A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis-Reference-Cited by-同舟云学术

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A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis

Published:1992-09 Issue:5 Volume:70 Page:821-828
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Chipev Constantin C.,Korge Bernhard P.,Markova Nedialka,Bale Sherri J.,DiGiovanna John J.,Compton John G.,Steinert Peter M.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference37 articles.

1. The fibrillar structure of keratin filaments unravelled;Aebi;J. Cell Biol.,1983

2. Genetically induced abnormalities of epidermal differentiation and ultrastructure in ichthyoses and epidermolyses; pathogenesis, heterogeneity, fetal manifestation, and prenatal diagnosis;Anton-Lamprecht;J. Invest. Dermatol.,1983

3. Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities;Bonifas;Science,1991

4. Intermediate filament reorganization during mitosis is mediated by p34cdc2 phosphorylation of vimentin;Chou;Cell,1990

5. Linkage of epidermolytic hyperkeratosis to the type Il keratin gene cluster on chromosome 12q;Compton;Nature Genetics,1992

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