PMC Links for Gene (Select 2706) - PMC

Result Filters

Links from Gene

Items: 1 to 20 of 221

<< First< Prev

Page of 12

Next >Last >>

Select item 111475071.

Structures of wild-type and a constitutively closed mutant of connexin26 shed light on channel regulation by CO₂

Deborah H Brotherton, Sarbjit Nijjar, Christos G Savva, Nicholas Dale, Alexander David Cameron

eLife. 2024; 13: RP93686. Published online 2024 Jun 3. doi: 10.7554/eLife.93686

PMCID:: PMC11147507

Abstract Article PDF–12M

Select item 110838312.

Structural basis for pathogenic variants of GJB2 and hearing levels of patients with hearing loss

Kazunori Namba, Hideki Mutai, Tatsuo Matsunaga, Hiroki Kaneko

BMC Res Notes. 2024; 17: 131. Published online 2024 May 10. doi: 10.1186/s13104-024-06793-w

PMCID:: PMC11083831

Abstract Article PDF–1.1M

Select item 109358543.

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 107059334.

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 106709655.

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 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 1017645711.

Programming Levels and Speech Perception in Pediatric Cochlear Implant Recipients with Enlarged Vestibular Aqueduct or GJB2 Mutation

Kelly N. Jahn, Charlotte Morse-Fortier, Amanda M. Griffin, David Faller, Michael S. Cohen, Margaret A. Kenna, Elizabeth Doney, Julie G. Arenberg

Otol Neurotol. Author manuscript; available in PMC 2024 Jun 1.

Published in final edited form as: Otol Neurotol. 2023 Jun 1; 44(5): e273–e280. doi: 10.1097/MAO.0000000000003879

PMCID:: PMC10176457

Abstract Article PDF–1.0M

Select item 985861112.

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 974097613.

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 961668314.

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 959255815.

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 944283116.

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 889192317.

Analysis of GJB2 Gene Mutations in 1330 Deafness Cases of Major Ethnic Groups in Northwest China

Panpan Bian, Baicheng Xu, Xiaoyun Zhao, YiMing Zhu, Chi Chen, XingJian Chen, Xiaowen Liu, Yanli Wang, Yufen Guo

Inquiry. 2022 Jan-Dec; 59: 00469580211055571. Published online 2022 Feb 25. doi: 10.1177/00469580211055571

PMCID:: PMC8891923

Abstract Article PDF–932K

Select item 881167518.

Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population

Anwar Madlool Al-janabi, Habeeb Shuhaib Ahmmed, Salih Mahdi Al-Khafaji

J Med Life. 2021 Nov-Dec; 14(6): 841–846. doi: 10.25122/jml-2021-0152

PMCID:: PMC8811675

Abstract Article PDF–613K

Select item 854486719.

Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan

Nabila Kausar, Asma Haque, Muhammad Shareef Masoud, Nazia Nahid, Usman Ali Ashfaq, Ali Muhammad Waryah, Rashid Bhatti, Muhammad Qasim

PLoS One. 2021; 16(10): e0259083. Published online 2021 Oct 25. doi: 10.1371/journal.pone.0259083

PMCID:: PMC8544867

Abstract Article PDF–1.2M

Select item 839192620.

Whole-Genome Sequencing Improves the Diagnosis of DFNB1 Monoallelic Patients

Anaïs Le Nabec, Mégane Collobert, Cédric Le Maréchal, Rémi Marianowski, Claude Férec, Stéphanie Moisan

Genes (Basel) 2021 Aug; 12(8): 1267. Published online 2021 Aug 19. doi: 10.3390/genes12081267

PMCID:: PMC8391926

Abstract Article PDF–4.0M

<< First< Prev

Page of 12

Next >Last >>

Supplemental Content

Filter your results:

Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

PMC Links for Gene (Select 2706) (221)
PMC
PREDICTED: Homo sapiens mevalonate kinase (MVK), transcript variant X2, mRNA
PREDICTED: Homo sapiens mevalonate kinase (MVK), transcript variant X2, mRNA
gi|2217289136|ref|XM_017019313.3|

Nucleotide
PREDICTED: Homo sapiens protein C, inactivator of coagulation factors Va and VII...
PREDICTED: Homo sapiens protein C, inactivator of coagulation factors Va and VIIIa (PROC), transcript variant X4, mRNA
gi|2217329629|ref|XM_047445117.1|

Nucleotide
Homo sapiens zinc finger, AN1-type domain 5, mRNA (cDNA clone MGC:87987 IMAGE:61...
Homo sapiens zinc finger, AN1-type domain 5, mRNA (cDNA clone MGC:87987 IMAGE:6137219), complete cds
gi|49116163|gb|BC073131.1|

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to: