PMC Links for GEO Profiles (Select 94286938) - PMC

Select item 112183121.

Impairment of α-tubulin and F-actin interactions of GJB3 induces aneuploidy in urothelial cells and promotes bladder cancer cell invasion

Junnan Liu, Xue Wang, Wencheng Jiang, Anca Azoitei, Tim Eiseler, Markus Eckstein, Arndt Hartmann, Stephan Stilgenbauer, Mohamed Elati, Meike Hohwieler, Alexander Kleger, Axel John, Felix Wezel, Friedemann Zengerling, Christian Bolenz, Cagatay Günes

Cell Mol Biol Lett. 2024; 29: 94. Published online 2024 Jul 2. doi: 10.1186/s11658-024-00609-2

PMCID:: PMC11218312

Abstract Article PDF–4.9M

Select item 81650302.

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

Abstract Article PDF–2.2M

Select item 71699833.

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

Abstract Article PDF–5.4M

Select item 68171134.

GJB3/GJB6 screening in GJB2 carriers with idiopathic hearing loss: Is it necessary?

Kaitian Chen, Xuan Wu, Ling Zong, Hongyan Jiang

J Clin Lab Anal. 2018 Nov; 32(9): e22592. Published online 2018 Jun 21. doi: 10.1002/jcla.22592

PMCID:: PMC6817113

Abstract Article PDF–625K

Select item 65856965.

Exome sequencing identifies novel compound heterozygous mutations in GJB3 gene that cause erythrokeratodermia variabilis et progressiva

Yongqiong Deng, Hong Wang, Yunzhu Mou, Qi Zeng, Xia Xiong

Australas J Dermatol. 2019 Feb; 60(1): e87–e89. Published online 2018 Jul 10. doi: 10.1111/ajd.12887

PMCID:: PMC6585696

Article PDF–352K

Select item 61601446.

Analysis of mutation spectrum of common deafness-causing genes in Hakka newborns in southern China by semiconductor sequencing

Pingsen Zhao, Lifang Lin, Liubing Lan

Medicine (Baltimore) 2018 Sep; 97(38): e12285. Published online 2018 Sep 21. doi: 10.1097/MD.0000000000012285

PMCID:: PMC6160144

Abstract Article PDF–234K

Select item 46479417.

hORFeome v3.1: A resource of human open reading frames representing over 10,000 human genes

Philippe Lamesch, Ning Li, Stuart Milstein, Changyu Fan, Tong Hao, Gabor Szabo, Zhenjun Hu, Kavitha Venkatesan, Graeme Bethel, Paul Martin, Jane Rogers, Stephanie Lawlor, Stuart McLaren, Amélie Dricot, Heather Borick, Michael E. Cusick, Jean Vandenhaute, Ian Dunham, David E. Hill, Marc Vidal

Genomics. 2007 Mar; 89(3): 307–315. doi: 10.1016/j.ygeno.2006.11.012

PMCID:: PMC4647941

Abstract Article

Select item 32905838.

Pathogenic Connexin-31 Forms Constitutively Active Hemichannels to Promote Necrotic Cell Death

Jingwei Chi, Li Li, Mujun Liu, Jieqiong Tan, Chengyuan Tang, Qian Pan, Danling Wang, Zhuohua Zhang

PLoS One. 2012; 7(2): e32531. Published online 2012 Feb 29. doi: 10.1371/journal.pone.0032531

PMCID:: PMC3290583

Abstract Article PDF–2.5M

Select item 32617089.

Toward an understanding of the protein interaction network of the human liver

Jian Wang, Keke Huo, Lixin Ma, Liujun Tang, Dong Li, Xiaobi Huang, Yanzhi Yuan, Chunhua Li, Wei Wang, Wei Guan, Hui Chen, Chaozhi Jin, Junchen Wei, Wanqiao Zhang, Yongsheng Yang, Qiongming Liu, Ying Zhou, Cuili Zhang, Zhihao Wu, Wangxiang Xu, Ying Zhang, Tao Liu, Donghui Yu, Yaping Zhang, Liang Chen, Dewu Zhu, Xing Zhong, Lixin Kang, Xiang Gan, Xiaolan Yu, Qi Ma, Jing Yan, Li Zhou, Zhongyang Liu, Yunping Zhu, Tao Zhou, Fuchu He, Xiaoming Yang

Mol Syst Biol. 2011; 7: 536. Published online 2011 Oct 11. doi: 10.1038/msb.2011.67

Correction in:: Mol Syst Biol. 2017 Dec; 13(12): 965.

PMCID:: PMC3261708

Abstract Article PDF–2.0M

Select item 317805910.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 290991511.

Genotyping with a 198 Mutation Arrayed Primer Extension Array for Hereditary Hearing Loss: Assessment of Its Diagnostic Value for Medical Practice

Juan Rodriguez-Paris, Lynn Pique, Tahl Colen, Joseph Roberson, Phyllis Gardner, Iris Schrijver

PLoS One. 2010; 5(7): e11804. Published online 2010 Jul 26. doi: 10.1371/journal.pone.0011804

PMCID:: PMC2909915

Abstract Article PDF–137K

Select item 279689112.

Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins

Francisco J. del Castillo, Martine Cohen-Salmon, Anne Charollais, Dorothée Caille, Paul D. Lampe, Philippe Chavrier, Paolo Meda, Christine Petit

Hum Mol Genet. 2010 Jan 15; 19(2): 262–275. Published online 2009 Nov 11. doi: 10.1093/hmg/ddp490

PMCID:: PMC2796891

Abstract Article PDF–643K

Select item 277837013.

EKV mutant connexin 31 associated cell death is mediated by ER stress

Daniel Tattersall, Claire A. Scott, Colin Gray, Daniel Zicha, David P. Kelsell

Hum Mol Genet. 2009 Dec 15; 18(24): 4734–4745. Published online 2009 Sep 14. doi: 10.1093/hmg/ddp436

PMCID:: PMC2778370

Abstract Article PDF–789K

Select item 275498414.

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

Yongyi Yuan, Yiwen You, Deliang Huang, Jinghong Cui, Yong Wang, Qiang Wang, Fei Yu, Dongyang Kang, Huijun Yuan, Dongyi Han, Pu Dai

J Transl Med. 2009; 7: 79. Published online 2009 Sep 10. doi: 10.1186/1479-5876-7-79

PMCID:: PMC2754984

Abstract Article PDF–331K

Select item 273770015.

Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31

Xue Zhong Liu, Yongyi Yuan, Denise Yan, Emilie Hong Ding, Xiao Mei Ouyang, Yu Fei, Wenxue Tang, Huijun Yuan, Qing Chang, LiLin Du, Xin Zhang, Guojian Wang, Shoeb Ahmad, Dongyang Kang, Xi Lin, Pu Dai

Hum Genet. Author manuscript; available in PMC 2009 Sep 4.

Published in final edited form as: Hum Genet. 2009 Feb; 125(1): 53–62. Published online 2008 Dec 3. doi: 10.1007/s00439-008-0602-9

PMCID:: PMC2737700

Abstract Article PDF–879K

Select item 145882016.

Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness

Charles K. Abrams, Mona M. Freidin, Vytas K. Verselis, Thaddeus A. Bargiello, David P. Kelsell, Gabriele Richard, Michael V. L. Bennett, Feliksas F. Bukauskas

Proc Natl Acad Sci U S A. 2006 Mar 28; 103(13): 5213–5218. Published online 2006 Mar 20. doi: 10.1073/pnas.0511091103

PMCID:: PMC1458820

Abstract Article PDF–1.2M

Select item 52892817.

The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)

Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504

Correction in:: Genome Res. 2006 Jun; 16(6): 804.

PMCID:: PMC528928

Abstract Article PDF–140K

Select item 13924118.

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Mammalian Gene Collection (MGC) Program Team

Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899

PMCID:: PMC139241

Abstract Article PDF–118K

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