A type VII collagen subdomain mutant is thermolabile and shows enhanced proteolytic degradability — Implications for the pathogenesis of recessive dystrophic epidermolysis bullosa?
Author:
Funder
Else Kröner-Fresenius-Stiftung
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference51 articles.
1. Type VII collagen is a major structural component of anchoring fibrils;Sakai;J. Cell Biol.,1986
2. Type VII collagen is a normal component of epidermal basement membrane, which shows altered expression in recessive dystrophic epidermolysis bullosa;Leigh;J. Invest. Dermatol.,1988
3. Lack of type VII collagen in unaffected skin of patients with severe recessive dystrophic epidermolysis bullosa;Bruckner-Tuderman;Dermatology,1988
4. Epidermolysis bullosa acquisita antigen is the globular carboxyl terminus of type VII procollagen;Woodley;J. Clin. Invest.,1988
5. Laminin 5 binds the NC-1 domain of type VII collagen;Rousselle;J. Cell Biol.,1997
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