Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the α3(VI) N10-N7 domains-Reference-Cited by-同舟云学术

Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the α3(VI) N10-N7 domains

Published:2005-06-17 Issue:1 Volume:206 Page:160-166
ISSN:0021-9541
Container-title:Journal of Cellular Physiology
language:en
Short-container-title:J. Cell. Physiol.

Author:

Squarzoni Stefano,Sabatelli Patrizia,Bergamin Natascha,Guicheney Pascale,Demir Ercan,Merlini Luciano,Lattanzi Giovanna,Ognibene Andrea,Capanni Cristina,Mattioli Elisabetta,Columbaro Marta,Bonaldo Paolo,Maraldi Nadir Mario

Funder

Association Française contre les Myopathies (AFM)

Telethon Italy

Italian Health Ministry

Italian Ministry for University and Research (FIRB Project)

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Physiology

Reference19 articles.

1. Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy;Baker;Hum Mol Genet,2005

2. The supramolecular organization of collagen VI microfibrils;Baldock;J Mol Biol,2003

3. Type VI collagen in extracellular, 100-nm periodic filaments and fibrils: Identification by immunoelectron microscopy;Bruns;J Cell Biol,1986

4. Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI;Camacho Vanegas;Proc Natl Acad Sci USA,2001

5. The superfamily of proteins with von Willebrand factor type A-like domains: One theme common to components of extracellular matrix, hemostasis, cellular adhesion, and defense mechanisms;Colombatti;Blood,1991

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