Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia-Reference-Cited by-同舟云学术

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Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

Published:1995-06 Issue:2 Volume:10 Page:229-234
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Vidal Frédérique,Aberdam Daniel,Miquel Corinne,Christiano Angela M.,Pulkkinen Leena,Uitto Jouni,Ortonne Jean-Paul,Meneguzzi Guerrino

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0695-229.pdf

Reference50 articles.

1. Hynes, R.O. Integrins: versatility, modulation and signaling in cell adhesion. Cell. 69, 11–25 (1992).

2. Anderson, D.C. & Springer, T.A. Leukocyte adhesion deficiency: an inherited defect in the Mac-1, LFA-1, and p150,95 glycoproteins. A. Rev. Med. 38, 175–194 (1987).

3. George, J.N., Caen, J.P. & Nurden, A.T. Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood. 75, 1383–1395 (1990).

4. De Luca, M. et al. Polarized integrin mediates human keratinocyte adhesion to basal lamina. Proc. natn. Acad. Sci. U.S.A. 87, 6888–6892 (1990).

5. Marchisio, P.C., Bondanza, S., Cremona, O., Cancedda, R. & De Luca, M. Polarized expression of integrin receptors ( α6β4, α2β1 and αvβ5) and their relationship with the cytoskeleton and basement membrane matrix in cultured human keratinocytes. J. Cell Biol. 112, 761–773 (1991).

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