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Select item 109358541.

Reconstructing the ancestral gene pool to uncover the origins and genetic links of Hmong–Mien speakers

Yang Gao, Xiaoxi Zhang, Hao Chen, Yan Lu, Sen Ma, Yajun Yang, Menghan Zhang, Shuhua Xu

BMC Biol. 2024; 22: 59. Published online 2024 Mar 13. doi: 10.1186/s12915-024-01838-9

PMCID:: PMC10935854

Abstract Article PDF–7.4M

Select item 107854072.

Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China

Shan Wu, Zhidan Wu, Manlian Chen, Xiangbin Zhong, Haoyan Gu, Wenjing Du, Weidong Liu, Li Lang, Junyi Wang

BMC Med Genomics. 2024; 17: 18. Published online 2024 Jan 11. doi: 10.1186/s12920-023-01790-7

PMCID:: PMC10785407

Abstract Article PDF–1.4M

Select item 107059333.

Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up

Aki Sakata, Akinori Kashio, Misaki Koyama, Shinji Urata, Hajime Koyama, Tatsuya Yamasoba

Int J Mol Sci. 2023 Dec; 24(23): 16763. Published online 2023 Nov 25. doi: 10.3390/ijms242316763

PMCID:: PMC10705933

Abstract Article PDF–2.4M

Select item 106709654.

Genotypic and Allelic Frequencies of GJB2 Variants and Features of Hearing Phenotypes in the Chinese Population of the Dongfeng-Tongji Cohort

Lanlai Yuan, Xiaohui Wang, Xiaozhou Liu, Sen Chen, Weijia Kong, Meian He, Yu Sun

Genes (Basel) 2023 Nov; 14(11): 2007. Published online 2023 Oct 27. doi: 10.3390/genes14112007

PMCID:: PMC10670965

Abstract Article PDF–1.3M

Select item 106683745.

Dispersed DNA variants underlie hearing loss in South Florida’s minority population

LéShon Peart, Joanna Gonzalez, Dayna Morel Swols, Duygu Duman, Turcin Saridogan, Memoona Ramzan, Mohammad Faraz Zafeer, Xue Zhong Liu, Adrien A. Eshraghi, Michael E. Hoffer, Simon I. Angeli, Guney Bademci, Susan Blanton, Carson Smith, Fred F. Telischi, Mustafa Tekin

Hum Genomics. 2023; 17: 103. Published online 2023 Nov 24. doi: 10.1186/s40246-023-00556-7

PMCID:: PMC10668374

Abstract Article PDF–1.3M

Select item 106049056.

Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains

Olga L. Posukh, Ekaterina A. Maslova, Valeriia Yu. Danilchenko, Marina V. Zytsar, Konstantin E. Orishchenko

Biomolecules. 2023 Oct; 13(10): 1521. Published online 2023 Oct 13. doi: 10.3390/biom13101521

PMCID:: PMC10604905

Abstract Article PDF–2.5M

Select item 105193717.

GJB2 – The Spectrum of Deafness-Causing Allele Variants and Their Phenotype

Hela Azaiez, G. Parker Chamberlin, Stephanie M. Fischer, Chelsea L. Welp, Sai D. Prasad, R. Thomas Taggart, Ignacio del Castillo, Guy Van Camp, Richard J. H. Smith

Hum Mutat. Author manuscript; available in PMC 2023 Sep 25.

Published in final edited form as: Hum Mutat. 2004 Oct; 24(4): 305–311. doi: 10.1002/humu.20084

PMCID:: PMC10519371

Abstract Article PDF–317K

Select item 104754268.

硒-甲基硒代半胱氨酸通过增强缝隙连接蛋白26构成的同型缝隙连接提高依托泊苷的细胞毒性

振宇吕, 文斌季, 倩倩程, 雪丽周, 威王, 燕杨

Sichuan Da Xue Xue Bao Yi Xue Ban. 2023 May 20; 54(3): 532–538. Chinese. doi: 10.12182/20230560205

PMCID:: PMC10475426

Abstract Article PDF–1.3M

Select item 104220659.

Analysis of GJB2 gene mutations spectrum and the characteristics of individuals with c.109G>A in Western Guangdong

Shaoming Liang, Weihong Li, Zhichao Chen, Shimin Yuan, Zhao Wang

Mol Genet Genomic Med. 2023 Aug; 11(8): e2185. Published online 2023 Apr 18. doi: 10.1002/mgg3.2185

PMCID:: PMC10422065

Abstract Article PDF–1.1M

Select item 1021860910.

The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia)

Vera G. Pshennikova, Fedor M. Teryutin, Alexandra M. Cherdonova, Tuyara V. Borisova, Aisen V. Solovyev, Georgii P. Romanov, Igor V. Morozov, Alexander A. Bondar, Olga L. Posukh, Sardana A. Fedorova, Nikolay A. Barashkov

Genes (Basel) 2023 May; 14(5): 1001. Published online 2023 Apr 28. doi: 10.3390/genes14051001

PMCID:: PMC10218609

Abstract Article PDF–2.1M

Select item 1003393711.

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

Abstract Article PDF–1.5M

Select item 1000858412.

Cryo-EM structures of human Cx36/GJD2 neuronal gap junction channel

Seu-Na Lee, Hwa-Jin Cho, Hyeongseop Jeong, Bumhan Ryu, Hyuk-Joon Lee, Minsoo Kim, Jejoong Yoo, Jae-Sung Woo, Hyung Ho Lee

Nat Commun. 2023; 14: 1347. Published online 2023 Mar 11. doi: 10.1038/s41467-023-37040-8

PMCID:: PMC10008584

Abstract Article PDF–7.3M

Select item 985861113.

Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene

Anca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, Andrei Pîrvu, Diana Miclea, Gheorghe Mihuț, Răzvan-Mihail Pleșea, Delia Ștefan, Mihaela Drodar, Călin Lazăr, on behalf of the HINT Study, on behalf of the FUSE Study, Mihai Ioana, Radu Popp

Genes (Basel) 2023 Jan; 14(1): 69. Published online 2022 Dec 26. doi: 10.3390/genes14010069

PMCID:: PMC9858611

Abstract Article PDF–639K

Select item 974097614.

The Expression of Connexin 26 Regulates the Radiosensitivity of Hepatocellular Carcinoma Cells through a Mitogen-Activated Protein Kinases Signal Pathway

Yuan Li, Li Yang, Rui Tao, Yajing Shang, Minqiong Sun, Shichao Peng, Guoping Zhao, Ye Zhao

Int J Mol Sci. 2022 Dec; 23(23): 14644. Published online 2022 Nov 24. doi: 10.3390/ijms232314644

PMCID:: PMC9740976

Abstract Article PDF–3.2M

Select item 961668315.

Cryo-EM structure of an open conformation of a gap junction hemichannel in lipid bilayer nanodiscs

Ali K. Khan, Maciej Jagielnicki, Brad.C. Bennett, Michael D. Purdy, Mark Yeager

Structure. Author manuscript; available in PMC 2022 Oct 28.

Published in final edited form as: Structure. 2021 Sep 2; 29(9): 1040–1047.e3. Published online 2021 Jun 14. doi: 10.1016/j.str.2021.05.010

PMCID:: PMC9616683

Abstract Article PDF–1.4M

Select item 959255816.

Conformational changes and CO₂-induced channel gating in connexin26

Deborah H. Brotherton, Christos G. Savva, Timothy J. Ragan, Nicholas Dale, Alexander D. Cameron

Structure. 2022 May 5; 30(5): 697–706.e4. doi: 10.1016/j.str.2022.02.010

PMCID:: PMC9592558

Abstract Article

Select item 945086517.

A study of GJB2 and delGJB6-D13S1830 mutations in Brazilian non-syndromic deaf children from the Amazon region

Luciana Santos Serrão de Castro, Anderson Nonato do Rosario Marinho, Elzemar Martins Ribeiro Rodrigues, Giorgio Christie Tavares Marques, Tarcísio André Amorim de Carvalho, Luiz Carlos Santana da Silva, Sidney Emanuel Batista dos Santos

Braz J Otorhinolaryngol. 2013 Jan-Feb; 79(1): 95–99. Published online 2015 Oct 14. doi: 10.5935/1808-8694.20130016

PMCID:: PMC9450865

Abstract Article PDF–179K

Select item 944617218.

Prevalence of 35de1G/GJB2 and del (GJB6-D13S1830) mutations in patients with non-syndromic deafness from a population of Espírito Santo - Brazil

Melissa de Freitas Cordeiro-Silva, Andressa Barbosa, Marília Santiago, Mariana Provetti, Eliete Rabbi-Bortolini

Braz J Otorhinolaryngol. 2010 Jul-Aug; 76(4): 428–432. Published online 2015 Oct 19. doi: 10.1590/S1808-86942010000400004

PMCID:: PMC9446172

Abstract Article PDF–174K

Select item 944283119.

Frequency of GJB2 mutations in patients with nonsyndromic hearing loss from an ethnically characterized Brazilian population

Felippe Felix, Marcia Gonçalves Ribeiro, Shiro Tomita, Mariano Gustavo Zalis

Braz J Otorhinolaryngol. 2019 Jan-Feb; 85(1): 92–98. Published online 2017 Nov 21. doi: 10.1016/j.bjorl.2017.10.013

PMCID:: PMC9442831

Abstract Article PDF–461K

Select item 926688020.

3D Chromatin Organization Involving MEIS1 Factor in the cis-Regulatory Landscape of GJB2

Anaïs Le Nabec, Clara Blotas, Alinéor Briset, Mégane Collobert, Claude Férec, Stéphanie Moisan

Int J Mol Sci. 2022 Jul; 23(13): 6964. Published online 2022 Jun 23. doi: 10.3390/ijms23136964

PMCID:: PMC9266880

Abstract Article PDF–2.0M

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