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Items: 1 to 20 of 41

1.
Protective roles of peroxiporins AQP0 and AQP11 in human astrocyte and neuronal cell lines in response to oxidative and inflammatory stressors
Zein Amro, Lyndsey E. Collins-Praino, Andrea J. Yool
Biosci Rep. 2024 Mar 29; 44(3): BSR20231725. Published online 2024 Mar 22. doi: 10.1042/BSR20231725
PMCID:
PMC10965398
AbstractArticlePDF–12M
2.
The role of phosphorylation in calmodulin-mediated gating of human AQP0
Stefan Kreida, Jennifer Virginia Roche, Julie Winkel Missel, Tamim Al-Jubair, Carl Johan Hagströmer, Veronika Wittenbecher, Sara Linse, Pontus Gourdon, Susanna Törnroth-Horsefield
Biochem J. 2024 Jan 10; 481(1): 17–32. Published online 2024 Jan 4. doi: 10.1042/BCJ20230158
PMCID:
PMC10903448
AbstractArticlePDF–2.5M
3.
Assessment of community efforts to advance network-based prediction of protein–protein interactions
Xu-Wen Wang, Lorenzo Madeddu, Kerstin Spirohn, Leonardo Martini, Adriano Fazzone, Luca Becchetti, Thomas P. Wytock, István A. Kovács, Olivér M. Balogh, Bettina Benczik, Mátyás Pétervári, Bence Ágg, Péter Ferdinandy, Loan Vulliard, Jörg Menche, Stefania Colonnese, Manuela Petti, Gaetano Scarano, Francesca Cuomo, Tong Hao, Florent Laval, Luc Willems, Jean-Claude Twizere, Marc Vidal, Michael A. Calderwood, Enrico Petrillo, Albert-László Barabási, Edwin K. Silverman, Joseph Loscalzo, Paola Velardi, Yang-Yu Liu
Nat Commun. 2023; 14: 1582. Published online 2023 Mar 22. doi: 10.1038/s41467-023-37079-7
PMCID:
PMC10033937
AbstractArticlePDF–1.5M
4.
Anterior Umbilication of Lens in a Family with Congenital Cataracts Associated with a Missense Mutation of MIP Gene
Zhixing Cheng, Xun Wang, Qiwei Wang, Xulin Zhang, Dongni Wang, Weiming Huang, Meimei Dongye, Xiaocheng Feng, Danying Zheng, Haotian Lin
Genes (Basel) 2022 Nov; 13(11): 1987. Published online 2022 Oct 31. doi: 10.3390/genes13111987
PMCID:
PMC9690445
AbstractArticlePDF–1.2M
5.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
6.
AQP0 is a novel surface marker for deciphering abnormal erythropoiesis
Tso-Fu Wang, Guan-Ling Lin, Sung-Chao Chu, Chang-Chin Chen, Yu-Shan Liou, Hsin-Hou Chang, Der-Shan Sun
Stem Cell Res Ther. 2021; 12: 274. Published online 2021 May 6. doi: 10.1186/s13287-021-02343-4
PMCID:
PMC8101103
AbstractArticlePDF–2.0M
7.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
8.
Identification of a novel MIP frameshift mutation associated with congenital cataract in a Chinese family by whole-exome sequencing and functional analysis
Xigui Long, Yanru Huang, Hu Tan, Zhuo Li, Rui Zhang, Siyuan Linpeng, Weigang Lv, Yingxi Cao, Haoxian Li, Desheng Liang, Lingqian Wu
Eye (Lond) 2018 Aug; 32(8): 1359–1364. Published online 2018 Apr 26. doi: 10.1038/s41433-018-0084-5
PMCID:
PMC6085365
AbstractArticlePDF–864K
9.
Identification of a novel missense mutation of MIP in a Chinese family with congenital cataracts by target region capture sequencing
Bo Jiang, Yanhua chen, Baisheng Xu, Nan Hong, Rongrong Liu, Ming Qi, Liping Shen
Sci Rep. 2017; 7: 40129. Published online 2017 Jan 6. doi: 10.1038/srep40129
PMCID:
PMC5216388
AbstractArticlePDF–790K
10.
Identification and Functional Analysis of a Novel MIP Gene Mutation Associated with Congenital Cataract in a Chinese Family
Xingchao Shentu, Qi Miao, Xiajing Tang, Houfa Yin, Yingying Zhao
PLoS One. 2015; 10(5): e0126679. Published online 2015 May 6. doi: 10.1371/journal.pone.0126679
PMCID:
PMC4422749
AbstractArticlePDF–3.7M
11.
A Novel Nonsense Mutation in the MIP Gene Linked to Congenital Posterior Polar Cataracts in a Chinese Family
Zixun Song, Lianqing Wang, Yaping Liu, Wei Xiao
PLoS One. 2015; 10(3): e0119296. Published online 2015 Mar 24. doi: 10.1371/journal.pone.0119296
PMCID:
PMC4372439
AbstractArticlePDF–955K
12.
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected with Congenital Progressive Punctate Cataract
Xuchen Ding, Nan Zhou, Hui Lin, Jianjun Chen, Chunyuan Zhao, Guangkai Zhou, J. Fielding Hejtmancik, Yanhua Qi
PLoS One. 2014; 9(7): e102733. Published online 2014 Jul 17. doi: 10.1371/journal.pone.0102733
PMCID:
PMC4102541
AbstractArticlePDF–918K
13.
Systematic identification of pathological lamin A interactors
Travis A. Dittmer, Nidhi Sahni, Nard Kubben, David E. Hill, Marc Vidal, Rebecca C. Burgess, Vassilis Roukos, Tom Misteli
Mol Biol Cell. 2014 May 1; 25(9): 1493–1510. doi: 10.1091/mbc.E14-02-0733
PMCID:
PMC4004598
AbstractArticlePDF–3.5M
14.
A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family
Yibo Yu, Yinhui Yu, Peiqing Chen, Jinyu Li, Yanan Zhu, Yi Zhai, Ke Yao
BMC Med Genet. 2014; 15: 6. Published online 2014 Jan 9. doi: 10.1186/1471-2350-15-6
PMCID:
PMC3890554
AbstractArticlePDF–2.9M
15.
Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion
Sindhu S. Kumari, Jason Gandhi, Mohammed H. Mustehsan, Semih Eren, Kulandaiappan Varadaraj
Exp Eye Res. Author manuscript; available in PMC 2014 Nov 1.
Published in final edited form as: Exp Eye Res. 2013 Nov; 116: 10.1016/j.exer.2013.09.019. Published online 2013 Oct 9. doi: 10.1016/j.exer.2013.09.019
PMCID:
PMC3864651
AbstractArticlePDF–7.1M
16.
A novel donor splice-site mutation of major intrinsic protein gene associated with congenital cataract in a Chinese family
Lu Zeng, Wenqiang Liu, Wenguo Feng, Xing Wang, Hui Dang, Luna Gao, Jing Yao, Xianqin Zhang
Mol Vis. 2013; 19: 2244–2249. Published online 2013 Nov 14.
PMCID:
PMC3834598
AbstractArticlePDF–704K
17.
Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error
Ching-Yu Cheng, Maria Schache, M. Kamran Ikram, Terri L. Young, Jeremy A. Guggenheim, Veronique Vitart, Stuart MacGregor, Virginie J.M. Verhoeven, Veluchamy A. Barathi, Jiemin Liao, Pirro G. Hysi, Joan E. Bailey-Wilson, Beate St. Pourcain, John P. Kemp, George McMahon, Nicholas J. Timpson, David M. Evans, Grant W. Montgomery, Aniket Mishra, Ya Xing Wang, Jie Jin Wang, Elena Rochtchina, Ozren Polasek, Alan F. Wright, Najaf Amin, Elisabeth M. van Leeuwen, James F. Wilson, Craig E. Pennell, Cornelia M. van Duijn, Paulus T.V.M. de Jong, Johannes R. Vingerling, Xin Zhou, Peng Chen, Ruoying Li, Wan-Ting Tay, Yingfeng Zheng, Merwyn Chew, Consortium for Refractive Error and Myopia, Kathryn P. Burdon, Jamie E. Craig, Sudha K. Iyengar, Robert P. Igo, Jr., Jonathan H. Lass, Jr., The Fuchs’ Genetics Multi-Center Study Group, Emily Y. Chew, Toomas Haller, Evelin Mihailov, Andres Metspalu, Juho Wedenoja, Claire L. Simpson, Robert Wojciechowski, René Höhn, Alireza Mirshahi, Tanja Zeller, Norbert Pfeiffer, Karl J. Lackner, Wellcome Trust Case Control Consortium 2, Thomas Bettecken, Thomas Meitinger, Konrad Oexle, Mario Pirastu, Laura Portas, Abhishek Nag, Katie M. Williams, Ekaterina Yonova-Doing, Ronald Klein, Barbara E. Klein, S. Mohsen Hosseini, Andrew D. Paterson, The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group, Kari-Matti Makela, Terho Lehtimaki, Mika Kahonen, Olli Raitakari, Nagahisa Yoshimura, Fumihiko Matsuda, Li Jia Chen, Chi Pui Pang, Shea Ping Yip, Maurice K.H. Yap, Akira Meguro, Nobuhisa Mizuki, Hidetoshi Inoko, Paul J. Foster, Jing Hua Zhao, Eranga Vithana, E-Shyong Tai, Qiao Fan, Liang Xu, Harry Campbell, Brian Fleck, Igor Rudan, Tin Aung, Albert Hofman, André G. Uitterlinden, Goran Bencic, Chiea-Chuen Khor, Hannah Forward, Olavi Pärssinen, Paul Mitchell, Fernando Rivadeneira, Alex W. Hewitt, Cathy Williams, Ben A. Oostra, Yik-Ying Teo, Christopher J. Hammond, Dwight Stambolian, David A. Mackey, Caroline C.W. Klaver, Tien-Yin Wong, Seang-Mei Saw, Paul N. Baird
Am J Hum Genet. 2013 Aug 8; 93(2): 264–277. doi: 10.1016/j.ajhg.2013.06.016
PMCID:
PMC3772747
AbstractArticlePDF–959K
18.
An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract
G. Senthil Kumar, John W. Kyle, Peter J. Minogue, K. Dinesh Kumar, K. Vasantha, Viviana M. Berthoud, Eric C. Beyer, Santhiya T. Sathiyavedu
Exp Eye Res. Author manuscript; available in PMC 2014 May 1.
Published in final edited form as: Exp Eye Res. 2013 May; 110: 136–141. Published online 2012 Oct 29. doi: 10.1016/j.exer.2012.10.010
PMCID:
PMC3570674
AbstractArticlePDF–1.4M
19.
The Arg233Lys AQP0 Mutation Disturbs Aquaporin0-Calmodulin Interaction Causing Polymorphic Congenital Cataract
Shanshan Hu, Binbin Wang, Yanhua Qi, Hui Lin
PLoS One. 2012; 7(5): e37637. Published online 2012 May 25. doi: 10.1371/journal.pone.0037637
PMCID:
PMC3360748
AbstractArticlePDF–190K
20.
Spatial analysis of human lens aquaporin-0 post-translational modifications by MALDI mass spectrometry tissue profiling
Danielle B. Gutierrez, Donita Garland, Kevin L. Schey
Exp Eye Res. Author manuscript; available in PMC 2012 Dec 1.
Published in final edited form as: Exp Eye Res. 2011 Dec; 93(6): 912–920. Published online 2011 Oct 25. doi: 10.1016/j.exer.2011.10.007
PMCID:
PMC3267704
AbstractArticlePDF–1.0M

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