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Items: 1 to 20 of 69

1.
GJB1 variants in Charcot-Marie-Tooth disease X-linked type 1 in Mali
Abdoulaye Yalcouyé, Seybou H. Diallo, Lassana Cissé, Mamadou Karembé, Salimata Diallo, Thomas Coulibaly, Salimata Diarra, Dramane Coulibaly, Mohamed Keita, Cheick O. Guinto, Kenneth H. Fischbeck, Ambroise Wonkam, Guida Landouré, The H3Africa Consortium
J Peripher Nerv Syst. Author manuscript; available in PMC 2024 Apr 8.
Published in final edited form as: J Peripher Nerv Syst. 2022 Jun; 27(2): 113–119. Published online 2022 Apr 5. doi: 10.1111/jns.12486
PMCID:
PMC11000073
AbstractArticlePDF–695K
2.
Connexin32 gap junction channels deliver miR155-3p to mediate pyroptosis in renal ischemia-reperfusion injury
Liubing Chen, Hongyi Fang, Xiaoyun Li, Peiling Yu, Yu Guan, Cuicui Xiao, Zhizhao Deng, Ziqing Hei, Chaojin Chen, Chenfang Luo
Cell Commun Signal. 2024; 22: 121. Published online 2024 Feb 12. doi: 10.1186/s12964-023-01443-3
PMCID:
PMC10863161
AbstractArticlePDF–2.7M
3.
Role of connexin 32 in the directional differentiation of induced pluripotent stem cells into hepatocytes
Yan Xu, Yufeng Wang, Ran Qi, Kun Li, Xiuyan Wang, Xinbo Li, Baomin Shi
Int J Med Sci. 2024; 21(3): 508–518. Published online 2024 Jan 12. doi: 10.7150/ijms.83973
PMCID:
PMC10797672
AbstractArticlePDF–4.7M
4.
A novel splicing mutation in 5'UTR of GJB1 causes X‐linked Charcot—Marie–tooth disease
MeiYi Li, Minna Yin, Li Yang, Zhiheng Chen, Peng Du, Ling Sun, Juan Chen
Mol Genet Genomic Med. 2023 Mar; 11(3): e2108. Published online 2022 Nov 17. doi: 10.1002/mgg3.2108
PMCID:
PMC10009907
AbstractArticlePDF–2.9M
5.
Identification of a rare missense mutation in GJB1 and prenatal diagnosis in a Chinese family with CMT: A case report
Xinyi Huang, Xiaoli Wu, Bei Wu, Jing Mou, Xingwei Ma
Medicine (Baltimore) 2022 Nov 11; 101(45): e31733. Published online 2022 Nov 11. doi: 10.1097/MD.0000000000031733
PMCID:
PMC9666213
AbstractArticlePDF–819K
6.
Connexin32 regulates expansion of liver cancer stem cells via the PI3K/Akt signaling pathway
Hongyu Li, Boying Wang, Benquan Qi, Guojun Jiang, Min Qin, Meiling Yu
Oncol Rep. 2022 Sep; 48(3): 166. Published online 2022 Jul 25. doi: 10.3892/or.2022.8381
PMCID:
PMC9351005
AbstractArticlePDF–4.2M
7.
Expression and Functionality of Connexin-Based Channels in Human Liver Cancer Cell Lines
Kaat Leroy, Cícero Júlio Silva Costa, Alanah Pieters, Bruna dos Santos Rodrigues, Raf Van Campenhout, Axelle Cooreman, Andrés Tabernilla, Bruno Cogliati, Mathieu Vinken
Int J Mol Sci. 2021 Nov; 22(22): 12187. Published online 2021 Nov 10. doi: 10.3390/ijms222212187
PMCID:
PMC8623148
AbstractArticlePDF–4.5M
8.
Cx32 inhibits the autophagic effect of Nur77 in SH-SY5Y cells and rat brain with ischemic stroke
Fengfeng Ping, Chao Zhang, Xue Wang, Yan Wang, Danli Zhou, Jing Hu, Yanhua Chen, Jingjing Ling, Jia Zhou
Aging (Albany NY) 2021 Sep 30; 13(18): 22188–22207. Published online 2021 Sep 22. doi: 10.18632/aging.203526
PMCID:
PMC8507301
AbstractArticlePDF–2.2M
9.
Connexin32 activates necroptosis through Src‐mediated inhibition of caspase 8 in hepatocellular carcinoma
Yu‐ke Xiang, Fu‐hua Peng, Yun‐quan Guo, Hui Ge, Shao‐yi Cai, Li‐xia Fan, Yue‐xia Peng, Hao Wen, Qin Wang, Liang Tao
Cancer Sci. 2021 Sep; 112(9): 3507–3519. Published online 2021 Jul 16. doi: 10.1111/cas.14994
PMCID:
PMC8409421
AbstractArticlePDF–2.3M
10.
Crosstalk Between Connexin32 and Mitochondrial Apoptotic Signaling Pathway Plays a Pivotal Role in Renal Ischemia Reperfusion-Induced Acute Kidney Injury
Chaojin Chen, Weifeng Yao, Shan Wu, Shaoli Zhou, Mian Ge, Yu Gu, Xiang Li, Guihua Chen, Joseph A. Bellanti, Song Guo Zheng, Dongdong Yuan, Ziqing Hei
Antioxid Redox Signal. 2019 Apr 20; 30(12): 1521–1538. Published online 2019 Mar 11. doi: 10.1089/ars.2017.7375
PMCID:
PMC7364332
AbstractArticlePDF–2.4M
11.
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
12.
A novel GJB1 mutation associated with X‐linked Charcot–Marie–Tooth disease in a large Chinese family pedigree
Yingdi Liu, Jinjie Xue, Zhuo Li, Siyuan Linpeng, Hu Tan, Yanling Teng, Desheng Liang, Lingqian Wu
Mol Genet Genomic Med. 2020 Mar; 8(3): e1127. Published online 2020 Jan 14. doi: 10.1002/mgg3.1127
PMCID:
PMC7057093
AbstractArticlePDF–697K
13.
Recurrent episodes of reversible posterior leukoencephalopathy in three Chinese families with GJB1 mutations in X-linked Charcot-Marie-tooth type 1 disease: cases report
Youlong Liang, Jingli Liu, Daobin Cheng, Yu Wu, Liuhong Mo, Wen Huang
BMC Neurol. 2019; 19: 325. Published online 2019 Dec 16. doi: 10.1186/s12883-019-1563-4
PMCID:
PMC6912941
AbstractArticlePDF–1.4M
14.
Connexin32 Mutations Associated with X-Linked Charcot–Marie–Tooth Disease Show Two Distinct Behaviors: Loss of Function and Altered Gating Properties
Catherine Ressot, Danielle Gomès, André Dautigny, Danielle Pham-Dinh, Roberto Bruzzone
J Neurosci. 1998 Jun 1; 18(11): 4063–4075. doi: 10.1523/JNEUROSCI.18-11-04063.1998
PMCID:
PMC6792797
AbstractArticlePDF–250K
15.
Altered Formation of Hemichannels and Gap Junction Channels Caused by C-Terminal Connexin-32 Mutations
Carmen Castro, Juan M. Gómez-Hernandez, Kaisa Silander, Luis C. Barrio
J Neurosci. 1999 May 15; 19(10): 3752–3760. doi: 10.1523/JNEUROSCI.19-10-03752.1999
PMCID:
PMC6782695
AbstractArticlePDF–173K
16.
Transgenic Expression of Human Connexin32 in Myelinating Schwann Cells Prevents Demyelination in Connexin32-Null Mice
Steven S. Scherer, Yi-Tian Xu, Albee Messing, Klaus Willecke, Kenneth H. Fischbeck, Linda Jo Bone Jeng
J Neurosci. 2005 Feb 9; 25(6): 1550–1559. doi: 10.1523/JNEUROSCI.3082-04.2005
PMCID:
PMC6725992
AbstractArticlePDF–824K
17.
Prenylation-Defective Human Connexin32 Mutants Are Normally Localized and Function Equivalently to Wild-Type Connexin32 in Myelinating Schwann Cells
Yan Huang, Erich E. Sirkowski, John T. Stickney, Steven S. Scherer
J Neurosci. 2005 Aug 3; 25(31): 7111–7120. doi: 10.1523/JNEUROSCI.1319-05.2005
PMCID:
PMC6725241
AbstractArticlePDF–539K
18.
A network of chaperones prevents and detects failures in membrane protein lipid bilayer integration
João P. L. Coelho, Matthias Stahl, Nicolas Bloemeke, Kevin Meighen-Berger, Carlos Piedrafita Alvira, Zai-Rong Zhang, Stephan A. Sieber, Matthias J. Feige
Nat Commun. 2019; 10: 672. Published online 2019 Feb 8. doi: 10.1038/s41467-019-08632-0
Correction in:
Nat Commun. 2019; 10: 1908.
PMCID:
PMC6368539
AbstractArticlePDF–1.6M
19.
Regulation of Connexin32 by ephrin receptors and T-cell protein-tyrosine phosphatase
Andrew J. Trease, Hanjun Li, Gaelle Spagnol, Li Zheng, Kelly L. Stauch, Paul L. Sorgen
J Biol Chem. 2019 Jan 4; 294(1): 341–350. Published online 2018 Nov 6. doi: 10.1074/jbc.RA118.003883
PMCID:
PMC6322898
AbstractArticlePDF–1.6M
20.
An Eight Generation Family With CMTX: Confirmation Of The Pathogenicity Of A 3′ Untranslated Region Mutation In GJB1 And Its Clinical Features
Dong-Hui Chen, Maxwell Ma, Mena Scavina, Elizabeth Blue, John Wolff, Prasanthi Karna, Michael O. Dorschner, Wendy H. Raskind, Thomas D. Bird
Muscle Nerve. Author manuscript; available in PMC 2019 May 1.
Published in final edited form as: Muscle Nerve. 2018 May; 57(5): 859–862. Published online 2017 Dec 28. doi: 10.1002/mus.26037
PMCID:
PMC5910283
AbstractArticlePDF–455K

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