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D J Prockop

Showing results (221-230 of 266) with videos related to

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The Journal of Biological Chemistry|June 25, 1985
cDNA clones coding for the pro-alpha1(IV) chain of human type IV procollagen reveal an unusual homology of amino acid sequences in two halves of the carboxyl-terminal domainT Pihlajaniemi, K Tryggvason, J C Myers, et al.
Molecular Medicine (Cambridge, Mass.)|May 1, 1996
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritanceL D Spotila, J Caminis, M Devoto, et al.
The American Review of Respiratory Disease|January 1, 1982
beta-Aminopropionitrile prevents bleomycin-induced pulmonary fibrosis in the hamsterD J Riley, J S Kerr, R A Berg, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.
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.
Pageof 27

Showing results (221-230 of 266) with videos related to

Sort By:
Pageof 27
The Journal of Biological Chemistry|June 25, 1985
cDNA clones coding for the pro-alpha1(IV) chain of human type IV procollagen reveal an unusual homology of amino acid sequences in two halves of the carboxyl-terminal domainT Pihlajaniemi, K Tryggvason, J C Myers, et al.
Molecular Medicine (Cambridge, Mass.)|May 1, 1996
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritanceL D Spotila, J Caminis, M Devoto, et al.
The American Review of Respiratory Disease|January 1, 1982
beta-Aminopropionitrile prevents bleomycin-induced pulmonary fibrosis in the hamsterD J Riley, J S Kerr, R A Berg, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.
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.
Pageof 27