Literature DB >> 10099690

Genetic diseases and gene knockouts reveal diverse connexin functions.

T W White1, D L Paul.   

Abstract

Intercellular channels present in gap junctions allow cells to share small molecules and thus coordinate a wide range of behaviors. Remarkably, although junctions provide similar functions in all multicellular organisms, vertebrates and invertebrates use unrelated gene families to encode these channels. The recent identification of the invertebrate innexin family opens up powerful genetic systems to studies of intercellular communication. At the same time, new information on the physiological roles of vertebrate connexins has emerged from genetic studies. Mutations in connexin genes underlie a variety of human diseases, including deafness, demyelinating neuropathies, and lens cataracts. In addition, gene targeting of connexins in mice has provided new insights into connexin function and the significance of connexin diversity.

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Year:  1999        PMID: 10099690     DOI: 10.1146/annurev.physiol.61.1.283

Source DB:  PubMed          Journal:  Annu Rev Physiol        ISSN: 0066-4278            Impact factor:   19.318


  88 in total

1.  Inhibition of endothelial wound repair by dominant negative connexin inhibitors.

Authors:  B R Kwak; M S Pepper; D B Gros; P Meda
Journal:  Mol Biol Cell       Date:  2001-04       Impact factor: 4.138

Review 2.  Connexin mutations in skin disease and hearing loss.

Authors:  D P Kelsell; W L Di; M J Houseman
Journal:  Am J Hum Genet       Date:  2001-01-25       Impact factor: 11.025

3.  Quinine blocks specific gap junction channel subtypes.

Authors:  M Srinivas; M G Hopperstad; D C Spray
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-04       Impact factor: 11.205

4.  Connexin 39.9 protein is necessary for coordinated activation of slow-twitch muscle and normal behavior in zebrafish.

Authors:  Hiromi Hirata; Hua Wen; Yu Kawakami; Yuriko Naganawa; Kazutoyo Ogino; Kenta Yamada; Louis Saint-Amant; Sean E Low; Wilson W Cui; Weibin Zhou; Shawn M Sprague; Kazuhide Asakawa; Akira Muto; Koichi Kawakami; John Y Kuwada
Journal:  J Biol Chem       Date:  2011-11-10       Impact factor: 5.157

Review 5.  Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.

Authors:  Noah A Levit; Gulistan Mese; Mena-George R Basaly; Thomas W White
Journal:  Biochim Biophys Acta       Date:  2011-09-10

6.  Regulation of ion fluxes, cell volume and gap junctional coupling by cGMP in GFSHR-17 granulosa cells.

Authors:  A Ngezahayo; B Altmann; H-A Kolb
Journal:  J Membr Biol       Date:  2003-08-01       Impact factor: 1.843

7.  Sequence and phylogenetic analyses of 4 TMS junctional proteins of animals: connexins, innexins, claudins and occludins.

Authors:  V B Hua; A B Chang; J H Tchieu; N M Kumar; P A Nielsen; M H Saier
Journal:  J Membr Biol       Date:  2003-07-01       Impact factor: 1.843

8.  The role of gap junctions in Charcot-Marie-Tooth disease.

Authors:  Kleopas A Kleopa
Journal:  J Neurosci       Date:  2011-12-07       Impact factor: 6.167

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.  Properties of connexin26 hemichannels expressed in Xenopus oocytes.

Authors:  Harris Ripps; Haohua Qian; Jane Zakevicius
Journal:  Cell Mol Neurobiol       Date:  2004-10       Impact factor: 5.046

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