Anti-type VII collagen autoantibodies, detected by enzyme-linked immunosorbent assay, fluctuate in parallel with clinical severity in patients with epidermolysis bullosa acquisita-Reference-Cited by-同舟云学术

Anti-type VII collagen autoantibodies, detected by enzyme-linked immunosorbent assay, fluctuate in parallel with clinical severity in patients with epidermolysis bullosa acquisita

Published:2013-10-16 Issue:11 Volume:40 Page:864-868
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Ito Yoshihiro¹,Kasai Hiroko¹,Yoshida Tetsuya¹,Saleh Marwah A.¹²,Amagai Masayuki¹,Yamagami Jun¹

Affiliation:

1. Department of Dermatology; Keio University School of Medicine; Tokyo Japan

2. Department of Dermatology; Faculty of Medicine; Cairo University; Cairo Egypt

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference18 articles.

1. Identification of the skin basement-membrane auto-antigen in epidermolysis bullosa-acquisita;Woodley;N Engl J Med,1984

2. Epidermolysis bullosa acquisita antigen, a new major component of cutaneous basement membrane, is a glycoprotein with collagenous domains;Woodley;J Invest Dermatol,1986

3. Type VII collagen: the anchoring fibril protein at fault in dystrophic epidermolysis bullosa;Chung;Dermatol Clin,2010

4. The large non-collagenous domain (NC-1) of type VII collagen is amino-terminal and chimeric. Homology to cartilage matrix protein, the type III domains of fibronectin and the A domains of von Willebrand factor;Christiano;Hum Mol Genet,1992

5. The carboxyl-terminal half of type VII collagen, including the non-collagenous NC-2 domain and intron/exon organization of the corresponding region of the COL7A1 gene;Greenspan;Hum Mol Genet,1993

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