Preprint","pmid":1,"abstract":[{"text":"An electro-optomechanical device capable of microwave-to-optics conversion has recently been demonstrated, with the vision of enabling optical networks of superconducting qubits. Here we present an improved converter design that uses a three-dimensional microwave cavity for coupling between the microwave transmission line and an integrated LC resonator on the converter chip. The new design simplifies the optical assembly and decouples it from the microwave part of the setup. Experimental demonstrations show that the modular device assembly allows us to flexibly tune the microwave coupling to the converter chip while maintaining small loss. We also find that electromechanical experiments are not impacted by the additional microwave cavity. Our design is compatible with a high-finesse optical cavity and will improve optical performance.","lang":"eng"}],"intvolume":" 88","month":"09","main_file_link":[{"url":"https://arxiv.org/abs/1703.06470","open_access":"1"}],"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"mla":"Menke, Tim, et al. “Reconfigurable Re-Entrant Cavity for Wireless Coupling to an Electro-Optomechanical Device.” Review of Scientific Instruments, vol. 88, no. 9, 094701, American Institute of Physics, 2017, doi:10.1063/1.5000973.","ieee":"T. Menke et al., “Reconfigurable re-entrant cavity for wireless coupling to an electro-optomechanical device,” Review of Scientific Instruments, vol. 88, no. 9. American Institute of Physics, 2017.","short":"T. Menke, P. Burns, A.P. Higginbotham, N.S. Kampel, R. Peterson, K. Cicak, R. Simmonds, C. Regal, K. Lehnert, Review of Scientific Instruments 88 (2017).","apa":"Menke, T., Burns, P., Higginbotham, A. P., Kampel, N. S., Peterson, R., Cicak, K., … Lehnert, K. (2017). Reconfigurable re-entrant cavity for wireless coupling to an electro-optomechanical device. Review of Scientific Instruments. American Institute of Physics. https://doi.org/10.1063/1.5000973","ama":"Menke T, Burns P, Higginbotham AP, et al. Reconfigurable re-entrant cavity for wireless coupling to an electro-optomechanical device. Review of Scientific Instruments. 2017;88(9). doi:10.1063/1.5000973","chicago":"Menke, Tim, Peter Burns, Andrew P Higginbotham, N S Kampel, Robert Peterson, Katarina Cicak, Raymond Simmonds, Cindy Regal, and Konrad Lehnert. “Reconfigurable Re-Entrant Cavity for Wireless Coupling to an Electro-Optomechanical Device.” Review of Scientific Instruments. American Institute of Physics, 2017. https://doi.org/10.1063/1.5000973.","ista":"Menke T, Burns P, Higginbotham AP, Kampel NS, Peterson R, Cicak K, Simmonds R, Regal C, Lehnert K. 2017. Reconfigurable re-entrant cavity for wireless coupling to an electro-optomechanical device. Review of Scientific Instruments. 88(9), 094701."},"title":"Reconfigurable re-entrant cavity for wireless coupling to an electro-optomechanical device","external_id":{"pmid":["28964202"],"arxiv":["1703.06470"]},"publist_id":"7961","author":[{"full_name":"Menke, Tim","last_name":"Menke","first_name":"Tim"},{"last_name":"Burns","full_name":"Burns, Peter","first_name":"Peter"},{"last_name":"Higginbotham","full_name":"Higginbotham, Andrew P","orcid":"0000-0003-2607-2363","id":"4AD6785A-F248-11E8-B48F-1D18A9856A87","first_name":"Andrew P"},{"first_name":"N S","full_name":"Kampel, N S","last_name":"Kampel"},{"last_name":"Peterson","full_name":"Peterson, Robert","first_name":"Robert"},{"first_name":"Katarina","last_name":"Cicak","full_name":"Cicak, Katarina"},{"last_name":"Simmonds","full_name":"Simmonds, Raymond","first_name":"Raymond"},{"last_name":"Regal","full_name":"Regal, Cindy","first_name":"Cindy"},{"first_name":"Konrad","full_name":"Lehnert, Konrad","last_name":"Lehnert"}],"article_number":"094701","publication":"Review of Scientific Instruments","day":"08","year":"2017","date_created":"2018-12-11T11:44:35Z","date_published":"2017-09-08T00:00:00Z","doi":"10.1063/1.5000973","oa":1,"quality_controlled":"1","publisher":"American Institute of Physics"},{"title":"Breaking Lorentz reciprocity with frequency conversion and delay","publist_id":"7960","author":[{"last_name":"Rosenthal","full_name":"Rosenthal, Eric","first_name":"Eric"},{"full_name":"Chapman, Benjamin","last_name":"Chapman","first_name":"Benjamin"},{"id":"4AD6785A-F248-11E8-B48F-1D18A9856A87","first_name":"Andrew P","last_name":"Higginbotham","full_name":"Higginbotham, Andrew P","orcid":"0000-0003-2607-2363"},{"full_name":"Kerckhoff, Joseph","last_name":"Kerckhoff","first_name":"Joseph"},{"first_name":"Konrad","full_name":"Lehnert, Konrad","last_name":"Lehnert"}],"external_id":{"arxiv":["1705.09548"]},"extern":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","date_updated":"2021-01-12T08:22:04Z","citation":{"chicago":"Rosenthal, Eric, Benjamin Chapman, Andrew P Higginbotham, Joseph Kerckhoff, and Konrad Lehnert. “Breaking Lorentz Reciprocity with Frequency Conversion and Delay.” APS Physics, Physical Review Letters. American Physical Society, 2017. https://doi.org/10.1103/PhysRevLett.119.147703.","ista":"Rosenthal E, Chapman B, Higginbotham AP, Kerckhoff J, Lehnert K. 2017. Breaking Lorentz reciprocity with frequency conversion and delay. APS Physics, Physical Review Letters. 119(14), 147703.","mla":"Rosenthal, Eric, et al. “Breaking Lorentz Reciprocity with Frequency Conversion and Delay.” APS Physics, Physical Review Letters, vol. 119, no. 14, 147703, American Physical Society, 2017, doi:10.1103/PhysRevLett.119.147703.","ama":"Rosenthal E, Chapman B, Higginbotham AP, Kerckhoff J, Lehnert K. Breaking Lorentz reciprocity with frequency conversion and delay. APS Physics, Physical Review Letters. 2017;119(14). doi:10.1103/PhysRevLett.119.147703","apa":"Rosenthal, E., Chapman, B., Higginbotham, A. P., Kerckhoff, J., & Lehnert, K. (2017). Breaking Lorentz reciprocity with frequency conversion and delay. APS Physics, Physical Review Letters. American Physical Society. https://doi.org/10.1103/PhysRevLett.119.147703","short":"E. Rosenthal, B. Chapman, A.P. Higginbotham, J. Kerckhoff, K. Lehnert, APS Physics, Physical Review Letters 119 (2017).","ieee":"E. Rosenthal, B. Chapman, A. P. Higginbotham, J. Kerckhoff, and K. Lehnert, “Breaking Lorentz reciprocity with frequency conversion and delay,” APS Physics, Physical Review Letters, vol. 119, no. 14. American Physical Society, 2017."},"status":"public","type":"journal_article","article_number":"147703","_id":"94","doi":"10.1103/PhysRevLett.119.147703","date_published":"2017-10-06T00:00:00Z","volume":119,"issue":"14","date_created":"2018-12-11T11:44:35Z","day":"06","publication":"APS Physics, Physical Review Letters","language":[{"iso":"eng"}],"year":"2017","publication_status":"published","month":"10","intvolume":" 119","publisher":"American Physical Society","quality_controlled":"1","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1705.09548"}],"oa":1,"oa_version":"Submitted Version","abstract":[{"text":"We introduce a method for breaking Lorentz reciprocity based upon the noncommutation of frequency conversion and delay. The method requires no magnetic materials or resonant physics, allowing for the design of scalable and broadband nonreciprocal circuits. With this approach, two types of gyrators - universal building blocks for linear, nonreciprocal circuits - are constructed. Using one of these gyrators, we create a circulator with >15 dB of isolation across the 5-9 GHz band. Our designs may be readily extended to any platform with suitable frequency conversion elements, including semiconducting devices for telecommunication or an on-chip superconducting implementation for quantum information processing.","lang":"eng"}]},{"publisher":"eLife Sciences Publications","quality_controlled":"1","oa":1,"date_published":"2017-11-15T00:00:00Z","doi":"10.7554/elife.30674","date_created":"2021-06-02T14:28:58Z","has_accepted_license":"1","year":"2017","day":"15","publication":"eLife","article_number":"e30674","author":[{"first_name":"David B","full_name":"Lyons, David B","last_name":"Lyons"},{"full_name":"Zilberman, Daniel","orcid":"0000-0002-0123-8649","last_name":"Zilberman","first_name":"Daniel","id":"6973db13-dd5f-11ea-814e-b3e5455e9ed1"}],"article_processing_charge":"No","external_id":{"pmid":["29140247"]},"title":"DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes","citation":{"apa":"Lyons, D. B., & Zilberman, D. (2017). DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes. ELife. eLife Sciences Publications. https://doi.org/10.7554/elife.30674","ama":"Lyons DB, Zilberman D. DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes. eLife. 2017;6. doi:10.7554/elife.30674","short":"D.B. Lyons, D. Zilberman, ELife 6 (2017).","ieee":"D. B. Lyons and D. Zilberman, “DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes,” eLife, vol. 6. eLife Sciences Publications, 2017.","mla":"Lyons, David B., and Daniel Zilberman. “DDM1 and Lsh Remodelers Allow Methylation of DNA Wrapped in Nucleosomes.” ELife, vol. 6, e30674, eLife Sciences Publications, 2017, doi:10.7554/elife.30674.","ista":"Lyons DB, Zilberman D. 2017. DDM1 and Lsh remodelers allow methylation of DNA wrapped in nucleosomes. eLife. 6, e30674.","chicago":"Lyons, David B, and Daniel Zilberman. “DDM1 and Lsh Remodelers Allow Methylation of DNA Wrapped in Nucleosomes.” ELife. eLife Sciences Publications, 2017. https://doi.org/10.7554/elife.30674."},"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","scopus_import":"1","month":"11","intvolume":" 6","abstract":[{"lang":"eng","text":"Cytosine methylation regulates essential genome functions across eukaryotes, but the fundamental question of whether nucleosomal or naked DNA is the preferred substrate of plant and animal methyltransferases remains unresolved. Here, we show that genetic inactivation of a single DDM1/Lsh family nucleosome remodeler biases methylation toward inter-nucleosomal linker DNA in Arabidopsis thaliana and mouse. We find that DDM1 enables methylation of DNA bound to the nucleosome, suggesting that nucleosome-free DNA is the preferred substrate of eukaryotic methyltransferases in vivo. Furthermore, we show that simultaneous mutation of DDM1 and linker histone H1 in Arabidopsis reproduces the strong linker-specific methylation patterns of species that diverged from flowering plants and animals over a billion years ago. Our results indicate that in the absence of remodeling, nucleosomes are strong barriers to DNA methyltransferases. Linker-specific methylation can evolve simply by breaking the connection between nucleosome remodeling and DNA methylation."}],"pmid":1,"oa_version":"Published Version","volume":6,"publication_identifier":{"eissn":["2050-084X"]},"publication_status":"published","file":[{"creator":"cziletti","date_updated":"2021-06-02T14:33:36Z","file_size":1603102,"date_created":"2021-06-02T14:33:36Z","file_name":"2017_eLife_Lyons.pdf","access_level":"open_access","relation":"main_file","content_type":"application/pdf","file_id":"9446","checksum":"4cfcdd67511ae4aed3d993550e46e146","success":1}],"language":[{"iso":"eng"}],"type":"journal_article","article_type":"original","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public","_id":"9445","file_date_updated":"2021-06-02T14:33:36Z","department":[{"_id":"DaZi"}],"date_updated":"2021-12-14T07:54:36Z","extern":"1","ddc":["570"]},{"project":[{"grant_number":"RGY0084/2012","name":"In situ real-time imaging of neurotransmitter signaling using designer optical sensors (HFSP Young Investigator)","_id":"255BFFFA-B435-11E9-9278-68D0E5697425"}],"citation":{"mla":"Clifton, Ben, et al. “Ancestral Protein Reconstruction and Circular Permutation for Improving the Stability and Dynamic Range of FRET Sensors.” Synthetic Protein Switches, edited by Viktor Stein, vol. 1596, Springer, 2017, pp. 71–87, doi:10.1007/978-1-4939-6940-1_5.","ieee":"B. Clifton et al., “Ancestral protein reconstruction and circular permutation for improving the stability and dynamic range of FRET sensors,” in Synthetic Protein Switches, vol. 1596, V. Stein, Ed. Springer, 2017, pp. 71–87.","short":"B. Clifton, J. Whitfield, I. Sanchez-Romero, M. Herde, C. Henneberger, H.L. Janovjak, C. Jackson, in:, V. Stein (Ed.), Synthetic Protein Switches, Springer, 2017, pp. 71–87.","apa":"Clifton, B., Whitfield, J., Sanchez-Romero, I., Herde, M., Henneberger, C., Janovjak, H. L., & Jackson, C. (2017). Ancestral protein reconstruction and circular permutation for improving the stability and dynamic range of FRET sensors. In V. Stein (Ed.), Synthetic Protein Switches (Vol. 1596, pp. 71–87). Springer. https://doi.org/10.1007/978-1-4939-6940-1_5","ama":"Clifton B, Whitfield J, Sanchez-Romero I, et al. Ancestral protein reconstruction and circular permutation for improving the stability and dynamic range of FRET sensors. In: Stein V, ed. Synthetic Protein Switches. Vol 1596. Synthetic Protein Switches. Springer; 2017:71-87. doi:10.1007/978-1-4939-6940-1_5","chicago":"Clifton, Ben, Jason Whitfield, Inmaculada Sanchez-Romero, Michel Herde, Christian Henneberger, Harald L Janovjak, and Colin Jackson. “Ancestral Protein Reconstruction and Circular Permutation for Improving the Stability and Dynamic Range of FRET Sensors.” In Synthetic Protein Switches, edited by Viktor Stein, 1596:71–87. Synthetic Protein Switches. Springer, 2017. https://doi.org/10.1007/978-1-4939-6940-1_5.","ista":"Clifton B, Whitfield J, Sanchez-Romero I, Herde M, Henneberger C, Janovjak HL, Jackson C. 2017.Ancestral protein reconstruction and circular permutation for improving the stability and dynamic range of FRET sensors. In: Synthetic Protein Switches. Methods in Molecular Biology, vol. 1596, 71–87."},"user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Ben","last_name":"Clifton","full_name":"Clifton, Ben"},{"last_name":"Whitfield","full_name":"Whitfield, Jason","first_name":"Jason"},{"last_name":"Sanchez Romero","full_name":"Sanchez Romero, Inmaculada","id":"3D9C5D30-F248-11E8-B48F-1D18A9856A87","first_name":"Inmaculada"},{"last_name":"Herde","full_name":"Herde, Michel","first_name":"Michel"},{"first_name":"Christian","last_name":"Henneberger","full_name":"Henneberger, Christian"},{"first_name":"Harald L","id":"33BA6C30-F248-11E8-B48F-1D18A9856A87","last_name":"Janovjak","orcid":"0000-0002-8023-9315","full_name":"Janovjak, Harald L"},{"first_name":"Colin","full_name":"Jackson, Colin","last_name":"Jackson"}],"publist_id":"6451","editor":[{"first_name":"Viktor","full_name":"Stein, Viktor","last_name":"Stein"}],"title":"Ancestral protein reconstruction and circular permutation for improving the stability and dynamic range of FRET sensors","quality_controlled":"1","publisher":"Springer","year":"2017","day":"15","publication":"Synthetic Protein Switches","page":"71 - 87","doi":"10.1007/978-1-4939-6940-1_5","date_published":"2017-03-15T00:00:00Z","date_created":"2018-12-11T11:49:24Z","_id":"957","series_title":"Synthetic Protein Switches","type":"book_chapter","status":"public","date_updated":"2021-01-12T08:22:13Z","department":[{"_id":"HaJa"}],"abstract":[{"lang":"eng","text":"Small molecule biosensors based on Forster resonance energy transfer (FRET) enable small molecule signaling to be monitored with high spatial and temporal resolution in complex cellular environments. FRET sensors can be constructed by fusing a pair of fluorescent proteins to a suitable recognition domain, such as a member of the solute-binding protein (SBP) superfamily. However, naturally occurring SBPs may be unsuitable for incorporation into FRET sensors due to their low thermostability, which may preclude imaging under physiological conditions, or because the positions of their N- and C-termini may be suboptimal for fusion of fluorescent proteins, which may limit the dynamic range of the resulting sensors. Here, we show how these problems can be overcome using ancestral protein reconstruction and circular permutation. Ancestral protein reconstruction, used as a protein engineering strategy, leverages phylogenetic information to improve the thermostability of proteins, while circular permutation enables the termini of an SBP to be repositioned to maximize the dynamic range of the resulting FRET sensor. We also provide a protocol for cloning the engineered SBPs into FRET sensor constructs using Golden Gate assembly and discuss considerations for in situ characterization of the FRET sensors."}],"oa_version":"None","scopus_import":1,"alternative_title":["Methods in Molecular Biology"],"month":"03","intvolume":" 1596","publication_identifier":{"issn":["10643745"]},"publication_status":"published","language":[{"iso":"eng"}],"volume":1596},{"article_type":"original","type":"journal_article","status":"public","_id":"9574","date_updated":"2023-02-23T14:01:26Z","extern":"1","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1609.08136"}],"scopus_import":"1","intvolume":" 61","month":"08","abstract":[{"lang":"eng","text":"Consider the sum X(ξ)=∑ni=1aiξi, where a=(ai)ni=1 is a sequence of non-zero reals and ξ=(ξi)ni=1 is a sequence of i.i.d. Rademacher random variables (that is, Pr[ξi=1]=Pr[ξi=−1]=1/2). The classical Littlewood-Offord problem asks for the best possible upper bound on the concentration probabilities Pr[X=x]. In this paper we study a resilience version of the Littlewood-Offord problem: how many of the ξi is an adversary typically allowed to change without being able to force concentration on a particular value? We solve this problem asymptotically, and present a few interesting open problems."}],"oa_version":"Preprint","volume":61,"publication_status":"published","publication_identifier":{"issn":["1571-0653"]},"language":[{"iso":"eng"}],"article_processing_charge":"No","external_id":{"arxiv":["1609.08136"]},"author":[{"full_name":"Bandeira, Afonso S.","last_name":"Bandeira","first_name":"Afonso S."},{"first_name":"Asaf","full_name":"Ferber, Asaf","last_name":"Ferber"},{"last_name":"Kwan","orcid":"0000-0002-4003-7567","full_name":"Kwan, Matthew Alan","id":"5fca0887-a1db-11eb-95d1-ca9d5e0453b3","first_name":"Matthew Alan"}],"title":"Resilience for the Littlewood-Offord problem","citation":{"chicago":"Bandeira, Afonso S., Asaf Ferber, and Matthew Alan Kwan. “Resilience for the Littlewood-Offord Problem.” Electronic Notes in Discrete Mathematics. Elsevier, 2017. https://doi.org/10.1016/j.endm.2017.06.025.","ista":"Bandeira AS, Ferber A, Kwan MA. 2017. Resilience for the Littlewood-Offord problem. Electronic Notes in Discrete Mathematics. 61, 93–99.","mla":"Bandeira, Afonso S., et al. “Resilience for the Littlewood-Offord Problem.” Electronic Notes in Discrete Mathematics, vol. 61, Elsevier, 2017, pp. 93–99, doi:10.1016/j.endm.2017.06.025.","ama":"Bandeira AS, Ferber A, Kwan MA. Resilience for the Littlewood-Offord problem. Electronic Notes in Discrete Mathematics. 2017;61:93-99. doi:10.1016/j.endm.2017.06.025","apa":"Bandeira, A. S., Ferber, A., & Kwan, M. A. (2017). Resilience for the Littlewood-Offord problem. Electronic Notes in Discrete Mathematics. Elsevier. https://doi.org/10.1016/j.endm.2017.06.025","ieee":"A. S. Bandeira, A. Ferber, and M. A. Kwan, “Resilience for the Littlewood-Offord problem,” Electronic Notes in Discrete Mathematics, vol. 61. Elsevier, pp. 93–99, 2017.","short":"A.S. Bandeira, A. Ferber, M.A. Kwan, Electronic Notes in Discrete Mathematics 61 (2017) 93–99."},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","oa":1,"quality_controlled":"1","publisher":"Elsevier","page":"93-99","date_created":"2021-06-21T06:31:10Z","date_published":"2017-08-01T00:00:00Z","doi":"10.1016/j.endm.2017.06.025","year":"2017","publication":"Electronic Notes in Discrete Mathematics","day":"01"},{"publication_status":"published","publication_identifier":{"eissn":["1095-7146"],"issn":["0895-4801"]},"language":[{"iso":"eng"}],"issue":"1","volume":31,"abstract":[{"lang":"eng","text":"We show that for any fixed dense graph G and bounded-degree tree T on the same number of vertices, a modest random perturbation of G will typically contain a copy of T . This combines the viewpoints of the well-studied problems of embedding trees into fixed dense graphs and into random graphs, and extends a sizeable body of existing research on randomly perturbed graphs. Specifically, we show that there is c=c(α,Δ) such that if G is an n-vertex graph with minimum degree at least αn, and T is an n-vertex tree with maximum degree at most Δ , then if we add cn uniformly random edges to G, the resulting graph will contain T asymptotically almost surely (as n→∞ ). Our proof uses a lemma concerning the decomposition of a dense graph into super-regular pairs of comparable sizes, which may be of independent interest."}],"oa_version":"Preprint","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1507.07960"}],"scopus_import":"1","intvolume":" 31","month":"01","date_updated":"2023-02-23T14:02:05Z","extern":"1","_id":"9590","type":"journal_article","article_type":"original","status":"public","year":"2017","publication":"SIAM Journal on Discrete Mathematics","day":"12","page":"155-171","date_created":"2021-06-22T12:26:25Z","doi":"10.1137/15m1032910","date_published":"2017-01-12T00:00:00Z","oa":1,"quality_controlled":"1","publisher":"Society for Industrial & Applied Mathematics","citation":{"mla":"Krivelevich, Michael, et al. “Bounded-Degree Spanning Trees in Randomly Perturbed Graphs.” SIAM Journal on Discrete Mathematics, vol. 31, no. 1, Society for Industrial & Applied Mathematics, 2017, pp. 155–71, doi:10.1137/15m1032910.","apa":"Krivelevich, M., Kwan, M. A., & Sudakov, B. (2017). Bounded-degree spanning trees in randomly perturbed graphs. SIAM Journal on Discrete Mathematics. Society for Industrial & Applied Mathematics. https://doi.org/10.1137/15m1032910","ama":"Krivelevich M, Kwan MA, Sudakov B. Bounded-degree spanning trees in randomly perturbed graphs. SIAM Journal on Discrete Mathematics. 2017;31(1):155-171. doi:10.1137/15m1032910","ieee":"M. Krivelevich, M. A. Kwan, and B. Sudakov, “Bounded-degree spanning trees in randomly perturbed graphs,” SIAM Journal on Discrete Mathematics, vol. 31, no. 1. Society for Industrial & Applied Mathematics, pp. 155–171, 2017.","short":"M. Krivelevich, M.A. Kwan, B. Sudakov, SIAM Journal on Discrete Mathematics 31 (2017) 155–171.","chicago":"Krivelevich, Michael, Matthew Alan Kwan, and Benny Sudakov. “Bounded-Degree Spanning Trees in Randomly Perturbed Graphs.” SIAM Journal on Discrete Mathematics. Society for Industrial & Applied Mathematics, 2017. https://doi.org/10.1137/15m1032910.","ista":"Krivelevich M, Kwan MA, Sudakov B. 2017. Bounded-degree spanning trees in randomly perturbed graphs. SIAM Journal on Discrete Mathematics. 31(1), 155–171."},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","article_processing_charge":"No","external_id":{"arxiv":["1507.07960"]},"author":[{"full_name":"Krivelevich, Michael","last_name":"Krivelevich","first_name":"Michael"},{"last_name":"Kwan","orcid":"0000-0002-4003-7567","full_name":"Kwan, Matthew Alan","id":"5fca0887-a1db-11eb-95d1-ca9d5e0453b3","first_name":"Matthew Alan"},{"last_name":"Sudakov","full_name":"Sudakov, Benny","first_name":"Benny"}],"title":"Bounded-degree spanning trees in randomly perturbed graphs"},{"oa":1,"publisher":"Elsevier","quality_controlled":"1","year":"2017","publication":"Advances in Mathematics","day":"15","page":"292-312","date_created":"2021-06-22T11:51:27Z","doi":"10.1016/j.aim.2017.08.031","date_published":"2017-10-15T00:00:00Z","citation":{"apa":"Bandeira, A. S., Ferber, A., & Kwan, M. A. (2017). Resilience for the Littlewood–Offord problem. Advances in Mathematics. Elsevier. https://doi.org/10.1016/j.aim.2017.08.031","ama":"Bandeira AS, Ferber A, Kwan MA. Resilience for the Littlewood–Offord problem. Advances in Mathematics. 2017;319:292-312. doi:10.1016/j.aim.2017.08.031","ieee":"A. S. Bandeira, A. Ferber, and M. A. Kwan, “Resilience for the Littlewood–Offord problem,” Advances in Mathematics, vol. 319. Elsevier, pp. 292–312, 2017.","short":"A.S. Bandeira, A. Ferber, M.A. Kwan, Advances in Mathematics 319 (2017) 292–312.","mla":"Bandeira, Afonso S., et al. “Resilience for the Littlewood–Offord Problem.” Advances in Mathematics, vol. 319, Elsevier, 2017, pp. 292–312, doi:10.1016/j.aim.2017.08.031.","ista":"Bandeira AS, Ferber A, Kwan MA. 2017. Resilience for the Littlewood–Offord problem. Advances in Mathematics. 319, 292–312.","chicago":"Bandeira, Afonso S., Asaf Ferber, and Matthew Alan Kwan. “Resilience for the Littlewood–Offord Problem.” Advances in Mathematics. Elsevier, 2017. https://doi.org/10.1016/j.aim.2017.08.031."},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","article_processing_charge":"No","external_id":{"arxiv":["1609.08136"]},"author":[{"first_name":"Afonso S.","full_name":"Bandeira, Afonso S.","last_name":"Bandeira"},{"first_name":"Asaf","last_name":"Ferber","full_name":"Ferber, Asaf"},{"first_name":"Matthew Alan","id":"5fca0887-a1db-11eb-95d1-ca9d5e0453b3","last_name":"Kwan","orcid":"0000-0002-4003-7567","full_name":"Kwan, Matthew Alan"}],"title":"Resilience for the Littlewood–Offord problem","abstract":[{"lang":"eng","text":"Consider the sum X(ξ)=∑ni=1aiξi , where a=(ai)ni=1 is a sequence of non-zero reals and ξ=(ξi)ni=1 is a sequence of i.i.d. Rademacher random variables (that is, Pr[ξi=1]=Pr[ξi=−1]=1/2 ). The classical Littlewood-Offord problem asks for the best possible upper bound on the concentration probabilities Pr[X=x] . In this paper we study a resilience version of the Littlewood-Offord problem: how many of the ξi is an adversary typically allowed to change without being able to force concentration on a particular value? We solve this problem asymptotically, and present a few interesting open problems."}],"oa_version":"Preprint","main_file_link":[{"url":"https://arxiv.org/abs/1609.08136","open_access":"1"}],"scopus_import":"1","intvolume":" 319","month":"10","publication_status":"published","publication_identifier":{"issn":["0001-8708"]},"language":[{"iso":"eng"}],"volume":319,"_id":"9588","type":"journal_article","article_type":"original","status":"public","date_updated":"2023-02-23T14:01:57Z","extern":"1"},{"month":"06","intvolume":" 63","scopus_import":"1","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1016/j.ejc.2017.02.003"}],"oa_version":"Published Version","abstract":[{"lang":"eng","text":"We give an asymptotic expression for the expected number of spanning trees in a random graph with a given degree sequence , provided that the number of edges is at least , where is the maximum degree. A key part of our argument involves establishing a concentration result for a certain family of functions over random trees with given degrees, using Prüfer codes."}],"volume":63,"language":[{"iso":"eng"}],"publication_identifier":{"issn":["0195-6698"]},"publication_status":"published","status":"public","type":"journal_article","article_type":"original","_id":"9589","extern":"1","date_updated":"2023-02-23T14:02:00Z","quality_controlled":"1","publisher":"Elsevier","oa":1,"doi":"10.1016/j.ejc.2017.02.003","date_published":"2017-06-01T00:00:00Z","date_created":"2021-06-22T12:18:59Z","page":"6-25","day":"01","publication":"European Journal of Combinatorics","year":"2017","title":"The average number of spanning trees in sparse graphs with given degrees","author":[{"last_name":"Greenhill","full_name":"Greenhill, Catherine","first_name":"Catherine"},{"first_name":"Mikhail","last_name":"Isaev","full_name":"Isaev, Mikhail"},{"id":"5fca0887-a1db-11eb-95d1-ca9d5e0453b3","first_name":"Matthew Alan","full_name":"Kwan, Matthew Alan","orcid":"0000-0002-4003-7567","last_name":"Kwan"},{"last_name":"McKay","full_name":"McKay, Brendan D.","first_name":"Brendan D."}],"article_processing_charge":"No","external_id":{"arxiv":["1606.01586"]},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","citation":{"mla":"Greenhill, Catherine, et al. “The Average Number of Spanning Trees in Sparse Graphs with given Degrees.” European Journal of Combinatorics, vol. 63, Elsevier, 2017, pp. 6–25, doi:10.1016/j.ejc.2017.02.003.","ieee":"C. Greenhill, M. Isaev, M. A. Kwan, and B. D. McKay, “The average number of spanning trees in sparse graphs with given degrees,” European Journal of Combinatorics, vol. 63. Elsevier, pp. 6–25, 2017.","short":"C. Greenhill, M. Isaev, M.A. Kwan, B.D. McKay, European Journal of Combinatorics 63 (2017) 6–25.","apa":"Greenhill, C., Isaev, M., Kwan, M. A., & McKay, B. D. (2017). The average number of spanning trees in sparse graphs with given degrees. European Journal of Combinatorics. Elsevier. https://doi.org/10.1016/j.ejc.2017.02.003","ama":"Greenhill C, Isaev M, Kwan MA, McKay BD. The average number of spanning trees in sparse graphs with given degrees. European Journal of Combinatorics. 2017;63:6-25. doi:10.1016/j.ejc.2017.02.003","chicago":"Greenhill, Catherine, Mikhail Isaev, Matthew Alan Kwan, and Brendan D. McKay. “The Average Number of Spanning Trees in Sparse Graphs with given Degrees.” European Journal of Combinatorics. Elsevier, 2017. https://doi.org/10.1016/j.ejc.2017.02.003.","ista":"Greenhill C, Isaev M, Kwan MA, McKay BD. 2017. The average number of spanning trees in sparse graphs with given degrees. European Journal of Combinatorics. 63, 6–25."}},{"doi":"10.4230/LIPIcs.MFCS.2017.37","date_published":"2017-06-01T00:00:00Z","date_created":"2018-12-11T11:49:26Z","has_accepted_license":"1","year":"2017","day":"01","publisher":"Schloss Dagstuhl - Leibniz-Zentrum für Informatik","quality_controlled":"1","oa":1,"author":[{"last_name":"Avni","orcid":"0000-0001-5588-8287","full_name":"Avni, Guy","id":"463C8BC2-F248-11E8-B48F-1D18A9856A87","first_name":"Guy"},{"first_name":"Shibashis","last_name":"Guha","full_name":"Guha, Shibashis"},{"first_name":"Orna","last_name":"Kupferman","full_name":"Kupferman, Orna"}],"publist_id":"6438","title":"Timed network games with clocks","citation":{"mla":"Avni, Guy, et al. Timed Network Games with Clocks. Vol. 83, 37, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017, doi:10.4230/LIPIcs.MFCS.2017.37.","ieee":"G. Avni, S. Guha, and O. Kupferman, “Timed network games with clocks,” presented at the MFCS: Mathematical Foundations of Computer Science (SG), Aalborg, Denmark, 2017, vol. 83.","short":"G. Avni, S. Guha, O. Kupferman, in:, Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017.","apa":"Avni, G., Guha, S., & Kupferman, O. (2017). Timed network games with clocks (Vol. 83). Presented at the MFCS: Mathematical Foundations of Computer Science (SG), Aalborg, Denmark: Schloss Dagstuhl - Leibniz-Zentrum für Informatik. https://doi.org/10.4230/LIPIcs.MFCS.2017.37","ama":"Avni G, Guha S, Kupferman O. Timed network games with clocks. In: Vol 83. Schloss Dagstuhl - Leibniz-Zentrum für Informatik; 2017. doi:10.4230/LIPIcs.MFCS.2017.37","chicago":"Avni, Guy, Shibashis Guha, and Orna Kupferman. “Timed Network Games with Clocks,” Vol. 83. Schloss Dagstuhl - Leibniz-Zentrum für Informatik, 2017. https://doi.org/10.4230/LIPIcs.MFCS.2017.37.","ista":"Avni G, Guha S, Kupferman O. 2017. Timed network games with clocks. MFCS: Mathematical Foundations of Computer Science (SG), LIPIcs, vol. 83, 37."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","project":[{"grant_number":"S11402-N23","name":"Moderne Concurrency Paradigms","call_identifier":"FWF","_id":"25F5A88A-B435-11E9-9278-68D0E5697425"}],"article_number":"37","related_material":{"record":[{"id":"6005","status":"public","relation":"later_version"}]},"volume":83,"publication_identifier":{"issn":["18688969"]},"publication_status":"published","file":[{"relation":"main_file","access_level":"open_access","content_type":"application/pdf","checksum":"f55eaf7f3c36ea07801112acfedd17d5","file_id":"5059","creator":"system","file_size":369730,"date_updated":"2020-07-14T12:48:18Z","file_name":"IST-2017-829-v1+1_mfcs-cr.pdf","date_created":"2018-12-12T10:14:10Z"}],"language":[{"iso":"eng"}],"alternative_title":["LIPIcs"],"scopus_import":1,"month":"06","intvolume":" 83","abstract":[{"text":"Network games are widely used as a model for selfish resource-allocation problems. In the classical model, each player selects a path connecting her source and target vertex. The cost of traversing an edge depends on the number of players that traverse it. Thus, it abstracts the fact that different users may use a resource at different times and for different durations, which plays an important role in defining the costs of the users in reality. For example, when transmitting packets in a communication network, routing traffic in a road network, or processing a task in a production system, the traversal of the network involves an inherent delay, and so sharing and congestion of resources crucially depends on time. We study timed network games , which add a time component to network games. Each vertex v in the network is associated with a cost function, mapping the load on v to the price that a player pays for staying in v for one time unit with this load. In addition, each edge has a guard, describing time intervals in which the edge can be traversed, forcing the players to spend time on vertices. Unlike earlier work that add a time component to network games, the time in our model is continuous and cannot be discretized. In particular, players have uncountably many strategies, and a game may have uncountably many pure Nash equilibria. We study properties of timed network games with cost-sharing or congestion cost functions: their stability, equilibrium inefficiency, and complexity. In particular, we show that the answer to the question whether we can restrict attention to boundary strategies, namely ones in which edges are traversed only at the boundaries of guards, is mixed. ","lang":"eng"}],"oa_version":"Published Version","file_date_updated":"2020-07-14T12:48:18Z","department":[{"_id":"ToHe"}],"date_updated":"2023-02-23T12:35:50Z","ddc":["004"],"type":"conference","conference":{"name":"MFCS: Mathematical Foundations of Computer Science (SG)","start_date":"2017-08-21","end_date":"2017-08-25","location":"Aalborg, Denmark"},"tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"status":"public","pubrep_id":"829","_id":"963"},{"day":"18","year":"2017","date_created":"2021-07-23T11:34:34Z","date_published":"2017-10-18T00:00:00Z","doi":"10.5061/dryad.1f1rc","related_material":{"record":[{"id":"1197","status":"public","relation":"used_in_publication"}]},"oa_version":"Published Version","abstract":[{"text":"Across the nervous system, certain population spiking patterns are observed far more frequently than others. A hypothesis about this structure is that these collective activity patterns function as population codewords–collective modes–carrying information distinct from that of any single cell. We investigate this phenomenon in recordings of ∼150 retinal ganglion cells, the retina’s output. We develop a novel statistical model that decomposes the population response into modes; it predicts the distribution of spiking activity in the ganglion cell population with high accuracy. We found that the modes represent localized features of the visual stimulus that are distinct from the features represented by single neurons. Modes form clusters of activity states that are readily discriminated from one another. When we repeated the same visual stimulus, we found that the same mode was robustly elicited. These results suggest that retinal ganglion cells’ collective signaling is endowed with a form of error-correcting code–a principle that may hold in brain areas beyond retina.","lang":"eng"}],"month":"10","oa":1,"main_file_link":[{"url":"https://doi.org/10.5061/dryad.1f1rc","open_access":"1"}],"publisher":"Dryad","user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","citation":{"ama":"Prentice J, Marre O, Ioffe M, Loback A, Tkačik G, Berry M. Data from: Error-robust modes of the retinal population code. 2017. doi:10.5061/dryad.1f1rc","apa":"Prentice, J., Marre, O., Ioffe, M., Loback, A., Tkačik, G., & Berry, M. (2017). Data from: Error-robust modes of the retinal population code. Dryad. https://doi.org/10.5061/dryad.1f1rc","ieee":"J. Prentice, O. Marre, M. Ioffe, A. Loback, G. Tkačik, and M. Berry, “Data from: Error-robust modes of the retinal population code.” Dryad, 2017.","short":"J. Prentice, O. Marre, M. Ioffe, A. Loback, G. Tkačik, M. Berry, (2017).","mla":"Prentice, Jason, et al. 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Such metabolic specialization could be driven by stochastic gene expression and could provide individual cells with growth benefits of specialization. We measured the degree of phenotypic specialization in two parallel metabolic pathways, the assimilation of glucose and arabinose. We grew Escherichia coli in chemostats, and used isotope-labeled sugars in combination with nanometer-scale secondary ion mass spectrometry and mathematical modeling to quantify sugar assimilation at the single-cell level. We found large variation in metabolic activities between single cells, both in absolute assimilation and in the degree to which individual cells specialize in the assimilation of different sugars. Analysis of transcriptional reporters indicated that this variation was at least partially based on cell-to-cell variation in gene expression. Metabolic differences between cells in clonal populations could potentially reduce metabolic incompatibilities between different pathways, and increase the rate at which parallel reactions can be performed."}],"month":"12","intvolume":" 13","scopus_import":1,"file":[{"file_id":"5088","checksum":"22426d9382f21554bad5fa5967afcfd0","access_level":"open_access","relation":"main_file","content_type":"application/pdf","date_created":"2018-12-12T10:14:35Z","file_name":"IST-2018-959-v1+1_2017_Nikolic_Cell-to-cell.pdf","creator":"system","date_updated":"2020-07-14T12:46:46Z","file_size":1308475}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["15537390"]},"publication_status":"published","volume":13,"related_material":{"record":[{"status":"public","id":"9844","relation":"research_data"},{"relation":"research_data","id":"9845","status":"public"},{"relation":"research_data","status":"public","id":"9846"}]},"issue":"12","ec_funded":1,"article_number":"e1007122","project":[{"_id":"25681D80-B435-11E9-9278-68D0E5697425","call_identifier":"FP7","grant_number":"291734","name":"International IST Postdoc Fellowship Programme"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"short":"N. 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Sensory noise predicts divisive reshaping of receptive fields. PLoS Computational Biology. 13(6), e1005582."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","article_number":"e1005582","date_created":"2018-12-11T11:47:53Z","doi":"10.1371/journal.pcbi.1005582","date_published":"2017-06-01T00:00:00Z","year":"2017","has_accepted_license":"1","publication":"PLoS Computational Biology","day":"01","oa":1,"quality_controlled":"1","publisher":"Public Library of Science","file_date_updated":"2020-07-14T12:47:40Z","department":[{"_id":"GaTk"}],"date_updated":"2023-02-23T14:10:54Z","ddc":["571"],"tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"type":"journal_article","pubrep_id":"898","status":"public","_id":"680","volume":13,"issue":"6","related_material":{"record":[{"status":"public","id":"9855","relation":"research_data"}]},"publication_status":"published","publication_identifier":{"issn":["1553734X"]},"language":[{"iso":"eng"}],"file":[{"creator":"system","date_updated":"2020-07-14T12:47:40Z","file_size":14555676,"date_created":"2018-12-12T10:07:47Z","file_name":"IST-2017-898-v1+1_journal.pcbi.1005582.pdf","access_level":"open_access","relation":"main_file","content_type":"application/pdf","checksum":"796a1026076af6f4405a47d985bc7b68","file_id":"4645"}],"scopus_import":1,"intvolume":" 13","month":"06","abstract":[{"text":"In order to respond reliably to specific features of their environment, sensory neurons need to integrate multiple incoming noisy signals. Crucially, they also need to compete for the interpretation of those signals with other neurons representing similar features. The form that this competition should take depends critically on the noise corrupting these signals. In this study we show that for the type of noise commonly observed in sensory systems, whose variance scales with the mean signal, sensory neurons should selectively divide their input signals by their predictions, suppressing ambiguous cues while amplifying others. Any change in the stimulus context alters which inputs are suppressed, leading to a deep dynamic reshaping of neural receptive fields going far beyond simple surround suppression. Paradoxically, these highly variable receptive fields go alongside and are in fact required for an invariant representation of external sensory features. In addition to offering a normative account of context-dependent changes in sensory responses, perceptual inference in the presence of signal-dependent noise accounts for ubiquitous features of sensory neurons such as divisive normalization, gain control and contrast dependent temporal dynamics.","lang":"eng"}],"oa_version":"Published Version"},{"year":"2017","day":"18","related_material":{"record":[{"relation":"used_in_publication","status":"public","id":"696"}]},"doi":"10.1371/journal.pcbi.1005609.s003","date_published":"2017-07-18T00:00:00Z","date_created":"2021-08-09T14:08:14Z","abstract":[{"text":"Based on the intuitive derivation of the dynamics of SIM allele frequency pM in the main text, we present a heuristic prediction for the long-term SIM allele frequencies with χ > 1 stresses and compare it to numerical simulations.","lang":"eng"}],"oa_version":"Published Version","publisher":"Public Library of Science","month":"07","date_updated":"2023-02-23T12:55:39Z","citation":{"ista":"Lukacisinova M, Novak S, Paixao T. 2017. Heuristic prediction for multiple stresses, Public Library of Science, 10.1371/journal.pcbi.1005609.s003.","chicago":"Lukacisinova, Marta, Sebastian Novak, and Tiago Paixao. “Heuristic Prediction for Multiple Stresses.” Public Library of Science, 2017. https://doi.org/10.1371/journal.pcbi.1005609.s003.","apa":"Lukacisinova, M., Novak, S., & Paixao, T. (2017). Heuristic prediction for multiple stresses. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1005609.s003","ama":"Lukacisinova M, Novak S, Paixao T. Heuristic prediction for multiple stresses. 2017. doi:10.1371/journal.pcbi.1005609.s003","ieee":"M. Lukacisinova, S. Novak, and T. Paixao, “Heuristic prediction for multiple stresses.” Public Library of Science, 2017.","short":"M. Lukacisinova, S. Novak, T. Paixao, (2017).","mla":"Lukacisinova, Marta, et al. Heuristic Prediction for Multiple Stresses. Public Library of Science, 2017, doi:10.1371/journal.pcbi.1005609.s003."},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","author":[{"last_name":"Lukacisinova","orcid":"0000-0002-2519-8004","full_name":"Lukacisinova, Marta","first_name":"Marta","id":"4342E402-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Novak, Sebastian","last_name":"Novak","first_name":"Sebastian","id":"461468AE-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Paixao","full_name":"Paixao, Tiago","orcid":"0000-0003-2361-3953","id":"2C5658E6-F248-11E8-B48F-1D18A9856A87","first_name":"Tiago"}],"article_processing_charge":"No","department":[{"_id":"ToBo"},{"_id":"CaGu"},{"_id":"NiBa"}],"title":"Heuristic prediction for multiple stresses","_id":"9851","type":"research_data_reference","status":"public"},{"type":"research_data_reference","status":"public","_id":"9852","author":[{"orcid":"0000-0002-2519-8004","full_name":"Lukacisinova, Marta","last_name":"Lukacisinova","id":"4342E402-F248-11E8-B48F-1D18A9856A87","first_name":"Marta"},{"full_name":"Novak, Sebastian","last_name":"Novak","id":"461468AE-F248-11E8-B48F-1D18A9856A87","first_name":"Sebastian"},{"full_name":"Paixao, Tiago","orcid":"0000-0003-2361-3953","last_name":"Paixao","id":"2C5658E6-F248-11E8-B48F-1D18A9856A87","first_name":"Tiago"}],"article_processing_charge":"No","department":[{"_id":"ToBo"},{"_id":"CaGu"},{"_id":"NiBa"}],"title":"Resistance frequencies for different combination strategies","date_updated":"2023-02-23T12:55:39Z","citation":{"chicago":"Lukacisinova, Marta, Sebastian Novak, and Tiago Paixao. “Resistance Frequencies for Different Combination Strategies.” Public Library of Science, 2017. https://doi.org/10.1371/journal.pcbi.1005609.s004.","ista":"Lukacisinova M, Novak S, Paixao T. 2017. Resistance frequencies for different combination strategies, Public Library of Science, 10.1371/journal.pcbi.1005609.s004.","mla":"Lukacisinova, Marta, et al. Resistance Frequencies for Different Combination Strategies. Public Library of Science, 2017, doi:10.1371/journal.pcbi.1005609.s004.","ama":"Lukacisinova M, Novak S, Paixao T. Resistance frequencies for different combination strategies. 2017. doi:10.1371/journal.pcbi.1005609.s004","apa":"Lukacisinova, M., Novak, S., & Paixao, T. (2017). Resistance frequencies for different combination strategies. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1005609.s004","ieee":"M. Lukacisinova, S. Novak, and T. Paixao, “Resistance frequencies for different combination strategies.” Public Library of Science, 2017.","short":"M. Lukacisinova, S. Novak, T. Paixao, (2017)."},"user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","publisher":"Public Library of Science","month":"07","abstract":[{"lang":"eng","text":"We show how different combination strategies affect the fraction of individuals that are multi-resistant."}],"oa_version":"Published Version","date_published":"2017-07-18T00:00:00Z","doi":"10.1371/journal.pcbi.1005609.s004","related_material":{"record":[{"status":"public","id":"696","relation":"used_in_publication"}]},"date_created":"2021-08-09T14:11:40Z","year":"2017","day":"18"},{"status":"public","type":"research_data_reference","_id":"9855","department":[{"_id":"GaTk"}],"title":"Supplementary appendix","author":[{"last_name":"Chalk","full_name":"Chalk, Matthew J","orcid":"0000-0001-7782-4436","first_name":"Matthew J","id":"2BAAC544-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Paul","last_name":"Masset","full_name":"Masset, Paul"},{"first_name":"Boris","full_name":"Gutkin, Boris","last_name":"Gutkin"},{"last_name":"Denève","full_name":"Denève, Sophie","first_name":"Sophie"}],"article_processing_charge":"No","user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","date_updated":"2023-02-23T12:52:17Z","citation":{"ista":"Chalk MJ, Masset P, Gutkin B, Denève S. 2017. Supplementary appendix, Public Library of Science, 10.1371/journal.pcbi.1005582.s001.","chicago":"Chalk, Matthew J, Paul Masset, Boris Gutkin, and Sophie Denève. “Supplementary Appendix.” Public Library of Science, 2017. https://doi.org/10.1371/journal.pcbi.1005582.s001.","short":"M.J. Chalk, P. Masset, B. Gutkin, S. Denève, (2017).","ieee":"M. J. Chalk, P. Masset, B. Gutkin, and S. Denève, “Supplementary appendix.” Public Library of Science, 2017.","apa":"Chalk, M. J., Masset, P., Gutkin, B., & Denève, S. (2017). Supplementary appendix. Public Library of Science. https://doi.org/10.1371/journal.pcbi.1005582.s001","ama":"Chalk MJ, Masset P, Gutkin B, Denève S. Supplementary appendix. 2017. doi:10.1371/journal.pcbi.1005582.s001","mla":"Chalk, Matthew J., et al. Supplementary Appendix. Public Library of Science, 2017, doi:10.1371/journal.pcbi.1005582.s001."},"month":"06","publisher":"Public Library of Science","oa_version":"Published Version","abstract":[{"lang":"eng","text":"Includes derivation of optimal estimation algorithm, generalisation to non-poisson noise statistics, correlated input noise, and implementation of in a multi-layer neural network."}],"related_material":{"record":[{"status":"public","id":"680","relation":"used_in_publication"}]},"doi":"10.1371/journal.pcbi.1005582.s001","date_published":"2017-06-01T00:00:00Z","date_created":"2021-08-10T07:05:10Z","day":"01","year":"2017"},{"page":"175-209","date_published":"2017-12-08T00:00:00Z","doi":"10.1215/00127094-2017-0038","date_created":"2020-09-17T10:42:42Z","year":"2017","day":"08","publication":"Duke Mathematical Journal","publisher":"Duke University Press","quality_controlled":"1","oa":1,"author":[{"last_name":"Huang","full_name":"Huang, Guan","first_name":"Guan"},{"full_name":"Kaloshin, Vadim","orcid":"0000-0002-6051-2628","last_name":"Kaloshin","id":"FE553552-CDE8-11E9-B324-C0EBE5697425","first_name":"Vadim"},{"full_name":"Sorrentino, Alfonso","last_name":"Sorrentino","first_name":"Alfonso"}],"external_id":{"arxiv":["1603.08838"]},"article_processing_charge":"No","title":"On the marked length spectrum of generic strictly convex billiard tables","citation":{"chicago":"Huang, Guan, Vadim Kaloshin, and Alfonso Sorrentino. “On the Marked Length Spectrum of Generic Strictly Convex Billiard Tables.” Duke Mathematical Journal. Duke University Press, 2017. https://doi.org/10.1215/00127094-2017-0038.","ista":"Huang G, Kaloshin V, Sorrentino A. 2017. On the marked length spectrum of generic strictly convex billiard tables. Duke Mathematical Journal. 167(1), 175–209.","mla":"Huang, Guan, et al. “On the Marked Length Spectrum of Generic Strictly Convex Billiard Tables.” Duke Mathematical Journal, vol. 167, no. 1, Duke University Press, 2017, pp. 175–209, doi:10.1215/00127094-2017-0038.","apa":"Huang, G., Kaloshin, V., & Sorrentino, A. (2017). On the marked length spectrum of generic strictly convex billiard tables. Duke Mathematical Journal. Duke University Press. https://doi.org/10.1215/00127094-2017-0038","ama":"Huang G, Kaloshin V, Sorrentino A. On the marked length spectrum of generic strictly convex billiard tables. Duke Mathematical Journal. 2017;167(1):175-209. doi:10.1215/00127094-2017-0038","ieee":"G. Huang, V. Kaloshin, and A. Sorrentino, “On the marked length spectrum of generic strictly convex billiard tables,” Duke Mathematical Journal, vol. 167, no. 1. Duke University Press, pp. 175–209, 2017.","short":"G. Huang, V. Kaloshin, A. Sorrentino, Duke Mathematical Journal 167 (2017) 175–209."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","volume":167,"issue":"1","publication_identifier":{"issn":["0012-7094"]},"publication_status":"published","language":[{"iso":"eng"}],"main_file_link":[{"url":"https://arxiv.org/abs/1603.08838","open_access":"1"}],"month":"12","intvolume":" 167","abstract":[{"lang":"eng","text":"In this paper we show that for a generic strictly convex domain, one can recover the eigendata corresponding to Aubry–Mather periodic orbits of the induced billiard map from the (maximal) marked length spectrum of the domain."}],"oa_version":"Preprint","date_updated":"2021-01-12T08:19:11Z","extern":"1","article_type":"original","type":"journal_article","status":"public","_id":"8423"},{"extern":"1","date_updated":"2021-01-12T08:19:12Z","status":"public","type":"journal_article","article_type":"original","_id":"8427","volume":186,"issue":"1","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["0003-486X"]},"intvolume":" 186","month":"07","main_file_link":[{"url":"https://arxiv.org/abs/1606.00230","open_access":"1"}],"oa_version":"Preprint","abstract":[{"text":"We show that any sufficiently (finitely) smooth ℤ₂-symmetric strictly convex domain sufficiently close to a circle is dynamically spectrally rigid; i.e., all deformations among domains in the same class that preserve the length of all periodic orbits of the associated billiard flow must necessarily be isometric deformations. This gives a partial answer to a question of P. Sarnak.","lang":"eng"}],"title":"Dynamical spectral rigidity among Z2-symmetric strictly convex domains close to a circle","external_id":{"arxiv":["1606.00230"]},"article_processing_charge":"No","author":[{"first_name":"Jacopo","last_name":"De Simoi","full_name":"De Simoi, Jacopo"},{"id":"FE553552-CDE8-11E9-B324-C0EBE5697425","first_name":"Vadim","last_name":"Kaloshin","full_name":"Kaloshin, Vadim","orcid":"0000-0002-6051-2628"},{"full_name":"Wei, Qiaoling","last_name":"Wei","first_name":"Qiaoling"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ieee":"J. De Simoi, V. Kaloshin, and Q. Wei, “Dynamical spectral rigidity among Z2-symmetric strictly convex domains close to a circle,” Annals of Mathematics, vol. 186, no. 1. Annals of Mathematics, pp. 277–314, 2017.","short":"J. De Simoi, V. Kaloshin, Q. Wei, Annals of Mathematics 186 (2017) 277–314.","ama":"De Simoi J, Kaloshin V, Wei Q. Dynamical spectral rigidity among Z2-symmetric strictly convex domains close to a circle. Annals of Mathematics. 2017;186(1):277-314. doi:10.4007/annals.2017.186.1.7","apa":"De Simoi, J., Kaloshin, V., & Wei, Q. (2017). Dynamical spectral rigidity among Z2-symmetric strictly convex domains close to a circle. Annals of Mathematics. Annals of Mathematics. https://doi.org/10.4007/annals.2017.186.1.7","mla":"De Simoi, Jacopo, et al. “Dynamical Spectral Rigidity among Z2-Symmetric Strictly Convex Domains Close to a Circle.” Annals of Mathematics, vol. 186, no. 1, Annals of Mathematics, 2017, pp. 277–314, doi:10.4007/annals.2017.186.1.7.","ista":"De Simoi J, Kaloshin V, Wei Q. 2017. Dynamical spectral rigidity among Z2-symmetric strictly convex domains close to a circle. Annals of Mathematics. 186(1), 277–314.","chicago":"De Simoi, Jacopo, Vadim Kaloshin, and Qiaoling Wei. “Dynamical Spectral Rigidity among Z2-Symmetric Strictly Convex Domains Close to a Circle.” Annals of Mathematics. Annals of Mathematics, 2017. https://doi.org/10.4007/annals.2017.186.1.7."},"date_created":"2020-09-17T10:46:42Z","doi":"10.4007/annals.2017.186.1.7","date_published":"2017-07-01T00:00:00Z","page":"277-314","publication":"Annals of Mathematics","day":"01","year":"2017","oa":1,"quality_controlled":"1","publisher":"Annals of Mathematics"},{"citation":{"ista":"Rennella E, Sára T, Juen M, Wunderlich C, Imbert L, Solyom Z, Favier A, Ayala I, Weinhäupl K, Schanda P, Konrat R, Kreutz C, Brutscher B. 2017. RNA binding and chaperone activity of the E.coli cold-shock protein CspA. Nucleic Acids Research. 45(7), 4255–4268.","chicago":"Rennella, Enrico, Tomáš Sára, Michael Juen, Christoph Wunderlich, Lionel Imbert, Zsofia Solyom, Adrien Favier, et al. “RNA Binding and Chaperone Activity of the E.Coli Cold-Shock Protein CspA.” Nucleic Acids Research. Oxford University Press, 2017. https://doi.org/10.1093/nar/gkx044.","ama":"Rennella E, Sára T, Juen M, et al. RNA binding and chaperone activity of the E.coli cold-shock protein CspA. Nucleic Acids Research. 2017;45(7):4255-4268. doi:10.1093/nar/gkx044","apa":"Rennella, E., Sára, T., Juen, M., Wunderlich, C., Imbert, L., Solyom, Z., … Brutscher, B. (2017). RNA binding and chaperone activity of the E.coli cold-shock protein CspA. Nucleic Acids Research. Oxford University Press. https://doi.org/10.1093/nar/gkx044","short":"E. Rennella, T. Sára, M. Juen, C. Wunderlich, L. Imbert, Z. Solyom, A. Favier, I. Ayala, K. Weinhäupl, P. Schanda, R. Konrat, C. Kreutz, B. Brutscher, Nucleic Acids Research 45 (2017) 4255–4268.","ieee":"E. Rennella et al., “RNA binding and chaperone activity of the E.coli cold-shock protein CspA,” Nucleic Acids Research, vol. 45, no. 7. Oxford University Press, pp. 4255–4268, 2017.","mla":"Rennella, Enrico, et al. “RNA Binding and Chaperone Activity of the E.Coli Cold-Shock Protein CspA.” Nucleic Acids Research, vol. 45, no. 7, Oxford University Press, 2017, pp. 4255–68, doi:10.1093/nar/gkx044."},"date_updated":"2021-01-12T08:19:20Z","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","article_processing_charge":"No","author":[{"full_name":"Rennella, Enrico","last_name":"Rennella","first_name":"Enrico"},{"first_name":"Tomáš","full_name":"Sára, Tomáš","last_name":"Sára"},{"last_name":"Juen","full_name":"Juen, Michael","first_name":"Michael"},{"first_name":"Christoph","full_name":"Wunderlich, Christoph","last_name":"Wunderlich"},{"first_name":"Lionel","last_name":"Imbert","full_name":"Imbert, Lionel"},{"first_name":"Zsofia","full_name":"Solyom, Zsofia","last_name":"Solyom"},{"first_name":"Adrien","full_name":"Favier, Adrien","last_name":"Favier"},{"last_name":"Ayala","full_name":"Ayala, Isabel","first_name":"Isabel"},{"first_name":"Katharina","full_name":"Weinhäupl, Katharina","last_name":"Weinhäupl"},{"last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul"},{"first_name":"Robert","full_name":"Konrat, Robert","last_name":"Konrat"},{"first_name":"Christoph","last_name":"Kreutz","full_name":"Kreutz, Christoph"},{"first_name":"Bernhard","last_name":"Brutscher","full_name":"Brutscher, Bernhard"}],"title":"RNA binding and chaperone activity of the E.coli cold-shock protein CspA","_id":"8449","type":"journal_article","article_type":"original","status":"public","publication_status":"published","year":"2017","publication_identifier":{"issn":["0305-1048","1362-4962"]},"publication":"Nucleic Acids Research","language":[{"iso":"eng"}],"day":"20","page":"4255-4268","date_created":"2020-09-18T10:06:34Z","date_published":"2017-04-20T00:00:00Z","doi":"10.1093/nar/gkx044","issue":"7","volume":45,"abstract":[{"text":"Ensuring the correct folding of RNA molecules in the cell is of major importance for a large variety of biological functions. Therefore, chaperone proteins that assist RNA in adopting their functionally active states are abundant in all living organisms. An important feature of RNA chaperone proteins is that they do not require an external energy source to perform their activity, and that they interact transiently and non-specifically with their RNA targets. So far, little is known about the mechanistic details of the RNA chaperone activity of these proteins. Prominent examples of RNA chaperones are bacterial cold shock proteins (Csp) that have been reported to bind single-stranded RNA and DNA. Here, we have used advanced NMR spectroscopy techniques to investigate at atomic resolution the RNA-melting activity of CspA, the major cold shock protein of Escherichia coli, upon binding to different RNA hairpins. Real-time NMR provides detailed information on the folding kinetics and folding pathways. Finally, comparison of wild-type CspA with single-point mutants and small peptides yields insights into the complementary roles of aromatic and positively charged amino-acid side chains for the RNA chaperone activity of the protein.","lang":"eng"}],"oa_version":"None","quality_controlled":"1","publisher":"Oxford University Press","intvolume":" 45","month":"04"},{"title":"Protein conformational dynamics studied by 15N and 1HR1ρ relaxation dispersion: Application to wild-type and G53A ubiquitin crystals","author":[{"first_name":"Diego F.","last_name":"Gauto","full_name":"Gauto, Diego F."},{"last_name":"Hessel","full_name":"Hessel, Audrey","first_name":"Audrey"},{"last_name":"Rovó","full_name":"Rovó, Petra","first_name":"Petra"},{"last_name":"Kurauskas","full_name":"Kurauskas, Vilius","first_name":"Vilius"},{"full_name":"Linser, Rasmus","last_name":"Linser","first_name":"Rasmus"},{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","last_name":"Schanda"}],"article_processing_charge":"No","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_updated":"2021-01-12T08:19:20Z","citation":{"apa":"Gauto, D. F., Hessel, A., Rovó, P., Kurauskas, V., Linser, R., & Schanda, P. (2017). Protein conformational dynamics studied by 15N and 1HR1ρ relaxation dispersion: Application to wild-type and G53A ubiquitin crystals. Solid State Nuclear Magnetic Resonance. Elsevier. https://doi.org/10.1016/j.ssnmr.2017.04.002","ama":"Gauto DF, Hessel A, Rovó P, Kurauskas V, Linser R, Schanda P. Protein conformational dynamics studied by 15N and 1HR1ρ relaxation dispersion: Application to wild-type and G53A ubiquitin crystals. Solid State Nuclear Magnetic Resonance. 2017;87(10):86-95. doi:10.1016/j.ssnmr.2017.04.002","short":"D.F. Gauto, A. Hessel, P. Rovó, V. Kurauskas, R. Linser, P. Schanda, Solid State Nuclear Magnetic Resonance 87 (2017) 86–95.","ieee":"D. F. Gauto, A. Hessel, P. Rovó, V. Kurauskas, R. Linser, and P. Schanda, “Protein conformational dynamics studied by 15N and 1HR1ρ relaxation dispersion: Application to wild-type and G53A ubiquitin crystals,” Solid State Nuclear Magnetic Resonance, vol. 87, no. 10. Elsevier, pp. 86–95, 2017.","mla":"Gauto, Diego F., et al. “Protein Conformational Dynamics Studied by 15N and 1HR1ρ Relaxation Dispersion: Application to Wild-Type and G53A Ubiquitin Crystals.” Solid State Nuclear Magnetic Resonance, vol. 87, no. 10, Elsevier, 2017, pp. 86–95, doi:10.1016/j.ssnmr.2017.04.002.","ista":"Gauto DF, Hessel A, Rovó P, Kurauskas V, Linser R, Schanda P. 2017. Protein conformational dynamics studied by 15N and 1HR1ρ relaxation dispersion: Application to wild-type and G53A ubiquitin crystals. Solid State Nuclear Magnetic Resonance. 87(10), 86–95.","chicago":"Gauto, Diego F., Audrey Hessel, Petra Rovó, Vilius Kurauskas, Rasmus Linser, and Paul Schanda. “Protein Conformational Dynamics Studied by 15N and 1HR1ρ Relaxation Dispersion: Application to Wild-Type and G53A Ubiquitin Crystals.” Solid State Nuclear Magnetic Resonance. Elsevier, 2017. https://doi.org/10.1016/j.ssnmr.2017.04.002."},"status":"public","keyword":["Nuclear and High Energy Physics","Instrumentation","General Chemistry","Radiation"],"type":"journal_article","article_type":"original","_id":"8447","doi":"10.1016/j.ssnmr.2017.04.002","volume":87,"issue":"10","date_published":"2017-10-01T00:00:00Z","date_created":"2020-09-18T10:06:18Z","page":"86-95","day":"01","publication":"Solid State Nuclear Magnetic Resonance","language":[{"iso":"eng"}],"publication_identifier":{"issn":["0926-2040"]},"publication_status":"published","year":"2017","month":"10","intvolume":" 87","publisher":"Elsevier","quality_controlled":"1","oa_version":"None","abstract":[{"lang":"eng","text":"Solid-state NMR spectroscopy can provide site-resolved information about protein dynamics over many time scales. Here we combine protein deuteration, fast magic-angle spinning (~45–60 kHz) and proton detection to study dynamics of ubiquitin in microcrystals, and in particular a mutant in a region that undergoes microsecond motions in a β-turn region in the wild-type protein. We use 15N R1ρ relaxation measurements as a function of the radio-frequency (RF) field strength, i.e. relaxation dispersion, to probe how the G53A mutation alters these dynamics. We report a population-inversion of conformational states: the conformation that in the wild-type protein is populated only sparsely becomes the predominant state. We furthermore explore the potential to use amide-1H R1ρ relaxation to obtain insight into dynamics. We show that while quantitative interpretation of 1H relaxation remains beyond reach under the experimental conditions, due to coherent contributions to decay, one may extract qualitative information about flexibility."}]},{"oa_version":"None","abstract":[{"lang":"eng","text":"We present an improved fast mixing device based on the rapid mixing of two solutions inside the NMR probe, as originally proposed by Hore and coworkers (J. Am. Chem. Soc. 125 (2003) 12484–12492). Such a device is important for off-equilibrium studies of molecular kinetics by multidimensional real-time NMR spectrsocopy. The novelty of this device is that it allows removing the injector from the NMR detection volume after mixing, and thus provides good magnetic field homogeneity independently of the initial sample volume placed in the NMR probe. The apparatus is simple to build, inexpensive, and can be used without any hardware modification on any type of liquid-state NMR spectrometer. We demonstrate the performance of our fast mixing device in terms of improved magnetic field homogeneity, and show an application to the study of protein folding and the structural characterization of transiently populated folding intermediates."}],"month":"08","intvolume":" 281","publisher":"Elsevier","quality_controlled":"1","day":"01","language":[{"iso":"eng"}],"publication":"Journal of Magnetic Resonance","publication_identifier":{"issn":["1090-7807"]},"publication_status":"published","year":"2017","doi":"10.1016/j.jmr.2017.05.016","issue":"8","volume":281,"date_published":"2017-08-01T00:00:00Z","date_created":"2020-09-18T10:06:27Z","page":"125-129","_id":"8448","status":"public","keyword":["Nuclear and High Energy Physics","Biophysics","Biochemistry","Condensed Matter Physics"],"type":"journal_article","article_type":"original","extern":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Franco, Rémi, Adrien Favier, Paul Schanda, and Bernhard Brutscher. “Optimized Fast Mixing Device for Real-Time NMR Applications.” Journal of Magnetic Resonance. Elsevier, 2017. https://doi.org/10.1016/j.jmr.2017.05.016.","ista":"Franco R, Favier A, Schanda P, Brutscher B. 2017. Optimized fast mixing device for real-time NMR applications. Journal of Magnetic Resonance. 281(8), 125–129.","mla":"Franco, Rémi, et al. “Optimized Fast Mixing Device for Real-Time NMR Applications.” Journal of Magnetic Resonance, vol. 281, no. 8, Elsevier, 2017, pp. 125–29, doi:10.1016/j.jmr.2017.05.016.","short":"R. Franco, A. Favier, P. Schanda, B. Brutscher, Journal of Magnetic Resonance 281 (2017) 125–129.","ieee":"R. Franco, A. Favier, P. Schanda, and B. Brutscher, “Optimized fast mixing device for real-time NMR applications,” Journal of Magnetic Resonance, vol. 281, no. 8. Elsevier, pp. 125–129, 2017.","ama":"Franco R, Favier A, Schanda P, Brutscher B. Optimized fast mixing device for real-time NMR applications. Journal of Magnetic Resonance. 2017;281(8):125-129. doi:10.1016/j.jmr.2017.05.016","apa":"Franco, R., Favier, A., Schanda, P., & Brutscher, B. (2017). Optimized fast mixing device for real-time NMR applications. Journal of Magnetic Resonance. Elsevier. https://doi.org/10.1016/j.jmr.2017.05.016"},"date_updated":"2021-01-12T08:19:20Z","title":"Optimized fast mixing device for real-time NMR applications","author":[{"last_name":"Franco","full_name":"Franco, Rémi","first_name":"Rémi"},{"full_name":"Favier, Adrien","last_name":"Favier","first_name":"Adrien"},{"first_name":"Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul","last_name":"Schanda"},{"last_name":"Brutscher","full_name":"Brutscher, Bernhard","first_name":"Bernhard"}],"article_processing_charge":"No"},{"intvolume":" 56","month":"01","quality_controlled":"1","publisher":"Wiley","oa_version":"None","abstract":[{"lang":"eng","text":"The structure, dynamics, and function of membrane proteins are intimately linked to the properties of the membrane environment in which the proteins are embedded. For structural and biophysical characterization, membrane proteins generally need to be extracted from the membrane and reconstituted in a suitable membrane‐mimicking environment. Ensuring functional and structural integrity in these environments is often a major concern. The styrene/maleic acid co‐polymer has recently been shown to be able to extract lipid/membrane protein patches directly from native membranes to form nanosize discoidal proteolipid particles, also referred to as native nanodiscs. In this work, we show that high‐resolution solid‐state NMR spectra can be obtained from an integral membrane protein in native nanodiscs, as exemplified by the 2×34 kDa bacterial cation diffusion facilitator CzcD."}],"date_created":"2020-09-18T10:06:50Z","date_published":"2017-01-27T00:00:00Z","volume":56,"doi":"10.1002/anie.201610441","issue":"9","page":"2508-2512","language":[{"iso":"eng"}],"publication":"Angewandte Chemie International Edition","day":"27","year":"2017","publication_status":"published","publication_identifier":{"issn":["1433-7851"]},"status":"public","type":"journal_article","article_type":"original","_id":"8451","title":"Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs","article_processing_charge":"No","author":[{"full_name":"Bersch, Beate","last_name":"Bersch","first_name":"Beate"},{"first_name":"Jonas M.","last_name":"Dörr","full_name":"Dörr, Jonas M."},{"first_name":"Audrey","last_name":"Hessel","full_name":"Hessel, Audrey"},{"first_name":"J. Antoinette","last_name":"Killian","full_name":"Killian, J. Antoinette"},{"full_name":"Schanda, Paul","orcid":"0000-0002-9350-7606","last_name":"Schanda","first_name":"Paul","id":"7B541462-FAF6-11E9-A490-E8DFE5697425"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:19:22Z","citation":{"chicago":"Bersch, Beate, Jonas M. Dörr, Audrey Hessel, J. Antoinette Killian, and Paul Schanda. “Proton-Detected Solid-State NMR Spectroscopy of a Zinc Diffusion Facilitator Protein in Native Nanodiscs.” Angewandte Chemie International Edition. Wiley, 2017. https://doi.org/10.1002/anie.201610441.","ista":"Bersch B, Dörr JM, Hessel A, Killian JA, Schanda P. 2017. Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs. Angewandte Chemie International Edition. 56(9), 2508–2512.","mla":"Bersch, Beate, et al. “Proton-Detected Solid-State NMR Spectroscopy of a Zinc Diffusion Facilitator Protein in Native Nanodiscs.” Angewandte Chemie International Edition, vol. 56, no. 9, Wiley, 2017, pp. 2508–12, doi:10.1002/anie.201610441.","ama":"Bersch B, Dörr JM, Hessel A, Killian JA, Schanda P. Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs. Angewandte Chemie International Edition. 2017;56(9):2508-2512. doi:10.1002/anie.201610441","apa":"Bersch, B., Dörr, J. M., Hessel, A., Killian, J. A., & Schanda, P. (2017). Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs. Angewandte Chemie International Edition. Wiley. https://doi.org/10.1002/anie.201610441","short":"B. Bersch, J.M. Dörr, A. Hessel, J.A. Killian, P. Schanda, Angewandte Chemie International Edition 56 (2017) 2508–2512.","ieee":"B. Bersch, J. M. Dörr, A. Hessel, J. A. Killian, and P. Schanda, “Proton-detected solid-state NMR spectroscopy of a Zinc diffusion facilitator protein in native nanodiscs,” Angewandte Chemie International Edition, vol. 56, no. 9. Wiley, pp. 2508–2512, 2017."}},{"article_processing_charge":"No","author":[{"full_name":"Kurauskas, Vilius","last_name":"Kurauskas","first_name":"Vilius"},{"id":"7B541462-FAF6-11E9-A490-E8DFE5697425","first_name":"Paul","last_name":"Schanda","orcid":"0000-0002-9350-7606","full_name":"Schanda, Paul"},{"last_name":"Sounier","full_name":"Sounier, Remy","first_name":"Remy"}],"title":"Methyl-specific isotope labeling strategies for NMR studies of membrane proteins","citation":{"ista":"Kurauskas V, Schanda P, Sounier R. 2017.Methyl-specific isotope labeling strategies for NMR studies of membrane proteins. In: Membrane protein structure and function characterization. Methods in Molecular Biology, vol. 1635, 109–123.","chicago":"Kurauskas, Vilius, Paul Schanda, and Remy Sounier. “Methyl-Specific Isotope Labeling Strategies for NMR Studies of Membrane Proteins.” In Membrane Protein Structure and Function Characterization, 1635:109–23. Springer Nature, 2017. https://doi.org/10.1007/978-1-4939-7151-0_6.","short":"V. Kurauskas, P. Schanda, R. Sounier, in:, Membrane Protein Structure and Function Characterization, Springer Nature, 2017, pp. 109–123.","ieee":"V. Kurauskas, P. Schanda, and R. Sounier, “Methyl-specific isotope labeling strategies for NMR studies of membrane proteins,” in Membrane protein structure and function characterization, vol. 1635, Springer Nature, 2017, pp. 109–123.","ama":"Kurauskas V, Schanda P, Sounier R. Methyl-specific isotope labeling strategies for NMR studies of membrane proteins. In: Membrane Protein Structure and Function Characterization. Vol 1635. Springer Nature; 2017:109-123. doi:10.1007/978-1-4939-7151-0_6","apa":"Kurauskas, V., Schanda, P., & Sounier, R. (2017). Methyl-specific isotope labeling strategies for NMR studies of membrane proteins. In Membrane protein structure and function characterization (Vol. 1635, pp. 109–123). Springer Nature. https://doi.org/10.1007/978-1-4939-7151-0_6","mla":"Kurauskas, Vilius, et al. “Methyl-Specific Isotope Labeling Strategies for NMR Studies of Membrane Proteins.” Membrane Protein Structure and Function Characterization, vol. 1635, Springer Nature, 2017, pp. 109–23, doi:10.1007/978-1-4939-7151-0_6."},"date_updated":"2022-08-26T09:14:20Z","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","extern":"1","type":"book_chapter","status":"public","_id":"8450","page":"109-123","date_created":"2020-09-18T10:06:44Z","volume":1635,"doi":"10.1007/978-1-4939-7151-0_6","date_published":"2017-07-29T00:00:00Z","publication_status":"published","year":"2017","publication_identifier":{"issn":["1064-3745","1940-6029"],"isbn":["9781493971497","9781493971510"]},"publication":"Membrane protein structure and function characterization","language":[{"iso":"eng"}],"day":"29","publisher":"Springer Nature","alternative_title":["Methods in Molecular Biology"],"quality_controlled":"1","intvolume":" 1635","month":"07","abstract":[{"text":"Methyl groups are very useful probes of structure, dynamics, and interactions in protein NMR spectroscopy. In particular, methyl-directed experiments provide high sensitivity even in very large proteins, such as membrane proteins in a membrane-mimicking environment. In this chapter, we discuss the approach for labeling methyl groups in E. coli-based protein expression, as exemplified with the mitochondrial carrier GGC.","lang":"eng"}],"oa_version":"None"},{"article_type":"original","type":"journal_article","keyword":["Geochemistry and Petrology","Geophysics"],"status":"public","_id":"9137","date_updated":"2022-01-24T12:41:45Z","extern":"1","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1007/s10712-017-9447-x"}],"intvolume":" 38","month":"11","abstract":[{"text":"Pools of air cooled by partial rain evaporation span up to several hundreds of kilometers in nature and typically last less than 1 day, ultimately losing their identity to the large-scale flow. These fundamentally differ in character from the radiatively-driven dry pools defining convective aggregation. Advancement in remote sensing and in computer capabilities has promoted exploration of how precipitation-induced cold pool processes modify the convective spectrum and life cycle. This contribution surveys current understanding of such cold pools over the tropical and subtropical oceans. In shallow convection with low rain rates, the cold pools moisten, preserving the near-surface equivalent potential temperature or increasing it if the surface moisture fluxes cannot ventilate beyond the new surface layer; both conditions indicate downdraft origin air from within the boundary layer. When rain rates exceed ∼ 2 mm h−1, convective-scale downdrafts can bring down drier air of lower equivalent potential temperature from above the boundary layer. The resulting density currents facilitate the lifting of locally thermodynamically favorable air and can impose an arc-shaped mesoscale cloud organization. This organization allows clouds capable of reaching 4–5 km within otherwise dry environments. These are more commonly observed in the northern hemisphere trade wind regime, where the flow to the intertropical convergence zone is unimpeded by the equator. Their near-surface air properties share much with those shown from cold pools sampled in the equatorial Indian Ocean. Cold pools are most effective at influencing the mesoscale organization when the atmosphere is moist in the lower free troposphere and dry above, suggesting an optimal range of water vapor paths. Outstanding questions on the relationship between cold pools, their accompanying moisture distribution and cloud cover are detailed further. Near-surface water vapor rings are documented in one model inside but near the cold pool edge; these are not consistent with observations, but do improve with smaller horizontal grid spacings.","lang":"eng"}],"oa_version":"Published Version","issue":"6","volume":38,"publication_status":"published","publication_identifier":{"issn":["0169-3298","1573-0956"]},"language":[{"iso":"eng"}],"article_processing_charge":"No","author":[{"full_name":"Zuidema, Paquita","last_name":"Zuidema","first_name":"Paquita"},{"last_name":"Torri","full_name":"Torri, Giuseppe","first_name":"Giuseppe"},{"id":"f978ccb0-3f7f-11eb-b193-b0e2bd13182b","first_name":"Caroline J","full_name":"Muller, Caroline J","orcid":"0000-0001-5836-5350","last_name":"Muller"},{"first_name":"Arunchandra","last_name":"Chandra","full_name":"Chandra, Arunchandra"}],"title":"A survey of precipitation-induced atmospheric cold pools over oceans and their interactions with the larger-scale environment","citation":{"ieee":"P. Zuidema, G. Torri, C. J. Muller, and A. Chandra, “A survey of precipitation-induced atmospheric cold pools over oceans and their interactions with the larger-scale environment,” Surveys in Geophysics, vol. 38, no. 6. Springer Nature, pp. 1283–1305, 2017.","short":"P. Zuidema, G. Torri, C.J. Muller, A. Chandra, Surveys in Geophysics 38 (2017) 1283–1305.","ama":"Zuidema P, Torri G, Muller CJ, Chandra A. A survey of precipitation-induced atmospheric cold pools over oceans and their interactions with the larger-scale environment. Surveys in Geophysics. 2017;38(6):1283-1305. doi:10.1007/s10712-017-9447-x","apa":"Zuidema, P., Torri, G., Muller, C. J., & Chandra, A. (2017). A survey of precipitation-induced atmospheric cold pools over oceans and their interactions with the larger-scale environment. Surveys in Geophysics. Springer Nature. https://doi.org/10.1007/s10712-017-9447-x","mla":"Zuidema, Paquita, et al. “A Survey of Precipitation-Induced Atmospheric Cold Pools over Oceans and Their Interactions with the Larger-Scale Environment.” Surveys in Geophysics, vol. 38, no. 6, Springer Nature, 2017, pp. 1283–305, doi:10.1007/s10712-017-9447-x.","ista":"Zuidema P, Torri G, Muller CJ, Chandra A. 2017. A survey of precipitation-induced atmospheric cold pools over oceans and their interactions with the larger-scale environment. Surveys in Geophysics. 38(6), 1283–1305.","chicago":"Zuidema, Paquita, Giuseppe Torri, Caroline J Muller, and Arunchandra Chandra. “A Survey of Precipitation-Induced Atmospheric Cold Pools over Oceans and Their Interactions with the Larger-Scale Environment.” Surveys in Geophysics. Springer Nature, 2017. https://doi.org/10.1007/s10712-017-9447-x."},"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","oa":1,"publisher":"Springer Nature","quality_controlled":"1","page":"1283-1305","date_created":"2021-02-15T14:20:07Z","doi":"10.1007/s10712-017-9447-x","date_published":"2017-11-14T00:00:00Z","year":"2017","publication":"Surveys in Geophysics","day":"14"},{"title":"Observing convective aggregation","author":[{"first_name":"Christopher E.","last_name":"Holloway","full_name":"Holloway, Christopher E."},{"first_name":"Allison A.","last_name":"Wing","full_name":"Wing, Allison A."},{"last_name":"Bony","full_name":"Bony, Sandrine","first_name":"Sandrine"},{"full_name":"Muller, Caroline J","orcid":"0000-0001-5836-5350","last_name":"Muller","id":"f978ccb0-3f7f-11eb-b193-b0e2bd13182b","first_name":"Caroline J"},{"full_name":"Masunaga, Hirohiko","last_name":"Masunaga","first_name":"Hirohiko"},{"first_name":"Tristan S.","full_name":"L’Ecuyer, Tristan S.","last_name":"L’Ecuyer"},{"first_name":"David D.","full_name":"Turner, David D.","last_name":"Turner"},{"first_name":"Paquita","full_name":"Zuidema, Paquita","last_name":"Zuidema"}],"article_processing_charge":"No","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"mla":"Holloway, Christopher E., et al. “Observing Convective Aggregation.” Surveys in Geophysics, vol. 38, no. 6, Springer Nature, 2017, pp. 1199–236, doi:10.1007/s10712-017-9419-1.","ama":"Holloway CE, Wing AA, Bony S, et al. Observing convective aggregation. Surveys in Geophysics. 2017;38(6):1199-1236. doi:10.1007/s10712-017-9419-1","apa":"Holloway, C. E., Wing, A. A., Bony, S., Muller, C. J., Masunaga, H., L’Ecuyer, T. S., … Zuidema, P. (2017). Observing convective aggregation. Surveys in Geophysics. Springer Nature. https://doi.org/10.1007/s10712-017-9419-1","ieee":"C. E. Holloway et al., “Observing convective aggregation,” Surveys in Geophysics, vol. 38, no. 6. Springer Nature, pp. 1199–1236, 2017.","short":"C.E. Holloway, A.A. Wing, S. Bony, C.J. Muller, H. Masunaga, T.S. L’Ecuyer, D.D. Turner, P. Zuidema, Surveys in Geophysics 38 (2017) 1199–1236.","chicago":"Holloway, Christopher E., Allison A. Wing, Sandrine Bony, Caroline J Muller, Hirohiko Masunaga, Tristan S. L’Ecuyer, David D. Turner, and Paquita Zuidema. “Observing Convective Aggregation.” Surveys in Geophysics. Springer Nature, 2017. https://doi.org/10.1007/s10712-017-9419-1.","ista":"Holloway CE, Wing AA, Bony S, Muller CJ, Masunaga H, L’Ecuyer TS, Turner DD, Zuidema P. 2017. Observing convective aggregation. Surveys in Geophysics. 38(6), 1199–1236."},"date_published":"2017-11-01T00:00:00Z","doi":"10.1007/s10712-017-9419-1","date_created":"2021-02-15T14:20:38Z","page":"1199-1236","day":"01","publication":"Surveys in Geophysics","year":"2017","publisher":"Springer Nature","quality_controlled":"1","oa":1,"extern":"1","date_updated":"2022-01-24T12:43:13Z","status":"public","keyword":["Geochemistry and Petrology","Geophysics"],"type":"journal_article","article_type":"original","_id":"9138","volume":38,"issue":"6","language":[{"iso":"eng"}],"publication_identifier":{"issn":["0169-3298","1573-0956"]},"publication_status":"published","month":"11","intvolume":" 38","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1007/s10712-017-9419-1"}],"oa_version":"Published Version","abstract":[{"text":"Convective self-aggregation, the spontaneous organization of initially scattered convection into isolated convective clusters despite spatially homogeneous boundary conditions and forcing, was first recognized and studied in idealized numerical simulations. While there is a rich history of observational work on convective clustering and organization, there have been only a few studies that have analyzed observations to look specifically for processes related to self-aggregation in models. Here we review observational work in both of these categories and motivate the need for more of this work. We acknowledge that self-aggregation may appear to be far-removed from observed convective organization in terms of time scales, initial conditions, initiation processes, and mean state extremes, but we argue that these differences vary greatly across the diverse range of model simulations in the literature and that these comparisons are already offering important insights into real tropical phenomena. Some preliminary new findings are presented, including results showing that a self-aggregation simulation with square geometry has too broad distribution of humidity and is too dry in the driest regions when compared with radiosonde records from Nauru, while an elongated channel simulation has realistic representations of atmospheric humidity and its variability. We discuss recent work increasing our understanding of how organized convection and climate change may interact, and how model discrepancies related to this question are prompting interest in observational comparisons. We also propose possible future directions for observational work related to convective aggregation, including novel satellite approaches and a ground-based observational network.","lang":"eng"}]},{"publisher":"Springer Nature","quality_controlled":"1","intvolume":" 38","month":"11","abstract":[{"lang":"eng","text":"Organized convection in the tropics occurs across a range of spatial and temporal scales and strongly influences cloud cover and humidity. One mode of organization found is “self-aggregation,” in which moist convection spontaneously organizes into one or several isolated clusters despite spatially homogeneous boundary conditions and forcing. Self-aggregation is driven by interactions between clouds, moisture, radiation, surface fluxes, and circulation, and occurs in a wide variety of idealized simulations of radiative–convective equilibrium. Here we provide a review of convective self-aggregation in numerical simulations, including its character, causes, and effects. We describe the evolution of self-aggregation including its time and length scales and the physical mechanisms leading to its triggering and maintenance, and we also discuss possible links to climate and climate change."}],"oa_version":"None","page":"1173-1197","date_created":"2021-02-15T14:20:56Z","doi":"10.1007/s10712-017-9408-4","date_published":"2017-11-01T00:00:00Z","issue":"6","volume":38,"year":"2017","publication_status":"published","publication_identifier":{"issn":["0169-3298","1573-0956"]},"language":[{"iso":"eng"}],"publication":"Surveys in Geophysics","day":"01","article_type":"original","type":"journal_article","keyword":["Geochemistry and Petrology","Geophysics"],"status":"public","_id":"9139","article_processing_charge":"No","author":[{"first_name":"Allison A.","full_name":"Wing, Allison A.","last_name":"Wing"},{"full_name":"Emanuel, Kerry","last_name":"Emanuel","first_name":"Kerry"},{"first_name":"Christopher E.","last_name":"Holloway","full_name":"Holloway, Christopher E."},{"id":"f978ccb0-3f7f-11eb-b193-b0e2bd13182b","first_name":"Caroline J","last_name":"Muller","orcid":"0000-0001-5836-5350","full_name":"Muller, Caroline J"}],"title":"Convective self-aggregation in numerical simulations: A review","citation":{"chicago":"Wing, Allison A., Kerry Emanuel, Christopher E. Holloway, and Caroline J Muller. “Convective Self-Aggregation in Numerical Simulations: A Review.” Surveys in Geophysics. Springer Nature, 2017. https://doi.org/10.1007/s10712-017-9408-4.","ista":"Wing AA, Emanuel K, Holloway CE, Muller CJ. 2017. Convective self-aggregation in numerical simulations: A review. Surveys in Geophysics. 38(6), 1173–1197.","mla":"Wing, Allison A., et al. “Convective Self-Aggregation in Numerical Simulations: A Review.” Surveys in Geophysics, vol. 38, no. 6, Springer Nature, 2017, pp. 1173–97, doi:10.1007/s10712-017-9408-4.","short":"A.A. Wing, K. Emanuel, C.E. Holloway, C.J. Muller, Surveys in Geophysics 38 (2017) 1173–1197.","ieee":"A. A. Wing, K. Emanuel, C. E. Holloway, and C. J. Muller, “Convective self-aggregation in numerical simulations: A review,” Surveys in Geophysics, vol. 38, no. 6. Springer Nature, pp. 1173–1197, 2017.","apa":"Wing, A. A., Emanuel, K., Holloway, C. E., & Muller, C. J. (2017). Convective self-aggregation in numerical simulations: A review. Surveys in Geophysics. Springer Nature. https://doi.org/10.1007/s10712-017-9408-4","ama":"Wing AA, Emanuel K, Holloway CE, Muller CJ. Convective self-aggregation in numerical simulations: A review. Surveys in Geophysics. 2017;38(6):1173-1197. doi:10.1007/s10712-017-9408-4"},"date_updated":"2022-01-24T12:42:36Z","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","extern":"1"},{"author":[{"first_name":"O.","last_name":"Richet","full_name":"Richet, O."},{"id":"f978ccb0-3f7f-11eb-b193-b0e2bd13182b","first_name":"Caroline J","last_name":"Muller","orcid":"0000-0001-5836-5350","full_name":"Muller, Caroline J"},{"full_name":"Chomaz, J.-M.","last_name":"Chomaz","first_name":"J.-M."}],"article_processing_charge":"No","title":"Impact of a mean current on the internal tide energy dissipation at the critical latitude","citation":{"chicago":"Richet, O., Caroline J Muller, and J.-M. Chomaz. “Impact of a Mean Current on the Internal Tide Energy Dissipation at the Critical Latitude.” Journal of Physical Oceanography. American Meteorological Society, 2017. https://doi.org/10.1175/jpo-d-16-0197.1.","ista":"Richet O, Muller CJ, Chomaz J-M. 2017. Impact of a mean current on the internal tide energy dissipation at the critical latitude. Journal of Physical Oceanography. 47(6), 1457–1472.","mla":"Richet, O., et al. “Impact of a Mean Current on the Internal Tide Energy Dissipation at the Critical Latitude.” Journal of Physical Oceanography, vol. 47, no. 6, American Meteorological Society, 2017, pp. 1457–72, doi:10.1175/jpo-d-16-0197.1.","apa":"Richet, O., Muller, C. J., & Chomaz, J.-M. (2017). Impact of a mean current on the internal tide energy dissipation at the critical latitude. Journal of Physical Oceanography. American Meteorological Society. https://doi.org/10.1175/jpo-d-16-0197.1","ama":"Richet O, Muller CJ, Chomaz J-M. Impact of a mean current on the internal tide energy dissipation at the critical latitude. Journal of Physical Oceanography. 2017;47(6):1457-1472. doi:10.1175/jpo-d-16-0197.1","short":"O. Richet, C.J. Muller, J.-M. Chomaz, Journal of Physical Oceanography 47 (2017) 1457–1472.","ieee":"O. Richet, C. J. Muller, and J.-M. Chomaz, “Impact of a mean current on the internal tide energy dissipation at the critical latitude,” Journal of Physical Oceanography, vol. 47, no. 6. American Meteorological Society, pp. 1457–1472, 2017."},"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","page":"1457-1472","doi":"10.1175/jpo-d-16-0197.1","date_published":"2017-06-01T00:00:00Z","date_created":"2021-02-15T15:11:04Z","year":"2017","day":"01","publication":"Journal of Physical Oceanography","quality_controlled":"1","publisher":"American Meteorological Society","oa":1,"date_updated":"2022-01-24T13:36:31Z","extern":"1","article_type":"original","type":"journal_article","status":"public","keyword":["Oceanography"],"_id":"9152","issue":"6","volume":47,"publication_identifier":{"issn":["0022-3670","1520-0485"]},"publication_status":"published","language":[{"iso":"eng"}],"main_file_link":[{"url":"https://doi.org/10.1175/JPO-D-16-0197.1","open_access":"1"}],"month":"06","intvolume":" 47","abstract":[{"text":"Previous numerical studies of the dissipation of internal tides in idealized settings suggest the existence of a critical latitude (~29°) where dissipation is enhanced. But observations only indicate a modest enhancement at this latitude. To resolve this difference between observational and numerical results, the authors study the latitudinal dependence of internal tides’ dissipation in more realistic conditions. In particular, the ocean is not a quiescent medium; the presence of large-scale currents or mesoscale eddies can impact the propagation and dissipation of internal tides. This paper investigates the impact of a weak background mean current in numerical simulations. The authors focus on the local dissipation of high spatial mode internal waves near their generation site. The vertical profile of dissipation and its variation with latitude without the mean current are consistent with earlier studies. But adding a weak mean current has a major impact on the latitudinal distribution of dissipation. The peak at the critical latitude disappears, and the dissipation is closer to a constant, albeit with two weak peaks at ~25° and ~35° latitude. This disappearance results from the Doppler shift of the internal tides’ frequency, which hinders the nonlinear transfer of energy to small-scale secondary waves via the parametric subharmonic instability (PSI). The new two weak peaks correspond to the Doppler-shifted critical latitudes of the left- and right-propagating waves. The results are confirmed in simulations with simple sinusoidal topography. Thus, although nonlinear transfers via PSI are efficient at dissipating internal tides, the exact location of the dissipation is sensitive to large-scale oceanic conditions.","lang":"eng"}],"oa_version":"Published Version"},{"abstract":[{"text":"During puberty, the mouse mammary gland develops into a highly branched epithelial network. Owing to the absence of exclusive stem cell markers, the location, multiplicity, dynamics and fate of mammary stem cells (MaSCs), which drive branching morphogenesis, are unknown. Here we show that morphogenesis is driven by proliferative terminal end buds that terminate or bifurcate with near equal probability, in a stochastic and time-invariant manner, leading to a heterogeneous epithelial network. We show that the majority of terminal end bud cells function as highly proliferative, lineage-committed MaSCs that are heterogeneous in their expression profile and short-term contribution to ductal extension. Yet, through cell rearrangements during terminal end bud bifurcation, each MaSC is able to contribute actively to long-term growth. Our study shows that the behaviour of MaSCs is not directly linked to a single expression profile. Instead, morphogenesis relies upon lineage-restricted heterogeneous MaSC populations that function as single equipotent pools in the long term.","lang":"eng"}],"oa_version":"None","quality_controlled":"1","publisher":"Nature Publishing Group","month":"02","intvolume":" 542","publication_identifier":{"issn":["00280836"]},"year":"2017","publication_status":"published","day":"16","publication":"Nature","language":[{"iso":"eng"}],"page":"313 - 317","date_published":"2017-02-16T00:00:00Z","doi":"10.1038/nature21046","issue":"7641","volume":542,"date_created":"2018-12-11T11:49:17Z","_id":"934","type":"journal_article","status":"public","date_updated":"2021-01-12T08:22:01Z","citation":{"ieee":"C. Scheele et al., “Identity and dynamics of mammary stem cells during branching morphogenesis,” Nature, vol. 542, no. 7641. Nature Publishing Group, pp. 313–317, 2017.","short":"C. Scheele, E.B. Hannezo, M. Muraro, A. Zomer, N. Langedijk, A. Van Oudenaarden, B. Simons, J. Van Rheenen, Nature 542 (2017) 313–317.","ama":"Scheele C, Hannezo EB, Muraro M, et al. Identity and dynamics of mammary stem cells during branching morphogenesis. Nature. 2017;542(7641):313-317. doi:10.1038/nature21046","apa":"Scheele, C., Hannezo, E. B., Muraro, M., Zomer, A., Langedijk, N., Van Oudenaarden, A., … Van Rheenen, J. (2017). Identity and dynamics of mammary stem cells during branching morphogenesis. Nature. Nature Publishing Group. https://doi.org/10.1038/nature21046","mla":"Scheele, Colinda, et al. “Identity and Dynamics of Mammary Stem Cells during Branching Morphogenesis.” Nature, vol. 542, no. 7641, Nature Publishing Group, 2017, pp. 313–17, doi:10.1038/nature21046.","ista":"Scheele C, Hannezo EB, Muraro M, Zomer A, Langedijk N, Van Oudenaarden A, Simons B, Van Rheenen J. 2017. Identity and dynamics of mammary stem cells during branching morphogenesis. Nature. 542(7641), 313–317.","chicago":"Scheele, Colinda, Edouard B Hannezo, Mauro Muraro, Anoek Zomer, Nathalia Langedijk, Alexander Van Oudenaarden, Benjamin Simons, and Jacco Van Rheenen. “Identity and Dynamics of Mammary Stem Cells during Branching Morphogenesis.” Nature. Nature Publishing Group, 2017. https://doi.org/10.1038/nature21046."},"extern":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Colinda","last_name":"Scheele","full_name":"Scheele, Colinda"},{"first_name":"Edouard B","id":"3A9DB764-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-6005-1561","full_name":"Hannezo, Edouard B","last_name":"Hannezo"},{"first_name":"Mauro","full_name":"Muraro, Mauro","last_name":"Muraro"},{"full_name":"Zomer, Anoek","last_name":"Zomer","first_name":"Anoek"},{"last_name":"Langedijk","full_name":"Langedijk, Nathalia","first_name":"Nathalia"},{"last_name":"Van Oudenaarden","full_name":"Van Oudenaarden, Alexander","first_name":"Alexander"},{"first_name":"Benjamin","last_name":"Simons","full_name":"Simons, Benjamin"},{"first_name":"Jacco","last_name":"Van Rheenen","full_name":"Van Rheenen, Jacco"}],"publist_id":"6505","title":"Identity and dynamics of mammary stem cells during branching morphogenesis"},{"quality_controlled":"1","publisher":"Company of Biologists","month":"01","intvolume":" 130","abstract":[{"text":"Homeostatic replacement of epithelial cells from basal precursors is a multistep process involving progenitor cell specification, radial intercalation and, finally, apical surface emergence. Recent data demonstrate that actin-based pushing under the control of the formin protein Fmn1 drives apical emergence in nascent multiciliated epithelial cells (MCCs), but little else is known about this actin network or the control of Fmn1. Here, we explore the role of the small GTPase RhoA in MCC apical emergence. Disruption of RhoA function reduced the rate of apical surface expansion and decreased the final size of the apical domain. Analysis of cell shapes suggests that RhoA alters the balance of forces exerted on the MCC apical surface. Finally, quantitative time-lapse imaging and fluorescence recovery after photobleaching studies argue that RhoA works in concert with Fmn1 to control assembly of the specialized apical actin network in MCCs. These data provide new molecular insights into epithelial apical surface assembly and could also shed light on mechanisms of apical lumen formation","lang":"eng"}],"oa_version":"None","volume":130,"issue":"5","date_published":"2017-01-01T00:00:00Z","doi":"10.1242/jcs.202234","date_created":"2018-12-11T11:49:17Z","year":"2017","publication_status":"published","day":"01","publication":"Journal of Cell Science","language":[{"iso":"eng"}],"type":"journal_article","status":"public","_id":"936","publist_id":"6507","author":[{"first_name":"Jakub","last_name":"Sedzinski","full_name":"Sedzinski, Jakub"},{"last_name":"Hannezo","orcid":"0000-0001-6005-1561","full_name":"Hannezo, Edouard B","id":"3A9DB764-F248-11E8-B48F-1D18A9856A87","first_name":"Edouard B"},{"full_name":"Tu, Fan","last_name":"Tu","first_name":"Fan"},{"last_name":"Biro","full_name":"Biro, Maté","first_name":"Maté"},{"first_name":"John","full_name":"Wallingford, John","last_name":"Wallingford"}],"title":"RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells ","date_updated":"2021-01-12T08:22:02Z","citation":{"mla":"Sedzinski, Jakub, et al. “RhoA Regulates Actin Network Dynamics during Apical Surface Emergence in Multiciliated Epithelial Cells .” Journal of Cell Science, vol. 130, no. 5, Company of Biologists, 2017, doi:10.1242/jcs.202234.","ieee":"J. Sedzinski, E. B. Hannezo, F. Tu, M. Biro, and J. Wallingford, “RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells ,” Journal of Cell Science, vol. 130, no. 5. Company of Biologists, 2017.","short":"J. Sedzinski, E.B. Hannezo, F. Tu, M. Biro, J. Wallingford, Journal of Cell Science 130 (2017).","apa":"Sedzinski, J., Hannezo, E. B., Tu, F., Biro, M., & Wallingford, J. (2017). RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells . Journal of Cell Science. Company of Biologists. https://doi.org/10.1242/jcs.202234","ama":"Sedzinski J, Hannezo EB, Tu F, Biro M, Wallingford J. RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells . Journal of Cell Science. 2017;130(5). doi:10.1242/jcs.202234","chicago":"Sedzinski, Jakub, Edouard B Hannezo, Fan Tu, Maté Biro, and John Wallingford. “RhoA Regulates Actin Network Dynamics during Apical Surface Emergence in Multiciliated Epithelial Cells .” Journal of Cell Science. Company of Biologists, 2017. https://doi.org/10.1242/jcs.202234.","ista":"Sedzinski J, Hannezo EB, Tu F, Biro M, Wallingford J. 2017. RhoA regulates actin network dynamics during apical surface emergence in multiciliated epithelial cells . Journal of Cell Science. 130(5)."},"extern":"1","user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87"},{"_id":"937","status":"public","type":"journal_article","user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","extern":"1","date_updated":"2021-01-12T08:22:02Z","citation":{"chicago":"Pinheiro, Diana, Edouard B Hannezo, Sophie Herszterg, Floris Bosveld, Isabelle Gaugué, Maria Balakireva, Zhimin Wang, et al. “Transmission of Cytokinesis Forces via E Cadherin Dilution and Actomyosin Flows.” Nature. Nature Publishing Group, 2017. https://doi.org/10.1038/nature22041.","ista":"Pinheiro D, Hannezo EB, Herszterg S, Bosveld F, Gaugué I, Balakireva M, Wang Z, Cristo I, Rigaud S, Markova O, Bellaïche Y. 2017. Transmission of cytokinesis forces via E cadherin dilution and actomyosin flows. Nature. 545(7652), 103–107.","mla":"Pinheiro, Diana, et al. “Transmission of Cytokinesis Forces via E Cadherin Dilution and Actomyosin Flows.” Nature, vol. 545, no. 7652, Nature Publishing Group, 2017, pp. 103–07, doi:10.1038/nature22041.","apa":"Pinheiro, D., Hannezo, E. B., Herszterg, S., Bosveld, F., Gaugué, I., Balakireva, M., … Bellaïche, Y. (2017). Transmission of cytokinesis forces via E cadherin dilution and actomyosin flows. Nature. Nature Publishing Group. https://doi.org/10.1038/nature22041","ama":"Pinheiro D, Hannezo EB, Herszterg S, et al. Transmission of cytokinesis forces via E cadherin dilution and actomyosin flows. Nature. 2017;545(7652):103-107. doi:10.1038/nature22041","ieee":"D. Pinheiro et al., “Transmission of cytokinesis forces via E cadherin dilution and actomyosin flows,” Nature, vol. 545, no. 7652. Nature Publishing Group, pp. 103–107, 2017.","short":"D. Pinheiro, E.B. Hannezo, S. Herszterg, F. Bosveld, I. Gaugué, M. Balakireva, Z. Wang, I. Cristo, S. Rigaud, O. Markova, Y. Bellaïche, Nature 545 (2017) 103–107."},"title":"Transmission of cytokinesis forces via E cadherin dilution and actomyosin flows","publist_id":"6504","author":[{"last_name":"Pinheiro","full_name":"Pinheiro, Diana","first_name":"Diana"},{"first_name":"Edouard B","id":"3A9DB764-F248-11E8-B48F-1D18A9856A87","full_name":"Hannezo, Edouard B","orcid":"0000-0001-6005-1561","last_name":"Hannezo"},{"first_name":"Sophie","last_name":"Herszterg","full_name":"Herszterg, Sophie"},{"last_name":"Bosveld","full_name":"Bosveld, Floris","first_name":"Floris"},{"last_name":"Gaugué","full_name":"Gaugué, Isabelle","first_name":"Isabelle"},{"last_name":"Balakireva","full_name":"Balakireva, Maria","first_name":"Maria"},{"last_name":"Wang","full_name":"Wang, Zhimin","first_name":"Zhimin"},{"last_name":"Cristo","full_name":"Cristo, Inês","first_name":"Inês"},{"first_name":"Stéphane","last_name":"Rigaud","full_name":"Rigaud, Stéphane"},{"full_name":"Markova, Olga","last_name":"Markova","first_name":"Olga"},{"full_name":"Bellaïche, Yohanns","last_name":"Bellaïche","first_name":"Yohanns"}],"oa_version":"None","abstract":[{"text":"During epithelial cytokinesis, the remodelling of adhesive cell-cell contacts between the dividing cell and its neighbours has profound implications for the integrity, arrangement and morphogenesis of proliferative tissues. In both vertebrates and invertebrates, this remodelling requires the activity of non-muscle myosin II (MyoII) in the interphasic cells neighbouring the dividing cell. However, the mechanisms that coordinate cytokinesis and MyoII activity in the neighbours are unknown. Here we show that in the Drosophila notum epithelium, each cell division is associated with a mechanosensing and transmission event that controls MyoII dynamics in neighbouring cells. We find that the ring pulling forces promote local junction elongation, which results in local E-cadherin dilution at the ingressing adherens junction. In turn, the reduction in E-cadherin concentration and the contractility of the neighbouring cells promote self-organized actomyosin flows, ultimately leading to accumulation of MyoII at the base of the ingressing junction. Although force transduction has been extensively studied in the context of adherens junction reinforcement to stabilize adhesive cell-cell contacts, we propose an alternative mechanosensing mechanism that coordinates actomyosin dynamics between epithelial cells and sustains the remodelling of the adherens junction in response to mechanical forces.","lang":"eng"}],"intvolume":" 545","month":"05","publisher":"Nature Publishing Group","quality_controlled":"1","publication":"Nature","language":[{"iso":"eng"}],"day":"04","publication_status":"published","year":"2017","publication_identifier":{"issn":["00280836"]},"date_created":"2018-12-11T11:49:18Z","issue":"7652","date_published":"2017-05-04T00:00:00Z","volume":545,"doi":"10.1038/nature22041","page":"103 - 107"},{"project":[{"_id":"25832EC2-B435-11E9-9278-68D0E5697425","call_identifier":"FWF","name":"Rigorous Systems Engineering","grant_number":"S 11407_N23"},{"_id":"25F42A32-B435-11E9-9278-68D0E5697425","call_identifier":"FWF","grant_number":"Z211","name":"The Wittgenstein Prize"}],"status":"public","conference":{"name":"ISSTA: International Symposium on Software Testing and Analysis","location":"Santa Barbara, CA, United States","end_date":"2017-07-14","start_date":"2017-07-10"},"type":"conference","_id":"941","department":[{"_id":"ToHe"}],"title":"JFIX: Semantics-based repair of Java programs via symbolic PathFinder","publist_id":"6478","author":[{"full_name":"Le, Xuan","last_name":"Le","first_name":"Xuan"},{"first_name":"Duc Hiep","id":"3598E630-F248-11E8-B48F-1D18A9856A87","full_name":"Chu, Duc Hiep","last_name":"Chu"},{"full_name":"Lo, David","last_name":"Lo","first_name":"David"},{"first_name":"Claire","full_name":"Le Goues, Claire","last_name":"Le Goues"},{"last_name":"Visser","full_name":"Visser, Willem","first_name":"Willem"}],"user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","date_updated":"2021-01-12T08:22:05Z","citation":{"mla":"Le, Xuan, et al. “JFIX: Semantics-Based Repair of Java Programs via Symbolic PathFinder.” Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis, ACM, 2017, pp. 376–79, doi:10.1145/3092703.3098225.","ieee":"X. Le, D. H. Chu, D. Lo, C. Le Goues, and W. Visser, “JFIX: Semantics-based repair of Java programs via symbolic PathFinder,” in Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis, Santa Barbara, CA, United States, 2017, pp. 376–379.","short":"X. Le, D.H. Chu, D. Lo, C. Le Goues, W. Visser, in:, Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis, ACM, 2017, pp. 376–379.","ama":"Le X, Chu DH, Lo D, Le Goues C, Visser W. JFIX: Semantics-based repair of Java programs via symbolic PathFinder. In: Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis. ACM; 2017:376-379. doi:10.1145/3092703.3098225","apa":"Le, X., Chu, D. H., Lo, D., Le Goues, C., & Visser, W. (2017). JFIX: Semantics-based repair of Java programs via symbolic PathFinder. In Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis (pp. 376–379). Santa Barbara, CA, United States: ACM. https://doi.org/10.1145/3092703.3098225","chicago":"Le, Xuan, Duc Hiep Chu, David Lo, Claire Le Goues, and Willem Visser. “JFIX: Semantics-Based Repair of Java Programs via Symbolic PathFinder.” In Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis, 376–79. ACM, 2017. https://doi.org/10.1145/3092703.3098225.","ista":"Le X, Chu DH, Lo D, Le Goues C, Visser W. 2017. JFIX: Semantics-based repair of Java programs via symbolic PathFinder. Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis. ISSTA: International Symposium on Software Testing and Analysis, 376–379."},"month":"07","publisher":"ACM","quality_controlled":"1","scopus_import":1,"oa_version":"None","abstract":[{"text":"Recently there has been a proliferation of automated program repair (APR) techniques, targeting various programming languages. Such techniques can be generally classified into two families: syntactic- and semantics-based. Semantics-based APR, on which we focus, typically uses symbolic execution to infer semantic constraints and then program synthesis to construct repairs conforming to them. While syntactic-based APR techniques have been shown successful on bugs in real-world programs written in both C and Java, semantics-based APR techniques mostly target C programs. This leaves empirical comparisons of the APR families not fully explored, and developers without a Java-based semantics APR technique. We present JFix, a semantics-based APR framework that targets Java, and an associated Eclipse plugin. JFix is implemented atop Symbolic PathFinder, a well-known symbolic execution engine for Java programs. It extends one particular APR technique (Angelix), and is designed to be sufficiently generic to support a variety of such techniques. We demonstrate that semantics-based APR can indeed efficiently and effectively repair a variety of classes of bugs in large real-world Java programs. This supports our claim that the framework can both support developers seeking semantics-based repair of bugs in Java programs, as well as enable larger scale empirical studies comparing syntactic- and semantics-based APR targeting Java. The demonstration of our tool is available via the project website at: https://xuanbachle.github.io/semanticsrepair/ ","lang":"eng"}],"date_created":"2018-12-11T11:49:19Z","date_published":"2017-07-10T00:00:00Z","doi":"10.1145/3092703.3098225","page":"376 - 379 ","language":[{"iso":"eng"}],"publication":"Proceedings of the 26th ACM SIGSOFT International Symposium on Software Testing and Analysis","day":"10","publication_status":"published","year":"2017"},{"doi":"10.1186/s13059-017-1230-2","date_published":"2017-05-09T00:00:00Z","date_created":"2021-06-07T12:27:39Z","day":"09","publication":"Genome Biology","has_accepted_license":"1","year":"2017","quality_controlled":"1","publisher":"Springer Nature","oa":1,"title":"An evolutionary case for functional gene body methylation in plants and animals","author":[{"last_name":"Zilberman","full_name":"Zilberman, Daniel","orcid":"0000-0002-0123-8649","first_name":"Daniel","id":"6973db13-dd5f-11ea-814e-b3e5455e9ed1"}],"external_id":{"pmid":["28486944"]},"article_processing_charge":"No","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"chicago":"Zilberman, Daniel. “An Evolutionary Case for Functional Gene Body Methylation in Plants and Animals.” Genome Biology. Springer Nature, 2017. https://doi.org/10.1186/s13059-017-1230-2.","ista":"Zilberman D. 2017. An evolutionary case for functional gene body methylation in plants and animals. Genome Biology. 18(1), 87.","mla":"Zilberman, Daniel. “An Evolutionary Case for Functional Gene Body Methylation in Plants and Animals.” Genome Biology, vol. 18, no. 1, 87, Springer Nature, 2017, doi:10.1186/s13059-017-1230-2.","apa":"Zilberman, D. (2017). An evolutionary case for functional gene body methylation in plants and animals. Genome Biology. Springer Nature. https://doi.org/10.1186/s13059-017-1230-2","ama":"Zilberman D. An evolutionary case for functional gene body methylation in plants and animals. Genome Biology. 2017;18(1). doi:10.1186/s13059-017-1230-2","ieee":"D. Zilberman, “An evolutionary case for functional gene body methylation in plants and animals,” Genome Biology, vol. 18, no. 1. Springer Nature, 2017.","short":"D. Zilberman, Genome Biology 18 (2017)."},"article_number":"87","volume":18,"issue":"1","file":[{"content_type":"application/pdf","access_level":"open_access","relation":"main_file","file_id":"9507","checksum":"5a455ad914e7d225b1baa4ab07fd925e","success":1,"date_updated":"2021-06-07T12:31:36Z","file_size":278183,"creator":"asandaue","date_created":"2021-06-07T12:31:36Z","file_name":"2017_GenomeBiology_Zilberman.pdf"}],"language":[{"iso":"eng"}],"publication_identifier":{"eissn":["1465-6906"],"issn":["1474-760X"]},"publication_status":"published","month":"05","intvolume":" 18","scopus_import":"1","pmid":1,"oa_version":"Published Version","abstract":[{"lang":"eng","text":"Methylation in the bodies of active genes is common in animals and vascular plants. Evolutionary patterns indicate homeostatic functions for this type of methylation."}],"department":[{"_id":"DaZi"}],"file_date_updated":"2021-06-07T12:31:36Z","extern":"1","ddc":["570"],"date_updated":"2021-12-14T07:55:02Z","status":"public","type":"journal_article","tmp":{"legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","image":"/images/cc_by.png","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","short":"CC BY (4.0)"},"_id":"9506"},{"month":"05","intvolume":" 1596","alternative_title":["Methods in Molecular Biology"],"scopus_import":1,"oa_version":"None","abstract":[{"lang":"eng","text":"Biosensors that exploit Forster resonance energy transfer (FRET) can be used to visualize biological and physiological processes and are capable of providing detailed information in both spatial and temporal dimensions. In a FRET-based biosensor, substrate binding is associated with a change in the relative positions of two fluorophores, leading to a change in FRET efficiency that may be observed in the fluorescence spectrum. As a result, their design requires a ligand-binding protein that exhibits a conformational change upon binding. However, not all ligand-binding proteins produce responsive sensors upon conjugation to fluorescent proteins or dyes, and identifying the optimum locations for the fluorophores often involves labor-intensive iterative design or high-throughput screening. Combining the genetic fusion of a fluorescent protein to the ligand-binding protein with site-specific covalent attachment of a fluorescent dye can allow fine control over the positions of the two fluorophores, allowing the construction of very sensitive sensors. This relies upon the accurate prediction of the locations of the two fluorophores in bound and unbound states. In this chapter, we describe a method for computational identification of dye-attachment sites that allows the use of cysteine modification to attach synthetic dyes that can be paired with a fluorescent protein for the purposes of creating FRET sensors."}],"volume":1596,"language":[{"iso":"eng"}],"publication_identifier":{"issn":["10643745"]},"publication_status":"published","status":"public","type":"book_chapter","_id":"958","series_title":"Synthetic Protein Switches","department":[{"_id":"HaJa"}],"date_updated":"2021-01-12T08:22:13Z","quality_controlled":"1","publisher":"Springer","doi":"10.1007/978-1-4939-6940-1_6","date_published":"2017-05-15T00:00:00Z","date_created":"2018-12-11T11:49:24Z","page":"89 - 99","day":"15","publication":"Synthetic Protein Switches","year":"2017","title":"Method for developing optical sensors using a synthetic dye fluorescent protein FRET pair and computational modeling and assessment","editor":[{"full_name":"Stein, Viktor","last_name":"Stein","first_name":"Viktor"}],"author":[{"last_name":"Mitchell","full_name":"Mitchell, Joshua","first_name":"Joshua"},{"last_name":"Zhang","full_name":"Zhang, William","first_name":"William"},{"first_name":"Michel","last_name":"Herde","full_name":"Herde, Michel"},{"last_name":"Henneberger","full_name":"Henneberger, Christian","first_name":"Christian"},{"full_name":"Janovjak, Harald L","orcid":"0000-0002-8023-9315","last_name":"Janovjak","first_name":"Harald L","id":"33BA6C30-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Megan","full_name":"O'Mara, Megan","last_name":"O'Mara"},{"first_name":"Colin","full_name":"Jackson, Colin","last_name":"Jackson"}],"publist_id":"6450","user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Mitchell, Joshua, William Zhang, Michel Herde, Christian Henneberger, Harald L Janovjak, Megan O’Mara, and Colin Jackson. “Method for Developing Optical Sensors Using a Synthetic Dye Fluorescent Protein FRET Pair and Computational Modeling and Assessment.” In Synthetic Protein Switches, edited by Viktor Stein, 1596:89–99. Synthetic Protein Switches. Springer, 2017. https://doi.org/10.1007/978-1-4939-6940-1_6.","ista":"Mitchell J, Zhang W, Herde M, Henneberger C, Janovjak HL, O’Mara M, Jackson C. 2017.Method for developing optical sensors using a synthetic dye fluorescent protein FRET pair and computational modeling and assessment. In: Synthetic Protein Switches. Methods in Molecular Biology, vol. 1596, 89–99.","mla":"Mitchell, Joshua, et al. “Method for Developing Optical Sensors Using a Synthetic Dye Fluorescent Protein FRET Pair and Computational Modeling and Assessment.” Synthetic Protein Switches, edited by Viktor Stein, vol. 1596, Springer, 2017, pp. 89–99, doi:10.1007/978-1-4939-6940-1_6.","ieee":"J. Mitchell et al., “Method for developing optical sensors using a synthetic dye fluorescent protein FRET pair and computational modeling and assessment,” in Synthetic Protein Switches, vol. 1596, V. Stein, Ed. Springer, 2017, pp. 89–99.","short":"J. Mitchell, W. Zhang, M. Herde, C. Henneberger, H.L. Janovjak, M. O’Mara, C. Jackson, in:, V. Stein (Ed.), Synthetic Protein Switches, Springer, 2017, pp. 89–99.","ama":"Mitchell J, Zhang W, Herde M, et al. Method for developing optical sensors using a synthetic dye fluorescent protein FRET pair and computational modeling and assessment. In: Stein V, ed. Synthetic Protein Switches. Vol 1596. Synthetic Protein Switches. Springer; 2017:89-99. doi:10.1007/978-1-4939-6940-1_6","apa":"Mitchell, J., Zhang, W., Herde, M., Henneberger, C., Janovjak, H. L., O’Mara, M., & Jackson, C. (2017). Method for developing optical sensors using a synthetic dye fluorescent protein FRET pair and computational modeling and assessment. In V. Stein (Ed.), Synthetic Protein Switches (Vol. 1596, pp. 89–99). Springer. https://doi.org/10.1007/978-1-4939-6940-1_6"}},{"status":"public","article_type":"original","type":"journal_article","_id":"9660","extern":"1","date_updated":"2023-02-23T14:04:02Z","month":"09","intvolume":" 147","scopus_import":"1","main_file_link":[{"url":"https://pure.qub.ac.uk/en/publications/the-gibbs-free-energy-of-homogeneous-nucleation-from-atomistic-nuclei-to-the-planar-limit(4599cdb4-dcc4-4522-8763-7b2a165ebf12).html","open_access":"1"}],"oa_version":"Submitted Version","pmid":1,"abstract":[{"text":"In this paper we discuss how the information contained in atomistic simulations of homogeneous nucleation should be used when fitting the parameters in macroscopic nucleation models. We show how the number of solid and liquid atoms in such simulations can be determined unambiguously by using a Gibbs dividing surface and how the free energy as a function of the number of solid atoms in the nucleus can thus be extracted. We then show that the parameters (the chemical potential, the interfacial free energy, and a Tolman correction) of a model based on classical nucleation theory can be fitted using the information contained in these free-energy profiles but that the parameters in such models are highly correlated. This correlation is unfortunate as it ensures that small errors in the computed free energy surface can give rise to large errors in the extrapolated properties of the fitted model. To resolve this problem we thus propose a method for fitting macroscopic nucleation models that uses simulations of planar interfaces and simulations of three-dimensional nuclei in tandem. We show that when the chemical potentials and the interface energy are pinned to their planar-interface values, more precise estimates for the Tolman length are obtained. Extrapolating the free energy profile obtained from small simulation boxes to larger nuclei is thus more reliable.","lang":"eng"}],"issue":"10","volume":147,"language":[{"iso":"eng"}],"publication_identifier":{"issn":["0021-9606"],"eissn":["1089-7690"]},"publication_status":"published","article_number":"104707","title":"The Gibbs free energy of homogeneous nucleation: From atomistic nuclei to the planar limit","author":[{"first_name":"Bingqing","id":"cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9","last_name":"Cheng","full_name":"Cheng, Bingqing","orcid":"0000-0002-3584-9632"},{"last_name":"Tribello","full_name":"Tribello, Gareth A.","first_name":"Gareth A."},{"full_name":"Ceriotti, Michele","last_name":"Ceriotti","first_name":"Michele"}],"external_id":{"pmid":["28915742"],"arxiv":["1703.06062"]},"article_processing_charge":"No","user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","citation":{"mla":"Cheng, Bingqing, et al. “The Gibbs Free Energy of Homogeneous Nucleation: From Atomistic Nuclei to the Planar Limit.” The Journal of Chemical Physics, vol. 147, no. 10, 104707, AIP Publishing, 2017, doi:10.1063/1.4997180.","short":"B. Cheng, G.A. Tribello, M. Ceriotti, The Journal of Chemical Physics 147 (2017).","ieee":"B. Cheng, G. A. Tribello, and M. Ceriotti, “The Gibbs free energy of homogeneous nucleation: From atomistic nuclei to the planar limit,” The Journal of Chemical Physics, vol. 147, no. 10. AIP Publishing, 2017.","ama":"Cheng B, Tribello GA, Ceriotti M. The Gibbs free energy of homogeneous nucleation: From atomistic nuclei to the planar limit. The Journal of Chemical Physics. 2017;147(10). doi:10.1063/1.4997180","apa":"Cheng, B., Tribello, G. A., & Ceriotti, M. (2017). The Gibbs free energy of homogeneous nucleation: From atomistic nuclei to the planar limit. The Journal of Chemical Physics. AIP Publishing. https://doi.org/10.1063/1.4997180","chicago":"Cheng, Bingqing, Gareth A. Tribello, and Michele Ceriotti. “The Gibbs Free Energy of Homogeneous Nucleation: From Atomistic Nuclei to the Planar Limit.” The Journal of Chemical Physics. AIP Publishing, 2017. https://doi.org/10.1063/1.4997180.","ista":"Cheng B, Tribello GA, Ceriotti M. 2017. The Gibbs free energy of homogeneous nucleation: From atomistic nuclei to the planar limit. The Journal of Chemical Physics. 147(10), 104707."},"quality_controlled":"1","publisher":"AIP Publishing","oa":1,"doi":"10.1063/1.4997180","date_published":"2017-09-14T00:00:00Z","date_created":"2021-07-15T08:13:29Z","day":"14","publication":"The Journal of Chemical Physics","year":"2017"},{"title":"Bridging the gap between atomistic and macroscopic models of homogeneous nucleation","author":[{"first_name":"Bingqing","id":"cbe3cda4-d82c-11eb-8dc7-8ff94289fcc9","last_name":"Cheng","full_name":"Cheng, Bingqing","orcid":"0000-0002-3584-9632"},{"last_name":"Ceriotti","full_name":"Ceriotti, Michele","first_name":"Michele"}],"external_id":{"pmid":["28109231"],"arxiv":["1610.01322"]},"article_processing_charge":"No","user_id":"6785fbc1-c503-11eb-8a32-93094b40e1cf","citation":{"chicago":"Cheng, Bingqing, and Michele Ceriotti. “Bridging the Gap between Atomistic and Macroscopic Models of Homogeneous Nucleation.” The Journal of Chemical Physics. AIP Publishing, 2017. https://doi.org/10.1063/1.4973883.","ista":"Cheng B, Ceriotti M. 2017. Bridging the gap between atomistic and macroscopic models of homogeneous nucleation. The Journal of Chemical Physics. 146(3), 034106.","mla":"Cheng, Bingqing, and Michele Ceriotti. “Bridging the Gap between Atomistic and Macroscopic Models of Homogeneous Nucleation.” The Journal of Chemical Physics, vol. 146, no. 3, 034106, AIP Publishing, 2017, doi:10.1063/1.4973883.","ieee":"B. Cheng and M. Ceriotti, “Bridging the gap between atomistic and macroscopic models of homogeneous nucleation,” The Journal of Chemical Physics, vol. 146, no. 3. AIP Publishing, 2017.","short":"B. Cheng, M. Ceriotti, The Journal of Chemical Physics 146 (2017).","apa":"Cheng, B., & Ceriotti, M. (2017). Bridging the gap between atomistic and macroscopic models of homogeneous nucleation. The Journal of Chemical Physics. AIP Publishing. https://doi.org/10.1063/1.4973883","ama":"Cheng B, Ceriotti M. Bridging the gap between atomistic and macroscopic models of homogeneous nucleation. The Journal of Chemical Physics. 2017;146(3). doi:10.1063/1.4973883"},"article_number":"034106","doi":"10.1063/1.4973883","date_published":"2017-01-21T00:00:00Z","date_created":"2021-07-15T08:27:31Z","day":"21","publication":"The Journal of Chemical Physics","year":"2017","publisher":"AIP Publishing","quality_controlled":"1","oa":1,"extern":"1","date_updated":"2021-08-09T12:31:57Z","status":"public","type":"journal_article","article_type":"original","_id":"9661","volume":146,"issue":"3","language":[{"iso":"eng"}],"publication_identifier":{"issn":["0021-9606"],"eissn":["1089-7690"]},"publication_status":"published","month":"01","intvolume":" 146","scopus_import":"1","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1610.01322"}],"oa_version":"Preprint","pmid":1,"abstract":[{"lang":"eng","text":"Macroscopic theories of nucleation such as classical nucleation theory envision that clusters of the bulk stable phase form inside the bulk metastable phase. Molecular dynamics simulations are often used to elucidate nucleation mechanisms, by capturing the microscopic configurations of all the atoms. In this paper, we introduce a thermodynamic model that links macroscopic theories and atomic-scale simulations and thus provide a simple and elegant framework for testing the limits of classical nucleation theory."}]}]