Similar articles for PMID: 23756814

Year	Number of Results
1994	1
1995	1
1998	3
1999	7
2000	7
2001	8
2002	8
2003	13
2004	11
2005	14
2006	19
2007	12
2008	24
2009	22
2010	19
2011	25
2012	32
2013	30
2014	39
2015	22
2016	16
2017	16
2018	10
2019	18
2020	27
2021	33
2022	22
2023	15
2024	0

1

Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.

Zhang Y, Hao H. Zhang Y, et al. Biochem Biophys Res Commun. 2013 Jul 5;436(3):424-9. doi: 10.1016/j.bbrc.2013.05.118. Epub 2013 Jun 10. Biochem Biophys Res Commun. 2013. PMID: 23756814

2

Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.

Gerido DA, DeRosa AM, Richard G, White TW. Gerido DA, et al. Am J Physiol Cell Physiol. 2007 Jul;293(1):C337-45. doi: 10.1152/ajpcell.00626.2006. Epub 2007 Apr 11. Am J Physiol Cell Physiol. 2007. PMID: 17428836 Free article.

3

A novel mechanism for connexin 26 mutation linked deafness: cell death caused by leaky gap junction hemichannels.

Stong BC, Chang Q, Ahmad S, Lin X. Stong BC, et al. Laryngoscope. 2006 Dec;116(12):2205-10. doi: 10.1097/01.mlg.0000241944.77192.d2. Laryngoscope. 2006. PMID: 17146396

4

Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome.

Sánchez HA, Mese G, Srinivas M, White TW, Verselis VK. Sánchez HA, et al. J Gen Physiol. 2010 Jul;136(1):47-62. doi: 10.1085/jgp.201010433. J Gen Physiol. 2010. PMID: 20584891 Free PMC article.

5

Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.

García IE, Maripillán J, Jara O, Ceriani R, Palacios-Muñoz A, Ramachandran J, Olivero P, Perez-Acle T, González C, Sáez JC, Contreras JE, Martínez AD. García IE, et al. J Invest Dermatol. 2015 May;135(5):1338-1347. doi: 10.1038/jid.2015.20. Epub 2015 Jan 27. J Invest Dermatol. 2015. PMID: 25625422 Free PMC article.

6

The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions.

Sanchez HA, Villone K, Srinivas M, Verselis VK. Sanchez HA, et al. J Gen Physiol. 2013 Jul;142(1):3-22. doi: 10.1085/jgp.201310962. J Gen Physiol. 2013. PMID: 23797419 Free PMC article.

7

Altered inhibition of Cx26 hemichannels by pH and Zn2+ in the A40V mutation associated with keratitis-ichthyosis-deafness syndrome.

Sanchez HA, Bienkowski R, Slavi N, Srinivas M, Verselis VK. Sanchez HA, et al. J Biol Chem. 2014 Aug 1;289(31):21519-32. doi: 10.1074/jbc.M114.578757. Epub 2014 Jun 17. J Biol Chem. 2014. PMID: 24939841 Free PMC article.

8

The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.

Mese G, Sellitto C, Li L, Wang HZ, Valiunas V, Richard G, Brink PR, White TW. Mese G, et al. Mol Biol Cell. 2011 Dec;22(24):4776-86. doi: 10.1091/mbc.E11-09-0778. Epub 2011 Oct 26. Mol Biol Cell. 2011. PMID: 22031297 Free PMC article.

9

A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall.

Mei L, Chen J, Zong L, Zhu Y, Liang C, Jones RO, Zhao HB. Mei L, et al. Neurobiol Dis. 2017 Dec;108:195-203. doi: 10.1016/j.nbd.2017.08.002. Epub 2017 Aug 17. Neurobiol Dis. 2017. PMID: 28823936 Free PMC article.

10

Unique expression of connexins in the human cochlea.

Liu W, Boström M, Kinnefors A, Rask-Andersen H. Liu W, et al. Hear Res. 2009 Apr;250(1-2):55-62. doi: 10.1016/j.heares.2009.01.010. Epub 2009 Feb 6. Hear Res. 2009. PMID: 19450429

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