Literature DB >> 12064628

Connexin 26 expression and mutation analysis in epidermal disease.

W L Di1, J E Common, D P Kelsell.   

Abstract

Gap junctional communication has a key role in the co-ordination of keratinocyte differentiation. Multiple connexins are expressed in the epidermis and mutations in four of these connexins are associated with disorders of keratinisation. Specific autosomal dominant Cx26 mutations have been associated with syndromes of skin disease and hearing loss. Here we describe the characterization of a new Cx26 polyclonal antibody raised against the cytoplasmic region of the protein. It has been used to investigate Cx26 protein localization in epidermal disease and in the study of mutant Cx26 proteins.

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Year:  2001        PMID: 12064628     DOI: 10.3109/15419060109080763

Source DB:  PubMed          Journal:  Cell Commun Adhes        ISSN: 1543-5180


  7 in total

Review 1.  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

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.  Connexin channels in congenital skin disorders.

Authors:  Evelyn Lilly; Caterina Sellitto; Leonard M Milstone; Thomas W White
Journal:  Semin Cell Dev Biol       Date:  2016-01-13       Impact factor: 7.727

4.  Connexin43 carboxyl-terminal peptides reduce scar progenitor and promote regenerative healing following skin wounding.

Authors:  Gautam S Ghatnekar; Michael P O'Quinn; L Jane Jourdan; Abhijit A Gurjarpadhye; Robert L Draughn; Robert G Gourdie
Journal:  Regen Med       Date:  2009-03       Impact factor: 3.806

5.  Altered intercellular communication in lung fibroblast cultures from patients with idiopathic pulmonary fibrosis.

Authors:  Angela Trovato-Salinaro; Elisa Trovato-Salinaro; Marco Failla; Claudio Mastruzzo; Valerio Tomaselli; Elisa Gili; Nunzio Crimi; Daniele Filippo Condorelli; Carlo Vancheri
Journal:  Respir Res       Date:  2006-09-27

6.  Functional Evaluation of a Rare Variant c.516G>C (p.Trp172Cys) in the GJB2 (Connexin 26) Gene Associated with Nonsyndromic Hearing Loss.

Authors:  Ekaterina A Maslova; Konstantin E Orishchenko; Olga L Posukh
Journal:  Biomolecules       Date:  2021-01-05

7.  Connexin26 Modulates the Radiosensitivity of Cutaneous Squamous Cell Carcinoma by Regulating the Activation of the MAPK/NF-κB Signaling Pathway.

Authors:  Minqiong Sun; Yuan Li; Jing Qian; Siwei Ding; Mingyu Sun; Bowen Tan; Ye Zhao
Journal:  Front Cell Dev Biol       Date:  2021-07-05
  7 in total

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