Literature DB >> 12923422

The role of connexins in human disease.

Eugene H Chang1, Guy Van Camp, Richard J H Smith.   

Abstract

Connexins are the building blocks of gap junctions. In forming a gap junction, six connexins oligomerize to form a hexameric torus called a connexon. The number of gap junctions in a cell ranges from a few to over 105 and imparts to interconnected cells a uniform phenotype. The crucial role that gap junctions play in normal physiology is reflected by the diverse spectrum of human diseases in which allele variants of different gap junction genes are implicated. In particular, mutations in GJB2 are a major cause of autosomal recessive non-syndromic deafness. This discovery has impacted medical practice and makes it incumbent on clinicians to familiarize themselves with the genetic advances that are rapidly occurring in our field.

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Year:  2003        PMID: 12923422     DOI: 10.1097/01.AUD.0000079801.55588.13

Source DB:  PubMed          Journal:  Ear Hear        ISSN: 0196-0202            Impact factor:   3.570


  14 in total

1.  A low-cost exon capture method suitable for large-scale screening of genetic deafness by the massively-parallel sequencing approach.

Authors:  Wenxue Tang; Dong Qian; Shoeb Ahmad; Douglas Mattox; N Wendell Todd; Harrison Han; Shouting Huang; Yuhua Li; Yunfeng Wang; Huawei Li; Xi Lin
Journal:  Genet Test Mol Biomarkers       Date:  2012-04-05

2.  Advances in Auditory and Vestibular Medicine.

Authors:  Mohamed A Hamid; Dennis R Trune; Mayank B Dutia
Journal:  Audiol Med       Date:  2009-12-01

3.  Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness.

Authors:  Shoeb Ahmad; Wenxue Tang; Qing Chang; Yan Qu; Jill Hibshman; Yuhua Li; Goran Söhl; Klaus Willecke; Ping Chen; Xi Lin
Journal:  Proc Natl Acad Sci U S A       Date:  2007-01-16       Impact factor: 11.205

4.  Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions.

Authors:  Yanping Zhang; Wenxue Tang; Shoab Ahmad; James A Sipp; Ping Chen; Xi Lin
Journal:  Proc Natl Acad Sci U S A       Date:  2005-10-10       Impact factor: 11.205

Review 5.  Inner ear supporting cells: rethinking the silent majority.

Authors:  Guoqiang Wan; Gabriel Corfas; Jennifer S Stone
Journal:  Semin Cell Dev Biol       Date:  2013-03-29       Impact factor: 7.727

6.  Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane.

Authors:  Omar Akil; Stephanie L Rouse; Dylan K Chan; Lawrence R Lustig
Journal:  J Vis Exp       Date:  2015-03-16       Impact factor: 1.355

7.  Gap junction protein connexin 43 serves as a negative marker for a stem cell-containing population of human limbal epithelial cells.

Authors:  Zhuo Chen; W Howard Evans; Stephen C Pflugfelder; De-Quan Li
Journal:  Stem Cells       Date:  2006-01-19       Impact factor: 6.277

Review 8.  Do cell junction protein mutations cause an airway phenotype in mice or humans?

Authors:  Eugene H Chang; Alejandro A Pezzulo; Joseph Zabner
Journal:  Am J Respir Cell Mol Biol       Date:  2011-02-04       Impact factor: 6.914

Review 9.  Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Authors:  Emilie Hoang Dinh; Shoeb Ahmad; Qing Chang; Wenxue Tang; Benjamin Stong; Xi Lin
Journal:  Brain Res       Date:  2009-02-20       Impact factor: 3.252

10.  Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea.

Authors:  Yu Sun; Wenxue Tang; Qing Chang; Yunfeng Wang; Weijia Kong; Xi Lin
Journal:  J Comp Neurol       Date:  2009-10-20       Impact factor: 3.215

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