[{"date_published":"2013-12-11T00:00:00Z","doi":"10.1103/physrevlett.111.245702","date_created":"2021-11-29T13:29:31Z","day":"11","publication":"Physical Review Letters","year":"2013","quality_controlled":"1","publisher":"American Physical Society","oa":1,"acknowledgement":"This work was supported by the ERC Advanced Grant 227758, the National Science Foundation under Career Grant No. DMR-0846426, the Wolfson Merit Award 2007/R3 of the Royal Society of London and the EPSRC Programme Grant EP/I001352/1. BMM acknowledge T. Curk and A. Ballard for useful discussions. C. V. acknowledges financial support from a Juan de la Cierva Fellowship, from the Marie Curie Integration Grant PCIG-GA-2011-303941 ANISOKINEQ, and from the National Project FIS2010- 16159. S. A-U acknowledges support from the Alexander von Humboldt Foundation.","title":"Living clusters and crystals from low-density suspensions of active colloids","author":[{"full_name":"Mognetti, B. M.","last_name":"Mognetti","first_name":"B. M."},{"last_name":"Šarić","full_name":"Šarić, Anđela","orcid":"0000-0002-7854-2139","first_name":"Anđela","id":"bf63d406-f056-11eb-b41d-f263a6566d8b"},{"first_name":"S.","last_name":"Angioletti-Uberti","full_name":"Angioletti-Uberti, S."},{"last_name":"Cacciuto","full_name":"Cacciuto, A.","first_name":"A."},{"first_name":"C.","last_name":"Valeriani","full_name":"Valeriani, C."},{"full_name":"Frenkel, D.","last_name":"Frenkel","first_name":"D."}],"article_processing_charge":"No","external_id":{"arxiv":["1311.4681"],"pmid":["24483677"]},"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"chicago":"Mognetti, B. M., Anđela Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, and D. Frenkel. “Living Clusters and Crystals from Low-Density Suspensions of Active Colloids.” Physical Review Letters. American Physical Society, 2013. https://doi.org/10.1103/physrevlett.111.245702.","ista":"Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel D. 2013. Living clusters and crystals from low-density suspensions of active colloids. Physical Review Letters. 111(24), 245702.","mla":"Mognetti, B. M., et al. “Living Clusters and Crystals from Low-Density Suspensions of Active Colloids.” Physical Review Letters, vol. 111, no. 24, 245702, American Physical Society, 2013, doi:10.1103/physrevlett.111.245702.","ieee":"B. M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, and D. Frenkel, “Living clusters and crystals from low-density suspensions of active colloids,” Physical Review Letters, vol. 111, no. 24. American Physical Society, 2013.","short":"B.M. Mognetti, A. Šarić, S. Angioletti-Uberti, A. Cacciuto, C. Valeriani, D. Frenkel, Physical Review Letters 111 (2013).","apa":"Mognetti, B. M., Šarić, A., Angioletti-Uberti, S., Cacciuto, A., Valeriani, C., & Frenkel, D. (2013). Living clusters and crystals from low-density suspensions of active colloids. Physical Review Letters. American Physical Society. https://doi.org/10.1103/physrevlett.111.245702","ama":"Mognetti BM, Šarić A, Angioletti-Uberti S, Cacciuto A, Valeriani C, Frenkel D. Living clusters and crystals from low-density suspensions of active colloids. Physical Review Letters. 2013;111(24). doi:10.1103/physrevlett.111.245702"},"article_number":"245702","issue":"24","volume":111,"language":[{"iso":"eng"}],"publication_identifier":{"eissn":["1079-7114"],"issn":["0031-9007"]},"publication_status":"published","month":"12","intvolume":" 111","scopus_import":"1","main_file_link":[{"url":"https://arxiv.org/abs/1311.4681","open_access":"1"}],"pmid":1,"oa_version":"Preprint","abstract":[{"text":"Recent studies aimed at investigating artificial analogs of bacterial colonies have shown that low-density suspensions of self-propelled particles confined in two dimensions can assemble into finite aggregates that merge and split, but have a typical size that remains constant (living clusters). In this Letter, we address the problem of the formation of living clusters and crystals of active particles in three dimensions. We study two systems: self-propelled particles interacting via a generic attractive potential and colloids that can move toward each other as a result of active agents (e.g., by molecular motors). In both cases, fluidlike “living” clusters form. We explain this general feature in terms of the balance between active forces and regression to thermodynamic equilibrium. This balance can be quantified in terms of a dimensionless number that allows us to collapse the observed clustering behavior onto a universal curve. We also discuss how active motion affects the kinetics of crystal formation.","lang":"eng"}],"extern":"1","date_updated":"2021-11-29T14:05:19Z","status":"public","keyword":["general physics and astronomy"],"article_type":"original","type":"journal_article","_id":"10384"},{"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"mla":"Šarić, Anđela, and Angelo Cacciuto. “Self-Assembly of Nanoparticles Adsorbed on Fluid and Elastic Membranes.” Soft Matter, vol. 9, no. 29, 6677, Royal Society of Chemistry, 2013, doi:10.1039/c3sm50188d.","ieee":"A. Šarić and A. Cacciuto, “Self-assembly of nanoparticles adsorbed on fluid and elastic membranes,” Soft Matter, vol. 9, no. 29. Royal Society of Chemistry, 2013.","short":"A. Šarić, A. Cacciuto, Soft Matter 9 (2013).","apa":"Šarić, A., & Cacciuto, A. (2013). Self-assembly of nanoparticles adsorbed on fluid and elastic membranes. Soft Matter. Royal Society of Chemistry. https://doi.org/10.1039/c3sm50188d","ama":"Šarić A, Cacciuto A. Self-assembly of nanoparticles adsorbed on fluid and elastic membranes. Soft Matter. 2013;9(29). doi:10.1039/c3sm50188d","chicago":"Šarić, Anđela, and Angelo Cacciuto. “Self-Assembly of Nanoparticles Adsorbed on Fluid and Elastic Membranes.” Soft Matter. Royal Society of Chemistry, 2013. https://doi.org/10.1039/c3sm50188d.","ista":"Šarić A, Cacciuto A. 2013. Self-assembly of nanoparticles adsorbed on fluid and elastic membranes. Soft Matter. 9(29), 6677."},"title":"Self-assembly of nanoparticles adsorbed on fluid and elastic membranes","article_processing_charge":"No","author":[{"last_name":"Šarić","orcid":"0000-0002-7854-2139","full_name":"Šarić, Anđela","id":"bf63d406-f056-11eb-b41d-f263a6566d8b","first_name":"Anđela"},{"first_name":"Angelo","full_name":"Cacciuto, Angelo","last_name":"Cacciuto"}],"article_number":"6677","publication":"Soft Matter","day":"03","year":"2013","date_created":"2021-11-29T14:06:32Z","date_published":"2013-05-03T00:00:00Z","doi":"10.1039/c3sm50188d","acknowledgement":"This work was supported by the National Science Foundation under Career Grant No. DMR 0846426. The authors thank J. C. Pàmies for many fruitful discussions on the subject.","publisher":"Royal Society of Chemistry","quality_controlled":"1","extern":"1","date_updated":"2021-11-29T14:29:31Z","_id":"10386","keyword":["condensed matter physics","general chemistry"],"status":"public","type":"journal_article","article_type":"original","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"eissn":["1744-6848"],"issn":["1744-683X"]},"volume":9,"issue":"29","oa_version":"None","abstract":[{"lang":"eng","text":"In this paper we review recent numerical and theoretical developments of particle self-assembly on fluid and elastic membranes and compare them to available experimental realizations. We discuss the problem and its applications in biology and materials science, and give an overview of numerical models and strategies to study these systems across all length-scales. As this is a very broad field, this review focuses exclusively on surface-driven aggregation of nanoparticles that are at least one order of magnitude larger than the surface thickness and are adsorbed onto it. In this regime, all chemical details of the surface can be ignored in favor of a coarse-grained representation, and the collective behavior of many particles can be monitored and analyzed. We review the existing literature on how the mechanical properties and the geometry of the surface affect the structure of the particle aggregates and how these can drive shape deformation on the surface."}],"intvolume":" 9","month":"05","main_file_link":[{"url":"https://pubs.rsc.org/en/content/articlehtml/2013/sm/c3sm50188d"}],"scopus_import":"1"},{"citation":{"chicago":"Napoli, Joseph A., Anđela Šarić, and Angelo Cacciuto. “Collapsing Nanoparticle-Laden Nanotubes.” Soft Matter. Royal Society of Chemistry, 2013. https://doi.org/10.1039/c3sm51495a.","ista":"Napoli JA, Šarić A, Cacciuto A. 2013. Collapsing nanoparticle-laden nanotubes. Soft Matter. 9(37), 8881–8886.","mla":"Napoli, Joseph A., et al. “Collapsing Nanoparticle-Laden Nanotubes.” Soft Matter, vol. 9, no. 37, Royal Society of Chemistry, 2013, pp. 8881–86, doi:10.1039/c3sm51495a.","apa":"Napoli, J. A., Šarić, A., & Cacciuto, A. (2013). Collapsing nanoparticle-laden nanotubes. Soft Matter. Royal Society of Chemistry. https://doi.org/10.1039/c3sm51495a","ama":"Napoli JA, Šarić A, Cacciuto A. Collapsing nanoparticle-laden nanotubes. Soft Matter. 2013;9(37):8881-8886. doi:10.1039/c3sm51495a","short":"J.A. Napoli, A. Šarić, A. Cacciuto, Soft Matter 9 (2013) 8881–8886.","ieee":"J. A. Napoli, A. Šarić, and A. Cacciuto, “Collapsing nanoparticle-laden nanotubes,” Soft Matter, vol. 9, no. 37. Royal Society of Chemistry, pp. 8881–8886, 2013."},"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","article_processing_charge":"No","author":[{"full_name":"Napoli, Joseph A.","last_name":"Napoli","first_name":"Joseph A."},{"id":"bf63d406-f056-11eb-b41d-f263a6566d8b","first_name":"Anđela","last_name":"Šarić","full_name":"Šarić, Anđela","orcid":"0000-0002-7854-2139"},{"last_name":"Cacciuto","full_name":"Cacciuto, Angelo","first_name":"Angelo"}],"title":"Collapsing nanoparticle-laden nanotubes","acknowledgement":"This work was supported by the National Science Foundation under Career Grant no. DMR-0846426.","publisher":"Royal Society of Chemistry","quality_controlled":"1","year":"2013","publication":"Soft Matter","day":"08","page":"8881-8886","date_created":"2021-11-29T13:31:24Z","date_published":"2013-08-08T00:00:00Z","doi":"10.1039/c3sm51495a","_id":"10385","type":"journal_article","article_type":"original","keyword":["condensed matter physics","general chemistry"],"status":"public","date_updated":"2021-11-29T14:05:23Z","extern":"1","abstract":[{"text":"We show how self-assembly of sticky nanoparticles can drive radial collapse of thin-walled nanotubes. Using numerical simulations, we study the transition as a function of the geometric and elastic parameters of the nanotube and the binding strength of the nanoparticles. We find that it is possible to derive a simple scaling law relating all these parameters, and estimate bounds for the onset conditions leading to the collapse of the nanotube. We also study the reverse process – the nanoparticle release from the folded state – and find that the stability of the collapsed state can be greatly improved by increasing the bending rigidity of the nanotubes. Our results suggest ways to strengthen the mechanical properties of nanotubes, but also indicate that the control of nanoparticle self-assembly on these nanotubes can lead to nanoparticle-laden responsive materials.","lang":"eng"}],"oa_version":"None","scopus_import":"1","intvolume":" 9","month":"08","publication_status":"published","publication_identifier":{"eissn":["1744-6848"],"issn":["1744-683X"]},"language":[{"iso":"eng"}],"issue":"37","volume":9},{"oa":1,"publisher":"De Gruyter","quality_controlled":"1","date_created":"2021-12-01T14:35:35Z","doi":"10.1515/bmt-2013-4181","date_published":"2013-08-01T00:00:00Z","publication":"Biomedical Engineering / Biomedizinische Technik","day":"01","year":"2013","has_accepted_license":"1","article_number":"000010151520134181","title":"Stimfit: A fast visualization and analysis environment for cellular neurophysiology","article_processing_charge":"No","external_id":{"pmid":["24042795"]},"author":[{"last_name":"Schlögl","full_name":"Schlögl, Alois","orcid":"0000-0002-5621-8100","id":"45BF87EE-F248-11E8-B48F-1D18A9856A87","first_name":"Alois"},{"id":"353C1B58-F248-11E8-B48F-1D18A9856A87","first_name":"Peter M","orcid":"0000-0001-5001-4804","full_name":"Jonas, Peter M","last_name":"Jonas"},{"last_name":"Schmidt-Hieber","full_name":"Schmidt-Hieber, C.","first_name":"C."},{"full_name":"Guzman, S. J.","last_name":"Guzman","first_name":"S. J."}],"user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"ista":"Schlögl A, Jonas PM, Schmidt-Hieber C, Guzman SJ. 2013. Stimfit: A fast visualization and analysis environment for cellular neurophysiology. Biomedical Engineering / Biomedizinische Technik. 58(SI-1-Track-G), 000010151520134181.","chicago":"Schlögl, Alois, Peter M Jonas, C. Schmidt-Hieber, and S. J. Guzman. “Stimfit: A Fast Visualization and Analysis Environment for Cellular Neurophysiology.” Biomedical Engineering / Biomedizinische Technik. De Gruyter, 2013. https://doi.org/10.1515/bmt-2013-4181.","ama":"Schlögl A, Jonas PM, Schmidt-Hieber C, Guzman SJ. Stimfit: A fast visualization and analysis environment for cellular neurophysiology. Biomedical Engineering / Biomedizinische Technik. 2013;58(SI-1-Track-G). doi:10.1515/bmt-2013-4181","apa":"Schlögl, A., Jonas, P. M., Schmidt-Hieber, C., & Guzman, S. J. (2013). Stimfit: A fast visualization and analysis environment for cellular neurophysiology. Biomedical Engineering / Biomedizinische Technik. Graz, Austria: De Gruyter. https://doi.org/10.1515/bmt-2013-4181","short":"A. Schlögl, P.M. Jonas, C. Schmidt-Hieber, S.J. Guzman, Biomedical Engineering / Biomedizinische Technik 58 (2013).","ieee":"A. Schlögl, P. M. Jonas, C. Schmidt-Hieber, and S. J. Guzman, “Stimfit: A fast visualization and analysis environment for cellular neurophysiology,” Biomedical Engineering / Biomedizinische Technik, vol. 58, no. SI-1-Track-G. De Gruyter, 2013.","mla":"Schlögl, Alois, et al. “Stimfit: A Fast Visualization and Analysis Environment for Cellular Neurophysiology.” Biomedical Engineering / Biomedizinische Technik, vol. 58, no. SI-1-Track-G, 000010151520134181, De Gruyter, 2013, doi:10.1515/bmt-2013-4181."},"intvolume":" 58","month":"08","pmid":1,"oa_version":"Submitted Version","abstract":[{"lang":"eng","text":"Stimfit is a free cross-platform software package for viewing and analyzing electrophysiological data. It supports most standard file types for cellular neurophysiology and other biomedical formats. Its analysis algorithms have been used and validated in several experimental laboratories. Its embedded Python scripting interface makes Stimfit highly extensible and customizable."}],"issue":"SI-1-Track-G","volume":58,"language":[{"iso":"eng"}],"file":[{"date_created":"2021-12-01T14:38:08Z","file_name":"Schloegl_Abstract-BMT2013.pdf","creator":"schloegl","date_updated":"2021-12-01T14:38:08Z","file_size":149825,"checksum":"cdfc5339b530a25d6079f7223f0b1f16","file_id":"10397","success":1,"access_level":"open_access","relation":"main_file","content_type":"application/pdf"}],"publication_status":"published","publication_identifier":{"eissn":["1862-278X"],"issn":["0013-5585"]},"keyword":["biomedical engineering","data analysis","free software"],"status":"public","conference":{"name":"BMT: Biomedizinische Technik ","location":"Graz, Austria","end_date":"2013-09-21","start_date":"2013-09-19"},"article_type":"original","type":"journal_article","_id":"10396","department":[{"_id":"PeJo"}],"file_date_updated":"2021-12-01T14:38:08Z","ddc":["005","610"],"date_updated":"2021-12-02T12:51:12Z"},{"oa_version":"Published Version","abstract":[{"text":"Fluxoid quantization provides a direct means to study phase coherence. In cuprate superconductors, there have been observations which suggest that phase coherent superconducting fluctuations may persist at temperatures significantly above Tc. The focus of this work is to study the vortex states in mesoscopic cuprate superconducting samples to directly probe phase coherence over a wide range of temperatures. We present cantilever torque susceptometry measurements of micron and sub-micron size Bi2212 rings and disks. The high sensitivity of this technique allowed observation of transitions between different fluxoid states of a single ring, and the discrete vortex states of micron size disks. The dependence of magnetic susceptibility on diameter and wall thickness of the ring was investigated. Measurements were made at different values of the in-plane magnetic field, and over a wide range of temperatures.","lang":"eng"}],"intvolume":" 58","month":"03","main_file_link":[{"open_access":"1","url":"https://meetings.aps.org/Meeting/MAR13/Event/186873"}],"alternative_title":["Bulletin of the American Physical Society"],"language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["0003-0503"]},"issue":"1","volume":58,"_id":"10749","status":"public","conference":{"name":"APS: American Physical Society","end_date":"2013-03-22","location":"Baltimore, MD, United States","start_date":"2013-03-18"},"type":"conference","extern":"1","date_updated":"2022-02-08T10:48:06Z","acknowledgement":"This work was supported by the Center for Emergent Superconductivity, an Energy Frontier Research Center funded by the US DOE, Office of Science.","oa":1,"quality_controlled":"1","publisher":"American Physical Society","publication":"APS March Meeting 2013","day":"01","year":"2013","date_created":"2022-02-08T10:34:29Z","date_published":"2013-03-01T00:00:00Z","article_number":"N36.00001","user_id":"8b945eb4-e2f2-11eb-945a-df72226e66a9","citation":{"mla":"Polshyn, Hryhoriy, et al. “Cantilever Micro-Susceptometry of Mesoscopic Bi2212 Samples.” APS March Meeting 2013, vol. 58, no. 1, N36.00001, American Physical Society, 2013.","apa":"Polshyn, H., Budakian, R., & Gu, G. (2013). Cantilever micro-susceptometry of mesoscopic Bi2212 samples. In APS March Meeting 2013 (Vol. 58). Baltimore, MD, United States: American Physical Society.","ama":"Polshyn H, Budakian R, Gu G. Cantilever micro-susceptometry of mesoscopic Bi2212 samples. In: APS March Meeting 2013. Vol 58. American Physical Society; 2013.","short":"H. Polshyn, R. Budakian, G. Gu, in:, APS March Meeting 2013, American Physical Society, 2013.","ieee":"H. Polshyn, R. Budakian, and G. Gu, “Cantilever micro-susceptometry of mesoscopic Bi2212 samples,” in APS March Meeting 2013, Baltimore, MD, United States, 2013, vol. 58, no. 1.","chicago":"Polshyn, Hryhoriy, Raffi Budakian, and Genda Gu. “Cantilever Micro-Susceptometry of Mesoscopic Bi2212 Samples.” In APS March Meeting 2013, Vol. 58. American Physical Society, 2013.","ista":"Polshyn H, Budakian R, Gu G. 2013. Cantilever micro-susceptometry of mesoscopic Bi2212 samples. APS March Meeting 2013. APS: American Physical Society, Bulletin of the American Physical Society, vol. 58, N36.00001."},"title":"Cantilever micro-susceptometry of mesoscopic Bi2212 samples","article_processing_charge":"No","author":[{"id":"edfc7cb1-526e-11ec-b05a-e6ecc27e4e48","first_name":"Hryhoriy","orcid":"0000-0001-8223-8896","full_name":"Polshyn, Hryhoriy","last_name":"Polshyn"},{"first_name":"Raffi","full_name":"Budakian, Raffi","last_name":"Budakian"},{"first_name":"Genda","full_name":"Gu, Genda","last_name":"Gu"}]},{"publisher":"MDPI","quality_controlled":"1","oa":1,"date_published":"2013-10-21T00:00:00Z","doi":"10.3390/plants2040650","date_created":"2022-03-21T07:13:49Z","page":"650-675","day":"21","publication":"Plants","has_accepted_license":"1","year":"2013","title":"Calcium: The missing link in auxin action","author":[{"last_name":"Vanneste","full_name":"Vanneste, Steffen","first_name":"Steffen"},{"full_name":"Friml, Jiří","orcid":"0000-0002-8302-7596","last_name":"Friml","id":"4159519E-F248-11E8-B48F-1D18A9856A87","first_name":"Jiří"}],"article_processing_charge":"No","external_id":{"pmid":["27137397"]},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ieee":"S. Vanneste and J. Friml, “Calcium: The missing link in auxin action,” Plants, vol. 2, no. 4. MDPI, pp. 650–675, 2013.","short":"S. Vanneste, J. Friml, Plants 2 (2013) 650–675.","ama":"Vanneste S, Friml J. Calcium: The missing link in auxin action. Plants. 2013;2(4):650-675. doi:10.3390/plants2040650","apa":"Vanneste, S., & Friml, J. (2013). Calcium: The missing link in auxin action. Plants. MDPI. https://doi.org/10.3390/plants2040650","mla":"Vanneste, Steffen, and Jiří Friml. “Calcium: The Missing Link in Auxin Action.” Plants, vol. 2, no. 4, MDPI, 2013, pp. 650–75, doi:10.3390/plants2040650.","ista":"Vanneste S, Friml J. 2013. Calcium: The missing link in auxin action. Plants. 2(4), 650–675.","chicago":"Vanneste, Steffen, and Jiří Friml. “Calcium: The Missing Link in Auxin Action.” Plants. MDPI, 2013. https://doi.org/10.3390/plants2040650."},"month":"10","intvolume":" 2","scopus_import":"1","pmid":1,"oa_version":"Published Version","abstract":[{"text":"Due to their sessile lifestyles, plants need to deal with the limitations and stresses imposed by the changing environment. Plants cope with these by a remarkable developmental flexibility, which is embedded in their strategy to survive. Plants can adjust their size, shape and number of organs, bend according to gravity and light, and regenerate tissues that were damaged, utilizing a coordinating, intercellular signal, the plant hormone, auxin. Another versatile signal is the cation, Ca2+, which is a crucial second messenger for many rapid cellular processes during responses to a wide range of endogenous and environmental signals, such as hormones, light, drought stress and others. Auxin is a good candidate for one of these Ca2+-activating signals. However, the role of auxin-induced Ca2+ signaling is poorly understood. Here, we will provide an overview of possible developmental and physiological roles, as well as mechanisms underlying the interconnection of Ca2+ and auxin signaling. ","lang":"eng"}],"issue":"4","volume":2,"license":"https://creativecommons.org/licenses/by/3.0/","file":[{"relation":"main_file","access_level":"open_access","content_type":"application/pdf","success":1,"file_id":"10916","checksum":"fb4ff2e820e344e253c9197544610be6","creator":"dernst","file_size":670188,"date_updated":"2022-03-21T12:12:56Z","file_name":"2013_Plants_Vanneste.pdf","date_created":"2022-03-21T12:12:56Z"}],"language":[{"iso":"eng"}],"publication_identifier":{"issn":["2223-7747"]},"publication_status":"published","status":"public","keyword":["Plant Science","Ecology","Ecology","Evolution","Behavior and Systematics"],"type":"journal_article","article_type":"original","tmp":{"short":"CC BY (3.0)","image":"/images/cc_by.png","legal_code_url":"https://creativecommons.org/licenses/by/3.0/legalcode","name":"Creative Commons Attribution 3.0 Unported (CC BY 3.0)"},"_id":"10895","department":[{"_id":"JiFr"}],"file_date_updated":"2022-03-21T12:12:56Z","ddc":["580"],"date_updated":"2022-03-21T12:15:29Z"},{"date_created":"2022-03-21T07:33:22Z","issue":"5","doi":"10.1145/2482767.2482789","date_published":"2013-05-01T00:00:00Z","publication":"Proceedings of the ACM International Conference on Computing Frontiers - CF '13","language":[{"iso":"eng"}],"day":"01","publication_status":"published","year":"2013","publication_identifier":{"isbn":["978-145032053-5"]},"month":"05","quality_controlled":"1","publisher":"ACM Press","scopus_import":"1","oa_version":"None","abstract":[{"text":"A prominent remedy to multicore scalability issues in concurrent data structure implementations is to relax the sequential specification of the data structure. We present distributed queues (DQ), a new family of relaxed concurrent queue implementations. DQs implement relaxed queues with linearizable emptiness check and either configurable or bounded out-of-order behavior or pool behavior. Our experiments show that DQs outperform and outscale in micro- and macrobenchmarks all strict and relaxed queue as well as pool implementations that we considered.","lang":"eng"}],"department":[{"_id":"ToHe"}],"title":"Distributed queues in shared memory: Multicore performance and scalability through quantitative relaxation","article_processing_charge":"No","author":[{"first_name":"Andreas","full_name":"Haas, Andreas","last_name":"Haas"},{"first_name":"Michael","full_name":"Lippautz, Michael","last_name":"Lippautz"},{"id":"40876CD8-F248-11E8-B48F-1D18A9856A87","first_name":"Thomas A","last_name":"Henzinger","full_name":"Henzinger, Thomas A","orcid":"0000-0002-2985-7724"},{"full_name":"Payer, Hannes","last_name":"Payer","first_name":"Hannes"},{"last_name":"Sokolova","full_name":"Sokolova, Ana","first_name":"Ana"},{"last_name":"Kirsch","full_name":"Kirsch, Christoph M.","first_name":"Christoph M."},{"first_name":"Ali","id":"4C7638DA-F248-11E8-B48F-1D18A9856A87","last_name":"Sezgin","full_name":"Sezgin, Ali"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Haas, Andreas, Michael Lippautz, Thomas A Henzinger, Hannes Payer, Ana Sokolova, Christoph M. Kirsch, and Ali Sezgin. “Distributed Queues in Shared Memory: Multicore Performance and Scalability through Quantitative Relaxation.” In Proceedings of the ACM International Conference on Computing Frontiers - CF ’13. ACM Press, 2013. https://doi.org/10.1145/2482767.2482789.","ista":"Haas A, Lippautz M, Henzinger TA, Payer H, Sokolova A, Kirsch CM, Sezgin A. 2013. Distributed queues in shared memory: Multicore performance and scalability through quantitative relaxation. Proceedings of the ACM International Conference on Computing Frontiers - CF ’13. CF: Conference on Computing Frontiers, 17.","mla":"Haas, Andreas, et al. “Distributed Queues in Shared Memory: Multicore Performance and Scalability through Quantitative Relaxation.” Proceedings of the ACM International Conference on Computing Frontiers - CF ’13, no. 5, 17, ACM Press, 2013, doi:10.1145/2482767.2482789.","ieee":"A. Haas et al., “Distributed queues in shared memory: Multicore performance and scalability through quantitative relaxation,” in Proceedings of the ACM International Conference on Computing Frontiers - CF ’13, Ischia, Italy, 2013, no. 5.","short":"A. Haas, M. Lippautz, T.A. Henzinger, H. Payer, A. Sokolova, C.M. Kirsch, A. Sezgin, in:, Proceedings of the ACM International Conference on Computing Frontiers - CF ’13, ACM Press, 2013.","ama":"Haas A, Lippautz M, Henzinger TA, et al. Distributed queues in shared memory: Multicore performance and scalability through quantitative relaxation. In: Proceedings of the ACM International Conference on Computing Frontiers - CF ’13. ACM Press; 2013. doi:10.1145/2482767.2482789","apa":"Haas, A., Lippautz, M., Henzinger, T. A., Payer, H., Sokolova, A., Kirsch, C. M., & Sezgin, A. (2013). Distributed queues in shared memory: Multicore performance and scalability through quantitative relaxation. In Proceedings of the ACM International Conference on Computing Frontiers - CF ’13. Ischia, Italy: ACM Press. https://doi.org/10.1145/2482767.2482789"},"date_updated":"2022-06-21T08:01:19Z","status":"public","conference":{"name":"CF: Conference on Computing Frontiers","start_date":"2013-05-14","end_date":"2013-05-16","location":"Ischia, Italy"},"type":"conference","article_number":"17","_id":"10898"},{"_id":"10899","status":"public","keyword":["Adaptive landscape","Cline","Coalescent process","Gene flow","Hybrid zone","Local adaptation","Natural selection","Neutral theory","Population structure","Speciation"],"type":"book_chapter","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","date_updated":"2022-06-20T09:18:06Z","citation":{"chicago":"Barton, Nicholas H. “Differentiation.” In Encyclopedia of Biodiversity, 2nd ed., 508–15. Elsevier, 2013. https://doi.org/10.1016/b978-0-12-384719-5.00031-9.","ista":"Barton NH. 2013.Differentiation. In: Encyclopedia of Biodiversity. , 508–515.","mla":"Barton, Nicholas H. “Differentiation.” Encyclopedia of Biodiversity, 2nd ed., Elsevier, 2013, pp. 508–15, doi:10.1016/b978-0-12-384719-5.00031-9.","ieee":"N. H. Barton, “Differentiation,” in Encyclopedia of Biodiversity, 2nd ed., Elsevier, 2013, pp. 508–515.","short":"N.H. Barton, in:, Encyclopedia of Biodiversity, 2nd ed., Elsevier, 2013, pp. 508–515.","apa":"Barton, N. H. (2013). Differentiation. In Encyclopedia of Biodiversity (2nd ed., pp. 508–515). Elsevier. https://doi.org/10.1016/b978-0-12-384719-5.00031-9","ama":"Barton NH. Differentiation. In: Encyclopedia of Biodiversity. 2nd ed. Elsevier; 2013:508-515. doi:10.1016/b978-0-12-384719-5.00031-9"},"department":[{"_id":"NiBa"}],"title":"Differentiation","author":[{"first_name":"Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87","full_name":"Barton, Nicholas H","orcid":"0000-0002-8548-5240","last_name":"Barton"}],"article_processing_charge":"No","oa_version":"None","month":"01","scopus_import":"1","publisher":"Elsevier","quality_controlled":"1","edition":"2","day":"01","language":[{"iso":"eng"}],"publication":"Encyclopedia of Biodiversity","publication_identifier":{"isbn":["978-0-12-384720-1"]},"year":"2013","publication_status":"published","date_published":"2013-01-01T00:00:00Z","doi":"10.1016/b978-0-12-384719-5.00031-9","date_created":"2022-03-21T07:46:22Z","page":"508-515"},{"_id":"11086","keyword":["Cancer Research","Genetics (clinical)","Genetics","Molecular Biology","Ecology","Evolution","Behavior and Systematics"],"status":"public","type":"journal_article","article_type":"original","extern":"1","date_updated":"2022-07-18T08:45:58Z","oa_version":"Published Version","pmid":1,"abstract":[{"text":"Faithful execution of developmental gene expression programs occurs at multiple levels and involves many different components such as transcription factors, histone-modification enzymes, and mRNA processing proteins. Recent evidence suggests that nucleoporins, well known components that control nucleo-cytoplasmic trafficking, have wide-ranging functions in developmental gene regulation that potentially extend beyond their role in nuclear transport. Whether the unexpected role of nuclear pore proteins in transcription regulation, which initially has been described in fungi and flies, also applies to human cells is unknown. Here we show at a genome-wide level that the nuclear pore protein NUP98 associates with developmentally regulated genes active during human embryonic stem cell differentiation. Overexpression of a dominant negative fragment of NUP98 levels decreases expression levels of NUP98-bound genes. In addition, we identify two modes of developmental gene regulation by NUP98 that are differentiated by the spatial localization of NUP98 target genes. Genes in the initial stage of developmental induction can associate with NUP98 that is embedded in the nuclear pores at the nuclear periphery. Alternatively, genes that are highly induced can interact with NUP98 in the nuclear interior, away from the nuclear pores. This work demonstrates for the first time that NUP98 dynamically associates with the human genome during differentiation, revealing a role of a nuclear pore protein in regulating developmental gene expression programs.","lang":"eng"}],"intvolume":" 9","month":"02","main_file_link":[{"url":"https://doi.org/10.1371/journal.pgen.1003308","open_access":"1"}],"scopus_import":"1","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["1553-7404"]},"issue":"2","volume":9,"article_number":"e1003308","user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","citation":{"ieee":"Y. Liang, T. M. Franks, M. C. Marchetto, F. H. Gage, and M. Hetzer, “Dynamic association of NUP98 with the human genome,” PLoS Genetics, vol. 9, no. 2. Public Library of Science, 2013.","short":"Y. Liang, T.M. Franks, M.C. Marchetto, F.H. Gage, M. Hetzer, PLoS Genetics 9 (2013).","ama":"Liang Y, Franks TM, Marchetto MC, Gage FH, Hetzer M. Dynamic association of NUP98 with the human genome. PLoS Genetics. 2013;9(2). doi:10.1371/journal.pgen.1003308","apa":"Liang, Y., Franks, T. M., Marchetto, M. C., Gage, F. H., & Hetzer, M. (2013). Dynamic association of NUP98 with the human genome. PLoS Genetics. Public Library of Science. https://doi.org/10.1371/journal.pgen.1003308","mla":"Liang, Yun, et al. “Dynamic Association of NUP98 with the Human Genome.” PLoS Genetics, vol. 9, no. 2, e1003308, Public Library of Science, 2013, doi:10.1371/journal.pgen.1003308.","ista":"Liang Y, Franks TM, Marchetto MC, Gage FH, Hetzer M. 2013. Dynamic association of NUP98 with the human genome. PLoS Genetics. 9(2), e1003308.","chicago":"Liang, Yun, Tobias M. Franks, Maria C. Marchetto, Fred H. Gage, and Martin Hetzer. “Dynamic Association of NUP98 with the Human Genome.” PLoS Genetics. Public Library of Science, 2013. https://doi.org/10.1371/journal.pgen.1003308."},"title":"Dynamic association of NUP98 with the human genome","external_id":{"pmid":["23468646"]},"article_processing_charge":"No","author":[{"full_name":"Liang, Yun","last_name":"Liang","first_name":"Yun"},{"first_name":"Tobias M.","last_name":"Franks","full_name":"Franks, Tobias M."},{"last_name":"Marchetto","full_name":"Marchetto, Maria C.","first_name":"Maria C."},{"full_name":"Gage, Fred H.","last_name":"Gage","first_name":"Fred H."},{"last_name":"HETZER","full_name":"HETZER, Martin W","orcid":"0000-0002-2111-992X","id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","first_name":"Martin W"}],"oa":1,"quality_controlled":"1","publisher":"Public Library of Science","publication":"PLoS Genetics","day":"28","year":"2013","date_created":"2022-04-07T07:50:59Z","doi":"10.1371/journal.pgen.1003308","date_published":"2013-02-28T00:00:00Z"},{"date_updated":"2022-07-18T08:50:47Z","extern":"1","article_type":"original","type":"journal_article","keyword":["General Biochemistry","Genetics and Molecular Biology"],"status":"public","_id":"11087","volume":154,"issue":"5","publication_status":"published","publication_identifier":{"issn":["0092-8674"]},"language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"https://doi.org/10.1016/j.cell.2013.07.037"}],"scopus_import":"1","intvolume":" 154","month":"08","abstract":[{"lang":"eng","text":"Intracellular proteins with long lifespans have recently been linked to age-dependent defects, ranging from decreased fertility to the functional decline of neurons. Why long-lived proteins exist in metabolically active cellular environments and how they are maintained over time remains poorly understood. Here, we provide a system-wide identification of proteins with exceptional lifespans in the rat brain. These proteins are inefficiently replenished despite being translated robustly throughout adulthood. Using nucleoporins as a paradigm for long-term protein persistence, we found that nuclear pore complexes (NPCs) are maintained over a cell’s life through slow but finite exchange of even its most stable subcomplexes. This maintenance is limited, however, as some nucleoporin levels decrease during aging, providing a rationale for the previously observed age-dependent deterioration of NPC function. Our identification of a long-lived proteome reveals cellular components that are at increased risk for damage accumulation, linking long-term protein persistence to the cellular aging process."}],"pmid":1,"oa_version":"Published Version","article_processing_charge":"No","external_id":{"pmid":["23993091"]},"author":[{"first_name":"Brandon H.","full_name":"Toyama, Brandon H.","last_name":"Toyama"},{"first_name":"Jeffrey N.","full_name":"Savas, Jeffrey N.","last_name":"Savas"},{"full_name":"Park, Sung Kyu","last_name":"Park","first_name":"Sung Kyu"},{"first_name":"Michael S.","full_name":"Harris, Michael S.","last_name":"Harris"},{"full_name":"Ingolia, Nicholas T.","last_name":"Ingolia","first_name":"Nicholas T."},{"full_name":"Yates, John R.","last_name":"Yates","first_name":"John R."},{"id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","first_name":"Martin W","full_name":"HETZER, Martin W","orcid":"0000-0002-2111-992X","last_name":"HETZER"}],"title":"Identification of long-lived proteins reveals exceptional stability of essential cellular structures","citation":{"short":"B.H. Toyama, J.N. Savas, S.K. Park, M.S. Harris, N.T. Ingolia, J.R. Yates, M. Hetzer, Cell 154 (2013) 971–982.","ieee":"B. H. Toyama et al., “Identification of long-lived proteins reveals exceptional stability of essential cellular structures,” Cell, vol. 154, no. 5. Elsevier, pp. 971–982, 2013.","ama":"Toyama BH, Savas JN, Park SK, et al. Identification of long-lived proteins reveals exceptional stability of essential cellular structures. Cell. 2013;154(5):971-982. doi:10.1016/j.cell.2013.07.037","apa":"Toyama, B. H., Savas, J. N., Park, S. K., Harris, M. S., Ingolia, N. T., Yates, J. R., & Hetzer, M. (2013). Identification of long-lived proteins reveals exceptional stability of essential cellular structures. Cell. Elsevier. https://doi.org/10.1016/j.cell.2013.07.037","mla":"Toyama, Brandon H., et al. “Identification of Long-Lived Proteins Reveals Exceptional Stability of Essential Cellular Structures.” Cell, vol. 154, no. 5, Elsevier, 2013, pp. 971–82, doi:10.1016/j.cell.2013.07.037.","ista":"Toyama BH, Savas JN, Park SK, Harris MS, Ingolia NT, Yates JR, Hetzer M. 2013. Identification of long-lived proteins reveals exceptional stability of essential cellular structures. Cell. 154(5), 971–982.","chicago":"Toyama, Brandon H., Jeffrey N. Savas, Sung Kyu Park, Michael S. Harris, Nicholas T. Ingolia, John R. Yates, and Martin Hetzer. “Identification of Long-Lived Proteins Reveals Exceptional Stability of Essential Cellular Structures.” Cell. Elsevier, 2013. https://doi.org/10.1016/j.cell.2013.07.037."},"user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","page":"971-982","date_created":"2022-04-07T07:51:08Z","date_published":"2013-08-29T00:00:00Z","doi":"10.1016/j.cell.2013.07.037","year":"2013","publication":"Cell","day":"29","oa":1,"publisher":"Elsevier","quality_controlled":"1"},{"publication":"Cell","day":"03","year":"2013","date_created":"2022-04-07T07:50:51Z","date_published":"2013-07-03T00:00:00Z","doi":"10.1016/j.cell.2013.06.007","page":"47-60","oa":1,"quality_controlled":"1","publisher":"Elsevier","user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","citation":{"chicago":"Hatch, Emily M., Andrew H. Fischer, Thomas J. Deerinck, and Martin Hetzer. “Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei.” Cell. Elsevier, 2013. https://doi.org/10.1016/j.cell.2013.06.007.","ista":"Hatch EM, Fischer AH, Deerinck TJ, Hetzer M. 2013. Catastrophic nuclear envelope collapse in cancer cell micronuclei. Cell. 154(1), 47–60.","mla":"Hatch, Emily M., et al. “Catastrophic Nuclear Envelope Collapse in Cancer Cell Micronuclei.” Cell, vol. 154, no. 1, Elsevier, 2013, pp. 47–60, doi:10.1016/j.cell.2013.06.007.","ama":"Hatch EM, Fischer AH, Deerinck TJ, Hetzer M. Catastrophic nuclear envelope collapse in cancer cell micronuclei. Cell. 2013;154(1):47-60. doi:10.1016/j.cell.2013.06.007","apa":"Hatch, E. M., Fischer, A. H., Deerinck, T. J., & Hetzer, M. (2013). Catastrophic nuclear envelope collapse in cancer cell micronuclei. Cell. Elsevier. https://doi.org/10.1016/j.cell.2013.06.007","short":"E.M. Hatch, A.H. Fischer, T.J. Deerinck, M. Hetzer, Cell 154 (2013) 47–60.","ieee":"E. M. Hatch, A. H. Fischer, T. J. Deerinck, and M. Hetzer, “Catastrophic nuclear envelope collapse in cancer cell micronuclei,” Cell, vol. 154, no. 1. Elsevier, pp. 47–60, 2013."},"title":"Catastrophic nuclear envelope collapse in cancer cell micronuclei","article_processing_charge":"No","external_id":{"pmid":["23827674"]},"author":[{"last_name":"Hatch","full_name":"Hatch, Emily M.","first_name":"Emily M."},{"full_name":"Fischer, Andrew H.","last_name":"Fischer","first_name":"Andrew H."},{"full_name":"Deerinck, Thomas J.","last_name":"Deerinck","first_name":"Thomas J."},{"first_name":"Martin W","id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","last_name":"HETZER","orcid":"0000-0002-2111-992X","full_name":"HETZER, Martin W"}],"language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"issn":["0092-8674"]},"issue":"1","volume":154,"pmid":1,"oa_version":"Published Version","abstract":[{"text":"During mitotic exit, missegregated chromosomes can recruit their own nuclear envelope (NE) to form micronuclei (MN). MN have reduced functioning compared to primary nuclei in the same cell, although the two compartments appear to be structurally comparable. Here we show that over 60% of MN undergo an irreversible loss of compartmentalization during interphase due to NE collapse. This disruption of the MN, which is induced by defects in nuclear lamina assembly, drastically reduces nuclear functions and can trigger massive DNA damage. MN disruption is associated with chromatin compaction and invasion of endoplasmic reticulum (ER) tubules into the chromatin. We identified disrupted MN in both major subtypes of human non-small-cell lung cancer, suggesting that disrupted MN could be a useful objective biomarker for genomic instability in solid tumors. Our study shows that NE collapse is a key event underlying MN dysfunction and establishes a link between aberrant NE organization and aneuploidy.","lang":"eng"}],"intvolume":" 154","month":"07","main_file_link":[{"url":"https://doi.org/10.1016/j.cell.2013.06.007","open_access":"1"}],"scopus_import":"1","extern":"1","date_updated":"2022-07-18T08:45:47Z","_id":"11085","keyword":["General Biochemistry","Genetics and Molecular Biology"],"status":"public","article_type":"original","type":"journal_article"},{"_id":"11088","article_type":"original","type":"journal_article","keyword":["Biophysics"],"status":"public","date_updated":"2022-07-18T08:51:01Z","extern":"1","abstract":[{"text":"The crowded intracellular environment poses a formidable challenge to experimental and theoretical analyses of intracellular transport mechanisms. Our measurements of single-particle trajectories in cytoplasm and their random-walk interpretations elucidate two of these mechanisms: molecular diffusion in crowded environments and cytoskeletal transport along microtubules. We employed acousto-optic deflector microscopy to map out the three-dimensional trajectories of microspheres migrating in the cytosolic fraction of a cellular extract. Classical Brownian motion (BM), continuous time random walk, and fractional BM were alternatively used to represent these trajectories. The comparison of the experimental and numerical data demonstrates that cytoskeletal transport along microtubules and diffusion in the cytosolic fraction exhibit anomalous (nonFickian) behavior and posses statistically distinct signatures. Among the three random-walk models used, continuous time random walk provides the best representation of diffusion, whereas microtubular transport is accurately modeled with fractional BM.","lang":"eng"}],"pmid":1,"oa_version":"Published Version","main_file_link":[{"open_access":"1","url":"https://doi.org/10.1016/j.bpj.2013.01.049"}],"scopus_import":"1","intvolume":" 104","month":"04","publication_status":"published","publication_identifier":{"issn":["0006-3495"]},"language":[{"iso":"eng"}],"issue":"8","volume":104,"citation":{"chicago":"Regner, Benjamin M., Dejan Vučinić, Cristina Domnisoru, Thomas M. Bartol, Martin Hetzer, Daniel M. Tartakovsky, and Terrence J. Sejnowski. “Anomalous Diffusion of Single Particles in Cytoplasm.” Biophysical Journal. Elsevier, 2013. https://doi.org/10.1016/j.bpj.2013.01.049.","ista":"Regner BM, Vučinić D, Domnisoru C, Bartol TM, Hetzer M, Tartakovsky DM, Sejnowski TJ. 2013. Anomalous diffusion of single particles in cytoplasm. Biophysical Journal. 104(8), 1652–1660.","mla":"Regner, Benjamin M., et al. “Anomalous Diffusion of Single Particles in Cytoplasm.” Biophysical Journal, vol. 104, no. 8, Elsevier, 2013, pp. 1652–60, doi:10.1016/j.bpj.2013.01.049.","ieee":"B. M. Regner et al., “Anomalous diffusion of single particles in cytoplasm,” Biophysical Journal, vol. 104, no. 8. Elsevier, pp. 1652–1660, 2013.","short":"B.M. Regner, D. Vučinić, C. Domnisoru, T.M. Bartol, M. Hetzer, D.M. Tartakovsky, T.J. Sejnowski, Biophysical Journal 104 (2013) 1652–1660.","ama":"Regner BM, Vučinić D, Domnisoru C, et al. Anomalous diffusion of single particles in cytoplasm. Biophysical Journal. 2013;104(8):1652-1660. doi:10.1016/j.bpj.2013.01.049","apa":"Regner, B. M., Vučinić, D., Domnisoru, C., Bartol, T. M., Hetzer, M., Tartakovsky, D. M., & Sejnowski, T. J. (2013). Anomalous diffusion of single particles in cytoplasm. Biophysical Journal. Elsevier. https://doi.org/10.1016/j.bpj.2013.01.049"},"user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","external_id":{"pmid":["23601312"]},"article_processing_charge":"No","author":[{"first_name":"Benjamin M.","last_name":"Regner","full_name":"Regner, Benjamin M."},{"full_name":"Vučinić, Dejan","last_name":"Vučinić","first_name":"Dejan"},{"full_name":"Domnisoru, Cristina","last_name":"Domnisoru","first_name":"Cristina"},{"first_name":"Thomas M.","full_name":"Bartol, Thomas M.","last_name":"Bartol"},{"last_name":"HETZER","full_name":"HETZER, Martin W","orcid":"0000-0002-2111-992X","id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","first_name":"Martin W"},{"full_name":"Tartakovsky, Daniel M.","last_name":"Tartakovsky","first_name":"Daniel M."},{"full_name":"Sejnowski, Terrence J.","last_name":"Sejnowski","first_name":"Terrence J."}],"title":"Anomalous diffusion of single particles in cytoplasm","oa":1,"publisher":"Elsevier","quality_controlled":"1","year":"2013","publication":"Biophysical Journal","day":"16","page":"1652-1660","date_created":"2022-04-07T07:51:26Z","doi":"10.1016/j.bpj.2013.01.049","date_published":"2013-04-16T00:00:00Z"},{"_id":"11083","status":"public","keyword":["Cell Biology"],"article_type":"letter_note","type":"journal_article","extern":"1","date_updated":"2022-07-18T08:45:34Z","oa_version":"None","pmid":1,"abstract":[{"lang":"eng","text":"Nuclear pore complex (NPC) proteins are known for their critical roles in regulating nucleocytoplasmic traffic of macromolecules across the nuclear envelope. However, recent findings suggest that some nucleoporins (Nups), including Nup98, have additional functions in developmental gene regulation. Nup98, which exhibits transcription-dependent mobility at the NPC but can also bind chromatin away from the nuclear envelope, is frequently involved in chromosomal translocations in a subset of patients suffering from acute myeloid leukemia (AML). A common paradigm suggests that Nup98 translocations cause aberrant transcription when they are recuited to aberrant genomic loci. Importantly, this model fails to account for the potential loss of wild type (WT) Nup98 function in the presence of Nup98 translocation mutants. Here we examine how the cell might regulate Nup98 nucleoplasmic protein levels to control transcription in healthy cells. In addition, we discuss the possibility that dominant negative Nup98 fusion proteins disrupt the transcriptional activity of WT Nup98 in the nucleoplasm to drive AML."}],"month":"03","intvolume":" 23","scopus_import":"1","language":[{"iso":"eng"}],"publication_identifier":{"issn":["0962-8924"]},"publication_status":"published","volume":23,"issue":"3","user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","citation":{"ista":"Franks TM, Hetzer M. 2013. The role of Nup98 in transcription regulation in healthy and diseased cells. Trends in Cell Biology. 23(3), 112–117.","chicago":"Franks, Tobias M., and Martin Hetzer. “The Role of Nup98 in Transcription Regulation in Healthy and Diseased Cells.” Trends in Cell Biology. Elsevier, 2013. https://doi.org/10.1016/j.tcb.2012.10.013.","ama":"Franks TM, Hetzer M. The role of Nup98 in transcription regulation in healthy and diseased cells. Trends in Cell Biology. 2013;23(3):112-117. doi:10.1016/j.tcb.2012.10.013","apa":"Franks, T. M., & Hetzer, M. (2013). The role of Nup98 in transcription regulation in healthy and diseased cells. Trends in Cell Biology. Elsevier. https://doi.org/10.1016/j.tcb.2012.10.013","ieee":"T. M. Franks and M. Hetzer, “The role of Nup98 in transcription regulation in healthy and diseased cells,” Trends in Cell Biology, vol. 23, no. 3. Elsevier, pp. 112–117, 2013.","short":"T.M. Franks, M. Hetzer, Trends in Cell Biology 23 (2013) 112–117.","mla":"Franks, Tobias M., and Martin Hetzer. “The Role of Nup98 in Transcription Regulation in Healthy and Diseased Cells.” Trends in Cell Biology, vol. 23, no. 3, Elsevier, 2013, pp. 112–17, doi:10.1016/j.tcb.2012.10.013."},"title":"The role of Nup98 in transcription regulation in healthy and diseased cells","author":[{"full_name":"Franks, Tobias M.","last_name":"Franks","first_name":"Tobias M."},{"id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","first_name":"Martin W","orcid":"0000-0002-2111-992X","full_name":"HETZER, Martin W","last_name":"HETZER"}],"external_id":{"pmid":["23246429"]},"article_processing_charge":"No","publisher":"Elsevier","quality_controlled":"1","day":"01","publication":"Trends in Cell Biology","year":"2013","date_published":"2013-03-01T00:00:00Z","doi":"10.1016/j.tcb.2012.10.013","date_created":"2022-04-07T07:50:33Z","page":"112-117"},{"date_updated":"2022-07-18T08:37:53Z","extern":"1","type":"journal_article","article_type":"original","keyword":["Cell Biology","Molecular Biology"],"status":"public","_id":"11084","volume":14,"publication_status":"published","publication_identifier":{"issn":["1471-0072","1471-0080"]},"language":[{"iso":"eng"}],"scopus_import":"1","intvolume":" 14","month":"01","abstract":[{"lang":"eng","text":"Protein turnover is an effective way of maintaining a functional proteome, as old and potentially damaged polypeptides are destroyed and replaced by newly synthesized copies. An increasing number of intracellular proteins, however, have been identified that evade this turnover process and instead are maintained over a cell's lifetime. This diverse group of long-lived proteins might be particularly prone to accumulation of damage and thus have a crucial role in the functional deterioration of key regulatory processes during ageing."}],"oa_version":"None","pmid":1,"article_processing_charge":"No","external_id":{"pmid":["23258296"]},"author":[{"last_name":"Toyama","full_name":"Toyama, Brandon H.","first_name":"Brandon H."},{"id":"86c0d31b-b4eb-11ec-ac5a-eae7b2e135ed","first_name":"Martin W","full_name":"HETZER, Martin W","orcid":"0000-0002-2111-992X","last_name":"HETZER"}],"title":"Protein homeostasis: Live long, won't prosper","citation":{"mla":"Toyama, Brandon H., and Martin Hetzer. “Protein Homeostasis: Live Long, Won’t Prosper.” Nature Reviews Molecular Cell Biology, vol. 14, Springer Nature, 2013, pp. 55–61, doi:10.1038/nrm3496.","ama":"Toyama BH, Hetzer M. Protein homeostasis: Live long, won’t prosper. Nature Reviews Molecular Cell Biology. 2013;14:55-61. doi:10.1038/nrm3496","apa":"Toyama, B. H., & Hetzer, M. (2013). Protein homeostasis: Live long, won’t prosper. Nature Reviews Molecular Cell Biology. Springer Nature. https://doi.org/10.1038/nrm3496","short":"B.H. Toyama, M. Hetzer, Nature Reviews Molecular Cell Biology 14 (2013) 55–61.","ieee":"B. H. Toyama and M. Hetzer, “Protein homeostasis: Live long, won’t prosper,” Nature Reviews Molecular Cell Biology, vol. 14. Springer Nature, pp. 55–61, 2013.","chicago":"Toyama, Brandon H., and Martin Hetzer. “Protein Homeostasis: Live Long, Won’t Prosper.” Nature Reviews Molecular Cell Biology. Springer Nature, 2013. https://doi.org/10.1038/nrm3496.","ista":"Toyama BH, Hetzer M. 2013. Protein homeostasis: Live long, won’t prosper. Nature Reviews Molecular Cell Biology. 14, 55–61."},"user_id":"72615eeb-f1f3-11ec-aa25-d4573ddc34fd","page":"55-61","date_created":"2022-04-07T07:50:43Z","date_published":"2013-01-01T00:00:00Z","doi":"10.1038/nrm3496","year":"2013","publication":"Nature Reviews Molecular Cell Biology","day":"01","quality_controlled":"1","publisher":"Springer Nature"},{"quality_controlled":"1","publisher":"AIP","intvolume":" 84","month":"02","abstract":[{"text":"We present the design and performance characterization of a new experimental technique for measuring individual particle charges in large ensembles of macroscopic grains. The measurement principle is qualitatively similar to that used in determining the elementary charge by Millikan in that it follows individual particle trajectories. However, by taking advantage of new technology we are able to work with macroscopic grains and achieve several orders of magnitude better resolution in charge to mass ratios. By observing freely falling grains accelerated in a horizontal electric field with a co-falling, high-speed video camera, we dramatically increase particle tracking time and measurement precision. Keeping the granular medium under vacuum, we eliminate air drag, leaving the electrostatic force as the primary source of particle accelerations in the co-moving frame. Because the technique is based on direct imaging, we can distinguish between different particle types during the experiment, opening up the possibility of studying charge transfer processes between different particle species. For the ∼300 μm diameter grains reported here, we achieve an average acceleration resolution of ∼0.008 m/s2, a force resolution of ∼500 pN, and a median charge resolution ∼6× 104 elementary charges per grain (corresponding to surface charge densities ∼1 elementary charges per μm2). The primary source of error is indeterminacy in the grain mass, but with higher resolution cameras and better optics this can be further improved. The high degree of resolution and the ability to visually identify particles of different species or sizes with direct imaging make this a powerful new tool to characterize charging processes in granular media.","lang":"eng"}],"acknowledgement":"This work was supported financially by the National Science Foundation (NSF) through its Materials Research Science and Engineering Center (MRSEC) program (DMR-0820054) and by the US Army Research Office through Grant No. W911NF-12-1-0182. S.R.W. acknowledges support from a University of Chicago Millikan Fellowship.","oa_version":"None","date_created":"2018-12-11T11:44:42Z","date_published":"2013-02-07T00:00:00Z","volume":84,"doi":"10.1063/1.4789496","issue":"2","publication_status":"published","year":"2013","language":[{"iso":"eng"}],"publication":"Review of Scientific Instruments","day":"07","type":"journal_article","status":"public","_id":"115","article_number":"025104","author":[{"first_name":"Scott R","id":"3A1FFC16-F248-11E8-B48F-1D18A9856A87","last_name":"Waitukaitis","full_name":"Waitukaitis, Scott R","orcid":"0000-0002-2299-3176"},{"full_name":"Jaeger, Heinrich","last_name":"Jaeger","first_name":"Heinrich"}],"publist_id":"7939","title":"In situ granular charge measurement by free-fall videography","citation":{"ista":"Waitukaitis SR, Jaeger H. 2013. In situ granular charge measurement by free-fall videography. Review of Scientific Instruments. 84(2), 025104.","chicago":"Waitukaitis, Scott R, and Heinrich Jaeger. “In Situ Granular Charge Measurement by Free-Fall Videography.” Review of Scientific Instruments. AIP, 2013. https://doi.org/10.1063/1.4789496.","short":"S.R. Waitukaitis, H. Jaeger, Review of Scientific Instruments 84 (2013).","ieee":"S. R. Waitukaitis and H. Jaeger, “In situ granular charge measurement by free-fall videography,” Review of Scientific Instruments, vol. 84, no. 2. AIP, 2013.","apa":"Waitukaitis, S. R., & Jaeger, H. (2013). In situ granular charge measurement by free-fall videography. Review of Scientific Instruments. AIP. https://doi.org/10.1063/1.4789496","ama":"Waitukaitis SR, Jaeger H. In situ granular charge measurement by free-fall videography. Review of Scientific Instruments. 2013;84(2). doi:10.1063/1.4789496","mla":"Waitukaitis, Scott R., and Heinrich Jaeger. “In Situ Granular Charge Measurement by Free-Fall Videography.” Review of Scientific Instruments, vol. 84, no. 2, 025104, AIP, 2013, doi:10.1063/1.4789496."},"date_updated":"2021-01-12T06:48:39Z","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","extern":"1"},{"title":"The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS","external_id":{"arxiv":["1310.3822"]},"article_processing_charge":"No","author":[{"last_name":"Sobral","full_name":"Sobral, D.","first_name":"D."},{"first_name":"A. M.","last_name":"Swinbank","full_name":"Swinbank, A. M."},{"first_name":"J. P.","last_name":"Stott","full_name":"Stott, J. P."},{"orcid":"0000-0003-2871-127X","full_name":"Matthee, Jorryt J","last_name":"Matthee","first_name":"Jorryt J","id":"7439a258-f3c0-11ec-9501-9df22fe06720"},{"first_name":"R. G.","last_name":"Bower","full_name":"Bower, R. G."},{"full_name":"Smail, Ian","last_name":"Smail","first_name":"Ian"},{"full_name":"Best, P.","last_name":"Best","first_name":"P."},{"last_name":"Geach","full_name":"Geach, J. E.","first_name":"J. E."},{"first_name":"R. M.","full_name":"Sharples, R. M.","last_name":"Sharples"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Sobral D, Swinbank AM, Stott JP, Matthee JJ, Bower RG, Smail I, Best P, Geach JE, Sharples RM. 2013. The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS. The Astrophysical Journal. 779(2), 139.","chicago":"Sobral, D., A. M. Swinbank, J. P. Stott, Jorryt J Matthee, R. G. Bower, Ian Smail, P. Best, J. E. Geach, and R. M. Sharples. “The Dynamics of Z=0.8 H-Alpha-Selected Star-Forming Galaxies from KMOS/CF-HiZELS.” The Astrophysical Journal. IOP Publishing, 2013. https://doi.org/10.1088/0004-637x/779/2/139.","ama":"Sobral D, Swinbank AM, Stott JP, et al. The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS. The Astrophysical Journal. 2013;779(2). doi:10.1088/0004-637x/779/2/139","apa":"Sobral, D., Swinbank, A. M., Stott, J. P., Matthee, J. J., Bower, R. G., Smail, I., … Sharples, R. M. (2013). The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS. The Astrophysical Journal. IOP Publishing. https://doi.org/10.1088/0004-637x/779/2/139","short":"D. Sobral, A.M. Swinbank, J.P. Stott, J.J. Matthee, R.G. Bower, I. Smail, P. Best, J.E. Geach, R.M. Sharples, The Astrophysical Journal 779 (2013).","ieee":"D. Sobral et al., “The dynamics of z=0.8 H-alpha-selected star-forming galaxies from KMOS/CF-HiZELS,” The Astrophysical Journal, vol. 779, no. 2. IOP Publishing, 2013.","mla":"Sobral, D., et al. “The Dynamics of Z=0.8 H-Alpha-Selected Star-Forming Galaxies from KMOS/CF-HiZELS.” The Astrophysical Journal, vol. 779, no. 2, 139, IOP Publishing, 2013, doi:10.1088/0004-637x/779/2/139."},"article_number":"139","date_created":"2022-07-07T09:14:48Z","doi":"10.1088/0004-637x/779/2/139","date_published":"2013-12-03T00:00:00Z","publication":"The Astrophysical Journal","day":"03","year":"2013","oa":1,"publisher":"IOP Publishing","quality_controlled":"1","acknowledgement":"We thank the referee for many helpful comments and suggestions which greatly improved the clarity and quality of this work. D.S. acknowledges financial support from the Netherlands Organisation for Scientific research (NWO) through a Veni fellowship and also funding from the European Community Seventh Framework Programme (FP7/2007-2013) under grant agreement number RG226604 (OPTICON) which allowed access to CFHT time (proposals: 11BO29 & 12AO19). A.M.S. gratefully acknowledges an STFC Advanced Fellowship through grant number ST/H005234/1. I.R.S., J.P.S., and R.G.B. acknowledge support from the UK Science and Technology Facilities Council (STFC) under ST/I001573/1. I.R.S. acknowledges STFC (ST/J001422/1), the ERC Advanced Investigator program DUSTYGAL and a Royal Society/Wolfson Merit Award. P.N.B. acknowledges support from STFC. R.M.S. acknowledges support from the grant ST/1001573/1. The data presented here are based on observations with the KMOS spectrograph on the ESO/VLT under program 60.A-9460 and can be accessed through the ESO data archive. The authors also wish to acknowledge the help from Michael Hilker in preparing the KMOS observations.","extern":"1","date_updated":"2022-08-18T10:43:07Z","keyword":["Space and Planetary Science","Astronomy and Astrophysics","galaxies: evolution – galaxies","high-redshift – galaxies","starburst"],"status":"public","article_type":"original","type":"journal_article","_id":"11520","volume":779,"issue":"2","language":[{"iso":"eng"}],"publication_status":"published","publication_identifier":{"eissn":["1538-4357"],"issn":["0004-637X"]},"intvolume":" 779","month":"12","main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1310.3822"}],"scopus_import":"1","oa_version":"Preprint","abstract":[{"lang":"eng","text":"We present the spatially resolved Hα dynamics of 16 star-forming galaxies at z ∼ 0.81 using the new KMOS multi-object integral field spectrograph on the ESO Very Large Telescope. These galaxies, selected using 1.18 μm narrowband imaging from the 10 deg2 CFHT-HiZELS survey of the SA 22 hr field, are found in a ∼4 Mpc overdensity of Hα emitters and likely reside in a group/intermediate environment, but not a cluster. We confirm and identify a rich group of star-forming galaxies at z = 0.813 ± 0.003, with 13 galaxies within 1000 km s−1 of each other, and seven within a diameter of 3 Mpc. All of our galaxies are “typical” star-forming galaxies at their redshift, 0.8 ± 0.4 SFR$^*_{z = 0.8}$, spanning a range of specific star formation rates (sSFRs) of 0.2–1.1 Gyr−1 and have a median metallicity very close to solar of 12 + log(O/H) = 8.62 ± 0.06. We measure the spatially resolved Hα dynamics of the galaxies in our sample and show that 13 out of 16 galaxies can be described by rotating disks and use the data to derive inclination corrected rotation speeds of 50–275 km s−1. The fraction of disks within our sample is 75% ± 8%, consistent with previous results based on Hubble Space Telescope morphologies of Hα-selected galaxies at z ∼ 1 and confirming that disks dominate the SFR density at z ∼ 1. Our Hα galaxies are well fitted by the z ∼ 1–2 Tully–Fisher (TF) relation, confirming the evolution seen in the zero point. Apart from having, on average, higher stellar masses and lower sSFRs, our group galaxies at z = 0.81 present the same mass–metallicity and TF relation as z ∼ 1 field galaxies and are all disk galaxies."}]},{"status":"public","type":"journal_article","article_number":"44001","_id":"116","title":"Dynamic jamming fronts","publist_id":"7938","author":[{"first_name":"Scott R","id":"3A1FFC16-F248-11E8-B48F-1D18A9856A87","last_name":"Waitukaitis","full_name":"Waitukaitis, Scott R","orcid":"0000-0002-2299-3176"},{"first_name":"Leah","last_name":"Roth","full_name":"Roth, Leah"},{"last_name":"Vitelli","full_name":"Vitelli, Vincenzo","first_name":"Vincenzo"},{"full_name":"Jaeger, Heinrich","last_name":"Jaeger","first_name":"Heinrich"}],"extern":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"chicago":"Waitukaitis, Scott R, Leah Roth, Vincenzo Vitelli, and Heinrich Jaeger. “Dynamic Jamming Fronts.” EPL. Elsevier, 2013. https://doi.org/10.1209/0295-5075/102/44001.","ista":"Waitukaitis SR, Roth L, Vitelli V, Jaeger H. 2013. Dynamic jamming fronts. EPL. 102(4), 44001.","mla":"Waitukaitis, Scott R., et al. “Dynamic Jamming Fronts.” EPL, vol. 102, no. 4, 44001, Elsevier, 2013, doi:10.1209/0295-5075/102/44001.","short":"S.R. Waitukaitis, L. Roth, V. Vitelli, H. Jaeger, EPL 102 (2013).","ieee":"S. R. Waitukaitis, L. Roth, V. Vitelli, and H. Jaeger, “Dynamic jamming fronts,” EPL, vol. 102, no. 4. Elsevier, 2013.","ama":"Waitukaitis SR, Roth L, Vitelli V, Jaeger H. Dynamic jamming fronts. EPL. 2013;102(4). doi:10.1209/0295-5075/102/44001","apa":"Waitukaitis, S. R., Roth, L., Vitelli, V., & Jaeger, H. (2013). Dynamic jamming fronts. EPL. Elsevier. https://doi.org/10.1209/0295-5075/102/44001"},"date_updated":"2021-01-12T06:48:44Z","month":"05","intvolume":" 102","publisher":"Elsevier","quality_controlled":"1","oa_version":"None","acknowledgement":"This work was supported by the National Science Foundation (NSF) through its Materials Research Science and Engineering program (DMR-0820054). SRW was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award DE-FG02-03ER46088. LKR acknowledges support through the NSF Research Experience for Undergraduates program.","abstract":[{"lang":"eng","text":"We describe a model experiment for dynamic jamming: a two-dimensional collection of initially unjammed disks that are forced into the jammed state by uniaxial compression via a rake. This leads to a stable densification front that travels ahead of the rake, leaving regions behind it jammed. Using disk conservation in conjunction with an upper limit to the packing fraction at jamming onset, we predict the front speed as a function of packing fraction and rake speed. However, we find that the jamming front has a finite width, a feature that cannot be explained by disk conservation alone. This width appears to diverge on approach to jamming, which suggests that it may be related to growing lengthscales encountered in other jamming studies."}],"volume":102,"date_published":"2013-05-24T00:00:00Z","issue":"4","doi":"10.1209/0295-5075/102/44001","date_created":"2018-12-11T11:44:43Z","day":"24","publication":"EPL","language":[{"iso":"eng"}],"year":"2013","publication_status":"published"},{"citation":{"chicago":"Baykan, Eda, Ingmar Weber, and Monika H Henzinger. “A Comprehensive Study of Techniques for URL-Based Web Page Language Classification.” ACM Transactions on the Web. Association for Computing Machinery, 2013. https://doi.org/10.1145/2435215.2435218.","ista":"Baykan E, Weber I, Henzinger MH. 2013. A comprehensive study of techniques for URL-based web page language classification. ACM Transactions on the Web. 7(1), 3.","mla":"Baykan, Eda, et al. “A Comprehensive Study of Techniques for URL-Based Web Page Language Classification.” ACM Transactions on the Web, vol. 7, no. 1, 3, Association for Computing Machinery, 2013, doi:10.1145/2435215.2435218.","apa":"Baykan, E., Weber, I., & Henzinger, M. H. (2013). A comprehensive study of techniques for URL-based web page language classification. ACM Transactions on the Web. Association for Computing Machinery. https://doi.org/10.1145/2435215.2435218","ama":"Baykan E, Weber I, Henzinger MH. A comprehensive study of techniques for URL-based web page language classification. ACM Transactions on the Web. 2013;7(1). doi:10.1145/2435215.2435218","ieee":"E. Baykan, I. Weber, and M. H. Henzinger, “A comprehensive study of techniques for URL-based web page language classification,” ACM Transactions on the Web, vol. 7, no. 1. Association for Computing Machinery, 2013.","short":"E. Baykan, I. Weber, M.H. Henzinger, ACM Transactions on the Web 7 (2013)."},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","author":[{"first_name":"Eda","last_name":"Baykan","full_name":"Baykan, Eda"},{"first_name":"Ingmar","full_name":"Weber, Ingmar","last_name":"Weber"},{"orcid":"0000-0002-5008-6530","full_name":"Henzinger, Monika H","last_name":"Henzinger","id":"540c9bbd-f2de-11ec-812d-d04a5be85630","first_name":"Monika H"}],"article_processing_charge":"No","title":"A comprehensive study of techniques for URL-based web page language classification","article_number":"3","year":"2013","day":"01","publication":"ACM Transactions on the Web","date_published":"2013-03-01T00:00:00Z","doi":"10.1145/2435215.2435218","date_created":"2022-07-27T12:50:18Z","publisher":"Association for Computing Machinery","quality_controlled":"1","date_updated":"2022-09-12T08:51:57Z","extern":"1","_id":"11671","article_type":"original","type":"journal_article","status":"public","keyword":["Computer Networks and Communications"],"publication_identifier":{"issn":["1559-1131"],"eissn":["1559-114X"]},"publication_status":"published","language":[{"iso":"eng"}],"volume":7,"issue":"1","abstract":[{"text":"Given only the URL of a Web page, can we identify its language? In this article we examine this question. URL-based language classification is useful when the content of the Web page is not available or downloading the content is a waste of bandwidth and time.\r\nWe built URL-based language classifiers for English, German, French, Spanish, and Italian by applying a variety of algorithms and features. As algorithms we used machine learning algorithms which are widely applied for text classification and state-of-art algorithms for language identification of text. As features we used words, various sized n-grams, and custom-made features (our novel feature set). We compared our approaches with two baseline methods, namely classification by country code top-level domains and classification by IP addresses of the hosting Web servers.\r\n\r\nWe trained and tested our classifiers in a 10-fold cross-validation setup on a dataset obtained from the Open Directory Project and from querying a commercial search engine. We obtained the lowest F1-measure for English (94) and the highest F1-measure for German (98) with the best performing classifiers.\r\n\r\nWe also evaluated the performance of our methods: (i) on a set of Web pages written in Adobe Flash and (ii) as part of a language-focused crawler. In the first case, the content of the Web page is hard to extract and in the second page downloading pages of the “wrong” language constitutes a waste of bandwidth. In both settings the best classifiers have a high accuracy with an F1-measure between 95 (for English) and 98 (for Italian) for the Adobe Flash pages and a precision between 90 (for Italian) and 97 (for French) for the language-focused crawler.","lang":"eng"}],"oa_version":"None","scopus_import":"1","month":"03","intvolume":" 7"},{"title":"From nanoscale cohesion to macroscale entanglement: opportunities for designing granular aggregate behaviour by tailoring grain shape and interactions","publist_id":"7937","author":[{"last_name":"Jaeger","full_name":"Jaeger, Heinrich","first_name":"Heinrich"},{"first_name":"Marc","full_name":"Miskin, Marc","last_name":"Miskin"},{"id":"3A1FFC16-F248-11E8-B48F-1D18A9856A87","first_name":"Scott R","orcid":"0000-0002-2299-3176","full_name":"Waitukaitis, Scott R","last_name":"Waitukaitis"}],"extern":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","citation":{"ista":"Jaeger H, Miskin M, Waitukaitis SR. 2013. From nanoscale cohesion to macroscale entanglement: opportunities for designing granular aggregate behaviour by tailoring grain shape and interactions. AIP Conference Proceedings. Powders and Grains vol. 1542, 3–6.","chicago":"Jaeger, Heinrich, Marc Miskin, and Scott R Waitukaitis. “From Nanoscale Cohesion to Macroscale Entanglement: Opportunities for Designing Granular Aggregate Behaviour by Tailoring Grain Shape and Interactions.” In AIP Conference Proceedings, 1542:3–6. AIP, 2013. https://doi.org/10.1063/1.4811858.","ama":"Jaeger H, Miskin M, Waitukaitis SR. From nanoscale cohesion to macroscale entanglement: opportunities for designing granular aggregate behaviour by tailoring grain shape and interactions. In: AIP Conference Proceedings. Vol 1542. AIP; 2013:3-6. doi:10.1063/1.4811858","apa":"Jaeger, H., Miskin, M., & Waitukaitis, S. R. (2013). From nanoscale cohesion to macroscale entanglement: opportunities for designing granular aggregate behaviour by tailoring grain shape and interactions. In AIP Conference Proceedings (Vol. 1542, pp. 3–6). Sydney, Australia: AIP. https://doi.org/10.1063/1.4811858","short":"H. Jaeger, M. Miskin, S.R. Waitukaitis, in:, AIP Conference Proceedings, AIP, 2013, pp. 3–6.","ieee":"H. Jaeger, M. Miskin, and S. R. Waitukaitis, “From nanoscale cohesion to macroscale entanglement: opportunities for designing granular aggregate behaviour by tailoring grain shape and interactions,” in AIP Conference Proceedings, Sydney, Australia, 2013, vol. 1542, pp. 3–6.","mla":"Jaeger, Heinrich, et al. “From Nanoscale Cohesion to Macroscale Entanglement: Opportunities for Designing Granular Aggregate Behaviour by Tailoring Grain Shape and Interactions.” AIP Conference Proceedings, vol. 1542, AIP, 2013, pp. 3–6, doi:10.1063/1.4811858."},"date_updated":"2021-01-12T06:48:49Z","status":"public","type":"conference","conference":{"start_date":"2013-07-08","location":"Sydney, Australia","end_date":"2013-07-12","name":"Powders and Grains"},"_id":"117","doi":"10.1063/1.4811858","date_published":"2013-06-01T00:00:00Z","volume":1542,"date_created":"2018-12-11T11:44:43Z","page":"3 - 6","day":"01","publication":" AIP Conference Proceedings","language":[{"iso":"eng"}],"publication_status":"published","year":"2013","month":"06","intvolume":" 1542","quality_controlled":"1","publisher":"AIP","oa_version":"None","acknowledgement":"This work was supported by the NSF MRSEC program under DMR-0820054. Additional support came from the US Army Research Office through W911NF-12-1-0182.","abstract":[{"lang":"eng","text":"The packing arrangement of individual particles inside a granular material and the resulting response to applied stresses depend critically on particle-particle interactions. One aspect that recently received attention are nanoscale surface features of particles, which play an important role in determining the strength of cohesive van der Waals and capillary interactions and also affect tribo-charging of grains. We describe experiments on freely falling granular streams that can detect the contributions from all three of these forces. We show that it is possible to measure the charge of individual grains and build up distributions that are detailed enough to provide stringent tests of tribo-charging models currently available. A second aspect concerns particle shape. In this case steric interactions become important and new types of aggregate behavior can be expected when non-convex particle shapes are considered that can interlock or entangle. However, a general connection between the mechanical response of a granular material and the constituents\\' shape remains unknown. This has made it infeasible to tackle the "inverse packing problem", namely to start from a given, desired behavior for the aggregate as a whole and then find the particle shape the produces it. We discuss a new approach, using concepts rooted in artificial evolution that provides a way to solve this inverse problem. This approach facilitates exploring the role of arbitrary particle geometry in jammed systems and invites the discovery and design of granular matter with optimized properties."}]},{"article_processing_charge":"No","external_id":{"arxiv":["0912.1934"]},"author":[{"first_name":"Paul","last_name":"Dütting","full_name":"Dütting, Paul"},{"last_name":"Henzinger","full_name":"Henzinger, Monika H","orcid":"0000-0002-5008-6530","first_name":"Monika H","id":"540c9bbd-f2de-11ec-812d-d04a5be85630"},{"last_name":"Weber","full_name":"Weber, Ingmar","first_name":"Ingmar"}],"title":"Sponsored search, market equilibria, and the Hungarian Method","citation":{"chicago":"Dütting, Paul, Monika H Henzinger, and Ingmar Weber. “Sponsored Search, Market Equilibria, and the Hungarian Method.” Information Processing Letters. Elsevier, 2013. https://doi.org/10.1016/j.ipl.2012.11.006.","ista":"Dütting P, Henzinger MH, Weber I. 2013. Sponsored search, market equilibria, and the Hungarian Method. Information Processing Letters. 113(3), 67–73.","mla":"Dütting, Paul, et al. “Sponsored Search, Market Equilibria, and the Hungarian Method.” Information Processing Letters, vol. 113, no. 3, Elsevier, 2013, pp. 67–73, doi:10.1016/j.ipl.2012.11.006.","short":"P. Dütting, M.H. Henzinger, I. Weber, Information Processing Letters 113 (2013) 67–73.","ieee":"P. Dütting, M. H. Henzinger, and I. Weber, “Sponsored search, market equilibria, and the Hungarian Method,” Information Processing Letters, vol. 113, no. 3. Elsevier, pp. 67–73, 2013.","apa":"Dütting, P., Henzinger, M. H., & Weber, I. (2013). Sponsored search, market equilibria, and the Hungarian Method. Information Processing Letters. Elsevier. https://doi.org/10.1016/j.ipl.2012.11.006","ama":"Dütting P, Henzinger MH, Weber I. Sponsored search, market equilibria, and the Hungarian Method. Information Processing Letters. 2013;113(3):67-73. doi:10.1016/j.ipl.2012.11.006"},"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","page":"67-73","date_created":"2022-08-08T11:29:08Z","doi":"10.1016/j.ipl.2012.11.006","date_published":"2013-02-15T00:00:00Z","year":"2013","publication":"Information Processing Letters","day":"15","oa":1,"quality_controlled":"1","publisher":"Elsevier","date_updated":"2022-09-12T09:36:15Z","extern":"1","article_type":"original","type":"journal_article","status":"public","_id":"11759","volume":113,"issue":"3","publication_status":"published","publication_identifier":{"issn":["0020-0190"]},"language":[{"iso":"eng"}],"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/0912.1934"}],"scopus_import":"1","intvolume":" 113","month":"02","abstract":[{"text":"Matching markets play a prominent role in economic theory. A prime example of such a market is the sponsored search market. Here, as in other markets of that kind, market equilibria correspond to feasible, envy free, and bidder optimal outcomes. For settings without budgets such an outcome always exists and can be computed in polynomial-time by the so-called Hungarian Method. Moreover, every mechanism that computes such an outcome is incentive compatible. We show that the Hungarian Method can be modified so that it finds a feasible, envy free, and bidder optimal outcome for settings with budgets. We also show that in settings with budgets no mechanism that computes such an outcome can be incentive compatible for all inputs. For inputs in general position, however, the presented mechanism—as any other mechanism that computes such an outcome for settings with budgets—is incentive compatible.","lang":"eng"}],"oa_version":"Preprint"}]