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The American Review of Respiratory Disease|April 1, 1981
Prevention of bleomycin-induced pulmonary fibrosis in the hamster by cis-4-hydroxy-l-prolineD J Riley, J S Kerr, R A Berg, et al.Calcified Tissue International|October 1, 1996
Vitamin D receptor genotype is not associated with bone mineral density in three ethnic/regional groupsL D Spotila, J Caminis, R Johnston, et al.Human Mutation|January 1, 1994
A single base mutation in the type II procollagen gene (COL2A1) that converts glycine alpha 1-247 to serine in a family with late-onset spondyloepiphyseal dysplasiaP Ritvaniemi, B P Sokolov, C J Williams, et al.American Journal of Medical Genetics|September 1, 1989
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissueD J Prockop, C D Constantinou, K E Dombrowski, et al.The Journal of Clinical Investigation|May 1, 1985
Modulation of procollagen gene expression by retinoids. Inhibition of collagen production by retinoic acid accompanied by reduced type I procollagen messenger ribonucleic acid levels in human skin fibroblast culturesH Oikarinen, A I Oikarinen, E M Tan, et al.Journal of Molecular Biology|November 20, 1989
Pleomorphism in type I collagen fibrils produced by persistence of the procollagen N-propeptideD J Hulmes, K E Kadler, A P Mould, et al.The Biochemical Journal|January 6, 2000
Lack of a phenotype in transgenic mice aberrantly expressing COL2A1 mRNA because of highly selective post-transcriptional down-regulationC M Yuan, L Ala-Kokko, D Le Guellec, et al.Genes & Development|November 15, 1995
Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral boneS W Li, D J Prockop, H Helminen, et al.Human Genetics|November 1, 1993
Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1)C J Williams, E L Considine, R G Knowlton, et al.Genomics|July 1, 1989
Assignment of the human collagen alpha 1 (XIII) chain gene (COL13A1) to the q22 region of chromosome 10T B Shows, L Tikka, M G Byers, et al.Pageof 30