@inproceedings{9227, abstract = {In the multiway cut problem we are given a weighted undirected graph G=(V,E) and a set T⊆V of k terminals. The goal is to find a minimum weight set of edges E′⊆E with the property that by removing E′ from G all the terminals become disconnected. In this paper we present a simple local search approximation algorithm for the multiway cut problem with approximation ratio 2−2k . We present an experimental evaluation of the performance of our local search algorithm and show that it greatly outperforms the isolation heuristic of Dalhaus et al. and it has similar performance as the much more complex algorithms of Calinescu et al., Sharma and Vondrak, and Buchbinder et al. which have the currently best known approximation ratios for this problem.}, author = {Bloch-Hansen, Andrew and Samei, Nasim and Solis-Oba, Roberto}, booktitle = {Conference on Algorithms and Discrete Applied Mathematics}, isbn = {9783030678982}, issn = {1611-3349}, location = {Rupnagar, India}, pages = {346--358}, publisher = {Springer Nature}, title = {{Experimental evaluation of a local search approximation algorithm for the multiway cut problem}}, doi = {10.1007/978-3-030-67899-9_28}, volume = {12601}, year = {2021}, } @article{8817, abstract = {The paper introduces an inertial extragradient subgradient method with self-adaptive step sizes for solving equilibrium problems in real Hilbert spaces. Weak convergence of the proposed method is obtained under the condition that the bifunction is pseudomonotone and Lipchitz continuous. Linear convergence is also given when the bifunction is strongly pseudomonotone and Lipchitz continuous. Numerical implementations and comparisons with other related inertial methods are given using test problems including a real-world application to Nash–Cournot oligopolistic electricity market equilibrium model.}, author = {Shehu, Yekini and Iyiola, Olaniyi S. and Thong, Duong Viet and Van, Nguyen Thi Cam}, issn = {1432-5217}, journal = {Mathematical Methods of Operations Research}, number = {2}, pages = {213--242}, publisher = {Springer Nature}, title = {{An inertial subgradient extragradient algorithm extended to pseudomonotone equilibrium problems}}, doi = {10.1007/s00186-020-00730-w}, volume = {93}, year = {2021}, } @article{9315, abstract = {We consider inertial iteration methods for Fermat–Weber location problem and primal–dual three-operator splitting in real Hilbert spaces. To do these, we first obtain weak convergence analysis and nonasymptotic O(1/n) convergence rate of the inertial Krasnoselskii–Mann iteration for fixed point of nonexpansive operators in infinite dimensional real Hilbert spaces under some seemingly easy to implement conditions on the iterative parameters. One of our contributions is that the convergence analysis and rate of convergence results are obtained using conditions which appear not complicated and restrictive as assumed in other previous related results in the literature. We then show that Fermat–Weber location problem and primal–dual three-operator splitting are special cases of fixed point problem of nonexpansive mapping and consequently obtain the convergence analysis of inertial iteration methods for Fermat–Weber location problem and primal–dual three-operator splitting in real Hilbert spaces. Some numerical implementations are drawn from primal–dual three-operator splitting to support the theoretical analysis.}, author = {Iyiola, Olaniyi S. and Shehu, Yekini}, issn = {1420-9012}, journal = {Results in Mathematics}, number = {2}, publisher = {Springer Nature}, title = {{New convergence results for inertial Krasnoselskii–Mann iterations in Hilbert spaces with applications}}, doi = {10.1007/s00025-021-01381-x}, volume = {76}, year = {2021}, } @article{9365, abstract = {In this paper, we propose a new iterative method with alternated inertial step for solving split common null point problem in real Hilbert spaces. We obtain weak convergence of the proposed iterative algorithm. Furthermore, we introduce the notion of bounded linear regularity property for the split common null point problem and obtain the linear convergence property for the new algorithm under some mild assumptions. Finally, we provide some numerical examples to demonstrate the performance and efficiency of the proposed method.}, author = {Ogbuisi, Ferdinard U. and Shehu, Yekini and Yao, Jen Chih}, issn = {1029-4945}, journal = {Optimization}, publisher = {Taylor and Francis}, title = {{Convergence analysis of new inertial method for the split common null point problem}}, doi = {10.1080/02331934.2021.1914035}, year = {2021}, } @article{10365, abstract = {The early development of many organisms involves the folding of cell monolayers, but this behaviour is difficult to reproduce in vitro; therefore, both mechanistic causes and effects of local curvature remain unclear. Here we study epithelial cell monolayers on corrugated hydrogels engineered into wavy patterns, examining how concave and convex curvatures affect cellular and nuclear shape. We find that substrate curvature affects monolayer thickness, which is larger in valleys than crests. We show that this feature generically arises in a vertex model, leading to the hypothesis that cells may sense curvature by modifying the thickness of the tissue. We find that local curvature also affects nuclear morphology and positioning, which we explain by extending the vertex model to take into account membrane–nucleus interactions, encoding thickness modulation in changes to nuclear deformation and position. We propose that curvature governs the spatial distribution of yes-associated proteins via nuclear shape and density changes. We show that curvature also induces significant variations in lamins, chromatin condensation and cell proliferation rate in folded epithelial tissues. Together, this work identifies active cell mechanics and nuclear mechanoadaptation as the key players of the mechanistic regulation of epithelia to substrate curvature.}, author = {Luciano, Marine and Xue, Shi-lei and De Vos, Winnok H. and Redondo-Morata, Lorena and Surin, Mathieu and Lafont, Frank and Hannezo, Edouard B and Gabriele, Sylvain}, issn = {1745-2481}, journal = {Nature Physics}, number = {12}, pages = {1382–1390}, publisher = {Springer Nature}, title = {{Cell monolayers sense curvature by exploiting active mechanics and nuclear mechanoadaptation}}, doi = {10.1038/s41567-021-01374-1}, volume = {17}, year = {2021}, } @article{9298, abstract = {In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field. }, author = {Klionsky, Daniel J. and Abdel-Aziz, Amal Kamal and Abdelfatah, Sara and Abdellatif, Mahmoud and Abdoli, Asghar and Abel, Steffen and Abeliovich, Hagai and Abildgaard, Marie H. and Abudu, Yakubu Princely and Acevedo-Arozena, Abraham and Adamopoulos, Iannis E. and Adeli, Khosrow and Adolph, Timon E. and Adornetto, Annagrazia and Aflaki, Elma and Agam, Galila and Agarwal, Anupam and Aggarwal, Bharat B. and Agnello, Maria and Agostinis, Patrizia and Agrewala, Javed N. and Agrotis, Alexander and Aguilar, Patricia V. and Ahmad, S. Tariq and Ahmed, Zubair M. and Ahumada-Castro, Ulises and Aits, Sonja and Aizawa, Shu and Akkoc, Yunus and Akoumianaki, Tonia and Akpinar, Hafize Aysin and Al-Abd, Ahmed M. and Al-Akra, Lina and Al-Gharaibeh, Abeer and Alaoui-Jamali, Moulay A. and Alberti, Simon and Alcocer-Gómez, Elísabet and Alessandri, Cristiano and Ali, Muhammad and Alim Al-Bari, M. Abdul and Aliwaini, Saeb and Alizadeh, Javad and Almacellas, Eugènia and Almasan, Alexandru and Alonso, Alicia and Alonso, Guillermo D. and Altan-Bonnet, Nihal and Altieri, Dario C. and Álvarez, Élida M.C. and Alves, Sara and Alves Da Costa, Cristine and Alzaharna, Mazen M. and Amadio, Marialaura and Amantini, Consuelo and Amaral, Cristina and Ambrosio, Susanna and Amer, Amal O. and Ammanathan, Veena and An, Zhenyi and Andersen, Stig U. and Andrabi, Shaida A. and Andrade-Silva, Magaiver and Andres, Allen M. and Angelini, Sabrina and Ann, David and Anozie, Uche C. and Ansari, Mohammad Y. and Antas, Pedro and Antebi, Adam and Antón, Zuriñe and Anwar, Tahira and Apetoh, Lionel and Apostolova, Nadezda and Araki, Toshiyuki and Araki, Yasuhiro and Arasaki, Kohei and Araújo, Wagner L. and Araya, Jun and Arden, Catherine and Arévalo, Maria Angeles and Arguelles, Sandro and Arias, Esperanza and Arikkath, Jyothi and Arimoto, Hirokazu and Ariosa, Aileen R. and Armstrong-James, Darius and Arnauné-Pelloquin, Laetitia and Aroca, Angeles and Arroyo, Daniela S. and Arsov, Ivica and Artero, Rubén and Asaro, Dalia Maria Lucia and Aschner, Michael and Ashrafizadeh, Milad and Ashur-Fabian, Osnat and Atanasov, Atanas G. and Au, Alicia K. and Auberger, Patrick and Auner, Holger W. and Aurelian, Laure and Autelli, Riccardo and Avagliano, Laura and Ávalos, Yenniffer and Aveic, Sanja and Aveleira, Célia Alexandra and Avin-Wittenberg, Tamar and Aydin, Yucel and Ayton, Scott and Ayyadevara, Srinivas and Azzopardi, Maria and Baba, Misuzu and Backer, Jonathan M. and Backues, Steven K. and Bae, Dong Hun and Bae, Ok Nam and Bae, Soo Han and Baehrecke, Eric H. and Baek, Ahruem and Baek, Seung Hoon and Baek, Sung Hee and Bagetta, Giacinto and Bagniewska-Zadworna, Agnieszka and Bai, Hua and Bai, Jie and Bai, Xiyuan and Bai, Yidong and Bairagi, Nandadulal and Baksi, Shounak and Balbi, Teresa and Baldari, Cosima T. and Balduini, Walter and Ballabio, Andrea and Ballester, Maria and Balazadeh, Salma and Balzan, Rena and Bandopadhyay, Rina and Banerjee, Sreeparna and Banerjee, Sulagna and Bánréti, Ágnes and Bao, Yan and Baptista, Mauricio S. and Baracca, Alessandra and Barbati, Cristiana and Bargiela, Ariadna and Barilà, Daniela and Barlow, Peter G. and Barmada, Sami J. and Barreiro, Esther and Barreto, George E. and Bartek, Jiri and Bartel, Bonnie and Bartolome, Alberto and Barve, Gaurav R. and Basagoudanavar, Suresh H. and Bassham, Diane C. and Bast, Robert C. and Basu, Alakananda and Batoko, Henri and Batten, Isabella and Baulieu, Etienne E. and Baumgarner, Bradley L. and Bayry, Jagadeesh and Beale, Rupert and Beau, Isabelle and Beaumatin, Florian and Bechara, Luiz R.G. and Beck, George R. and Beers, Michael F. and Begun, Jakob and Behrends, Christian and Behrens, Georg M.N. and Bei, Roberto and Bejarano, Eloy and Bel, Shai and Behl, Christian and Belaid, Amine and Belgareh-Touzé, Naïma and Bellarosa, Cristina and Belleudi, Francesca and Belló Pérez, Melissa and Bello-Morales, Raquel and Beltran, Jackeline Soares De Oliveira and Beltran, Sebastián and Benbrook, Doris Mangiaracina and Bendorius, Mykolas and Benitez, Bruno A. and Benito-Cuesta, Irene and Bensalem, Julien and Berchtold, Martin W. and Berezowska, Sabina and Bergamaschi, Daniele and Bergami, Matteo and Bergmann, Andreas and Berliocchi, Laura and Berlioz-Torrent, Clarisse and Bernard, Amélie and Berthoux, Lionel and Besirli, Cagri G. and Besteiro, Sebastien and Betin, Virginie M. and Beyaert, Rudi and Bezbradica, Jelena S. and Bhaskar, Kiran and Bhatia-Kissova, Ingrid and Bhattacharya, Resham and Bhattacharya, Sujoy and Bhattacharyya, Shalmoli and Bhuiyan, Md Shenuarin and Bhutia, Sujit Kumar and Bi, Lanrong and Bi, Xiaolin and Biden, Trevor J. and Bijian, Krikor and Billes, Viktor A. and Binart, Nadine and Bincoletto, Claudia and Birgisdottir, Asa B. and Bjorkoy, Geir and Blanco, Gonzalo and Blas-Garcia, Ana and Blasiak, Janusz and Blomgran, Robert and Blomgren, Klas and Blum, Janice S. and Boada-Romero, Emilio and Boban, Mirta and Boesze-Battaglia, Kathleen and Boeuf, Philippe and Boland, Barry and Bomont, Pascale and Bonaldo, Paolo and Bonam, Srinivasa Reddy and Bonfili, Laura and Bonifacino, Juan S. and Boone, Brian A. and Bootman, Martin D. and Bordi, Matteo and Borner, Christoph and Bornhauser, Beat C. and Borthakur, Gautam and Bosch, Jürgen and Bose, Santanu and Botana, Luis M. and Botas, Juan and Boulanger, Chantal M. and Boulton, Michael E. and Bourdenx, Mathieu and Bourgeois, Benjamin and Bourke, Nollaig M. and Bousquet, Guilhem and Boya, Patricia and Bozhkov, Peter V. and Bozi, Luiz H.M. and Bozkurt, Tolga O. and Brackney, Doug E. and Brandts, Christian H. and Braun, Ralf J. and Braus, Gerhard H. and Bravo-Sagua, Roberto and Bravo-San Pedro, José M. and Brest, Patrick and Bringer, Marie Agnès and Briones-Herrera, Alfredo and Broaddus, V. Courtney and Brodersen, Peter and Brodsky, Jeffrey L. and Brody, Steven L. and Bronson, Paola G. and Bronstein, Jeff M. and Brown, Carolyn N. and Brown, Rhoderick E. and Brum, Patricia C. and Brumell, John H. and Brunetti-Pierri, Nicola and Bruno, Daniele and Bryson-Richardson, Robert J. and Bucci, Cecilia and Buchrieser, Carmen and Bueno, Marta and Buitrago-Molina, Laura Elisa and Buraschi, Simone and Buch, Shilpa and Buchan, J. Ross and Buckingham, Erin M. and Budak, Hikmet and Budini, Mauricio and Bultynck, Geert and Burada, Florin and Burgoyne, Joseph R. and Burón, M. Isabel and Bustos, Victor and Büttner, Sabrina and Butturini, Elena and Byrd, Aaron and Cabas, Isabel and Cabrera-Benitez, Sandra and Cadwell, Ken and Cai, Jingjing and Cai, Lu and Cai, Qian and Cairó, Montserrat and Calbet, Jose A. and Caldwell, Guy A. and Caldwell, Kim A. and Call, Jarrod A. and Calvani, Riccardo and Calvo, Ana C. and Calvo-Rubio Barrera, Miguel and Camara, Niels O.S. and Camonis, Jacques H. and Camougrand, Nadine and Campanella, Michelangelo and Campbell, Edward M. and Campbell-Valois, François Xavier and Campello, Silvia and Campesi, Ilaria and Campos, Juliane C. and Camuzard, Olivier and Cancino, Jorge and Candido De Almeida, Danilo and Canesi, Laura and Caniggia, Isabella and Canonico, Barbara and Cantí, Carles and Cao, Bin and Caraglia, Michele and Caramés, Beatriz and Carchman, Evie H. and Cardenal-Muñoz, Elena and Cardenas, Cesar and Cardenas, Luis and Cardoso, Sandra M. and Carew, Jennifer S. and Carle, Georges F. and Carleton, Gillian and Carloni, Silvia and Carmona-Gutierrez, Didac and Carneiro, Leticia A. and Carnevali, Oliana and Carosi, Julian M. and Carra, Serena and Carrier, Alice and Carrier, Lucie and Carroll, Bernadette and Carter, A. Brent and Carvalho, Andreia Neves and Casanova, Magali and Casas, Caty and Casas, Josefina and Cassioli, Chiara and Castillo, Eliseo F. and Castillo, Karen and Castillo-Lluva, Sonia and Castoldi, Francesca and Castori, Marco and Castro, Ariel F. and Castro-Caldas, Margarida and Castro-Hernandez, Javier and Castro-Obregon, Susana and Catz, Sergio D. and Cavadas, Claudia and Cavaliere, Federica and Cavallini, Gabriella and Cavinato, Maria and Cayuela, Maria L. and Cebollada Rica, Paula and Cecarini, Valentina and Cecconi, Francesco and Cechowska-Pasko, Marzanna and Cenci, Simone and Ceperuelo-Mallafré, Victòria and Cerqueira, João J. and Cerutti, Janete M. and Cervia, Davide and Cetintas, Vildan Bozok and Cetrullo, Silvia and Chae, Han Jung and Chagin, Andrei S. and Chai, Chee Yin and Chakrabarti, Gopal and Chakrabarti, Oishee and Chakraborty, Tapas and Chakraborty, Trinad and Chami, Mounia and Chamilos, Georgios and Chan, David W. and Chan, Edmond Y.W. and Chan, Edward D. and Chan, H. Y.Edwin and Chan, Helen H. and Chan, Hung and Chan, Matthew T.V. and Chan, Yau Sang and Chandra, Partha K. and Chang, Chih Peng and Chang, Chunmei and Chang, Hao Chun and Chang, Kai and Chao, Jie and Chapman, Tracey and Charlet-Berguerand, Nicolas and Chatterjee, Samrat and Chaube, Shail K. and Chaudhary, Anu and Chauhan, Santosh and Chaum, Edward and Checler, Frédéric and Cheetham, Michael E. and Chen, Chang Shi and Chen, Guang Chao and Chen, Jian Fu and Chen, Liam L. and Chen, Leilei and Chen, Lin and Chen, Mingliang and Chen, Mu Kuan and Chen, Ning and Chen, Quan and Chen, Ruey Hwa and Chen, Shi and Chen, Wei and Chen, Weiqiang and Chen, Xin Ming and Chen, Xiong Wen and Chen, Xu and Chen, Yan and Chen, Ye Guang and Chen, Yingyu and Chen, Yongqiang and Chen, Yu Jen and Chen, Yue Qin and Chen, Zhefan Stephen and Chen, Zhi and Chen, Zhi Hua and Chen, Zhijian J. and Chen, Zhixiang and Cheng, Hanhua and Cheng, Jun and Cheng, Shi Yuan and Cheng, Wei and Cheng, Xiaodong and Cheng, Xiu Tang and Cheng, Yiyun and Cheng, Zhiyong and Chen, Zhong and Cheong, Heesun and Cheong, Jit Kong and Chernyak, Boris V. and Cherry, Sara and Cheung, Chi Fai Randy and Cheung, Chun Hei Antonio and Cheung, King Ho and Chevet, Eric and Chi, Richard J. and Chiang, Alan Kwok Shing and Chiaradonna, Ferdinando and Chiarelli, Roberto and Chiariello, Mario and Chica, Nathalia and Chiocca, Susanna and Chiong, Mario and Chiou, Shih Hwa and Chiramel, Abhilash I. and Chiurchiù, Valerio and Cho, Dong Hyung and Choe, Seong Kyu and Choi, Augustine M.K. and Choi, Mary E. and Choudhury, Kamalika Roy and Chow, Norman S. and Chu, Charleen T. and Chua, Jason P. and Chua, John Jia En and Chung, Hyewon and Chung, Kin Pan and Chung, Seockhoon and Chung, So Hyang and Chung, Yuen Li and Cianfanelli, Valentina and Ciechomska, Iwona A. and Cifuentes, Mariana and Cinque, Laura and Cirak, Sebahattin and Cirone, Mara and Clague, Michael J. and Clarke, Robert and Clementi, Emilio and Coccia, Eliana M. and Codogno, Patrice and Cohen, Ehud and Cohen, Mickael M. and Colasanti, Tania and Colasuonno, Fiorella and Colbert, Robert A. and Colell, Anna and Čolić, Miodrag and Coll, Nuria S. and Collins, Mark O. and Colombo, María I. and Colón-Ramos, Daniel A. and Combaret, Lydie and Comincini, Sergio and Cominetti, Márcia R. and Consiglio, Antonella and Conte, Andrea and Conti, Fabrizio and Contu, Viorica Raluca and Cookson, Mark R. and Coombs, Kevin M. and Coppens, Isabelle and Corasaniti, Maria Tiziana and Corkery, Dale P. and Cordes, Nils and Cortese, Katia and Costa, Maria Do Carmo and Costantino, Sarah and Costelli, Paola and Coto-Montes, Ana and Crack, Peter J. and Crespo, Jose L. and Criollo, Alfredo and Crippa, Valeria and Cristofani, Riccardo and Csizmadia, Tamas and Cuadrado, Antonio and Cui, Bing and Cui, Jun and Cui, Yixian and Cui, Yong and Culetto, Emmanuel and Cumino, Andrea C. and Cybulsky, Andrey V. and Czaja, Mark J. and Czuczwar, Stanislaw J. and D’Adamo, Stefania and D’Amelio, Marcello and D’Arcangelo, Daniela and D’Lugos, Andrew C. and D’Orazi, Gabriella and Da Silva, James A. and Dafsari, Hormos Salimi and Dagda, Ruben K. and Dagdas, Yasin and Daglia, Maria and Dai, Xiaoxia and Dai, Yun and Dai, Yuyuan and Dal Col, Jessica and Dalhaimer, Paul and Dalla Valle, Luisa and Dallenga, Tobias and Dalmasso, Guillaume and Damme, Markus and Dando, Ilaria and Dantuma, Nico P. and Darling, April L. and Das, Hiranmoy and Dasarathy, Srinivasan and Dasari, Santosh K. and Dash, Srikanta and Daumke, Oliver and Dauphinee, Adrian N. and Davies, Jeffrey S. and Dávila, Valeria A. and Davis, Roger J. and Davis, Tanja and Dayalan Naidu, Sharadha and De Amicis, Francesca and De Bosscher, Karolien and De Felice, Francesca and De Franceschi, Lucia and De Leonibus, Chiara and De Mattos Barbosa, Mayara G. and De Meyer, Guido R.Y. and De Milito, Angelo and De Nunzio, Cosimo and De Palma, Clara and De Santi, Mauro and De Virgilio, Claudio and De Zio, Daniela and Debnath, Jayanta and Debosch, Brian J. and Decuypere, Jean Paul and Deehan, Mark A. and Deflorian, Gianluca and Degregori, James and Dehay, Benjamin and Del Rio, Gabriel and Delaney, Joe R. and Delbridge, Lea M.D. and Delorme-Axford, Elizabeth and Delpino, M. Victoria and Demarchi, Francesca and Dembitz, Vilma and Demers, Nicholas D. and Deng, Hongbin and Deng, Zhiqiang and Dengjel, Joern and Dent, Paul and Denton, Donna and Depamphilis, Melvin L. and Der, Channing J. and Deretic, Vojo and Descoteaux, Albert and Devis, Laura and Devkota, Sushil and Devuyst, Olivier and Dewson, Grant and Dharmasivam, Mahendiran and Dhiman, Rohan and Di Bernardo, Diego and Di Cristina, Manlio and Di Domenico, Fabio and Di Fazio, Pietro and Di Fonzo, Alessio and Di Guardo, Giovanni and Di Guglielmo, Gianni M. and Di Leo, Luca and Di Malta, Chiara and Di Nardo, Alessia and Di Rienzo, Martina and Di Sano, Federica and Diallinas, George and Diao, Jiajie and Diaz-Araya, Guillermo and Díaz-Laviada, Inés and Dickinson, Jared M. and Diederich, Marc and Dieudé, Mélanie and Dikic, Ivan and Ding, Shiping and Ding, Wen Xing and Dini, Luciana and Dinić, Jelena and Dinic, Miroslav and Dinkova-Kostova, Albena T. and Dionne, Marc S. and Distler, Jörg H.W. and Diwan, Abhinav and Dixon, Ian M.C. and Djavaheri-Mergny, Mojgan and Dobrinski, Ina and Dobrovinskaya, Oxana and Dobrowolski, Radek and Dobson, Renwick C.J. and Đokić, Jelena and Dokmeci Emre, Serap and Donadelli, Massimo and Dong, Bo and Dong, Xiaonan and Dong, Zhiwu and Dorn, Gerald W. and Dotsch, Volker and Dou, Huan and Dou, Juan and Dowaidar, Moataz and Dridi, Sami and Drucker, Liat and Du, Ailian and Du, Caigan and Du, Guangwei and Du, Hai Ning and Du, Li Lin and Du Toit, André and Duan, Shao Bin and Duan, Xiaoqiong and Duarte, Sónia P. and Dubrovska, Anna and Dunlop, Elaine A. and Dupont, Nicolas and Durán, Raúl V. and Dwarakanath, Bilikere S. and Dyshlovoy, Sergey A. and Ebrahimi-Fakhari, Darius and Eckhart, Leopold and Edelstein, Charles L. and Efferth, Thomas and Eftekharpour, Eftekhar and Eichinger, Ludwig and Eid, Nabil and Eisenberg, Tobias and Eissa, N. Tony and Eissa, Sanaa and Ejarque, Miriam and El Andaloussi, Abdeljabar and El-Hage, Nazira and El-Naggar, Shahenda and Eleuteri, Anna Maria and El-Shafey, Eman S. and Elgendy, Mohamed and Eliopoulos, Aristides G. and Elizalde, María M. and Elks, Philip M. and Elsasser, Hans Peter and Elsherbiny, Eslam S. and Emerling, Brooke M. and Emre, N. C.Tolga and Eng, Christina H. and Engedal, Nikolai and Engelbrecht, Anna Mart and Engelsen, Agnete S.T. and Enserink, Jorrit M. and Escalante, Ricardo and Esclatine, Audrey and Escobar-Henriques, Mafalda and Eskelinen, Eeva Liisa and Espert, Lucile and Eusebio, Makandjou Ola and Fabrias, Gemma and Fabrizi, Cinzia and Facchiano, Antonio and Facchiano, Francesco and Fadeel, Bengt and Fader, Claudio and Faesen, Alex C. and Fairlie, W. Douglas and Falcó, Alberto and Falkenburger, Bjorn H. and Fan, Daping and Fan, Jie and Fan, Yanbo and Fang, Evandro F. and Fang, Yanshan and Fang, Yognqi and Fanto, Manolis and Farfel-Becker, Tamar and Faure, Mathias and Fazeli, Gholamreza and Fedele, Anthony O. and Feldman, Arthur M. and Feng, Du and Feng, Jiachun and Feng, Lifeng and Feng, Yibin and Feng, Yuchen and Feng, Wei and Fenz Araujo, Thais and Ferguson, Thomas A. and Fernández, Álvaro F. and Fernandez-Checa, Jose C. and Fernández-Veledo, Sonia and Fernie, Alisdair R. and Ferrante, Anthony W. and Ferraresi, Alessandra and Ferrari, Merari F. and Ferreira, Julio C.B. and Ferro-Novick, Susan and Figueras, Antonio and Filadi, Riccardo and Filigheddu, Nicoletta and Filippi-Chiela, Eduardo and Filomeni, Giuseppe and Fimia, Gian Maria and Fineschi, Vittorio and Finetti, Francesca and Finkbeiner, Steven and Fisher, Edward A. and Fisher, Paul B. and Flamigni, Flavio and Fliesler, Steven J. and Flo, Trude H. and Florance, Ida and Florey, Oliver and Florio, Tullio and Fodor, Erika and Follo, Carlo and Fon, Edward A. and Forlino, Antonella and Fornai, Francesco and Fortini, Paola and Fracassi, Anna and Fraldi, Alessandro and Franco, Brunella and Franco, Rodrigo and Franconi, Flavia and Frankel, Lisa B. and Friedman, Scott L. and Fröhlich, Leopold F. and Frühbeck, Gema and Fuentes, Jose M. and Fujiki, Yukio and Fujita, Naonobu and Fujiwara, Yuuki and Fukuda, Mitsunori and Fulda, Simone and Furic, Luc and Furuya, Norihiko and Fusco, Carmela and Gack, Michaela U. and Gaffke, Lidia and Galadari, Sehamuddin and Galasso, Alessia and Galindo, Maria F. and Gallolu Kankanamalage, Sachith and Galluzzi, Lorenzo and Galy, Vincent and Gammoh, Noor and Gan, Boyi and Ganley, Ian G. and Gao, Feng and Gao, Hui and Gao, Minghui and Gao, Ping and Gao, Shou Jiang and Gao, Wentao and Gao, Xiaobo and Garcera, Ana and Garcia, Maria Noé and Garcia, Verónica E. and García-Del Portillo, Francisco and Garcia-Escudero, Vega and Garcia-Garcia, Aracely and Garcia-Macia, Marina and García-Moreno, Diana and Garcia-Ruiz, Carmen and García-Sanz, Patricia and Garg, Abhishek D. and Gargini, Ricardo and Garofalo, Tina and Garry, Robert F. and Gassen, Nils C. and Gatica, Damian and Ge, Liang and Ge, Wanzhong and Geiss-Friedlander, Ruth and Gelfi, Cecilia and Genschik, Pascal and Gentle, Ian E. and Gerbino, Valeria and Gerhardt, Christoph and Germain, Kyla and Germain, Marc and Gewirtz, David A. and Ghasemipour Afshar, Elham and Ghavami, Saeid and Ghigo, Alessandra and Ghosh, Manosij and Giamas, Georgios and Giampietri, Claudia and Giatromanolaki, Alexandra and Gibson, Gary E. and Gibson, Spencer B. and Ginet, Vanessa and Giniger, Edward and Giorgi, Carlotta and Girao, Henrique and Girardin, Stephen E. and Giridharan, Mridhula and Giuliano, Sandy and Giulivi, Cecilia and Giuriato, Sylvie and Giustiniani, Julien and Gluschko, Alexander and Goder, Veit and Goginashvili, Alexander and Golab, Jakub and Goldstone, David C. and Golebiewska, Anna and Gomes, Luciana R. and Gomez, Rodrigo and Gómez-Sánchez, Rubén and Gomez-Puerto, Maria Catalina and Gomez-Sintes, Raquel and Gong, Qingqiu and Goni, Felix M. and González-Gallego, Javier and Gonzalez-Hernandez, Tomas and Gonzalez-Polo, Rosa A. and Gonzalez-Reyes, Jose A. and González-Rodríguez, Patricia and Goping, Ing Swie and Gorbatyuk, Marina S. and Gorbunov, Nikolai V. and Görgülü, Kıvanç and Gorojod, Roxana M. and Gorski, Sharon M. and Goruppi, Sandro and Gotor, Cecilia and Gottlieb, Roberta A. and Gozes, Illana and Gozuacik, Devrim and Graef, Martin and Gräler, Markus H. and Granatiero, Veronica and Grasso, Daniel and Gray, Joshua P. and Green, Douglas R. and Greenhough, Alexander and Gregory, Stephen L. and Griffin, Edward F. and Grinstaff, Mark W. and Gros, Frederic and Grose, Charles and Gross, Angelina S. and Gruber, Florian and Grumati, Paolo and Grune, Tilman and Gu, Xueyan and Guan, Jun Lin and Guardia, Carlos M. and Guda, Kishore and Guerra, Flora and Guerri, Consuelo and Guha, Prasun and Guillén, Carlos and Gujar, Shashi and Gukovskaya, Anna and Gukovsky, Ilya and Gunst, Jan and Günther, Andreas and Guntur, Anyonya R. and Guo, Chuanyong and Guo, Chun and Guo, Hongqing and Guo, Lian Wang and Guo, Ming and Gupta, Pawan and Gupta, Shashi Kumar and Gupta, Swapnil and Gupta, Veer Bala and Gupta, Vivek and Gustafsson, Asa B. and Gutterman, David D. and H.B, Ranjitha and Haapasalo, Annakaisa and Haber, James E. and Hać, Aleksandra and Hadano, Shinji and Hafrén, Anders J. and Haidar, Mansour and Hall, Belinda S. and Halldén, Gunnel and Hamacher-Brady, Anne and Hamann, Andrea and Hamasaki, Maho and Han, Weidong and Hansen, Malene and Hanson, Phyllis I. . and Hao, Zijian and Harada, Masaru and Harhaji-Trajkovic, Ljubica and Hariharan, Nirmala and Haroon, Nigil and Harris, James and Hasegawa, Takafumi and Hasima Nagoor, Noor and Haspel, Jeffrey A. and Haucke, Volker and Hawkins, Wayne D. and Hay, Bruce A. and Haynes, Cole M. and Hayrabedyan, Soren B. and Hays, Thomas S. and He, Congcong and He, Qin and He, Rong Rong and He, You Wen and He, Yu Ying and Heakal, Yasser and Heberle, Alexander M. and Hejtmancik, J. 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and Kanthasamy, Anumantha G. and Kanthasamy, Arthi and Kantorow, Marc and Kapuy, Orsolya and Karamouzis, Michalis V. and Karim, Md Razaul and Karmakar, Parimal and Katare, Rajesh G. and Kato, Masaru and Kaufmann, Stefan H.E. and Kauppinen, Anu and Kaushal, Gur P. and Kaushik, Susmita and Kawasaki, Kiyoshi and Kazan, Kemal and Ke, Po Yuan and Keating, Damien J. and Keber, Ursula and Kehrl, John H. and Keller, Kate E. and Keller, Christian W. and Kemper, Jongsook Kim and Kenific, Candia M. and Kepp, Oliver and Kermorgant, Stephanie and Kern, Andreas and Ketteler, Robin and Keulers, Tom G. and Khalfin, Boris and Khalil, Hany and Khambu, Bilon and Khan, Shahid Y. and Khandelwal, Vinoth Kumar Megraj and Khandia, Rekha and Kho, Widuri and Khobrekar, Noopur V. and Khuansuwan, Sataree and Khundadze, Mukhran and Killackey, Samuel A. and Kim, Dasol and Kim, Deok Ryong and Kim, Do Hyung and Kim, Dong Eun and Kim, Eun Young and Kim, Eun Kyoung and Kim, Hak Rim and Kim, Hee Sik and Hyung-Ryong Kim, Unknown and Kim, Jeong Hun and Kim, Jin Kyung and Kim, Jin Hoi and Kim, Joungmok and Kim, Ju Hwan and Kim, Keun Il and Kim, Peter K. and Kim, Seong Jun and Kimball, Scot R. and Kimchi, Adi and Kimmelman, Alec C. and Kimura, Tomonori and King, Matthew A. and Kinghorn, Kerri J. and Kinsey, Conan G. and Kirkin, Vladimir and Kirshenbaum, Lorrie A. and Kiselev, Sergey L. and Kishi, Shuji and Kitamoto, Katsuhiko and Kitaoka, Yasushi and Kitazato, Kaio and Kitsis, Richard N. and Kittler, Josef T. and Kjaerulff, Ole and Klein, Peter S. and Klopstock, Thomas and Klucken, Jochen and Knævelsrud, Helene and Knorr, Roland L. and Ko, Ben C.B. and Ko, Fred and Ko, Jiunn Liang and Kobayashi, Hotaka and Kobayashi, Satoru and Koch, Ina and Koch, Jan C. and Koenig, Ulrich and Kögel, Donat and Koh, Young Ho and Koike, Masato and Kohlwein, Sepp D. and Kocaturk, Nur M. and Komatsu, Masaaki and König, Jeannette and Kono, Toru and Kopp, Benjamin T. and Korcsmaros, Tamas and Korkmaz, Gözde and Korolchuk, 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Guanghong and Liao, Lujian and Liao, Mingzhi and Liao, Yung Feng and Librizzi, Mariangela and Lie, Pearl P.Y. and Lilly, Mary A. and Lim, Hyunjung J. and Lima, Thania R.R. and Limana, Federica and Lin, Chao and Lin, Chih Wen and Lin, Dar Shong and Lin, Fu Cheng and Lin, Jiandie D. and Lin, Kurt M. and Lin, Kwang Huei and Lin, Liang Tzung and Lin, Pei Hui and Lin, Qiong and Lin, Shaofeng and Lin, Su Ju and Lin, Wenyu and Lin, Xueying and Lin, Yao Xin and Lin, Yee Shin and Linden, Rafael and Lindner, Paula and Ling, Shuo Chien and Lingor, Paul and Linnemann, Amelia K. and Liou, Yih Cherng and Lipinski, Marta M. and Lipovšek, Saška and Lira, Vitor A. and Lisiak, Natalia and Liton, Paloma B. and Liu, Chao and Liu, Ching Hsuan and Liu, Chun Feng and Liu, Cui Hua and Liu, Fang and Liu, Hao and Liu, Hsiao Sheng and Liu, Hua Feng and Liu, Huifang and Liu, Jia and Liu, Jing and Liu, Julia and Liu, Leyuan and Liu, Longhua and Liu, Meilian and Liu, Qin and Liu, Wei and Liu, Wende and Liu, Xiao 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and Manjili, Masoud H. and Manjithaya, Ravi and Manque, Patricio and Manshian, Bella B. and Manzano, Raquel and Manzoni, Claudia and Mao, Kai and Marchese, Cinzia and Marchetti, Sandrine and Marconi, Anna Maria and Marcucci, Fabrizio and Mardente, Stefania and Mareninova, Olga A. and Margeta, Marta and Mari, Muriel and Marinelli, Sara and Marinelli, Oliviero and Mariño, Guillermo and Mariotto, Sofia and Marshall, Richard S. and Marten, Mark R. and Martens, Sascha and Martin, Alexandre P.J. and Martin, Katie R. and Martin, Sara and Martin, Shaun and Martín-Segura, Adrián and Martín-Acebes, Miguel A. and Martin-Burriel, Inmaculada and Martin-Rincon, Marcos and Martin-Sanz, Paloma and Martina, José A. and Martinet, Wim and Martinez, Aitor and Martinez, Ana and Martinez, Jennifer and Martinez Velazquez, Moises and Martinez-Lopez, Nuria and Martinez-Vicente, Marta and Martins, Daniel O. and Martins, Joilson O. and Martins, Waleska K. and Martins-Marques, Tania and Marzetti, Emanuele and 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Patrick and Murthy, Aditya and Myöhänen, Timo T. and Mysorekar, Indira U. and Mytych, Jennifer and Nabavi, Seyed Mohammad and Nabissi, Massimo and Nagy, Péter and Nah, Jihoon and Nahimana, Aimable and Nakagawa, Ichiro and Nakamura, Ken and Nakatogawa, Hitoshi and Nandi, Shyam S. and Nanjundan, Meera and Nanni, Monica and Napolitano, Gennaro and Nardacci, Roberta and Narita, Masashi and Nassif, Melissa and Nathan, Ilana and Natsumeda, Manabu and Naude, Ryno J. and Naumann, Christin and Naveiras, Olaia and Navid, Fatemeh and Nawrocki, Steffan T. and Nazarko, Taras Y. and Nazio, Francesca and Negoita, Florentina and Neill, Thomas and Neisch, Amanda L. and Neri, Luca M. and Netea, Mihai G. and Neubert, Patrick and Neufeld, Thomas P. and Neumann, Dietbert and Neutzner, Albert and Newton, Phillip T. and Ney, Paul A. and Nezis, Ioannis P. and Ng, Charlene C.W. and Ng, Tzi Bun and Nguyen, Hang T.T. and Nguyen, Long T. and Ni, Hong Min and Ní Cheallaigh, Clíona and Ni, Zhenhong and Nicolao, M. Celeste and Nicoli, Francesco and Nieto-Diaz, Manuel and Nilsson, Per and Ning, Shunbin and Niranjan, Rituraj and Nishimune, Hiroshi and Niso-Santano, Mireia and Nixon, Ralph A. and Nobili, Annalisa and Nobrega, Clevio and Noda, Takeshi and Nogueira-Recalde, Uxía and Nolan, Trevor M. and Nombela, Ivan and Novak, Ivana and Novoa, Beatriz and Nozawa, Takashi and Nukina, Nobuyuki and Nussbaum-Krammer, Carmen and Nylandsted, Jesper and O’Donovan, Tracey R. and O’Leary, Seónadh M. and O’Rourke, Eyleen J. and O’Sullivan, Mary P. and O’Sullivan, Timothy E. and Oddo, Salvatore and Oehme, Ina and Ogawa, Michinaga and Ogier-Denis, Eric and Ogmundsdottir, Margret H. and Ogretmen, Besim and Oh, Goo Taeg and Oh, Seon Hee and Oh, Young J. and Ohama, Takashi and Ohashi, Yohei and Ohmuraya, Masaki and Oikonomou, Vasileios and Ojha, Rani and Okamoto, Koji and Okazawa, Hitoshi and Oku, Masahide and Oliván, Sara and Oliveira, Jorge M.A. and Ollmann, Michael and Olzmann, James A. and Omari, Shakib and Omary, M. 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Wei Lynn and Wu, An Guo and Wu, Chengbiao and Wu, Jian and Wu, Junfang and Wu, Kenneth K. and Wu, Min and Wu, Shan Ying and Wu, Shengzhou and Wu, Shu Yan and Wu, Shufang and Wu, William K.K. and Wu, Xiaohong and Wu, Xiaoqing and Wu, Yao Wen and Wu, Yihua and Xavier, Ramnik J. and Xia, Hongguang and Xia, Lixin and Xia, Zhengyuan and Xiang, Ge and Xiang, Jin and Xiang, Mingliang and Xiang, Wei and Xiao, Bin and Xiao, Guozhi and Xiao, Hengyi and Xiao, Hong Tao and Xiao, Jian and Xiao, Lan and Xiao, Shi and Xiao, Yin and Xie, Baoming and Xie, Chuan Ming and Xie, Min and Xie, Yuxiang and Xie, Zhiping and Xie, Zhonglin and Xilouri, Maria and Xu, Congfeng and Xu, En and Xu, Haoxing and Xu, Jing and Xu, Jin Rong and Xu, Liang and Xu, Wen Wen and Xu, Xiulong and Xue, Yu and Yakhine-Diop, Sokhna M.S. and Yamaguchi, Masamitsu and Yamaguchi, Osamu and Yamamoto, Ai and Yamashina, Shunhei and Yan, Shengmin and Yan, Shian Jang and Yan, Zhen and Yanagi, Yasuo and Yang, Chuanbin and Yang, Dun Sheng and Yang, Huan and Yang, Huang Tian and Yang, Hui and Yang, Jin Ming and Yang, Jing and Yang, Jingyu and Yang, Ling and Yang, Liu and Yang, Ming and Yang, Pei Ming and Yang, Qian and Yang, Seungwon and Yang, Shu and Yang, Shun Fa and Yang, Wannian and Yang, Wei Yuan and Yang, Xiaoyong and Yang, Xuesong and Yang, Yi and Yang, Ying and Yao, Honghong and Yao, Shenggen and Yao, Xiaoqiang and Yao, Yong Gang and Yao, Yong Ming and Yasui, Takahiro and Yazdankhah, Meysam and Yen, Paul M. and Yi, Cong and Yin, Xiao Ming and Yin, Yanhai and Yin, Zhangyuan and Yin, Ziyi and Ying, Meidan and Ying, Zheng and Yip, Calvin K. and Yiu, Stephanie Pei Tung and Yoo, Young H. and Yoshida, Kiyotsugu and Yoshii, Saori R. and Yoshimori, Tamotsu and Yousefi, Bahman and Yu, Boxuan and Yu, Haiyang and Yu, Jun and Yu, Jun and Yu, Li and Yu, Ming Lung and Yu, Seong Woon and Yu, Victor C. and Yu, W. Haung and Yu, Zhengping and Yu, Zhou and Yuan, Junying and Yuan, Ling Qing and Yuan, Shilin and Yuan, Shyng Shiou F. and Yuan, Yanggang and Yuan, Zengqiang and Yue, Jianbo and Yue, Zhenyu and Yun, Jeanho and Yung, Raymond L. and Zacks, David N. and Zaffagnini, Gabriele and Zambelli, Vanessa O. and Zanella, Isabella and Zang, Qun S. and Zanivan, Sara and Zappavigna, Silvia and Zaragoza, Pilar and Zarbalis, Konstantinos S. and Zarebkohan, Amir and Zarrouk, Amira and Zeitlin, Scott O. and Zeng, Jialiu and Zeng, Ju Deng and Žerovnik, Eva and Zhan, Lixuan and Zhang, Bin and Zhang, Donna D. and Zhang, Hanlin and Zhang, Hong and Zhang, Hong and Zhang, Honghe and Zhang, Huafeng and Zhang, Huaye and Zhang, Hui and Zhang, Hui Ling and Zhang, Jianbin and Zhang, Jianhua and Zhang, Jing Pu and Zhang, Kalin Y.B. and Zhang, Leshuai W. and Zhang, Lin and Zhang, Lisheng and Zhang, Lu and Zhang, Luoying and Zhang, Menghuan and Zhang, Peng and Zhang, Sheng and Zhang, Wei and Zhang, Xiangnan and Zhang, Xiao Wei and Zhang, Xiaolei and Zhang, Xiaoyan and Zhang, Xin and Zhang, Xinxin and Zhang, Xu Dong and Zhang, Yang and Zhang, Yanjin and Zhang, Yi and Zhang, Ying Dong and Zhang, Yingmei and Zhang, Yuan Yuan and Zhang, Yuchen and Zhang, Zhe and Zhang, Zhengguang and Zhang, Zhibing and Zhang, Zhihai and Zhang, Zhiyong and Zhang, Zili and Zhao, Haobin and Zhao, Lei and Zhao, Shuang and Zhao, Tongbiao and Zhao, Xiao Fan and Zhao, Ying and Zhao, Yongchao and Zhao, Yongliang and Zhao, Yuting and Zheng, Guoping and Zheng, Kai and Zheng, Ling and Zheng, Shizhong and Zheng, Xi Long and Zheng, Yi and Zheng, Zu Guo and Zhivotovsky, Boris and Zhong, Qing and Zhou, Ao and Zhou, Ben and Zhou, Cefan and Zhou, Gang and Zhou, Hao and Zhou, Hong and Zhou, Hongbo and Zhou, Jie and Zhou, Jing and Zhou, Jing and Zhou, Jiyong and Zhou, Kailiang and Zhou, Rongjia and Zhou, Xu Jie and Zhou, Yanshuang and Zhou, Yinghong and Zhou, Yubin and Zhou, Zheng Yu and Zhou, Zhou and Zhu, Binglin and Zhu, Changlian and Zhu, Guo Qing and Zhu, Haining and Zhu, Hongxin and Zhu, Hua and Zhu, Wei Guo and Zhu, Yanping and Zhu, Yushan and Zhuang, Haixia and Zhuang, Xiaohong and Zientara-Rytter, Katarzyna and Zimmermann, Christine M. and Ziviani, Elena and Zoladek, Teresa and Zong, Wei Xing and Zorov, Dmitry B. and Zorzano, Antonio and Zou, Weiping and Zou, Zhen and Zou, Zhengzhi and Zuryn, Steven and Zwerschke, Werner and Brand-Saberi, Beate and Dong, X. Charlie and Kenchappa, Chandra Shekar and Li, Zuguo and Lin, Yong and Oshima, Shigeru and Rong, Yueguang and Sluimer, Judith C. and Stallings, Christina L. and Tong, Chun Kit}, issn = {1554-8635}, journal = {Autophagy}, number = {1}, pages = {1--382}, publisher = {Taylor & Francis}, title = {{Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)}}, doi = {10.1080/15548627.2020.1797280}, volume = {17}, year = {2021}, } @article{8742, abstract = {We develop a version of Ekedahl’s geometric sieve for integral quadratic forms of rank at least five. As one ranges over the zeros of such quadratic forms, we use the sieve to compute the density of coprime values of polynomials, and furthermore, to address a question about local solubility in families of varieties parameterised by the zeros.}, author = {Browning, Timothy D and Heath-Brown, Roger}, issn = {1435-5337}, journal = {Forum Mathematicum}, number = {1}, pages = {147--165}, publisher = {De Gruyter}, title = {{The geometric sieve for quadrics}}, doi = {10.1515/forum-2020-0074}, volume = {33}, year = {2021}, } @phdthesis{10035, abstract = {Many security definitions come in two flavors: a stronger “adaptive” flavor, where the adversary can arbitrarily make various choices during the course of the attack, and a weaker “selective” flavor where the adversary must commit to some or all of their choices a-priori. For example, in the context of identity-based encryption, selective security requires the adversary to decide on the identity of the attacked party at the very beginning of the game whereas adaptive security allows the attacker to first see the master public key and some secret keys before making this choice. Often, it appears to be much easier to achieve selective security than it is to achieve adaptive security. A series of several recent works shows how to cleverly achieve adaptive security in several such scenarios including generalized selective decryption [Pan07][FJP15], constrained PRFs [FKPR14], and Yao’s garbled circuits [JW16]. Although the above works expressed vague intuition that they share a common technique, the connection was never made precise. In this work we present a new framework (published at Crypto ’17 [JKK+17a]) that connects all of these works and allows us to present them in a unified and simplified fashion. Having the framework in place, we show how to achieve adaptive security for proxy re-encryption schemes (published at PKC ’19 [FKKP19]) and provide the first adaptive security proofs for continuous group key agreement protocols (published at S&P ’21 [KPW+21]). Questioning optimality of our framework, we then show that currently used proof techniques cannot lead to significantly better security guarantees for "graph-building" games (published at TCC ’21 [KKPW21a]). These games cover generalized selective decryption, as well as the security of prominent constructions for constrained PRFs, continuous group key agreement, and proxy re-encryption. Finally, we revisit the adaptive security of Yao’s garbled circuits and extend the analysis of Jafargholi and Wichs in two directions: While they prove adaptive security only for a modified construction with increased online complexity, we provide the first positive results for the original construction by Yao (published at TCC ’21 [KKP21a]). On the negative side, we prove that the results of Jafargholi and Wichs are essentially optimal by showing that no black-box reduction can provide a significantly better security bound (published at Crypto ’21 [KKPW21c]).}, author = {Klein, Karen}, issn = {2663-337X}, pages = {276}, publisher = {Institute of Science and Technology Austria}, title = {{On the adaptive security of graph-based games}}, doi = {10.15479/at:ista:10035}, year = {2021}, } @inproceedings{10410, abstract = {The security of cryptographic primitives and protocols against adversaries that are allowed to make adaptive choices (e.g., which parties to corrupt or which queries to make) is notoriously difficult to establish. A broad theoretical framework was introduced by Jafargholi et al. [Crypto’17] for this purpose. In this paper we initiate the study of lower bounds on loss in adaptive security for certain cryptographic protocols considered in the framework. We prove lower bounds that almost match the upper bounds (proven using the framework) for proxy re-encryption, prefix-constrained PRFs and generalized selective decryption, a security game that captures the security of certain group messaging and broadcast encryption schemes. Those primitives have in common that their security game involves an underlying graph that can be adaptively built by the adversary. Some of our lower bounds only apply to a restricted class of black-box reductions which we term “oblivious” (the existing upper bounds are of this restricted type), some apply to the broader but still restricted class of non-rewinding reductions, while our lower bound for proxy re-encryption applies to all black-box reductions. The fact that some of our lower bounds seem to crucially rely on obliviousness or at least a non-rewinding reduction hints to the exciting possibility that the existing upper bounds can be improved by using more sophisticated reductions. Our main conceptual contribution is a two-player multi-stage game called the Builder-Pebbler Game. We can translate bounds on the winning probabilities for various instantiations of this game into cryptographic lower bounds for the above-mentioned primitives using oracle separation techniques.}, author = {Kamath Hosdurg, Chethan and Klein, Karen and Pietrzak, Krzysztof Z and Walter, Michael}, booktitle = {19th International Conference}, isbn = {9-783-0309-0452-4}, issn = {1611-3349}, location = {Raleigh, NC, United States}, pages = {550--581}, publisher = {Springer Nature}, title = {{The cost of adaptivity in security games on graphs}}, doi = {10.1007/978-3-030-90453-1_19}, volume = {13043}, year = {2021}, } @inproceedings{10048, abstract = {The security of cryptographic primitives and protocols against adversaries that are allowed to make adaptive choices (e.g., which parties to corrupt or which queries to make) is notoriously difficult to establish. A broad theoretical framework was introduced by Jafargholi et al. [Crypto’17] for this purpose. In this paper we initiate the study of lower bounds on loss in adaptive security for certain cryptographic protocols considered in the framework. We prove lower bounds that almost match the upper bounds (proven using the framework) for proxy re-encryption, prefix-constrained PRFs and generalized selective decryption, a security game that captures the security of certain group messaging and broadcast encryption schemes. Those primitives have in common that their security game involves an underlying graph that can be adaptively built by the adversary. Some of our lower bounds only apply to a restricted class of black-box reductions which we term “oblivious” (the existing upper bounds are of this restricted type), some apply to the broader but still restricted class of non-rewinding reductions, while our lower bound for proxy re-encryption applies to all black-box reductions. The fact that some of our lower bounds seem to crucially rely on obliviousness or at least a non-rewinding reduction hints to the exciting possibility that the existing upper bounds can be improved by using more sophisticated reductions. Our main conceptual contribution is a two-player multi-stage game called the Builder-Pebbler Game. We can translate bounds on the winning probabilities for various instantiations of this game into cryptographic lower bounds for the above-mentioned primitives using oracle separation techniques. }, author = {Kamath Hosdurg, Chethan and Klein, Karen and Pietrzak, Krzysztof Z and Walter, Michael}, booktitle = {19th Theory of Cryptography Conference 2021}, location = {Raleigh, NC, United States}, publisher = {International Association for Cryptologic Research}, title = {{The cost of adaptivity in security games on graphs}}, year = {2021}, } @article{10738, abstract = {We prove an adiabatic theorem for the Landau–Pekar equations. This allows us to derive new results on the accuracy of their use as effective equations for the time evolution generated by the Fröhlich Hamiltonian with large coupling constant α. In particular, we show that the time evolution of Pekar product states with coherent phonon field and the electron being trapped by the phonons is well approximated by the Landau–Pekar equations until times short compared to α2.}, author = {Leopold, Nikolai K and Rademacher, Simone Anna Elvira and Schlein, Benjamin and Seiringer, Robert}, issn = {1948-206X}, journal = {Analysis and PDE}, number = {7}, pages = {2079--2100}, publisher = {Mathematical Sciences Publishers}, title = {{ The Landau–Pekar equations: Adiabatic theorem and accuracy}}, doi = {10.2140/APDE.2021.14.2079}, volume = {14}, year = {2021}, } @phdthesis{10429, abstract = {The scalability of concurrent data structures and distributed algorithms strongly depends on reducing the contention for shared resources and the costs of synchronization and communication. We show how such cost reductions can be attained by relaxing the strict consistency conditions required by sequential implementations. In the first part of the thesis, we consider relaxation in the context of concurrent data structures. Specifically, in data structures such as priority queues, imposing strong semantics renders scalability impossible, since a correct implementation of the remove operation should return only the element with highest priority. Intuitively, attempting to invoke remove operations concurrently creates a race condition. This bottleneck can be circumvented by relaxing semantics of the affected data structure, thus allowing removal of the elements which are no longer required to have the highest priority. We prove that the randomized implementations of relaxed data structures provide provable guarantees on the priority of the removed elements even under concurrency. Additionally, we show that in some cases the relaxed data structures can be used to scale the classical algorithms which are usually implemented with the exact ones. In the second part, we study parallel variants of the stochastic gradient descent (SGD) algorithm, which distribute computation among the multiple processors, thus reducing the running time. Unfortunately, in order for standard parallel SGD to succeed, each processor has to maintain a local copy of the necessary model parameter, which is identical to the local copies of other processors; the overheads from this perfect consistency in terms of communication and synchronization can negate the speedup gained by distributing the computation. We show that the consistency conditions required by SGD can be relaxed, allowing the algorithm to be more flexible in terms of tolerating quantized communication, asynchrony, or even crash faults, while its convergence remains asymptotically the same.}, author = {Nadiradze, Giorgi}, issn = {2663-337X}, pages = {132}, publisher = {Institute of Science and Technology Austria}, title = {{On achieving scalability through relaxation}}, doi = {10.15479/at:ista:10429}, year = {2021}, } @inproceedings{10435, abstract = {Decentralized optimization is emerging as a viable alternative for scalable distributed machine learning, but also introduces new challenges in terms of synchronization costs. To this end, several communication-reduction techniques, such as non-blocking communication, quantization, and local steps, have been explored in the decentralized setting. Due to the complexity of analyzing optimization in such a relaxed setting, this line of work often assumes \emph{global} communication rounds, which require additional synchronization. In this paper, we consider decentralized optimization in the simpler, but harder to analyze, \emph{asynchronous gossip} model, in which communication occurs in discrete, randomly chosen pairings among nodes. Perhaps surprisingly, we show that a variant of SGD called \emph{SwarmSGD} still converges in this setting, even if \emph{non-blocking communication}, \emph{quantization}, and \emph{local steps} are all applied \emph{in conjunction}, and even if the node data distributions and underlying graph topology are both \emph{heterogenous}. Our analysis is based on a new connection with multi-dimensional load-balancing processes. We implement this algorithm and deploy it in a super-computing environment, showing that it can outperform previous decentralized methods in terms of end-to-end training time, and that it can even rival carefully-tuned large-batch SGD for certain tasks.}, author = {Nadiradze, Giorgi and Sabour, Amirmojtaba and Davies, Peter and Li, Shigang and Alistarh, Dan-Adrian}, booktitle = {35th Conference on Neural Information Processing Systems}, location = {Sydney, Australia}, publisher = {Neural Information Processing Systems Foundation}, title = {{Asynchronous decentralized SGD with quantized and local updates}}, year = {2021}, } @inproceedings{10593, abstract = {We study the problem of estimating a rank-$1$ signal in the presence of rotationally invariant noise-a class of perturbations more general than Gaussian noise. Principal Component Analysis (PCA) provides a natural estimator, and sharp results on its performance have been obtained in the high-dimensional regime. Recently, an Approximate Message Passing (AMP) algorithm has been proposed as an alternative estimator with the potential to improve the accuracy of PCA. However, the existing analysis of AMP requires an initialization that is both correlated with the signal and independent of the noise, which is often unrealistic in practice. In this work, we combine the two methods, and propose to initialize AMP with PCA. Our main result is a rigorous asymptotic characterization of the performance of this estimator. Both the AMP algorithm and its analysis differ from those previously derived in the Gaussian setting: at every iteration, our AMP algorithm requires a specific term to account for PCA initialization, while in the Gaussian case, PCA initialization affects only the first iteration of AMP. The proof is based on a two-phase artificial AMP that first approximates the PCA estimator and then mimics the true AMP. Our numerical simulations show an excellent agreement between AMP results and theoretical predictions, and suggest an interesting open direction on achieving Bayes-optimal performance.}, author = {Mondelli, Marco and Venkataramanan, Ramji}, booktitle = {35th Conference on Neural Information Processing Systems}, isbn = {9781713845393}, issn = {1049-5258}, location = {Virtual}, pages = {29616--29629}, publisher = {Neural Information Processing Systems Foundation}, title = {{PCA initialization for approximate message passing in rotationally invariant models}}, volume = {35}, year = {2021}, } @inproceedings{10594, abstract = {The question of how and why the phenomenon of mode connectivity occurs in training deep neural networks has gained remarkable attention in the research community. From a theoretical perspective, two possible explanations have been proposed: (i) the loss function has connected sublevel sets, and (ii) the solutions found by stochastic gradient descent are dropout stable. While these explanations provide insights into the phenomenon, their assumptions are not always satisfied in practice. In particular, the first approach requires the network to have one layer with order of N neurons (N being the number of training samples), while the second one requires the loss to be almost invariant after removing half of the neurons at each layer (up to some rescaling of the remaining ones). In this work, we improve both conditions by exploiting the quality of the features at every intermediate layer together with a milder over-parameterization condition. More specifically, we show that: (i) under generic assumptions on the features of intermediate layers, it suffices that the last two hidden layers have order of N−−√ neurons, and (ii) if subsets of features at each layer are linearly separable, then no over-parameterization is needed to show the connectivity. Our experiments confirm that the proposed condition ensures the connectivity of solutions found by stochastic gradient descent, even in settings where the previous requirements do not hold.}, author = {Nguyen, Quynh and Bréchet, Pierre and Mondelli, Marco}, booktitle = {35th Conference on Neural Information Processing Systems}, isbn = {9781713845393}, issn = {1049-5258}, location = {Virtual}, publisher = {Neural Information Processing Systems Foundation}, title = {{When are solutions connected in deep networks?}}, volume = {35}, year = {2021}, } @article{9815, abstract = {The quantum bits (qubits) on which superconducting quantum computers are based have energy scales corresponding to photons with GHz frequencies. The energy of photons in the gigahertz domain is too low to allow transmission through the noisy room-temperature environment, where the signal would be lost in thermal noise. Optical photons, on the other hand, have much higher energies, and signals can be detected using highly efficient single-photon detectors. Transduction from microwave to optical frequencies is therefore a potential enabling technology for quantum devices. However, in such a device the optical pump can be a source of thermal noise and thus degrade the fidelity; the similarity of input microwave state to the output optical state. In order to investigate the magnitude of this effect we model the sub-Kelvin thermal behavior of an electro-optic transducer based on a lithium niobate whispering gallery mode resonator. We find that there is an optimum power level for a continuous pump, whilst pulsed operation of the pump increases the fidelity of the conversion.}, author = {Mobassem, Sonia and Lambert, Nicholas J. and Rueda Sanchez, Alfredo R and Fink, Johannes M and Leuchs, Gerd and Schwefel, Harald G.L.}, issn = {2058-9565}, journal = {Quantum Science and Technology}, number = {4}, publisher = {IOP Publishing}, title = {{Thermal noise in electro-optic devices at cryogenic temperatures}}, doi = {10.1088/2058-9565/ac0f36}, volume = {6}, year = {2021}, } @unpublished{9978, abstract = {Redox mediators could catalyse otherwise slow and energy-inefficient cycling of Li-S and Li-O 2 batteries by shuttling electrons/holes between the electrode and the solid insulating storage materials. For mediators to work efficiently they need to oxidize the solid with fast kinetics yet the lowest possible overpotential. Here, we found that when the redox potentials of mediators are tuned via, e.g., Li + concentration in the electrolyte, they exhibit distinct threshold potentials, where the kinetics accelerate several-fold within a range as small as 10 mV. This phenomenon is independent of types of mediators and electrolyte. The acceleration originates from the overpotentials required to activate fast Li + /e – extraction and the following chemical step at specific abundant surface facets. Efficient redox catalysis at insulating solids requires therefore carefully considering the surface conditions of the storage materials and electrolyte-dependent redox potentials, which may be tuned by salt concentrations or solvents.}, author = {Cao, Deqing and Shen, Xiaoxiao and Wang, Aiping and Yu, Fengjiao and Wu, Yuping and Shi, Siqi and Freunberger, Stefan Alexander and Chen, Yuhui}, booktitle = {Research Square}, issn = {2693-5015}, keywords = {Catalysis, Energy engineering, Materials theory and modeling}, pages = {21}, publisher = {Research Square}, title = {{Sharp kinetic acceleration potentials during mediated redox catalysis of insulators}}, doi = {10.21203/rs.3.rs-750965/v1}, year = {2021}, } @article{8730, abstract = {P-glycoprotein (ABCB1) and breast cancer resistance protein (ABCG2) restrict at the blood–brain barrier (BBB) the brain distribution of the majority of currently known molecularly targeted anticancer drugs. To improve brain delivery of dual ABCB1/ABCG2 substrates, both ABCB1 and ABCG2 need to be inhibited simultaneously at the BBB. We examined the feasibility of simultaneous ABCB1/ABCG2 inhibition with i.v. co-infusion of erlotinib and tariquidar by studying brain distribution of the model ABCB1/ABCG2 substrate [11C]erlotinib in mice and rhesus macaques with PET. Tolerability of the erlotinib/tariquidar combination was assessed in human embryonic stem cell-derived cerebral organoids. In mice and macaques, baseline brain distribution of [11C]erlotinib was low (brain distribution volume, VT,brain < 0.3 mL/cm3). Co-infusion of erlotinib and tariquidar increased VT,brain in mice by 3.0-fold and in macaques by 3.4- to 5.0-fold, while infusion of erlotinib alone or tariquidar alone led to less pronounced VT,brain increases in both species. Treatment of cerebral organoids with erlotinib/tariquidar led to an induction of Caspase-3-dependent apoptosis. Co-infusion of erlotinib/tariquidar may potentially allow for complete ABCB1/ABCG2 inhibition at the BBB, while simultaneously achieving brain-targeted EGFR inhibition. Our protocol may be applicable to enhance brain delivery of molecularly targeted anticancer drugs for a more effective treatment of brain tumors.}, author = {Tournier, N and Goutal, S and Mairinger, S and Lozano, IH and Filip, T and Sauberer, M and Caillé, F and Breuil, L and Stanek, J and Freeman, AF and Novarino, Gaia and Truillet, C and Wanek, T and Langer, O}, issn = {1559-7016}, journal = {Journal of Cerebral Blood Flow and Metabolism}, number = {7}, pages = {1634--1646}, publisher = {SAGE Publications}, title = {{Complete inhibition of ABCB1 and ABCG2 at the blood-brain barrier by co-infusion of erlotinib and tariquidar to improve brain delivery of the model ABCB1/ABCG2 substrate [11C]erlotinib}}, doi = {10.1177/0271678X20965500}, volume = {41}, year = {2021}, } @article{9383, abstract = {A primary roadblock to our understanding of speciation is that it usually occurs over a timeframe that is too long to study from start to finish. The idea of a speciation continuum provides something of a solution to this problem; rather than observing the entire process, we can simply reconstruct it from the multitude of speciation events that surround us. But what do we really mean when we talk about the speciation continuum, and can it really help us understand speciation? We explored these questions using a literature review and online survey of speciation researchers. Although most researchers were familiar with the concept and thought it was useful, our survey revealed extensive disagreement about what the speciation continuum actually tells us. This is due partly to the lack of a clear definition. Here, we provide an explicit definition that is compatible with the Biological Species Concept. That is, the speciation continuum is a continuum of reproductive isolation. After outlining the logic of the definition in light of alternatives, we explain why attempts to reconstruct the speciation process from present‐day populations will ultimately fail. We then outline how we think the speciation continuum concept can continue to act as a foundation for understanding the continuum of reproductive isolation that surrounds us.}, author = {Stankowski, Sean and Ravinet, Mark}, issn = {1558-5646}, journal = {Evolution}, number = {6}, pages = {1256--1273}, publisher = {Oxford University Press}, title = {{Defining the speciation continuum}}, doi = {10.1111/evo.14215}, volume = {75}, year = {2021}, } @article{10223, abstract = {Growth regulation tailors development in plants to their environment. A prominent example of this is the response to gravity, in which shoots bend up and roots bend down1. This paradox is based on opposite effects of the phytohormone auxin, which promotes cell expansion in shoots while inhibiting it in roots via a yet unknown cellular mechanism2. Here, by combining microfluidics, live imaging, genetic engineering and phosphoproteomics in Arabidopsis thaliana, we advance understanding of how auxin inhibits root growth. We show that auxin activates two distinct, antagonistically acting signalling pathways that converge on rapid regulation of apoplastic pH, a causative determinant of growth. Cell surface-based TRANSMEMBRANE KINASE1 (TMK1) interacts with and mediates phosphorylation and activation of plasma membrane H+-ATPases for apoplast acidification, while intracellular canonical auxin signalling promotes net cellular H+ influx, causing apoplast alkalinization. Simultaneous activation of these two counteracting mechanisms poises roots for rapid, fine-tuned growth modulation in navigating complex soil environments.}, author = {Li, Lanxin and Verstraeten, Inge and Roosjen, Mark and Takahashi, Koji and Rodriguez Solovey, Lesia and Merrin, Jack and Chen, Jian and Shabala, Lana and Smet, Wouter and Ren, Hong and Vanneste, Steffen and Shabala, Sergey and De Rybel, Bert and Weijers, Dolf and Kinoshita, Toshinori and Gray, William M. and Friml, Jiří}, issn = {14764687}, journal = {Nature}, keywords = {Multidisciplinary}, number = {7884}, pages = {273--277}, publisher = {Springer Nature}, title = {{Cell surface and intracellular auxin signalling for H+ fluxes in root growth}}, doi = {10.1038/s41586-021-04037-6}, volume = {599}, year = {2021}, } @article{9379, abstract = {When B cells encounter membrane-bound antigens, the formation and coalescence of B cell antigen receptor (BCR) microclusters amplifies BCR signaling. The ability of B cells to probe the surface of antigen-presenting cells (APCs) and respond to APC-bound antigens requires remodeling of the actin cytoskeleton. Initial BCR signaling stimulates actin-related protein (Arp) 2/3 complex-dependent actin polymerization, which drives B cell spreading as well as the centripetal movement and coalescence of BCR microclusters at the B cell-APC synapse. Sustained actin polymerization depends on concomitant actin filament depolymerization, which enables the recycling of actin monomers and Arp2/3 complexes. Cofilin-mediated severing of actin filaments is a rate-limiting step in the morphological changes that occur during immune synapse formation. Hence, regulators of cofilin activity such as WD repeat-containing protein 1 (Wdr1), LIM domain kinase (LIMK), and coactosin-like 1 (Cotl1) may also be essential for actin-dependent processes in B cells. Wdr1 enhances cofilin-mediated actin disassembly. Conversely, Cotl1 competes with cofilin for binding to actin and LIMK phosphorylates cofilin and prevents it from binding to actin filaments. We now show that Wdr1 and LIMK have distinct roles in BCR-induced assembly of the peripheral actin structures that drive B cell spreading, and that cofilin, Wdr1, and LIMK all contribute to the actin-dependent amplification of BCR signaling at the immune synapse. Depleting Cotl1 had no effect on these processes. Thus, the Wdr1-LIMK-cofilin axis is critical for BCR-induced actin remodeling and for B cell responses to APC-bound antigens.}, author = {Bolger-Munro, Madison and Choi, Kate and Cheung, Faith and Liu, Yi Tian and Dang-Lawson, May and Deretic, Nikola and Keane, Connor and Gold, Michael R.}, issn = {2296-634X}, journal = {Frontiers in Cell and Developmental Biology}, keywords = {B cell, actin, immune synapse, cell spreading, cofilin, WDR1 (AIP1), LIM domain kinase, B cell receptor (BCR)}, publisher = {Frontiers Media}, title = {{The Wdr1-LIMK-Cofilin axis controls B cell antigen receptor-induced actin remodeling and signaling at the immune synapse}}, doi = {10.3389/fcell.2021.649433}, volume = {9}, year = {2021}, } @article{9362, abstract = {A central goal in systems neuroscience is to understand the functions performed by neural circuits. Previous top-down models addressed this question by comparing the behaviour of an ideal model circuit, optimised to perform a given function, with neural recordings. However, this requires guessing in advance what function is being performed, which may not be possible for many neural systems. To address this, we propose an inverse reinforcement learning (RL) framework for inferring the function performed by a neural network from data. We assume that the responses of each neuron in a network are optimised so as to drive the network towards ‘rewarded’ states, that are desirable for performing a given function. We then show how one can use inverse RL to infer the reward function optimised by the network from observing its responses. This inferred reward function can be used to predict how the neural network should adapt its dynamics to perform the same function when the external environment or network structure changes. This could lead to theoretical predictions about how neural network dynamics adapt to deal with cell death and/or varying sensory stimulus statistics.}, author = {Chalk, Matthew J and Tkačik, Gašper and Marre, Olivier}, issn = {19326203}, journal = {PLoS ONE}, number = {4}, publisher = {Public Library of Science}, title = {{Inferring the function performed by a recurrent neural network}}, doi = {10.1371/journal.pone.0248940}, volume = {16}, year = {2021}, } @article{9986, abstract = {Size control is a fundamental question in biology, showing incremental complexity in plants, whose cells possess a rigid cell wall. The phytohormone auxin is a vital growth regulator with central importance for differential growth control. Our results indicate that auxin-reliant growth programs affect the molecular complexity of xyloglucans, the major type of cell wall hemicellulose in eudicots. Auxin-dependent induction and repression of growth coincide with reduced and enhanced molecular complexity of xyloglucans, respectively. In agreement with a proposed function in growth control, genetic interference with xyloglucan side decorations distinctly modulates auxin-dependent differential growth rates. Our work proposes that auxin-dependent growth programs have a spatially defined effect on xyloglucan’s molecular structure, which in turn affects cell wall mechanics and specifies differential, gravitropic hypocotyl growth.}, author = {Velasquez, Silvia Melina and Guo, Xiaoyuan and Gallemi, Marçal and Aryal, Bibek and Venhuizen, Peter and Barbez, Elke and Dünser, Kai Alexander and Darino, Martin and Pӗnčík, Aleš and Novák, Ondřej and Kalyna, Maria and Mouille, Gregory and Benková, Eva and Bhalerao, Rishikesh P. and Mravec, Jozef and Kleine-Vehn, Jürgen}, issn = {1422-0067}, journal = {International Journal of Molecular Sciences}, keywords = {auxin, growth, cell wall, xyloglucans, hypocotyls, gravitropism}, number = {17}, publisher = {MDPI}, title = {{Xyloglucan remodeling defines auxin-dependent differential tissue expansion in plants}}, doi = {10.3390/ijms22179222}, volume = {22}, year = {2021}, } @article{9189, abstract = {Transposable elements exist widely throughout plant genomes and play important roles in plant evolution. Auxin is an important regulator that is traditionally associated with root development and drought stress adaptation. The DEEPER ROOTING 1 (DRO1) gene is a key component of rice drought avoidance. Here, we identified a transposon that acts as an autonomous auxin‐responsive promoter and its presence at specific genome positions conveys physiological adaptations related to drought avoidance. Rice varieties with high and auxin‐mediated transcription of DRO1 in the root tip show deeper and longer root phenotypes and are thus better adapted to drought. The INDITTO2 transposon contains an auxin response element and displays auxin‐responsive promoter activity; it is thus able to convey auxin regulation of transcription to genes in its proximity. In the rice Acuce, which displays DRO1‐mediated drought adaptation, the INDITTO2 transposon was found to be inserted at the promoter region of the DRO1 locus. Transgenesis‐based insertion of the INDITTO2 transposon into the DRO1 promoter of the non‐adapted rice variety Nipponbare was sufficient to promote its drought avoidance. Our data identify an example of how transposons can act as promoters and convey hormonal regulation to nearby loci, improving plant fitness in response to different abiotic stresses.}, author = {Zhao, Y and Wu, L and Fu, Q and Wang, D and Li, J and Yao, B and Yu, S and Jiang, L and Qian, J and Zhou, X and Han, L and Zhao, S and Ma, C and Zhang, Y and Luo, C and Dong, Q and Li, S and Zhang, L and Jiang, X and Li, Y and Luo, H and Li, K and Yang, J and Luo, Q and Li, L and Peng, S and Huang, H and Zuo, Z and Liu, C and Wang, L and Li, C and He, X and Friml, Jiří and Du, Y}, issn = {1365-3040}, journal = {Plant, Cell & Environment}, number = {6}, pages = {1846--1857}, publisher = {Wiley}, title = {{INDITTO2 transposon conveys auxin-mediated DRO1 transcription for rice drought avoidance}}, doi = {10.1111/pce.14029}, volume = {44}, year = {2021}, } @unpublished{9792, abstract = {This paper establishes new connections between many-body quantum systems, One-body Reduced Density Matrices Functional Theory (1RDMFT) and Optimal Transport (OT), by interpreting the problem of computing the ground-state energy of a finite dimensional composite quantum system at positive temperature as a non-commutative entropy regularized Optimal Transport problem. We develop a new approach to fully characterize the dual-primal solutions in such non-commutative setting. The mathematical formalism is particularly relevant in quantum chemistry: numerical realizations of the many-electron ground state energy can be computed via a non-commutative version of Sinkhorn algorithm. Our approach allows to prove convergence and robustness of this algorithm, which, to our best knowledge, were unknown even in the two marginal case. Our methods are based on careful a priori estimates in the dual problem, which we believe to be of independent interest. Finally, the above results are extended in 1RDMFT setting, where bosonic or fermionic symmetry conditions are enforced on the problem.}, author = {Feliciangeli, Dario and Gerolin, Augusto and Portinale, Lorenzo}, booktitle = {arXiv}, title = {{A non-commutative entropic optimal transport approach to quantum composite systems at positive temperature}}, doi = {10.48550/arXiv.2106.11217}, year = {2021}, } @article{10655, abstract = {Adeno-associated viruses (AAVs) are widely used to deliver genetic material in vivo to distinct cell types such as neurons or glial cells, allowing for targeted manipulation. Transduction of microglia is mostly excluded from this strategy, likely due to the cells’ heterogeneous state upon environmental changes, which makes AAV design challenging. Here, we established the retina as a model system for microglial AAV validation and optimization. First, we show that AAV2/6 transduced microglia in both synaptic layers, where layer preference corresponds to the intravitreal or subretinal delivery method. Surprisingly, we observed significantly enhanced microglial transduction during photoreceptor degeneration. Thus, we modified the AAV6 capsid to reduce heparin binding by introducing four point mutations (K531E, R576Q, K493S, and K459S), resulting in increased microglial transduction in the outer plexiform layer. Finally, to improve microglial-specific transduction, we validated a Cre-dependent transgene delivery cassette for use in combination with the Cx3cr1CreERT2 mouse line. Together, our results provide a foundation for future studies optimizing AAV-mediated microglia transduction and highlight that environmental conditions influence microglial transduction efficiency. }, author = {Maes, Margaret E and Wögenstein, Gabriele M. and Colombo, Gloria and Casado Polanco, Raquel and Siegert, Sandra}, issn = {2329-0501}, journal = {Molecular Therapy - Methods and Clinical Development}, pages = {210--224}, publisher = {Elsevier}, title = {{Optimizing AAV2/6 microglial targeting identified enhanced efficiency in the photoreceptor degenerative environment}}, doi = {10.1016/j.omtm.2021.09.006}, volume = {23}, year = {2021}, } @article{10565, abstract = {Enzymatic digestion of the extracellular matrix with chondroitinase-ABC reinstates juvenile-like plasticity in the adult cortex as it also disassembles the perineuronal nets (PNNs). The disadvantage of the enzyme is that it must be applied intracerebrally and it degrades the ECM for several weeks. Here, we provide two minimally invasive and transient protocols for microglia-enabled PNN disassembly in mouse cortex: repeated treatment with ketamine-xylazine-acepromazine (KXA) anesthesia and 60-Hz light entrainment. We also discuss how to analyze PNNs within microglial endosomes-lysosomes. For complete details on the use and execution of this protocol, please refer to Venturino et al. (2021).}, author = {Venturino, Alessandro and Siegert, Sandra}, issn = {2666-1667}, journal = {STAR Protocols}, number = {4}, publisher = {Elsevier ; Cell Press}, title = {{Minimally invasive protocols and quantification for microglia-mediated perineuronal net disassembly in mouse brain}}, doi = {10.1016/j.xpro.2021.101012}, volume = {2}, year = {2021}, } @article{10321, abstract = {Mosaic analysis with double markers (MADM) technology enables the generation of genetic mosaic tissue in mice. MADM enables concomitant fluorescent cell labeling and introduction of a mutation of a gene of interest with single-cell resolution. This protocol highlights major steps for the generation of genetic mosaic tissue and the isolation and processing of respective tissues for downstream histological analysis. For complete details on the use and execution of this protocol, please refer to Contreras et al. (2021).}, author = {Amberg, Nicole and Hippenmeyer, Simon}, issn = {2666-1667}, journal = {STAR Protocols}, number = {4}, publisher = {Cell Press}, title = {{Genetic mosaic dissection of candidate genes in mice using mosaic analysis with double markers}}, doi = {10.1016/j.xpro.2021.100939}, volume = {2}, year = {2021}, } @article{10290, abstract = {A precise quantitative description of the ultrastructural characteristics underlying biological mechanisms is often key to their understanding. This is particularly true for dynamic extra- and intracellular filamentous assemblies, playing a role in cell motility, cell integrity, cytokinesis, tissue formation and maintenance. For example, genetic manipulation or modulation of actin regulatory proteins frequently manifests in changes of the morphology, dynamics, and ultrastructural architecture of actin filament-rich cell peripheral structures, such as lamellipodia or filopodia. However, the observed ultrastructural effects often remain subtle and require sufficiently large datasets for appropriate quantitative analysis. The acquisition of such large datasets has been enabled by recent advances in high-throughput cryo-electron tomography (cryo-ET) methods. This also necessitates the development of complementary approaches to maximize the extraction of relevant biological information. We have developed a computational toolbox for the semi-automatic quantification of segmented and vectorized filamentous networks from pre-processed cryo-electron tomograms, facilitating the analysis and cross-comparison of multiple experimental conditions. GUI-based components simplify the processing of data and allow users to obtain a large number of ultrastructural parameters describing filamentous assemblies. We demonstrate the feasibility of this workflow by analyzing cryo-ET data of untreated and chemically perturbed branched actin filament networks and that of parallel actin filament arrays. In principle, the computational toolbox presented here is applicable for data analysis comprising any type of filaments in regular (i.e. parallel) or random arrangement. We show that it can ease the identification of key differences between experimental groups and facilitate the in-depth analysis of ultrastructural data in a time-efficient manner.}, author = {Dimchev, Georgi A and Amiri, Behnam and Fäßler, Florian and Falcke, Martin and Schur, Florian KM}, issn = {1047-8477}, journal = {Journal of Structural Biology}, keywords = {Structural Biology}, number = {4}, publisher = {Elsevier }, title = {{Computational toolbox for ultrastructural quantitative analysis of filament networks in cryo-ET data}}, doi = {10.1016/j.jsb.2021.107808}, volume = {213}, year = {2021}, } @inproceedings{9969, abstract = {Payment channel networks are a promising approach to improve the scalability of cryptocurrencies: they allow to perform transactions in a peer-to-peer fashion, along multihop routes in the network, without requiring consensus on the blockchain. However, during the discovery of cost-efficient routes for the transaction, critical information may be revealed about the transacting entities. This paper initiates the study of privacy-preserving route discovery mechanisms for payment channel networks. In particular, we present LightPIR, an approach which allows a client to learn the shortest (or cheapest in terms of fees) path between two nodes without revealing any information about the endpoints of the transaction to the servers. The two main observations which allow for an efficient solution in LightPIR are that: (1) surprisingly, hub labelling algorithms – which were developed to preprocess “street network like” graphs so one can later efficiently compute shortest paths – also perform well for the graphs underlying payment channel networks, and that (2) hub labelling algorithms can be conveniently combined with private information retrieval. LightPIR relies on a simple hub labeling heuristic on top of existing hub labeling algorithms which leverages the specific topological features of cryptocurrency networks to further minimize storage and bandwidth overheads. In a case study considering the Lightning network, we show that our approach is an order of magnitude more efficient compared to a privacy-preserving baseline based on using private information retrieval on a database that stores all pairs shortest paths.}, author = {Pietrzak, Krzysztof Z and Salem, Iosif and Schmid, Stefan and Yeo, Michelle X}, isbn = {978-1-6654-4501-6}, issn = {1861-2288}, location = {Espoo and Helsinki, Finland}, publisher = {IEEE}, title = {{LightPIR: Privacy-preserving route discovery for payment channel networks}}, doi = {10.23919/IFIPNetworking52078.2021.9472205}, year = {2021}, } @inproceedings{9644, abstract = {We present a new approach to proving non-termination of non-deterministic integer programs. Our technique is rather simple but efficient. It relies on a purely syntactic reversal of the program's transition system followed by a constraint-based invariant synthesis with constraints coming from both the original and the reversed transition system. The latter task is performed by a simple call to an off-the-shelf SMT-solver, which allows us to leverage the latest advances in SMT-solving. Moreover, our method offers a combination of features not present (as a whole) in previous approaches: it handles programs with non-determinism, provides relative completeness guarantees and supports programs with polynomial arithmetic. The experiments performed with our prototype tool RevTerm show that our approach, despite its simplicity and stronger theoretical guarantees, is at least on par with the state-of-the-art tools, often achieving a non-trivial improvement under a proper configuration of its parameters.}, author = {Chatterjee, Krishnendu and Goharshady, Ehsan Kafshdar and Novotný, Petr and Zikelic, Dorde}, booktitle = {Proceedings of the 42nd ACM SIGPLAN International Conference on Programming Language Design and Implementation}, isbn = {9781450383912}, location = {Online}, pages = {1033--1048}, publisher = {Association for Computing Machinery}, title = {{Proving non-termination by program reversal}}, doi = {10.1145/3453483.3454093}, year = {2021}, } @article{9760, abstract = {The quantum approximate optimization algorithm (QAOA) is a prospective near-term quantum algorithm due to its modest circuit depth and promising benchmarks. However, an external parameter optimization required in the QAOA could become a performance bottleneck. This motivates studies of the optimization landscape and search for heuristic ways of parameter initialization. In this work we visualize the optimization landscape of the QAOA applied to the MaxCut problem on random graphs, demonstrating that random initialization of the QAOA is prone to converging to local minima with suboptimal performance. We introduce the initialization of QAOA parameters based on the Trotterized quantum annealing (TQA) protocol, parameterized by the Trotter time step. We find that the TQA initialization allows to circumvent the issue of false minima for a broad range of time steps, yielding the same performance as the best result out of an exponentially scaling number of random initializations. Moreover, we demonstrate that the optimal value of the time step coincides with the point of proliferation of Trotter errors in quantum annealing. Our results suggest practical ways of initializing QAOA protocols on near-term quantum devices and reveal new connections between QAOA and quantum annealing.}, author = {Sack, Stefan and Serbyn, Maksym}, issn = {2521-327X}, journal = {Quantum}, publisher = {Verein zur Förderung des Open Access Publizierens in den Quantenwissenschaften}, title = {{Quantum annealing initialization of the quantum approximate optimization algorithm}}, doi = {10.22331/Q-2021-07-01-491}, volume = {5}, year = {2021}, } @inproceedings{10414, abstract = {We consider the almost-sure (a.s.) termination problem for probabilistic programs, which are a stochastic extension of classical imperative programs. Lexicographic ranking functions provide a sound and practical approach for termination of non-probabilistic programs, and their extension to probabilistic programs is achieved via lexicographic ranking supermartingales (LexRSMs). However, LexRSMs introduced in the previous work have a limitation that impedes their automation: all of their components have to be non-negative in all reachable states. This might result in LexRSM not existing even for simple terminating programs. Our contributions are twofold: First, we introduce a generalization of LexRSMs which allows for some components to be negative. This standard feature of non-probabilistic termination proofs was hitherto not known to be sound in the probabilistic setting, as the soundness proof requires a careful analysis of the underlying stochastic process. Second, we present polynomial-time algorithms using our generalized LexRSMs for proving a.s. termination in broad classes of linear-arithmetic programs.}, author = {Chatterjee, Krishnendu and Goharshady, Ehsan Kafshdar and Novotný, Petr and Zárevúcky, Jiří and Zikelic, Dorde}, booktitle = {24th International Symposium on Formal Methods}, isbn = {9-783-0309-0869-0}, issn = {1611-3349}, location = {Virtual}, pages = {619--639}, publisher = {Springer Nature}, title = {{On lexicographic proof rules for probabilistic termination}}, doi = {10.1007/978-3-030-90870-6_33}, volume = {13047}, year = {2021}, } @article{14800, abstract = {Research on two-dimensional (2D) materials has been explosively increasing in last seventeen years in varying subjects including condensed matter physics, electronic engineering, materials science, and chemistry since the mechanical exfoliation of graphene in 2004. Starting from graphene, 2D materials now have become a big family with numerous members and diverse categories. The unique structural features and physicochemical properties of 2D materials make them one class of the most appealing candidates for a wide range of potential applications. In particular, we have seen some major breakthroughs made in the field of 2D materials in last five years not only in developing novel synthetic methods and exploring new structures/properties but also in identifying innovative applications and pushing forward commercialisation. In this review, we provide a critical summary on the recent progress made in the field of 2D materials with a particular focus on last five years. After a brief background introduction, we first discuss the major synthetic methods for 2D materials, including the mechanical exfoliation, liquid exfoliation, vapor phase deposition, and wet-chemical synthesis as well as phase engineering of 2D materials belonging to the field of phase engineering of nanomaterials (PEN). We then introduce the superconducting/optical/magnetic properties and chirality of 2D materials along with newly emerging magic angle 2D superlattices. Following that, the promising applications of 2D materials in electronics, optoelectronics, catalysis, energy storage, solar cells, biomedicine, sensors, environments, etc. are described sequentially. Thereafter, we present the theoretic calculations and simulations of 2D materials. Finally, after concluding the current progress, we provide some personal discussions on the existing challenges and future outlooks in this rapidly developing field. }, author = {Chang, Cheng and Chen, Wei and Chen, Ye and Chen, Yonghua and Chen, Yu and Ding, Feng and Fan, Chunhai and Fan, Hong Jin and Fan, Zhanxi and Gong, Cheng and Gong, Yongji and He, Qiyuan and Hong, Xun and Hu, Sheng and Hu, Weida and Huang, Wei and Huang, Yuan and Ji, Wei and Li, Dehui and Li, Lain Jong and Li, Qiang and Lin, Li and Ling, Chongyi and Liu, Minghua and Liu, Nan and Liu, Zhuang and Loh, Kian Ping and Ma, Jianmin and Miao, Feng and Peng, Hailin and Shao, Mingfei and Song, Li and Su, Shao and Sun, Shuo and Tan, Chaoliang and Tang, Zhiyong and Wang, Dingsheng and Wang, Huan and Wang, Jinlan and Wang, Xin and Wang, Xinran and Wee, Andrew T.S. and Wei, Zhongming and Wu, Yuen and Wu, Zhong Shuai and Xiong, Jie and Xiong, Qihua and Xu, Weigao and Yin, Peng and Zeng, Haibo and Zeng, Zhiyuan and Zhai, Tianyou and Zhang, Han and Zhang, Hui and Zhang, Qichun and Zhang, Tierui and Zhang, Xiang and Zhao, Li Dong and Zhao, Meiting and Zhao, Weijie and Zhao, Yunxuan and Zhou, Kai Ge and Zhou, Xing and Zhou, Yu and Zhu, Hongwei and Zhang, Hua and Liu, Zhongfan}, issn = {1001-4861}, journal = {Acta Physico-Chimica Sinica}, number = {12}, publisher = {Peking University}, title = {{Recent progress on two-dimensional materials}}, doi = {10.3866/PKU.WHXB202108017}, volume = {37}, year = {2021}, } @inproceedings{10206, abstract = {Neural-network classifiers achieve high accuracy when predicting the class of an input that they were trained to identify. Maintaining this accuracy in dynamic environments, where inputs frequently fall outside the fixed set of initially known classes, remains a challenge. The typical approach is to detect inputs from novel classes and retrain the classifier on an augmented dataset. However, not only the classifier but also the detection mechanism needs to adapt in order to distinguish between newly learned and yet unknown input classes. To address this challenge, we introduce an algorithmic framework for active monitoring of a neural network. A monitor wrapped in our framework operates in parallel with the neural network and interacts with a human user via a series of interpretable labeling queries for incremental adaptation. In addition, we propose an adaptive quantitative monitor to improve precision. An experimental evaluation on a diverse set of benchmarks with varying numbers of classes confirms the benefits of our active monitoring framework in dynamic scenarios.}, author = {Lukina, Anna and Schilling, Christian and Henzinger, Thomas A}, booktitle = {21st International Conference on Runtime Verification}, isbn = {9-783-0308-8493-2}, issn = {1611-3349}, keywords = {monitoring, neural networks, novelty detection}, location = {Virtual}, pages = {42--61}, publisher = {Springer Nature}, title = {{Into the unknown: active monitoring of neural networks}}, doi = {10.1007/978-3-030-88494-9_3}, volume = {12974 }, year = {2021}, } @article{14889, abstract = {We consider the Fröhlich Hamiltonian with large coupling constant α. For initial data of Pekar product form with coherent phonon field and with the electron minimizing the corresponding energy, we provide a norm approximation of the evolution, valid up to times of order α2. The approximation is given in terms of a Pekar product state, evolved through the Landau-Pekar equations, corrected by a Bogoliubov dynamics taking quantum fluctuations into account. This allows us to show that the Landau-Pekar equations approximately describe the evolution of the electron- and one-phonon reduced density matrices under the Fröhlich dynamics up to times of order α2.}, author = {Leopold, Nikolai K and Mitrouskas, David Johannes and Rademacher, Simone Anna Elvira and Schlein, Benjamin and Seiringer, Robert}, issn = {2578-5885}, journal = {Pure and Applied Analysis}, number = {4}, pages = {653--676}, publisher = {Mathematical Sciences Publishers}, title = {{Landau–Pekar equations and quantum fluctuations for the dynamics of a strongly coupled polaron}}, doi = {10.2140/paa.2021.3.653}, volume = {3}, year = {2021}, } @article{14890, abstract = {We consider a system of N interacting bosons in the mean-field scaling regime and construct corrections to the Bogoliubov dynamics that approximate the true N-body dynamics in norm to arbitrary precision. The N-independent corrections are given in terms of the solutions of the Bogoliubov and Hartree equations and satisfy a generalized form of Wick's theorem. We determine the n-point correlation functions of the excitations around the condensate, as well as the reduced densities of the N-body system, to arbitrary accuracy, given only the knowledge of the two-point functions of a quasi-free state and the solution of the Hartree equation. In this way, the complex problem of computing all n-point correlation functions for an interacting N-body system is essentially reduced to the problem of solving the Hartree equation and the PDEs for the Bogoliubov two-point functions.}, author = {Bossmann, Lea and Petrat, Sören P and Pickl, Peter and Soffer, Avy}, issn = {2578-5885}, journal = {Pure and Applied Analysis}, number = {4}, pages = {677--726}, publisher = {Mathematical Sciences Publishers}, title = {{Beyond Bogoliubov dynamics}}, doi = {10.2140/paa.2021.3.677}, volume = {3}, year = {2021}, } @article{15013, abstract = {We consider random n×n matrices X with independent and centered entries and a general variance profile. We show that the spectral radius of X converges with very high probability to the square root of the spectral radius of the variance matrix of X when n tends to infinity. We also establish the optimal rate of convergence, that is a new result even for general i.i.d. matrices beyond the explicitly solvable Gaussian cases. The main ingredient is the proof of the local inhomogeneous circular law [arXiv:1612.07776] at the spectral edge.}, author = {Alt, Johannes and Erdös, László and Krüger, Torben H}, issn = {2690-1005}, journal = {Probability and Mathematical Physics}, number = {2}, pages = {221--280}, publisher = {Mathematical Sciences Publishers}, title = {{Spectral radius of random matrices with independent entries}}, doi = {10.2140/pmp.2021.2.221}, volume = {2}, year = {2021}, } @article{9887, abstract = {Clathrin-mediated endocytosis is the major route of entry of cargos into cells and thus underpins many physiological processes. During endocytosis, an area of flat membrane is remodeled by proteins to create a spherical vesicle against intracellular forces. The protein machinery which mediates this membrane bending in plants is unknown. However, it is known that plant endocytosis is actin independent, thus indicating that plants utilize a unique mechanism to mediate membrane bending against high-turgor pressure compared to other model systems. Here, we investigate the TPLATE complex, a plant-specific endocytosis protein complex. It has been thought to function as a classical adaptor functioning underneath the clathrin coat. However, by using biochemical and advanced live microscopy approaches, we found that TPLATE is peripherally associated with clathrin-coated vesicles and localizes at the rim of endocytosis events. As this localization is more fitting to the protein machinery involved in membrane bending during endocytosis, we examined cells in which the TPLATE complex was disrupted and found that the clathrin structures present as flat patches. This suggests a requirement of the TPLATE complex for membrane bending during plant clathrin–mediated endocytosis. Next, we used in vitro biophysical assays to confirm that the TPLATE complex possesses protein domains with intrinsic membrane remodeling activity. These results redefine the role of the TPLATE complex and implicate it as a key component of the evolutionarily distinct plant endocytosis mechanism, which mediates endocytic membrane bending against the high-turgor pressure in plant cells.}, author = {Johnson, Alexander J and Dahhan, Dana A and Gnyliukh, Nataliia and Kaufmann, Walter and Zheden, Vanessa and Costanzo, Tommaso and Mahou, Pierre and Hrtyan, Mónika and Wang, Jie and Aguilera Servin, Juan L and van Damme, Daniël and Beaurepaire, Emmanuel and Loose, Martin and Bednarek, Sebastian Y and Friml, Jiří}, issn = {1091-6490}, journal = {Proceedings of the National Academy of Sciences}, number = {51}, publisher = {National Academy of Sciences}, title = {{The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis}}, doi = {10.1073/pnas.2113046118}, volume = {118}, year = {2021}, } @inbook{14984, abstract = {Hybrid zones are narrow geographic regions where different populations, races or interbreeding species meet and mate, producing mixed ‘hybrid’ offspring. They are relatively common and can be found in a diverse range of organisms and environments. The study of hybrid zones has played an important role in our understanding of the origin of species, with hybrid zones having been described as ‘natural laboratories’. This is because they allow us to study,in situ, the conditions and evolutionary forces that enable divergent taxa to remain distinct despite some ongoing gene exchange between them.}, author = {Stankowski, Sean and Shipilina, Daria and Westram, Anja M}, booktitle = {Encyclopedia of Life Sciences}, isbn = {9780470016176}, publisher = {Wiley}, title = {{Hybrid Zones}}, doi = {10.1002/9780470015902.a0029355}, volume = {2}, year = {2021}, } @inbook{14987, abstract = {The goal of zero-shot learning is to construct a classifier that can identify object classes for which no training examples are available. When training data for some of the object classes is available but not for others, the name generalized zero-shot learning is commonly used. In a wider sense, the phrase zero-shot is also used to describe other machine learning-based approaches that require no training data from the problem of interest, such as zero-shot action recognition or zero-shot machine translation.}, author = {Lampert, Christoph}, booktitle = {Computer Vision}, editor = {Ikeuchi, Katsushi}, isbn = {9783030634155}, pages = {1395--1397}, publisher = {Springer}, title = {{Zero-Shot Learning}}, doi = {10.1007/978-3-030-63416-2_874}, year = {2021}, } @misc{14988, abstract = {Raw data generated from the publication - The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis by Johnson et al., 2021 In PNAS}, author = {Johnson, Alexander J}, publisher = {Zenodo}, title = {{Raw data from Johnson et al, PNAS, 2021}}, doi = {10.5281/ZENODO.5747100}, year = {2021}, } @unpublished{10029, abstract = {Superconductor-semiconductor hybrids are platforms for realizing effective p-wave superconductivity. Spin-orbit coupling, combined with the proximity effect, causes the two-dimensional semiconductor to inherit p±ip intraband pairing, and application of magnetic field can then result in transitions to the normal state, partial Bogoliubov Fermi surfaces, or topological phases with Majorana modes. Experimentally probing the hybrid superconductor-semiconductor interface is challenging due to the shunting effect of the conventional superconductor. Consequently, the nature of induced pairing remains an open question. Here, we use the circuit quantum electrodynamics architecture to probe induced superconductivity in a two dimensional Al-InAs hybrid system. We observe a strong suppression of superfluid density and enhanced dissipation driven by magnetic field, which cannot be accounted for by the depairing theory of an s-wave superconductor. These observations are explained by a picture of independent intraband p±ip superconductors giving way to partial Bogoliubov Fermi surfaces, and allow for the first characterization of key properties of the hybrid superconducting system.}, author = {Phan, Duc T and Senior, Jorden L and Ghazaryan, Areg and Hatefipour, M. and Strickland, W. M. and Shabani, J. and Serbyn, Maksym and Higginbotham, Andrew P}, booktitle = {arXiv}, title = {{Breakdown of induced p±ip pairing in a superconductor-semiconductor hybrid}}, year = {2021}, } @misc{9291, abstract = {This .zip File contains the transport data for figures presented in the main text and supplementary material of "Enhancement of Proximity Induced Superconductivity in Planar Germanium" by K. Aggarwal, et. al. The measurements were done using Labber Software and the data is stored in the hdf5 file format. The files can be opened using either the Labber Log Browser (https://labber.org/overview/) or Labber Python API (http://labber.org/online-doc/api/LogFile.html).}, author = {Katsaros, Georgios}, publisher = {Institute of Science and Technology Austria}, title = {{Raw transport data for: Enhancement of proximity induced superconductivity in planar germanium}}, doi = {10.15479/AT:ISTA:9291}, year = {2021}, } @misc{9636, author = {Higginbotham, Andrew P}, publisher = {Institute of Science and Technology Austria}, title = {{Data for "Breakdown of induced p ± ip pairing in a superconductor-semiconductor hybrid"}}, year = {2021}, } @article{8910, abstract = {A semiconducting nanowire fully wrapped by a superconducting shell has been proposed as a platform for obtaining Majorana modes at small magnetic fields. In this study, we demonstrate that the appearance of subgap states in such structures is actually governed by the junction region in tunneling spectroscopy measurements and not the full-shell nanowire itself. Short tunneling regions never show subgap states, whereas longer junctions always do. This can be understood in terms of quantum dots forming in the junction and hosting Andreev levels in the Yu-Shiba-Rusinov regime. The intricate magnetic field dependence of the Andreev levels, through both the Zeeman and Little-Parks effects, may result in robust zero-bias peaks—features that could be easily misinterpreted as originating from Majorana zero modes but are unrelated to topological superconductivity.}, author = {Valentini, Marco and Peñaranda, Fernando and Hofmann, Andrea C and Brauns, Matthias and Hauschild, Robert and Krogstrup, Peter and San-Jose, Pablo and Prada, Elsa and Aguado, Ramón and Katsaros, Georgios}, issn = {10959203}, journal = {Science}, number = {6550}, publisher = {American Association for the Advancement of Science}, title = {{Nontopological zero-bias peaks in full-shell nanowires induced by flux-tunable Andreev states}}, doi = {10.1126/science.abf1513}, volume = {373}, year = {2021}, } @misc{9323, abstract = {This .zip File contains the data for figures presented in the main text and supplementary material of "A singlet triplet hole spin qubit in planar Ge" by D. Jirovec, et. al. The measurements were done using Labber Software and the data is stored in the hdf5 file format. The files can be opened using either the Labber Log Browser (https://labber.org/overview/) or Labber Python API (http://labber.org/online-doc/api/LogFile.html). A single file is acquired with QCodes and features the corresponding data type. XRD data are in .dat format and a code to open the data is provided. The code for simulations is as well provided in Python.}, author = {Jirovec, Daniel}, publisher = {Institute of Science and Technology Austria}, title = {{Research data for "A singlet-triplet hole spin qubit planar Ge"}}, doi = {10.15479/AT:ISTA:9323}, year = {2021}, } @misc{9389, abstract = {This .zip File contains the transport data for "Non-topological zero bias peaks in full-shell nanowires induced by flux tunable Andreev states" by M. Valentini, et. al. The measurements were done using Labber Software and the data is stored in the hdf5 file format. Instructions of how to read the data are in "Notebook_Valentini.pdf".}, author = {Valentini, Marco}, publisher = {Institute of Science and Technology Austria}, title = {{Research data for "Non-topological zero bias peaks in full-shell nanowires induced by flux tunable Andreev states"}}, doi = {10.15479/AT:ISTA:9389}, year = {2021}, } @article{10559, abstract = {Hole gases in planar germanium can have high mobilities in combination with strong spin-orbit interaction and electrically tunable g factors, and are therefore emerging as a promising platform for creating hybrid superconductor-semiconductor devices. A key challenge towards hybrid Ge-based quantum technologies is the design of high-quality interfaces and superconducting contacts that are robust against magnetic fields. In this work, by combining the assets of aluminum, which provides good contact to the Ge, and niobium, which has a significant superconducting gap, we demonstrate highly transparent low-disordered JoFETs with relatively large ICRN products that are capable of withstanding high magnetic fields. We furthermore demonstrate the ability of phase-biasing individual JoFETs, opening up an avenue to explore topological superconductivity in planar Ge. The persistence of superconductivity in the reported hybrid devices beyond 1.8 T paves the way towards integrating spin qubits and proximity-induced superconductivity on the same chip.}, author = {Aggarwal, Kushagra and Hofmann, Andrea C and Jirovec, Daniel and Prieto Gonzalez, Ivan and Sammak, Amir and Botifoll, Marc and Martí-Sánchez, Sara and Veldhorst, Menno and Arbiol, Jordi and Scappucci, Giordano and Danon, Jeroen and Katsaros, Georgios}, issn = {2643-1564}, journal = {Physical Review Research}, keywords = {general engineering}, number = {2}, publisher = {American Physical Society}, title = {{Enhancement of proximity-induced superconductivity in a planar Ge hole gas}}, doi = {10.1103/physrevresearch.3.l022005}, volume = {3}, year = {2021}, } @article{10166, abstract = {While sexual reproduction is widespread among many taxa, asexual lineages have repeatedly evolved from sexual ancestors. Despite extensive research on the evolution of sex, it is still unclear whether this switch represents a major transition requiring major molecular reorganization, and how convergent the changes involved are. In this study, we investigated the phylogenetic relationship and patterns of gene expression of sexual and asexual lineages of Eurasian Artemia brine shrimp, to assess how gene expression patterns are affected by the transition to asexuality. We find only a few genes that are consistently associated with the evolution of asexuality, suggesting that this shift may not require an extensive overhauling of the meiotic machinery. While genes with sex-biased expression have high rates of expression divergence within Eurasian Artemia, neither female- nor male-biased genes appear to show unusual evolutionary patterns after sexuality is lost, contrary to theoretical expectations.}, author = {Huylmans, Ann K and Macon, Ariana and Hontoria, Francisco and Vicoso, Beatriz}, issn = {1471-2954}, journal = {Proceedings of the Royal Society B: Biological Sciences}, keywords = {asexual reproduction, parthenogenesis, sex-biased genes, sexual conflict, automixis, crustaceans}, number = {1959}, publisher = {The Royal Society}, title = {{Transitions to asexuality and evolution of gene expression in Artemia brine shrimp}}, doi = {10.1098/rspb.2021.1720}, volume = {288}, year = {2021}, } @misc{9192, abstract = {Here are the research data underlying the publication " Effects of fine-scale population structure on inbreeding in a long-term study of snapdragons (Antirrhinum majus)." Further information are summed up in the README document.}, author = {Surendranadh, Parvathy and Arathoon, Louise S and Baskett, Carina and Field, David and Pickup, Melinda and Barton, Nicholas H}, publisher = {Institute of Science and Technology Austria}, title = {{Effects of fine-scale population structure on the distribution of heterozygosity in a long-term study of Antirrhinum majus}}, doi = {10.15479/AT:ISTA:9192}, year = {2021}, } @misc{9949, author = {Vicoso, Beatriz}, publisher = {Institute of Science and Technology Austria}, title = {{Data from Hyulmans et al 2021, "Transitions to asexuality and evolution of gene expression in Artemia brine shrimp"}}, doi = {10.15479/AT:ISTA:9949}, year = {2021}, } @article{8997, abstract = {Phenomenological relations such as Ohm’s or Fourier’s law have a venerable history in physics but are still scarce in biology. This situation restrains predictive theory. Here, we build on bacterial “growth laws,” which capture physiological feedback between translation and cell growth, to construct a minimal biophysical model for the combined action of ribosome-targeting antibiotics. Our model predicts drug interactions like antagonism or synergy solely from responses to individual drugs. We provide analytical results for limiting cases, which agree well with numerical results. We systematically refine the model by including direct physical interactions of different antibiotics on the ribosome. In a limiting case, our model provides a mechanistic underpinning for recent predictions of higher-order interactions that were derived using entropy maximization. We further refine the model to include the effects of antibiotics that mimic starvation and the presence of resistance genes. We describe the impact of a starvation-mimicking antibiotic on drug interactions analytically and verify it experimentally. Our extended model suggests a change in the type of drug interaction that depends on the strength of resistance, which challenges established rescaling paradigms. We experimentally show that the presence of unregulated resistance genes can lead to altered drug interaction, which agrees with the prediction of the model. While minimal, the model is readily adaptable and opens the door to predicting interactions of second and higher-order in a broad range of biological systems.}, author = {Kavcic, Bor and Tkačik, Gašper and Bollenbach, Tobias}, issn = {1553-7358}, journal = {PLOS Computational Biology}, keywords = {Modelling and Simulation, Genetics, Molecular Biology, Antibiotics, Drug interactions}, publisher = {Public Library of Science}, title = {{Minimal biophysical model of combined antibiotic action}}, doi = {10.1371/journal.pcbi.1008529}, volume = {17}, year = {2021}, } @article{9283, abstract = {Gene expression levels are influenced by multiple coexisting molecular mechanisms. Some of these interactions such as those of transcription factors and promoters have been studied extensively. However, predicting phenotypes of gene regulatory networks (GRNs) remains a major challenge. Here, we use a well-defined synthetic GRN to study in Escherichia coli how network phenotypes depend on local genetic context, i.e. the genetic neighborhood of a transcription factor and its relative position. We show that one GRN with fixed topology can display not only quantitatively but also qualitatively different phenotypes, depending solely on the local genetic context of its components. Transcriptional read-through is the main molecular mechanism that places one transcriptional unit (TU) within two separate regulons without the need for complex regulatory sequences. We propose that relative order of individual TUs, with its potential for combinatorial complexity, plays an important role in shaping phenotypes of GRNs.}, author = {Nagy-Staron, Anna A and Tomasek, Kathrin and Caruso Carter, Caroline and Sonnleitner, Elisabeth and Kavcic, Bor and Paixão, Tiago and Guet, Calin C}, issn = {2050-084X}, journal = {eLife}, keywords = {Genetics and Molecular Biology}, publisher = {eLife Sciences Publications}, title = {{Local genetic context shapes the function of a gene regulatory network}}, doi = {10.7554/elife.65993}, volume = {10}, year = {2021}, } @article{10184, abstract = {We introduce a novel technique to automatically decompose an input object’s volume into a set of parts that can be represented by two opposite height fields. Such decomposition enables the manufacturing of individual parts using two-piece reusable rigid molds. Our decomposition strategy relies on a new energy formulation that utilizes a pre-computed signal on the mesh volume representing the accessibility for a predefined set of extraction directions. Thanks to this novel formulation, our method allows for efficient optimization of a fabrication-aware partitioning of volumes in a completely automatic way. We demonstrate the efficacy of our approach by generating valid volume partitionings for a wide range of complex objects and physically reproducing several of them.}, author = {Alderighi, Thomas and Malomo, Luigi and Bickel, Bernd and Cignoni, Paolo and Pietroni, Nico}, issn = {1557-7368 }, journal = {ACM Transactions on Graphics}, number = {6}, publisher = {Association for Computing Machinery}, title = {{Volume decomposition for two-piece rigid casting}}, doi = {10.1145/3478513.3480555}, volume = {40}, year = {2021}, } @article{9541, abstract = {The Massively Parallel Computation (MPC) model is an emerging model that distills core aspects of distributed and parallel computation, developed as a tool to solve combinatorial (typically graph) problems in systems of many machines with limited space. Recent work has focused on the regime in which machines have sublinear (in n, the number of nodes in the input graph) space, with randomized algorithms presented for the fundamental problems of Maximal Matching and Maximal Independent Set. However, there have been no prior corresponding deterministic algorithms. A major challenge underlying the sublinear space setting is that the local space of each machine might be too small to store all edges incident to a single node. This poses a considerable obstacle compared to classical models in which each node is assumed to know and have easy access to its incident edges. To overcome this barrier, we introduce a new graph sparsification technique that deterministically computes a low-degree subgraph, with the additional property that solving the problem on this subgraph provides significant progress towards solving the problem for the original input graph. Using this framework to derandomize the well-known algorithm of Luby [SICOMP’86], we obtain O(log Δ + log log n)-round deterministic MPC algorithms for solving the problems of Maximal Matching and Maximal Independent Set with O(nɛ) space on each machine for any constant ɛ > 0. These algorithms also run in O(log Δ) rounds in the closely related model of CONGESTED CLIQUE, improving upon the state-of-the-art bound of O(log 2Δ) rounds by Censor-Hillel et al. [DISC’17].}, author = {Czumaj, Artur and Davies, Peter and Parter, Merav}, issn = {1549-6333}, journal = {ACM Transactions on Algorithms}, number = {2}, publisher = {Association for Computing Machinery}, title = {{Graph sparsification for derandomizing massively parallel computation with low space}}, doi = {10.1145/3451992}, volume = {17}, year = {2021}, } @article{10134, abstract = {We investigate the effect of coupling between translational and internal degrees of freedom of composite quantum particles on their localization in a random potential. We show that entanglement between the two degrees of freedom weakens localization due to the upper bound imposed on the inverse participation ratio by purity of a quantum state. We perform numerical calculations for a two-particle system bound by a harmonic force in a 1D disordered lattice and a rigid rotor in a 2D disordered lattice. We illustrate that the coupling has a dramatic effect on localization properties, even with a small number of internal states participating in quantum dynamics.}, author = {Suzuki, Fumika and Lemeshko, Mikhail and Zurek, Wojciech H. and Krems, Roman V.}, issn = {1079-7114}, journal = {Physical Review Letters}, keywords = {General Physics and Astronomy}, number = {16}, publisher = {American Physical Society }, title = {{Anderson localization of composite particles}}, doi = {10.1103/physrevlett.127.160602}, volume = {127}, year = {2021}, } @inproceedings{9678, abstract = {We introduce a new graph problem, the token dropping game, and we show how to solve it efficiently in a distributed setting. We use the token dropping game as a tool to design an efficient distributed algorithm for stable orientations and more generally for locally optimal semi-matchings. The prior work by Czygrinow et al. (DISC 2012) finds a stable orientation in O(Δ^5) rounds in graphs of maximum degree Δ, while we improve it to O(Δ^4) and also prove a lower bound of Ω(Δ). For the more general problem of locally optimal semi-matchings, the prior upper bound is O(S^5) and our new algorithm runs in O(C · S^4) rounds, which is an improvement for C = o(S); here C and S are the maximum degrees of customers and servers, respectively.}, author = {Brandt, Sebastian and Keller, Barbara and Rybicki, Joel and Suomela, Jukka and Uitto, Jara}, booktitle = {Annual ACM Symposium on Parallelism in Algorithms and Architectures}, isbn = {9781450380706}, location = { Virtual Event, United States}, pages = {129--139}, title = {{Efficient load-balancing through distributed token dropping}}, doi = {10.1145/3409964.3461785}, year = {2021}, } @article{8286, abstract = {We consider the following dynamic load-balancing process: given an underlying graph G with n nodes, in each step t≥ 0, one unit of load is created, and placed at a randomly chosen graph node. In the same step, the chosen node picks a random neighbor, and the two nodes balance their loads by averaging them. We are interested in the expected gap between the minimum and maximum loads at nodes as the process progresses, and its dependence on n and on the graph structure. Variants of the above graphical balanced allocation process have been studied previously by Peres, Talwar, and Wieder [Peres et al., 2015], and by Sauerwald and Sun [Sauerwald and Sun, 2015]. These authors left as open the question of characterizing the gap in the case of cycle graphs in the dynamic case, where weights are created during the algorithm’s execution. For this case, the only known upper bound is of 𝒪(n log n), following from a majorization argument due to [Peres et al., 2015], which analyzes a related graphical allocation process. In this paper, we provide an upper bound of 𝒪 (√n log n) on the expected gap of the above process for cycles of length n. We introduce a new potential analysis technique, which enables us to bound the difference in load between k-hop neighbors on the cycle, for any k ≤ n/2. We complement this with a "gap covering" argument, which bounds the maximum value of the gap by bounding its value across all possible subsets of a certain structure, and recursively bounding the gaps within each subset. We provide analytical and experimental evidence that our upper bound on the gap is tight up to a logarithmic factor. }, author = {Alistarh, Dan-Adrian and Nadiradze, Giorgi and Sabour, Amirmojtaba}, issn = {1432-0541}, journal = {Algorithmica}, location = {Virtual, Online; Germany}, publisher = {Springer Nature}, title = {{Dynamic averaging load balancing on cycles}}, doi = {10.1007/s00453-021-00905-9}, year = {2021}, } @phdthesis{9733, abstract = {This thesis is the result of the research carried out by the author during his PhD at IST Austria between 2017 and 2021. It mainly focuses on the Fröhlich polaron model, specifically to its regime of strong coupling. This model, which is rigorously introduced and discussed in the introduction, has been of great interest in condensed matter physics and field theory for more than eighty years. It is used to describe an electron interacting with the atoms of a solid material (the strength of this interaction is modeled by the presence of a coupling constant α in the Hamiltonian of the system). The particular regime examined here, which is mathematically described by considering the limit α →∞, displays many interesting features related to the emergence of classical behavior, which allows for a simplified effective description of the system under analysis. The properties, the range of validity and a quantitative analysis of the precision of such classical approximations are the main object of the present work. We specify our investigation to the study of the ground state energy of the system, its dynamics and its effective mass. For each of these problems, we provide in the introduction an overview of the previously known results and a detailed account of the original contributions by the author.}, author = {Feliciangeli, Dario}, issn = {2663-337X}, pages = {180}, publisher = {Institute of Science and Technology Austria}, title = {{The polaron at strong coupling}}, doi = {10.15479/at:ista:9733}, year = {2021}, } @article{9571, abstract = {As the size and complexity of models and datasets grow, so does the need for communication-efficient variants of stochastic gradient descent that can be deployed to perform parallel model training. One popular communication-compression method for data-parallel SGD is QSGD (Alistarh et al., 2017), which quantizes and encodes gradients to reduce communication costs. The baseline variant of QSGD provides strong theoretical guarantees, however, for practical purposes, the authors proposed a heuristic variant which we call QSGDinf, which demonstrated impressive empirical gains for distributed training of large neural networks. In this paper, we build on this work to propose a new gradient quantization scheme, and show that it has both stronger theoretical guarantees than QSGD, and matches and exceeds the empirical performance of the QSGDinf heuristic and of other compression methods.}, author = {Ramezani-Kebrya, Ali and Faghri, Fartash and Markov, Ilya and Aksenov, Vitalii and Alistarh, Dan-Adrian and Roy, Daniel M.}, issn = {15337928}, journal = {Journal of Machine Learning Research}, number = {114}, pages = {1−43}, publisher = {Journal of Machine Learning Research}, title = {{NUQSGD: Provably communication-efficient data-parallel SGD via nonuniform quantization}}, volume = {22}, year = {2021}, } @article{8544, abstract = {The synaptotrophic hypothesis posits that synapse formation stabilizes dendritic branches, yet this hypothesis has not been causally tested in vivo in the mammalian brain. Presynaptic ligand cerebellin-1 (Cbln1) and postsynaptic receptor GluD2 mediate synaptogenesis between granule cells and Purkinje cells in the molecular layer of the cerebellar cortex. Here we show that sparse but not global knockout of GluD2 causes under-elaboration of Purkinje cell dendrites in the deep molecular layer and overelaboration in the superficial molecular layer. Developmental, overexpression, structure-function, and genetic epistasis analyses indicate that dendrite morphogenesis defects result from competitive synaptogenesis in a Cbln1/GluD2-dependent manner. A generative model of dendritic growth based on competitive synaptogenesis largely recapitulates GluD2 sparse and global knockout phenotypes. Our results support the synaptotrophic hypothesis at initial stages of dendrite development, suggest a second mode in which cumulative synapse formation inhibits further dendrite growth, and highlight the importance of competition in dendrite morphogenesis.}, author = {Takeo, Yukari H. and Shuster, S. Andrew and Jiang, Linnie and Hu, Miley and Luginbuhl, David J. and Rülicke, Thomas and Contreras, Ximena and Hippenmeyer, Simon and Wagner, Mark J. and Ganguli, Surya and Luo, Liqun}, issn = {1097-4199}, journal = {Neuron}, number = {4}, pages = {P629--644.E8}, publisher = {Elsevier}, title = {{GluD2- and Cbln1-mediated competitive synaptogenesis shapes the dendritic arbors of cerebellar Purkinje cells}}, doi = {10.1016/j.neuron.2020.11.028}, volume = {109}, year = {2021}, } @unpublished{9791, abstract = {We provide a definition of the effective mass for the classical polaron described by the Landau-Pekar equations. It is based on a novel variational principle, minimizing the energy functional over states with given (initial) velocity. The resulting formula for the polaron's effective mass agrees with the prediction by Landau and Pekar.}, author = {Feliciangeli, Dario and Rademacher, Simone Anna Elvira and Seiringer, Robert}, booktitle = {arXiv}, title = {{The effective mass problem for the Landau-Pekar equations}}, year = {2021}, } @article{7553, abstract = {Normative theories and statistical inference provide complementary approaches for the study of biological systems. A normative theory postulates that organisms have adapted to efficiently solve essential tasks, and proceeds to mathematically work out testable consequences of such optimality; parameters that maximize the hypothesized organismal function can be derived ab initio, without reference to experimental data. In contrast, statistical inference focuses on efficient utilization of data to learn model parameters, without reference to any a priori notion of biological function, utility, or fitness. Traditionally, these two approaches were developed independently and applied separately. Here we unify them in a coherent Bayesian framework that embeds a normative theory into a family of maximum-entropy “optimization priors.” This family defines a smooth interpolation between a data-rich inference regime (characteristic of “bottom-up” statistical models), and a data-limited ab inito prediction regime (characteristic of “top-down” normative theory). We demonstrate the applicability of our framework using data from the visual cortex, and argue that the flexibility it affords is essential to address a number of fundamental challenges relating to inference and prediction in complex, high-dimensional biological problems.}, author = {Mlynarski, Wiktor F and Hledik, Michal and Sokolowski, Thomas R and Tkačik, Gašper}, journal = {Neuron}, number = {7}, pages = {1227--1241.e5}, publisher = {Cell Press}, title = {{Statistical analysis and optimality of neural systems}}, doi = {10.1016/j.neuron.2021.01.020}, volume = {109}, year = {2021}, } @inproceedings{10598, abstract = { We consider the problem of estimating a signal from measurements obtained via a generalized linear model. We focus on estimators based on approximate message passing (AMP), a family of iterative algorithms with many appealing features: the performance of AMP in the high-dimensional limit can be succinctly characterized under suitable model assumptions; AMP can also be tailored to the empirical distribution of the signal entries, and for a wide class of estimation problems, AMP is conjectured to be optimal among all polynomial-time algorithms. However, a major issue of AMP is that in many models (such as phase retrieval), it requires an initialization correlated with the ground-truth signal and independent from the measurement matrix. Assuming that such an initialization is available is typically not realistic. In this paper, we solve this problem by proposing an AMP algorithm initialized with a spectral estimator. With such an initialization, the standard AMP analysis fails since the spectral estimator depends in a complicated way on the design matrix. Our main contribution is a rigorous characterization of the performance of AMP with spectral initialization in the high-dimensional limit. The key technical idea is to define and analyze a two-phase artificial AMP algorithm that first produces the spectral estimator, and then closely approximates the iterates of the true AMP. We also provide numerical results that demonstrate the validity of the proposed approach. }, author = {Mondelli, Marco and Venkataramanan, Ramji}, booktitle = {Proceedings of The 24th International Conference on Artificial Intelligence and Statistics}, editor = {Banerjee, Arindam and Fukumizu, Kenji}, issn = {2640-3498}, location = {Virtual, San Diego, CA, United States}, pages = {397--405}, publisher = {ML Research Press}, title = {{Approximate message passing with spectral initialization for generalized linear models}}, volume = {130}, year = {2021}, } @article{8196, abstract = {This paper aims to obtain a strong convergence result for a Douglas–Rachford splitting method with inertial extrapolation step for finding a zero of the sum of two set-valued maximal monotone operators without any further assumption of uniform monotonicity on any of the involved maximal monotone operators. Furthermore, our proposed method is easy to implement and the inertial factor in our proposed method is a natural choice. Our method of proof is of independent interest. Finally, some numerical implementations are given to confirm the theoretical analysis.}, author = {Shehu, Yekini and Dong, Qiao-Li and Liu, Lu-Lu and Yao, Jen-Chih}, issn = {1573-2924}, journal = {Optimization and Engineering}, pages = {2627--2653}, publisher = {Springer Nature}, title = {{New strong convergence method for the sum of two maximal monotone operators}}, doi = {10.1007/s11081-020-09544-5}, volume = {22}, year = {2021}, } @article{8911, abstract = {In the worldwide endeavor for disruptive quantum technologies, germanium is emerging as a versatile material to realize devices capable of encoding, processing, or transmitting quantum information. These devices leverage special properties of the germanium valence-band states, commonly known as holes, such as their inherently strong spin-orbit coupling and the ability to host superconducting pairing correlations. In this Review, we initially introduce the physics of holes in low-dimensional germanium structures with key insights from a theoretical perspective. We then examine the material science progress underpinning germanium-based planar heterostructures and nanowires. We review the most significant experimental results demonstrating key building blocks for quantum technology, such as an electrically driven universal quantum gate set with spin qubits in quantum dots and superconductor-semiconductor devices for hybrid quantum systems. We conclude by identifying the most promising prospects toward scalable quantum information processing. }, author = {Scappucci, Giordano and Kloeffel, Christoph and Zwanenburg, Floris A. and Loss, Daniel and Myronov, Maksym and Zhang, Jian-Jun and Franceschi, Silvano De and Katsaros, Georgios and Veldhorst, Menno}, issn = {2058-8437}, journal = {Nature Reviews Materials}, pages = {926–943 }, publisher = {Springer Nature}, title = {{The germanium quantum information route}}, doi = {10.1038/s41578-020-00262-z}, volume = {6}, year = {2021}, } @article{8338, abstract = {Canonical parametrisations of classical confocal coordinate systems are introduced and exploited to construct non-planar analogues of incircular (IC) nets on individual quadrics and systems of confocal quadrics. Intimate connections with classical deformations of quadrics that are isometric along asymptotic lines and circular cross-sections of quadrics are revealed. The existence of octahedral webs of surfaces of Blaschke type generated by asymptotic and characteristic lines that are diagonally related to lines of curvature is proved theoretically and established constructively. Appropriate samplings (grids) of these webs lead to three-dimensional extensions of non-planar IC nets. Three-dimensional octahedral grids composed of planes and spatially extending (checkerboard) IC-nets are shown to arise in connection with systems of confocal quadrics in Minkowski space. In this context, the Laguerre geometric notion of conical octahedral grids of planes is introduced. The latter generalise the octahedral grids derived from systems of confocal quadrics in Minkowski space. An explicit construction of conical octahedral grids is presented. The results are accompanied by various illustrations which are based on the explicit formulae provided by the theory.}, author = {Akopyan, Arseniy and Bobenko, Alexander I. and Schief, Wolfgang K. and Techter, Jan}, issn = {1432-0444}, journal = {Discrete and Computational Geometry}, pages = {938--976}, publisher = {Springer Nature}, title = {{On mutually diagonal nets on (confocal) quadrics and 3-dimensional webs}}, doi = {10.1007/s00454-020-00240-w}, volume = {66}, year = {2021}, } @article{7939, abstract = {We design fast deterministic algorithms for distance computation in the Congested Clique model. Our key contributions include: A (2+ϵ)-approximation for all-pairs shortest paths in O(log2n/ϵ) rounds on unweighted undirected graphs. With a small additional additive factor, this also applies for weighted graphs. This is the first sub-polynomial constant-factor approximation for APSP in this model. A (1+ϵ)-approximation for multi-source shortest paths from O(n−−√) sources in O(log2n/ϵ) rounds on weighted undirected graphs. This is the first sub-polynomial algorithm obtaining this approximation for a set of sources of polynomial size. Our main techniques are new distance tools that are obtained via improved algorithms for sparse matrix multiplication, which we leverage to construct efficient hopsets and shortest paths. Furthermore, our techniques extend to additional distance problems for which we improve upon the state-of-the-art, including diameter approximation, and an exact single-source shortest paths algorithm for weighted undirected graphs in O~(n1/6) rounds. }, author = {Censor-Hillel, Keren and Dory, Michal and Korhonen, Janne and Leitersdorf, Dean}, issn = {1432-0452}, journal = {Distributed Computing}, pages = {463--487}, publisher = {Springer Nature}, title = {{Fast approximate shortest paths in the congested clique}}, doi = {10.1007/s00446-020-00380-5}, volume = {34}, year = {2021}, } @article{8248, abstract = {We consider the following setting: suppose that we are given a manifold M in Rd with positive reach. Moreover assume that we have an embedded simplical complex A without boundary, whose vertex set lies on the manifold, is sufficiently dense and such that all simplices in A have sufficient quality. We prove that if, locally, interiors of the projection of the simplices onto the tangent space do not intersect, then A is a triangulation of the manifold, that is, they are homeomorphic.}, author = {Boissonnat, Jean-Daniel and Dyer, Ramsay and Ghosh, Arijit and Lieutier, Andre and Wintraecken, Mathijs}, issn = {1432-0444}, journal = {Discrete and Computational Geometry}, pages = {666--686}, publisher = {Springer Nature}, title = {{Local conditions for triangulating submanifolds of Euclidean space}}, doi = {10.1007/s00454-020-00233-9}, volume = {66}, year = {2021}, } @article{9002, abstract = { We prove that, for the binary erasure channel (BEC), the polar-coding paradigm gives rise to codes that not only approach the Shannon limit but do so under the best possible scaling of their block length as a function of the gap to capacity. This result exhibits the first known family of binary codes that attain both optimal scaling and quasi-linear complexity of encoding and decoding. Our proof is based on the construction and analysis of binary polar codes with large kernels. When communicating reliably at rates within ε>0 of capacity, the code length n often scales as O(1/εμ), where the constant μ is called the scaling exponent. It is known that the optimal scaling exponent is μ=2, and it is achieved by random linear codes. The scaling exponent of conventional polar codes (based on the 2×2 kernel) on the BEC is μ=3.63. This falls far short of the optimal scaling guaranteed by random codes. Our main contribution is a rigorous proof of the following result: for the BEC, there exist ℓ×ℓ binary kernels, such that polar codes constructed from these kernels achieve scaling exponent μ(ℓ) that tends to the optimal value of 2 as ℓ grows. We furthermore characterize precisely how large ℓ needs to be as a function of the gap between μ(ℓ) and 2. The resulting binary codes maintain the recursive structure of conventional polar codes, and thereby achieve construction complexity O(n) and encoding/decoding complexity O(nlogn).}, author = {Fazeli, Arman and Hassani, Hamed and Mondelli, Marco and Vardy, Alexander}, issn = {1557-9654}, journal = {IEEE Transactions on Information Theory}, number = {9}, pages = {5693--5710}, publisher = {IEEE}, title = {{Binary linear codes with optimal scaling: Polar codes with large kernels}}, doi = {10.1109/TIT.2020.3038806}, volume = {67}, year = {2021}, } @article{7883, abstract = {All vertebrates have a spinal cord with dimensions and shape specific to their species. Yet how species‐specific organ size and shape are achieved is a fundamental unresolved question in biology. The formation and sculpting of organs begins during embryonic development. As it develops, the spinal cord extends in anterior–posterior direction in synchrony with the overall growth of the body. The dorsoventral (DV) and apicobasal lengths of the spinal cord neuroepithelium also change, while at the same time a characteristic pattern of neural progenitor subtypes along the DV axis is established and elaborated. At the basis of these changes in tissue size and shape are biophysical determinants, such as the change in cell number, cell size and shape, and anisotropic tissue growth. These processes are controlled by global tissue‐scale regulators, such as morphogen signaling gradients as well as mechanical forces. Current challenges in the field are to uncover how these tissue‐scale regulatory mechanisms are translated to the cellular and molecular level, and how regulation of distinct cellular processes gives rise to an overall defined size. Addressing these questions will help not only to achieve a better understanding of how size is controlled, but also of how tissue size is coordinated with the specification of pattern.}, author = {Kuzmicz-Kowalska, Katarzyna and Kicheva, Anna}, issn = {17597692}, journal = {Wiley Interdisciplinary Reviews: Developmental Biology}, publisher = {Wiley}, title = {{Regulation of size and scale in vertebrate spinal cord development}}, doi = {10.1002/wdev.383}, year = {2021}, } @article{7905, abstract = {We investigate a sheaf-theoretic interpretation of stratification learning from geometric and topological perspectives. Our main result is the construction of stratification learning algorithms framed in terms of a sheaf on a partially ordered set with the Alexandroff topology. We prove that the resulting decomposition is the unique minimal stratification for which the strata are homogeneous and the given sheaf is constructible. In particular, when we choose to work with the local homology sheaf, our algorithm gives an alternative to the local homology transfer algorithm given in Bendich et al. (Proceedings of the 23rd Annual ACM-SIAM Symposium on Discrete Algorithms, pp. 1355–1370, ACM, New York, 2012), and the cohomology stratification algorithm given in Nanda (Found. Comput. Math. 20(2), 195–222, 2020). Additionally, we give examples of stratifications based on the geometric techniques of Breiding et al. (Rev. Mat. Complut. 31(3), 545–593, 2018), illustrating how the sheaf-theoretic approach can be used to study stratifications from both topological and geometric perspectives. This approach also points toward future applications of sheaf theory in the study of topological data analysis by illustrating the utility of the language of sheaf theory in generalizing existing algorithms.}, author = {Brown, Adam and Wang, Bei}, issn = {1432-0444}, journal = {Discrete and Computational Geometry}, pages = {1166--1198}, publisher = {Springer Nature}, title = {{Sheaf-theoretic stratification learning from geometric and topological perspectives}}, doi = {10.1007/s00454-020-00206-y}, volume = {65}, year = {2021}, } @article{8601, abstract = {We consider large non-Hermitian real or complex random matrices X with independent, identically distributed centred entries. We prove that their local eigenvalue statistics near the spectral edge, the unit circle, coincide with those of the Ginibre ensemble, i.e. when the matrix elements of X are Gaussian. This result is the non-Hermitian counterpart of the universality of the Tracy–Widom distribution at the spectral edges of the Wigner ensemble.}, author = {Cipolloni, Giorgio and Erdös, László and Schröder, Dominik J}, issn = {14322064}, journal = {Probability Theory and Related Fields}, publisher = {Springer Nature}, title = {{Edge universality for non-Hermitian random matrices}}, doi = {10.1007/s00440-020-01003-7}, year = {2021}, } @article{7925, abstract = {In this paper, we introduce a relaxed CQ method with alternated inertial step for solving split feasibility problems. We give convergence of the sequence generated by our method under some suitable assumptions. Some numerical implementations from sparse signal and image deblurring are reported to show the efficiency of our method.}, author = {Shehu, Yekini and Gibali, Aviv}, issn = {1862-4480}, journal = {Optimization Letters}, pages = {2109--2126}, publisher = {Springer Nature}, title = {{New inertial relaxed method for solving split feasibilities}}, doi = {10.1007/s11590-020-01603-1}, volume = {15}, year = {2021}, } @article{9438, abstract = {Rigorous investigation of synaptic transmission requires analysis of unitary synaptic events by simultaneous recording from presynaptic terminals and postsynaptic target neurons. However, this has been achieved at only a limited number of model synapses, including the squid giant synapse and the mammalian calyx of Held. Cortical presynaptic terminals have been largely inaccessible to direct presynaptic recording, due to their small size. Here, we describe a protocol for improved subcellular patch-clamp recording in rat and mouse brain slices, with the synapse in a largely intact environment. Slice preparation takes ~2 h, recording ~3 h and post hoc morphological analysis 2 d. Single presynaptic hippocampal mossy fiber terminals are stimulated minimally invasively in the bouton-attached configuration, in which the cytoplasmic content remains unperturbed, or in the whole-bouton configuration, in which the cytoplasmic composition can be precisely controlled. Paired pre–postsynaptic recordings can be integrated with biocytin labeling and morphological analysis, allowing correlative investigation of synapse structure and function. Paired recordings can be obtained from mossy fiber terminals in slices from both rats and mice, implying applicability to genetically modified synapses. Paired recordings can also be performed together with axon tract stimulation or optogenetic activation, allowing comparison of unitary and compound synaptic events in the same target cell. Finally, paired recordings can be combined with spontaneous event analysis, permitting collection of miniature events generated at a single identified synapse. In conclusion, the subcellular patch-clamp techniques detailed here should facilitate analysis of biophysics, plasticity and circuit function of cortical synapses in the mammalian central nervous system.}, author = {Vandael, David H and Okamoto, Yuji and Borges Merjane, Carolina and Vargas Barroso, Victor M and Suter, Benjamin and Jonas, Peter M}, issn = {17502799}, journal = {Nature Protocols}, number = {6}, pages = {2947–2967}, publisher = {Springer Nature}, title = {{Subcellular patch-clamp techniques for single-bouton stimulation and simultaneous pre- and postsynaptic recording at cortical synapses}}, doi = {10.1038/s41596-021-00526-0}, volume = {16}, year = {2021}, } @phdthesis{9992, abstract = {Blood – this is what animals use to heal wounds fast and efficient. Plants do not have blood circulation and their cells cannot move. However, plants have evolved remarkable capacities to regenerate tissues and organs preventing further damage. In my PhD research, I studied the wound healing in the Arabidopsis root. I used a UV laser to ablate single cells in the root tip and observed the consequent wound healing. Interestingly, the inner adjacent cells induced a division plane switch and subsequently adopted the cell type of the killed cell to replace it. We termed this form of wound healing “restorative divisions”. This initial observation triggered the questions of my PhD studies: How and why do cells orient their division planes, how do they feel the wound and why does this happen only in inner adjacent cells. For answering these questions, I used a quite simple experimental setup: 5 day - old seedlings were stained with propidium iodide to visualize cell walls and dead cells; ablation was carried out using a special laser cutter and a confocal microscope. Adaptation of the novel vertical microscope system made it possible to observe wounds in real time. This revealed that restorative divisions occur at increased frequency compared to normal divisions. Additionally, the major plant hormone auxin accumulates in wound adjacent cells and drives the expression of the wound-stress responsive transcription factor ERF115. Using this as a marker gene for wound responses, we found that an important part of wound signalling is the sensing of the collapse of the ablated cell. The collapse causes a radical pressure drop, which results in strong tissue deformations. These deformations manifest in an invasion of the now free spot specifically by the inner adjacent cells within seconds, probably because of higher pressure of the inner tissues. Long-term imaging revealed that those deformed cells continuously expand towards the wound hole and that this is crucial for the restorative division. These wound-expanding cells exhibit an abnormal, biphasic polarity of microtubule arrays before the division. Experiments inhibiting cell expansion suggest that it is the biphasic stretching that induces those MT arrays. Adapting the micromanipulator aspiration system from animal scientists at our institute confirmed the hypothesis that stretching influences microtubule stability. In conclusion, this shows that microtubules react to tissue deformation and this facilitates the observed division plane switch. This puts mechanical cues and tensions at the most prominent position for explaining the growth and wound healing properties of plants. Hence, it shines light onto the importance of understanding mechanical signal transduction. }, author = {Hörmayer, Lukas}, issn = {2663-337X}, pages = {168}, publisher = {Institute of Science and Technology Austria}, title = {{Wound healing in the Arabidopsis root meristem}}, doi = {10.15479/at:ista:9992}, year = {2021}, } @article{10816, abstract = {Pattern separation is a fundamental brain computation that converts small differences in input patterns into large differences in output patterns. Several synaptic mechanisms of pattern separation have been proposed, including code expansion, inhibition and plasticity; however, which of these mechanisms play a role in the entorhinal cortex (EC)–dentate gyrus (DG)–CA3 circuit, a classical pattern separation circuit, remains unclear. Here we show that a biologically realistic, full-scale EC–DG–CA3 circuit model, including granule cells (GCs) and parvalbumin-positive inhibitory interneurons (PV+-INs) in the DG, is an efficient pattern separator. Both external gamma-modulated inhibition and internal lateral inhibition mediated by PV+-INs substantially contributed to pattern separation. Both local connectivity and fast signaling at GC–PV+-IN synapses were important for maximum effectiveness. Similarly, mossy fiber synapses with conditional detonator properties contributed to pattern separation. By contrast, perforant path synapses with Hebbian synaptic plasticity and direct EC–CA3 connection shifted the network towards pattern completion. Our results demonstrate that the specific properties of cells and synapses optimize higher-order computations in biological networks and might be useful to improve the deep learning capabilities of technical networks.}, author = {Guzmán, José and Schlögl, Alois and Espinoza Martinez, Claudia and Zhang, Xiaomin and Suter, Benjamin and Jonas, Peter M}, issn = {2662-8457}, journal = {Nature Computational Science}, keywords = {general medicine}, number = {12}, pages = {830--842}, publisher = {Springer Nature}, title = {{How connectivity rules and synaptic properties shape the efficacy of pattern separation in the entorhinal cortex–dentate gyrus–CA3 network}}, doi = {10.1038/s43588-021-00157-1}, volume = {1}, year = {2021}, } @misc{10110, abstract = {Pattern separation is a fundamental brain computation that converts small differences in input patterns into large differences in output patterns. Several synaptic mechanisms of pattern separation have been proposed, including code expansion, inhibition and plasticity; however, which of these mechanisms play a role in the entorhinal cortex (EC)–dentate gyrus (DG)–CA3 circuit, a classical pattern separation circuit, remains unclear. Here we show that a biologically realistic, full-scale EC–DG–CA3 circuit model, including granule cells (GCs) and parvalbumin-positive inhibitory interneurons (PV+-INs) in the DG, is an efficient pattern separator. Both external gamma-modulated inhibition and internal lateral inhibition mediated by PV+-INs substantially contributed to pattern separation. Both local connectivity and fast signaling at GC–PV+-IN synapses were important for maximum effectiveness. Similarly, mossy fiber synapses with conditional detonator properties contributed to pattern separation. By contrast, perforant path synapses with Hebbian synaptic plasticity and direct EC–CA3 connection shifted the network towards pattern completion. Our results demonstrate that the specific properties of cells and synapses optimize higher-order computations in biological networks and might be useful to improve the deep learning capabilities of technical networks.}, author = {Guzmán, José and Schlögl, Alois and Espinoza Martinez, Claudia and Zhang, Xiaomin and Suter, Benjamin and Jonas, Peter M}, publisher = {IST Austria}, title = {{How connectivity rules and synaptic properties shape the efficacy of pattern separation in the entorhinal cortex–dentate gyrus–CA3 network}}, doi = {10.15479/AT:ISTA:10110}, year = {2021}, } @unpublished{10077, abstract = {Although much is known about how single neurons in the hippocampus represent an animal’s position, how cell-cell interactions contribute to spatial coding remains poorly understood. Using a novel statistical estimator and theoretical modeling, both developed in the framework of maximum entropy models, we reveal highly structured cell-to-cell interactions whose statistics depend on familiar vs. novel environment. In both conditions the circuit interactions optimize the encoding of spatial information, but for regimes that differ in the signal-to-noise ratio of their spatial inputs. Moreover, the topology of the interactions facilitates linear decodability, making the information easy to read out by downstream circuits. These findings suggest that the efficient coding hypothesis is not applicable only to individual neuron properties in the sensory periphery, but also to neural interactions in the central brain.}, author = {Nardin, Michele and Csicsvari, Jozsef L and Tkačik, Gašper and Savin, Cristina}, booktitle = {bioRxiv}, publisher = {Cold Spring Harbor Laboratory}, title = {{The structure of hippocampal CA1 interactions optimizes spatial coding across experience}}, doi = {10.1101/2021.09.28.460602}, year = {2021}, } @article{9250, abstract = {Aprotic alkali metal–O2 batteries face two major obstacles to their chemistry occurring efficiently, the insulating nature of the formed alkali superoxides/peroxides and parasitic reactions that are caused by the highly reactive singlet oxygen (1O2). Redox mediators are recognized to be key for improving rechargeability. However, it is unclear how they affect 1O2 formation, which hinders strategies for their improvement. Here we clarify the mechanism of mediated peroxide and superoxide oxidation and thus explain how redox mediators either enhance or suppress 1O2 formation. We show that charging commences with peroxide oxidation to a superoxide intermediate and that redox potentials above ~3.5 V versus Li/Li+ drive 1O2 evolution from superoxide oxidation, while disproportionation always generates some 1O2. We find that 1O2 suppression requires oxidation to be faster than the generation of 1O2 from disproportionation. Oxidation rates decrease with growing driving force following Marcus inverted-region behaviour, establishing a region of maximum rate.}, author = {Petit, Yann K. and Mourad, Eléonore and Prehal, Christian and Leypold, Christian and Windischbacher, Andreas and Mijailovic, Daniel and Slugovc, Christian and Borisov, Sergey M. and Zojer, Egbert and Brutti, Sergio and Fontaine, Olivier and Freunberger, Stefan Alexander}, issn = {1755-4349}, journal = {Nature Chemistry}, keywords = {General Chemistry, General Chemical Engineering}, number = {5}, pages = {465--471}, publisher = {Springer Nature}, title = {{Mechanism of mediated alkali peroxide oxidation and triplet versus singlet oxygen formation}}, doi = {10.1038/s41557-021-00643-z}, volume = {13}, year = {2021}, } @phdthesis{9623, abstract = {Cytoplasmic reorganizations are essential for morphogenesis. In large cells like oocytes, these reorganizations become crucial in patterning the oocyte for later stages of embryonic development. Ascidians oocytes reorganize their cytoplasm (ooplasm) in a spectacular manner. Ooplasmic reorganization is initiated at fertilization with the contraction of the actomyosin cortex along the animal-vegetal axis of the oocyte, driving the accumulation of cortical endoplasmic reticulum (cER), maternal mRNAs associated to it and a mitochondria-rich subcortical layer – the myoplasm – in a region of the vegetal pole termed contraction pole (CP). Here we have used the species Phallusia mammillata to investigate the changes in cell shape that accompany these reorganizations and the mechanochemical mechanisms underlining CP formation. We report that the length of the animal-vegetal (AV) axis oscillates upon fertilization: it first undergoes a cycle of fast elongation-lengthening followed by a slow expansion of mainly the vegetal pole (VP) of the cell. We show that the fast oscillation corresponds to a dynamic polarization of the actin cortex as a result of a fertilization-induced increase in cortical tension in the oocyte that triggers a rupture of the cortex at the animal pole and the establishment of vegetal-directed cortical flows. These flows are responsible for the vegetal accumulation of actin causing the VP to flatten. We find that the slow expansion of the VP, leading to CP formation, correlates with a relaxation of the vegetal cortex and that the myoplasm plays a role in the expansion. We show that the myoplasm is a solid-like layer that buckles under compression forces arising from the contracting actin cortex at the VP. Straightening of the myoplasm when actin flows stops, facilitates the expansion of the VP and the CP. Altogether, our results present a previously unrecognized role for the myoplasm in ascidian ooplasmic segregation. }, author = {Caballero Mancebo, Silvia}, isbn = {978-3-99078-012-1}, issn = {2663-337X}, pages = {111}, publisher = {Institute of Science and Technology Austria}, title = {{Fertilization-induced deformations are controlled by the actin cortex and a mitochondria-rich subcortical layer in ascidian oocytes}}, doi = {10.15479/at:ista:9623}, year = {2021}, } @article{9006, abstract = {Cytoplasm is a gel-like crowded environment composed of various macromolecules, organelles, cytoskeletal networks, and cytosol. The structure of the cytoplasm is highly organized and heterogeneous due to the crowding of its constituents and their effective compartmentalization. In such an environment, the diffusive dynamics of the molecules are restricted, an effect that is further amplified by clustering and anchoring of molecules. Despite the crowded nature of the cytoplasm at the microscopic scale, large-scale reorganization of the cytoplasm is essential for important cellular functions, such as cell division and polarization. How such mesoscale reorganization of the cytoplasm is achieved, especially for large cells such as oocytes or syncytial tissues that can span hundreds of micrometers in size, is only beginning to be understood. In this review, we will discuss recent advances in elucidating the molecular, cellular, and biophysical mechanisms by which the cytoskeleton drives cytoplasmic reorganization across different scales, structures, and species.}, author = {Shamipour, Shayan and Caballero Mancebo, Silvia and Heisenberg, Carl-Philipp J}, issn = {18781551}, journal = {Developmental Cell}, number = {2}, pages = {P213--226}, publisher = {Elsevier}, title = {{Cytoplasm's got moves}}, doi = {10.1016/j.devcel.2020.12.002}, volume = {56}, year = {2021}, } @article{9429, abstract = {De novo loss of function mutations in the ubiquitin ligase-encoding gene Cullin3 lead to autism spectrum disorder (ASD). In mouse, constitutive haploinsufficiency leads to motor coordination deficits as well as ASD-relevant social and cognitive impairments. However, induction of Cul3 haploinsufficiency later in life does not lead to ASD-relevant behaviors, pointing to an important role of Cul3 during a critical developmental window. Here we show that Cul3 is essential to regulate neuronal migration and, therefore, constitutive Cul3 heterozygous mutant mice display cortical lamination abnormalities. At the molecular level, we found that Cul3 controls neuronal migration by tightly regulating the amount of Plastin3 (Pls3), a previously unrecognized player of neural migration. Furthermore, we found that Pls3 cell-autonomously regulates cell migration by regulating actin cytoskeleton organization, and its levels are inversely proportional to neural migration speed. Finally, we provide evidence that cellular phenotypes associated with autism-linked gene haploinsufficiency can be rescued by transcriptional activation of the intact allele in vitro, offering a proof of concept for a potential therapeutic approach for ASDs.}, author = {Morandell, Jasmin and Schwarz, Lena A and Basilico, Bernadette and Tasciyan, Saren and Dimchev, Georgi A and Nicolas, Armel and Sommer, Christoph M and Kreuzinger, Caroline and Dotter, Christoph and Knaus, Lisa and Dobler, Zoe and Cacci, Emanuele and Schur, Florian KM and Danzl, Johann G and Novarino, Gaia}, issn = {2041-1723}, journal = {Nature Communications}, keywords = {General Biochemistry, Genetics and Molecular Biology}, number = {1}, publisher = {Springer Nature}, title = {{Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development}}, doi = {10.1038/s41467-021-23123-x}, volume = {12}, year = {2021}, } @phdthesis{10058, abstract = {Quantum information and computation has become a vast field paved with opportunities for researchers and investors. As large multinational companies and international funds are heavily investing in quantum technologies it is still a question which platform is best suited for the task of realizing a scalable quantum processor. In this work we investigate hole spins in Ge quantum wells. These hold great promise as they possess several favorable properties: a small effective mass, a strong spin-orbit coupling, long relaxation time and an inherent immunity to hyperfine noise. All these characteristics helped Ge hole spin qubits to evolve from a single qubit to a fully entangled four qubit processor in only 3 years. Here, we investigated a qubit approach leveraging the large out-of-plane g-factors of heavy hole states in Ge quantum dots. We found this qubit to be reproducibly operable at extremely low magnetic field and at large speeds while maintaining coherence. This was possible because large differences of g-factors in adjacent dots can be achieved in the out-of-plane direction. In the in-plane direction the small g-factors, on the other hand, can be altered very effectively by the confinement potentials. Here, we found that this can even lead to a sign change of the g-factors. The resulting g-factor difference alters the dynamics of the system drastically and produces effects typically attributed to a spin-orbit induced spin-flip term. The investigations carried out in this thesis give further insights into the possibilities of holes in Ge and reveal new physical properties that need to be considered when designing future spin qubit experiments.}, author = {Jirovec, Daniel}, issn = {2663-337X}, keywords = {qubits, quantum computing, holes}, pages = {151}, publisher = {Institute of Science and Technology Austria}, title = {{Singlet-Triplet qubits and spin-orbit interaction in 2-dimensional Ge hole gases}}, doi = {10.15479/at:ista:10058}, year = {2021}, } @article{8909, abstract = {Spin qubits are considered to be among the most promising candidates for building a quantum processor. Group IV hole spin qubits have moved into the focus of interest due to the ease of operation and compatibility with Si technology. In addition, Ge offers the option for monolithic superconductor-semiconductor integration. Here we demonstrate a hole spin qubit operating at fields below 10 mT, the critical field of Al, by exploiting the large out-of-plane hole g-factors in planar Ge and by encoding the qubit into the singlet-triplet states of a double quantum dot. We observe electrically controlled X and Z-rotations with tunable frequencies exceeding 100 MHz and dephasing times of 1μs which we extend beyond 15μs with echo techniques. These results show that Ge hole singlet triplet qubits outperform their electronic Si and GaAs based counterparts in speed and coherence, respectively. In addition, they are on par with Ge single spin qubits, but can be operated at much lower fields underlining their potential for on chip integration with superconducting technologies.}, author = {Jirovec, Daniel and Hofmann, Andrea C and Ballabio, Andrea and Mutter, Philipp M. and Tavani, Giulio and Botifoll, Marc and Crippa, Alessandro and Kukucka, Josip and Sagi, Oliver and Martins, Frederico and Saez Mollejo, Jaime and Prieto Gonzalez, Ivan and Borovkov, Maksim and Arbiol, Jordi and Chrastina, Daniel and Isella, Giovanni and Katsaros, Georgios}, issn = {1476-4660}, journal = {Nature Materials}, number = {8}, pages = {1106–1112}, publisher = {Springer Nature}, title = {{A singlet triplet hole spin qubit in planar Ge}}, doi = {10.1038/s41563-021-01022-2}, volume = {20}, year = {2021}, } @phdthesis{9397, abstract = {Accumulation of interstitial fluid (IF) between embryonic cells is a common phenomenon in vertebrate embryogenesis. Unlike other model systems, where these accumulations coalesce into a large central cavity – the blastocoel, in zebrafish, IF is more uniformly distributed between the deep cells (DC) before the onset of gastrulation. This is likely due to the presence of a large extraembryonic structure – the yolk cell (YC) at the position where the blastocoel typically forms in other model organisms. IF has long been speculated to play a role in tissue morphogenesis during embryogenesis, but direct evidence supporting such function is still sparse. Here we show that the relocalization of IF to the interface between the YC and DC/epiblast is critical for axial mesendoderm (ME) cell protrusion formation and migration along this interface, a key process in embryonic axis formation. We further demonstrate that axial ME cell migration and IF relocalization engage in a positive feedback loop, where axial ME migration triggers IF accumulation ahead of the advancing axial ME tissue by mechanically compressing the overlying epiblast cell layer. Upon compression, locally induced flow relocalizes the IF through the porous epiblast tissue resulting in an IF accumulation ahead of the leading axial ME. This IF accumulation, in turn, promotes cell protrusion formation and migration of the leading axial ME cells, thereby facilitating axial ME extension. Our findings reveal a central role of dynamic IF relocalization in orchestrating germ layer morphogenesis during gastrulation.}, author = {Huljev, Karla}, issn = {2663-337X}, pages = {101}, publisher = {Institute of Science and Technology Austria}, title = {{Coordinated spatiotemporal reorganization of interstitial fluid is required for axial mesendoderm migration in zebrafish gastrulation}}, doi = {10.15479/at:ista:9397}, year = {2021}, } @unpublished{10066, abstract = {The potential of Si and SiGe-based devices for the scaling of quantum circuits is tainted by device variability. Each device needs to be tuned to operation conditions. We give a key step towards tackling this variability with an algorithm that, without modification, is capable of tuning a 4-gate Si FinFET, a 5-gate GeSi nanowire and a 7-gate SiGe heterostructure double quantum dot device from scratch. We achieve tuning times of 30, 10, and 92 minutes, respectively. The algorithm also provides insight into the parameter space landscape for each of these devices. These results show that overarching solutions for the tuning of quantum devices are enabled by machine learning.}, author = {Severin, B. and Lennon, D. T. and Camenzind, L. C. and Vigneau, F. and Fedele, F. and Jirovec, Daniel and Ballabio, A. and Chrastina, D. and Isella, G. and Kruijf, M. de and Carballido, M. J. and Svab, S. and Kuhlmann, A. V. and Braakman, F. R. and Geyer, S. and Froning, F. N. M. and Moon, H. and Osborne, M. A. and Sejdinovic, D. and Katsaros, Georgios and Zumbühl, D. M. and Briggs, G. A. D. and Ares, N.}, booktitle = {arXiv}, title = {{Cross-architecture tuning of silicon and SiGe-based quantum devices using machine learning}}, doi = {10.48550/arXiv.2107.12975}, year = {2021}, } @article{9437, abstract = {The synaptic connection from medial habenula (MHb) to interpeduncular nucleus (IPN) is critical for emotion-related behaviors and uniquely expresses R-type Ca2+ channels (Cav2.3) and auxiliary GABAB receptor (GBR) subunits, the K+-channel tetramerization domain-containing proteins (KCTDs). Activation of GBRs facilitates or inhibits transmitter release from MHb terminals depending on the IPN subnucleus, but the role of KCTDs is unknown. We therefore examined the localization and function of Cav2.3, GBRs, and KCTDs in this pathway in mice. We show in heterologous cells that KCTD8 and KCTD12b directly bind to Cav2.3 and that KCTD8 potentiates Cav2.3 currents in the absence of GBRs. In the rostral IPN, KCTD8, KCTD12b, and Cav2.3 co-localize at the presynaptic active zone. Genetic deletion indicated a bidirectional modulation of Cav2.3-mediated release by these KCTDs with a compensatory increase of KCTD8 in the active zone in KCTD12b-deficient mice. The interaction of Cav2.3 with KCTDs therefore scales synaptic strength independent of GBR activation.}, author = {Bhandari, Pradeep and Vandael, David H and Fernández-Fernández, Diego and Fritzius, Thorsten and Kleindienst, David and Önal, Hüseyin C and Montanaro-Punzengruber, Jacqueline-Claire and Gassmann, Martin and Jonas, Peter M and Kulik, Akos and Bettler, Bernhard and Shigemoto, Ryuichi and Koppensteiner, Peter}, issn = {2050-084X}, journal = {eLife}, publisher = {eLife Sciences Publications}, title = {{GABAB receptor auxiliary subunits modulate Cav2.3-mediated release from medial habenula terminals}}, doi = {10.7554/ELIFE.68274}, volume = {10}, year = {2021}, } @phdthesis{9562, abstract = {Left-right asymmetries can be considered a fundamental organizational principle of the vertebrate central nervous system. The hippocampal CA3-CA1 pyramidal cell synaptic connection shows an input-side dependent asymmetry where the hemispheric location of the presynaptic CA3 neuron determines the synaptic properties. Left-input synapses terminating on apical dendrites in stratum radiatum have a higher density of NMDA receptor subunit GluN2B, a lower density of AMPA receptor subunit GluA1 and smaller areas with less often perforated PSDs. On the other hand, left-input synapses terminating on basal dendrites in stratum oriens have lower GluN2B densities than right-input ones. Apical and basal synapses further employ different signaling pathways involved in LTP. SDS-digested freeze-fracture replica labeling can visualize synaptic membrane proteins with high sensitivity and resolution, and has been used to reveal the asymmetry at the electron microscopic level. However, it requires time-consuming manual demarcation of the synaptic surface for quantitative measurements. To facilitate the analysis of replica labeling, I first developed a software named Darea, which utilizes deep-learning to automatize this demarcation. With Darea I characterized the synaptic distribution of NMDA and AMPA receptors as well as the voltage-gated Ca2+ channels in CA1 stratum radiatum and oriens. Second, I explored the role of GluN2B and its carboxy-terminus in the establishment of input-side dependent hippocampal asymmetry. In conditional knock-out mice lacking GluN2B expression in CA1 and GluN2B-2A swap mice, where GluN2B carboxy-terminus was exchanged to that of GluN2A, no significant asymmetries of GluN2B, GluA1 and PSD area were detected. We further discovered a previously unknown functional asymmetry of GluN2A, which was also lost in the swap mouse. These results demonstrate that GluN2B carboxy-terminus plays a critical role in normal formation of input-side dependent asymmetry.}, author = {Kleindienst, David}, issn = {2663-337X}, pages = {124}, publisher = {Institute of Science and Technology Austria}, title = {{2B or not 2B: Hippocampal asymmetries mediated by NMDA receptor subunit GluN2B C-terminus and high-throughput image analysis by Deep-Learning}}, doi = {10.15479/at:ista:9562}, year = {2021}, } @inbook{9756, abstract = {High-resolution visualization and quantification of membrane proteins contribute to the understanding of their functions and the roles they play in physiological and pathological conditions. Sodium dodecyl sulfate-digested freeze-fracture replica labeling (SDS-FRL) is a powerful electron microscopy method to study quantitatively the two-dimensional distribution of transmembrane proteins and their tightly associated proteins. During treatment with SDS, intracellular organelles and proteins not anchored to the replica are dissolved, whereas integral membrane proteins captured and stabilized by carbon/platinum deposition remain on the replica. Their intra- and extracellular domains become exposed on the surface of the replica, facilitating the accessibility of antibodies and, therefore, providing higher labeling efficiency than those obtained with other immunoelectron microscopy techniques. In this chapter, we describe the protocols of SDS-FRL adapted for mammalian brain samples, and optimization of the SDS treatment to increase the labeling efficiency for quantification of Cav2.1, the alpha subunit of P/Q-type voltage-dependent calcium channels utilizing deep learning algorithms.}, author = {Kaufmann, Walter and Kleindienst, David and Harada, Harumi and Shigemoto, Ryuichi}, booktitle = { Receptor and Ion Channel Detection in the Brain}, isbn = {9781071615218}, keywords = {Freeze-fracture replica: Deep learning, Immunogold labeling, Integral membrane protein, Electron microscopy}, pages = {267--283}, publisher = {Humana}, title = {{High-Resolution localization and quantitation of membrane proteins by SDS-digested freeze-fracture replica labeling (SDS-FRL)}}, doi = {10.1007/978-1-0716-1522-5_19}, volume = {169}, year = {2021}, } @phdthesis{8934, abstract = {In this thesis, we consider several of the most classical and fundamental problems in static analysis and formal verification, including invariant generation, reachability analysis, termination analysis of probabilistic programs, data-flow analysis, quantitative analysis of Markov chains and Markov decision processes, and the problem of data packing in cache management. We use techniques from parameterized complexity theory, polyhedral geometry, and real algebraic geometry to significantly improve the state-of-the-art, in terms of both scalability and completeness guarantees, for the mentioned problems. In some cases, our results are the first theoretical improvements for the respective problems in two or three decades.}, author = {Goharshady, Amir Kafshdar}, issn = {2663-337X}, pages = {278}, publisher = {Institute of Science and Technology Austria}, title = {{Parameterized and algebro-geometric advances in static program analysis}}, doi = {10.15479/AT:ISTA:8934}, year = {2021}, } @phdthesis{10307, abstract = {Bacteria-host interactions represent a continuous trade-off between benefit and risk. Thus, the host immune response is faced with a non-trivial problem – accommodate beneficial commensals and remove harmful pathogens. This is especially difficult as molecular patterns, such as lipopolysaccharide or specific surface organelles such as pili, are conserved in both, commensal and pathogenic bacteria. Type 1 pili, tightly regulated by phase variation, are considered an important virulence factor of pathogenic bacteria as they facilitate invasion into host cells. While invasion represents a de facto passive mechanism for pathogens to escape the host immune response, we demonstrate a fundamental role of type 1 pili as active modulators of the innate and adaptive immune response.}, author = {Tomasek, Kathrin}, issn = {2663-337X}, pages = {73}, publisher = {Institute of Science and Technology Austria}, title = {{Pathogenic Escherichia coli hijack the host immune response}}, doi = {10.15479/at:ista:10307}, year = {2021}, } @unpublished{10316, abstract = {A key attribute of persistent or recurring bacterial infections is the ability of the pathogen to evade the host’s immune response. Many Enterobacteriaceae express type 1 pili, a pre-adapted virulence trait, to invade host epithelial cells and establish persistent infections. However, the molecular mechanisms and strategies by which bacteria actively circumvent the immune response of the host remain poorly understood. Here, we identified CD14, the major co-receptor for lipopolysaccharide detection, on dendritic cells as a previously undescribed binding partner of FimH, the protein located at the tip of the type 1 pilus of Escherichia coli. The FimH amino acids involved in CD14 binding are highly conserved across pathogenic and non-pathogenic strains. Binding of pathogenic bacteria to CD14 lead to reduced dendritic cell migration and blunted expression of co-stimulatory molecules, both rate-limiting factors of T cell activation. While defining an active molecular mechanism of immune evasion by pathogens, the interaction between FimH and CD14 represents a potential target to interfere with persistent and recurrent infections, such as urinary tract infections or Crohn’s disease.}, author = {Tomasek, Kathrin and Leithner, Alexander F and Glatzová, Ivana and Lukesch, Michael S. and Guet, Calin C and Sixt, Michael K}, booktitle = {bioRxiv}, publisher = {Cold Spring Harbor Laboratory}, title = {{Type 1 piliated uropathogenic Escherichia coli hijack the host immune response by binding to CD14}}, doi = {10.1101/2021.10.18.464770}, year = {2021}, } @article{9010, abstract = {Availability of the essential macronutrient nitrogen in soil plays a critical role in plant growth, development, and impacts agricultural productivity. Plants have evolved different strategies for sensing and responding to heterogeneous nitrogen distribution. Modulation of root system architecture, including primary root growth and branching, is among the most essential plant adaptions to ensure adequate nitrogen acquisition. However, the immediate molecular pathways coordinating the adjustment of root growth in response to distinct nitrogen sources, such as nitrate or ammonium, are poorly understood. Here, we show that growth as manifested by cell division and elongation is synchronized by coordinated auxin flux between two adjacent outer tissue layers of the root. This coordination is achieved by nitrate‐dependent dephosphorylation of the PIN2 auxin efflux carrier at a previously uncharacterized phosphorylation site, leading to subsequent PIN2 lateralization and thereby regulating auxin flow between adjacent tissues. A dynamic computer model based on our experimental data successfully recapitulates experimental observations. Our study provides mechanistic insights broadening our understanding of root growth mechanisms in dynamic environments.}, author = {Ötvös, Krisztina and Marconi, Marco and Vega, Andrea and O’Brien, Jose and Johnson, Alexander J and Abualia, Rashed and Antonielli, Livio and Montesinos López, Juan C and Zhang, Yuzhou and Tan, Shutang and Cuesta, Candela and Artner, Christina and Bouguyon, Eleonore and Gojon, Alain and Friml, Jiří and Gutiérrez, Rodrigo A. and Wabnik, Krzysztof T and Benková, Eva}, issn = {14602075}, journal = {EMBO Journal}, number = {3}, publisher = {Embo Press}, title = {{Modulation of plant root growth by nitrogen source-defined regulation of polar auxin transport}}, doi = {10.15252/embj.2020106862}, volume = {40}, year = {2021}, } @article{9913, abstract = {Nitrate commands genome-wide gene expression changes that impact metabolism, physiology, plant growth, and development. In an effort to identify new components involved in nitrate responses in plants, we analyze the Arabidopsis thaliana root phosphoproteome in response to nitrate treatments via liquid chromatography coupled to tandem mass spectrometry. 176 phosphoproteins show significant changes at 5 or 20 min after nitrate treatments. Proteins identified by 5 min include signaling components such as kinases or transcription factors. In contrast, by 20 min, proteins identified were associated with transporter activity or hormone metabolism functions, among others. The phosphorylation profile of NITRATE TRANSPORTER 1.1 (NRT1.1) mutant plants was significantly altered as compared to wild-type plants, confirming its key role in nitrate signaling pathways that involves phosphorylation changes. Integrative bioinformatics analysis highlights auxin transport as an important mechanism modulated by nitrate signaling at the post-translational level. We validated a new phosphorylation site in PIN2 and provide evidence that it functions in primary and lateral root growth responses to nitrate.}, author = {Vega, Andrea and Fredes, Isabel and O’Brien, José and Shen, Zhouxin and Ötvös, Krisztina and Abualia, Rashed and Benková, Eva and Briggs, Steven P. and Gutiérrez, Rodrigo A.}, issn = {1469-3178}, journal = {EMBO Reports}, number = {9}, publisher = {Wiley}, title = {{Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture}}, doi = {10.15252/embr.202051813}, volume = {22}, year = {2021}, } @phdthesis{10303, abstract = {Nitrogen is an essential macronutrient determining plant growth, development and affecting agricultural productivity. Root, as a hub that perceives and integrates local and systemic signals on the plant’s external and endogenous nitrogen resources, communicates with other plant organs to consolidate their physiology and development in accordance with actual nitrogen balance. Over the last years, numerous studies demonstrated that these comprehensive developmental adaptations rely on the interaction between pathways controlling nitrogen homeostasis and hormonal networks acting globally in the plant body. However, molecular insights into how the information about the nitrogen status is translated through hormonal pathways into specific developmental output are lacking. In my work, I addressed so far poorly understood mechanisms underlying root-to-shoot communication that lead to a rapid re-adjustment of shoot growth and development after nitrate provision. Applying a combination of molecular, cell, and developmental biology approaches, genetics and grafting experiments as well as hormonal analytics, I identified and characterized an unknown molecular framework orchestrating shoot development with a root nitrate sensory system. }, author = {Abualia, Rashed}, issn = {2663-337X}, pages = {139}, publisher = {Institute of Science and Technology Austria}, title = {{Role of hormones in nitrate regulated growth}}, doi = {10.15479/at:ista:10303}, year = {2021}, } @phdthesis{9962, abstract = {The brain is one of the largest and most complex organs and it is composed of billions of neurons that communicate together enabling e.g. consciousness. The cerebral cortex is the largest site of neural integration in the central nervous system. Concerted radial migration of newly born cortical projection neurons, from their birthplace to their final position, is a key step in the assembly of the cerebral cortex. The cellular and molecular mechanisms regulating radial neuronal migration in vivo are however still unclear. Recent evidence suggests that distinct signaling cues act cell-autonomously but differentially at certain steps during the overall migration process. Moreover, functional analysis of genetic mosaics (mutant neurons present in wild-type/heterozygote environment) using the MADM (Mosaic Analysis with Double Markers) analyses in comparison to global knockout also indicate a significant degree of non-cell-autonomous and/or community effects in the control of cortical neuron migration. The interactions of cell-intrinsic (cell-autonomous) and cell-extrinsic (non-cell-autonomous) components are largely unknown. In part of this thesis work we established a MADM-based experimental strategy for the quantitative analysis of cell-autonomous gene function versus non-cell-autonomous and/or community effects. The direct comparison of mutant neurons from the genetic mosaic (cell-autonomous) to mutant neurons in the conditional and/or global knockout (cell-autonomous + non-cell-autonomous) allows to quantitatively analyze non-cell-autonomous effects. Such analysis enable the high-resolution analysis of projection neuron migration dynamics in distinct environments with concomitant isolation of genomic and proteomic profiles. Using these experimental paradigms and in combination with computational modeling we show and characterize the nature of non-cell-autonomous effects to coordinate radial neuron migration. Furthermore, this thesis discusses recent developments in neurodevelopment with focus on neuronal polarization and non-cell-autonomous mechanisms in neuronal migration.}, author = {Hansen, Andi H}, issn = {2663-337X}, keywords = {Neuronal migration, Non-cell-autonomous, Cell-autonomous, Neurodevelopmental disease}, pages = {182}, publisher = {Institute of Science and Technology Austria}, title = {{Cell-autonomous gene function and non-cell-autonomous effects in radial projection neuron migration}}, doi = {10.15479/at:ista:9962}, year = {2021}, } @article{9428, abstract = {Thermalization is the inevitable fate of many complex quantum systems, whose dynamics allow them to fully explore the vast configuration space regardless of the initial state---the behaviour known as quantum ergodicity. In a quest for experimental realizations of coherent long-time dynamics, efforts have focused on ergodicity-breaking mechanisms, such as integrability and localization. The recent discovery of persistent revivals in quantum simulators based on Rydberg atoms have pointed to the existence of a new type of behaviour where the system rapidly relaxes for most initial conditions, while certain initial states give rise to non-ergodic dynamics. This collective effect has been named ”quantum many-body scarring’by analogy with a related form of weak ergodicity breaking that occurs for a single particle inside a stadium billiard potential. In this Review, we provide a pedagogical introduction to quantum many-body scars and highlight the emerging connections with the semiclassical quantization of many-body systems. We discuss the relation between scars and more general routes towards weak violations of ergodicity due to embedded algebras and non-thermal eigenstates, and highlight possible applications of scars in quantum technology.}, author = {Serbyn, Maksym and Abanin, Dmitry A. and Papić, Zlatko}, issn = {1745-2481}, journal = {Nature Physics}, number = {6}, pages = {675–685}, publisher = {Nature Research}, title = {{Quantum many-body scars and weak breaking of ergodicity}}, doi = {10.1038/s41567-021-01230-2}, volume = {17}, year = {2021}, } @article{8931, abstract = {Auxin is a major plant growth regulator, but current models on auxin perception and signaling cannot explain the whole plethora of auxin effects, in particular those associated with rapid responses. A possible candidate for a component of additional auxin perception mechanisms is the AUXIN BINDING PROTEIN 1 (ABP1), whose function in planta remains unclear. Here we combined expression analysis with gain- and loss-of-function approaches to analyze the role of ABP1 in plant development. ABP1 shows a broad expression largely overlapping with, but not regulated by, transcriptional auxin response activity. Furthermore, ABP1 activity is not essential for the transcriptional auxin signaling. Genetic in planta analysis revealed that abp1 loss-of-function mutants show largely normal development with minor defects in bolting. On the other hand, ABP1 gain-of-function alleles show a broad range of growth and developmental defects, including root and hypocotyl growth and bending, lateral root and leaf development, bolting, as well as response to heat stress. At the cellular level, ABP1 gain-of-function leads to impaired auxin effect on PIN polar distribution and affects BFA-sensitive PIN intracellular aggregation. The gain-of-function analysis suggests a broad, but still mechanistically unclear involvement of ABP1 in plant development, possibly masked in abp1 loss-of-function mutants by a functional redundancy.}, author = {Gelová, Zuzana and Gallei, Michelle C and Pernisová, Markéta and Brunoud, Géraldine and Zhang, Xixi and Glanc, Matous and Li, Lanxin and Michalko, Jaroslav and Pavlovicova, Zlata and Verstraeten, Inge and Han, Huibin and Hajny, Jakub and Hauschild, Robert and Čovanová, Milada and Zwiewka, Marta and Hörmayer, Lukas and Fendrych, Matyas and Xu, Tongda and Vernoux, Teva and Friml, Jiří}, issn = {0168-9452}, journal = {Plant Science}, keywords = {Agronomy and Crop Science, Plant Science, Genetics, General Medicine}, publisher = {Elsevier}, title = {{Developmental roles of auxin binding protein 1 in Arabidopsis thaliana}}, doi = {10.1016/j.plantsci.2020.110750}, volume = {303}, year = {2021}, }