Meşe G - Search Results

1

The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epithelium.

DeRosa AM, Meşe G, Li L, Sellitto C, Brink PR, Gong X, White TW. DeRosa AM, et al. Among authors: mese g. Exp Cell Res. 2009 Apr 1;315(6):1063-75. doi: 10.1016/j.yexcr.2009.01.017. Epub 2009 Jan 30. Exp Cell Res. 2009. PMID: 19331825 Free PMC article.

2

Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

Meşe G, Londin E, Mui R, Brink PR, White TW. Meşe G, et al. Hum Genet. 2004 Aug;115(3):191-9. doi: 10.1007/s00439-004-1142-6. Epub 2004 Jul 7. Hum Genet. 2004. PMID: 15241677

3

Gap junctions: basic structure and function.

Meşe G, Richard G, White TW. Meşe G, et al. J Invest Dermatol. 2007 Nov;127(11):2516-24. doi: 10.1038/sj.jid.5700770. J Invest Dermatol. 2007. PMID: 17934503 Free article. Review.

4

Gap junction channels exhibit connexin-specific permeability to cyclic nucleotides.

Kanaporis G, Mese G, Valiuniene L, White TW, Brink PR, Valiunas V. Kanaporis G, et al. Among authors: mese g. J Gen Physiol. 2008 Apr;131(4):293-305. doi: 10.1085/jgp.200709934. J Gen Physiol. 2008. PMID: 18378798 Free PMC article.

5

Connexin26 deafness associated mutations show altered permeability to large cationic molecules.

Meşe G, Valiunas V, Brink PR, White TW. Meşe G, et al. Am J Physiol Cell Physiol. 2008 Oct;295(4):C966-74. doi: 10.1152/ajpcell.00008.2008. Epub 2008 Aug 6. Am J Physiol Cell Physiol. 2008. PMID: 18684989 Free PMC article.

6

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.

7

Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.

Levit NA, Mese G, Basaly MG, White TW. Levit NA, et al. Among authors: mese g. Biochim Biophys Acta. 2012 Aug;1818(8):2014-9. doi: 10.1016/j.bbamem.2011.09.003. Epub 2011 Sep 10. Biochim Biophys Acta. 2012. PMID: 21933663 Free PMC article. Review.

8

Altered conductance and permeability of Cx40 mutations associated with atrial fibrillation.

Santa Cruz A, Meşe G, Valiuniene L, Brink PR, White TW, Valiunas V. Santa Cruz A, et al. Among authors: mese g. J Gen Physiol. 2015 Nov;146(5):387-98. doi: 10.1085/jgp.201511475. J Gen Physiol. 2015. PMID: 26503720 Free PMC article.

9

Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel Properties.

Shuja Z, Li L, Gupta S, Meşe G, White TW. Shuja Z, et al. Among authors: mese g. J Invest Dermatol. 2016 Jan;136(1):225-235. doi: 10.1038/JID.2015.389. J Invest Dermatol. 2016. PMID: 26763442 Free PMC article.

10

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. Among authors: mese g. J Gen Physiol. 2010 Jul;136(1):47-62. doi: 10.1085/jgp.201010433. J Gen Physiol. 2010. PMID: 20584891 Free PMC article.

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