Three Novel Collagen VI Chains, α4(VI), α5(VI), and α6(VI)

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منابع مشابه

Non-basement membrane collagen A, B and C alpha-chains: types V and VI collagen? [proceedings].

Eibl, H. & Lands, W. E. M. (1969) Anal. Blochem. 30,5 1-57 Furthmayr, H. (1978) J. Supramol. Struct. 9,79-95 Grant, C. W. M. & McConnell, H. M. (1974) Proc. Natl. Acad. Sci. U S A . 17,46534657 Hesketh, T. R., Smith, G. A., Houslay, M. D., McGill, K. A., Birdsall, N. N. J., Metcalfe, J. and Warren, G. B. (1976) Biochemistry IS, 4145-415 1 Commun. 68,363-368 Lowry, 0. H., Rosebrough, N. J., Farr...

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Collagen VI-related myopathy

Synonyms Spectrum of phenotypes: Mild: Bethlem myopathy/ benign congenital muscular dystrophy Intermediate: Limb-girdle muscular dystrophy; myosclerosis myopathy Severe: Ullrich myopathy/ congenital atonic sclerotic muscular dystrophy First described by Ullrich in 1930 and Bethlem in 1976 respectively [1]. Caused by mutations in any of the 3 genes which code for collagen type VI synthesis, COL6...

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Collagen VI related muscle disorders.

Mutations in the genes encoding collagen VI (COL6A1, COL6A2, and COL6A3) cause Bethlem myopathy (BM) and Ullrich congenital muscular dystrophy (UCMD), two conditions which were previously believed to be completely separate entities. BM is a relatively mild dominantly inherited disorder characterised by proximal weakness and distal joint contractures. UCMD was originally described as an autosoma...

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Col6a1 Null Mice as a Model to Study Skin Phenotypes in Patients with Collagen VI Related Myopathies: Expression of Classical and Novel Collagen VI Variants during Wound Healing

Patients suffering from collagen VI related myopathies caused by mutations in COL6A1, COL6A2 and COL6A3 often also display skin abnormalities, like formation of keloids or "cigarette paper" scars, dry skin, striae rubrae and keratosis pilaris (follicular keratosis). Here we evaluated if Col6a1 null mice, an established animal model for the muscle changes in collagen VI related myopathies, are a...

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H-1 Collagen VI myopathies: pathogenic mechanisms and novel therapeutic perspectives

Mutations in any of the three genes coding for the extracellular matrix protein collagen VI cause different types of muscle diseases, including Bethlem Myopathy (BM), Ullrich Congenital Muscular Dystrophy (UCMD) and Congenital Myosclerosis (1). Collagen VI null (Col6a1–/–) mice display a myopathic phenotype with organelle defects, mitochondrial dysfunction and spontaneous apoptosis of muscle fi...

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ژورنال

عنوان ژورنال: Journal of Biological Chemistry

سال: 2008

ISSN: 0021-9258

DOI: 10.1074/jbc.m710139200