Literature DB >> 12823303

Connexin gene pathology.

G Richard1.   

Abstract

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Year:  2003        PMID： 12823303     DOI： 10.1046/j.1365-2230.2003.01312.x

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN： 0307-6938            Impact factor:   3.470


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  8 in total

Review 1.  Life cycle of connexins in health and disease.

Authors:  Dale W Laird
Journal:  Biochem J       Date:  2006-03-15       Impact factor: 3.857

2.  Differentiation of organotypic epidermis in the presence of skin disease-linked dominant-negative Cx26 mutants and knockdown Cx26.

Authors:  Tamsin Thomas; Qing Shao; Dale W Laird
Journal:  J Membr Biol       Date:  2007-07-20       Impact factor: 1.843

Review 3.  Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.

Authors:  Iris Schrijver
Journal:  J Mol Diagn       Date:  2004-11       Impact factor: 5.568

Review 4.  Connexin37: a potential modifier gene of inflammatory disease.

Authors:  Marc Chanson; Brenda R Kwak
Journal:  J Mol Med (Berl)       Date:  2007-02-22       Impact factor: 4.599

5.  Properties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.

Authors:  Charles K Abrams; Mona M Freidin; Vytas K Verselis; Thaddeus A Bargiello; David P Kelsell; Gabriele Richard; Michael V L Bennett; Feliksas F Bukauskas
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-20       Impact factor: 11.205

Review 6.  Possible involvement of different connexin43 domains in plasma membrane permeabilization induced by ischemia-reperfusion.

Authors:  Mauricio A Retamal; Kurt A Schalper; Kenji F Shoji; Juan A Orellana; Michael V L Bennett; Juan C Sáez
Journal:  J Membr Biol       Date:  2007-08-20       Impact factor: 1.843

7.  Novel mutations in GJA1 cause oculodentodigital syndrome.

Authors:  A Fenwick; R J Richardson; J Butterworth; M J Barron; M J Dixon
Journal:  J Dent Res       Date:  2008-11       Impact factor: 6.116

8.  Evaluation of electrocardiographic parameters in patients with hearing loss genotyped for the connexin 26 gene (GJB2) mutations.

Authors:  Agnieszka Sanecka; Elzbieta Katarzyna Biernacka; Magdalena Sosna; Malgorzata Mueller-Malesinska; Rafal Ploski; Henryk Skarzynski; Ryszard Piotrowicz
Journal:  Braz J Otorhinolaryngol       Date:  2016-04-22
  8 in total

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