Bone fragility in transgenic mice expressing a mutated gene for type I procollagen (COL1A1) parallels the age-dependent phenotype of human osteogenesis imperfecta-Reference-Cited by-同舟云学术

Bone fragility in transgenic mice expressing a mutated gene for type I procollagen (COL1A1) parallels the age-dependent phenotype of human osteogenesis imperfecta

Published:2009-12-03 Issue:12 Volume:10 Page:1837-1843
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Pereira Ruth F.,Hume Eric L.,Halford Kenneth W.,Prockop Darwin J.

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jbmr.5650101202/fullpdf

Reference17 articles.

1. Molecular basis of hereditary disorders of connective tissues;Tilstra;Ann Rev Med,1994

2. Mutation analysis of coding sequences for type I procollagen in individuals with low bone density;Spotila;J Bone Miner Res,1994

3. Embryonic lethal mutation in mouse collagen I gene causes rupture of blood vessels and is associated with erythropoietic and mesenchymal cell death;Lohler;Cell,1984

4. A transgenic mouse model of osteogenesis imperfecta type I;Bonadio;Proc Natl Acad Sci USA,1990

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