Phenotypic and biochemical consequences of collagen X mutations in mice and humans-Reference-Cited by-同舟云学术

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Phenotypic and biochemical consequences of collagen X mutations in mice and humans

Published:1998-07 Issue:3 Volume:17 Page:169-184
ISSN:0945-053X
Container-title:Matrix Biology
language:en
Short-container-title:Matrix Biology

Author:

Chan Danny,Jacenko Olena

Publisher

Elsevier BV

Subject

Molecular Biology

Reference80 articles.

1. Characterization of the mouse type X collagen gene;Apte;Matrix,1993

2. Collagens of the chicken eggshell membranes;Arias;Connect. Tissue Res.,1991

3. Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta;Bateman;Biochem. J.,1984

4. Mutations in three subdomains of the carboxyl-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias;Bonaventure;Hum. Genet.,1995

5. The fibrillar collagens, collagen VIII, collagen X and C1q complement proteins share a similar domain in their C-terminal non-collagenous regions;Brass;FEBS Lett.,1992

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