The N-terminal N5 Subdomain of the α3(VI) Chain Is Important for Collagen VI Microfibril Formation

This publication has 31 references indexed in Scilit:

• Bethlem Myopathy and Engineered Collagen VI Triple Helical Deletions Prevent Intracellular Multimer Assembly and Protein Secretion
  Published by Elsevier ,1999
• Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy
  Human Molecular Genetics, 1998
• Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiency
  Human Molecular Genetics, 1998
• Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy
  Human Molecular Genetics, 1998
• The Role of the α3(VI) Chain in Collagen VI Assembly
  Journal of Biological Chemistry, 1998
• Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
  Nature Genetics, 1996
• Primary structure of the long and short splice variants of mouse collagen XII and their tissue‐specific expression during embryonic development
  Developmental Dynamics, 1995
• 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
  Blood, 1991
• Structure and Macromolecular Organization of Type VI Collagena
  Annals of the New York Academy of Sciences, 1985
• Electron-microscopical approach to a structural model of intima collagen
  Biochemical Journal, 1983