J D Schofield|D J Prockop - JoVE Visualize

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Osteoarthritis and Cartilage|July 4, 2012

Intra-articular injection of human mesenchymal stem cells (MSCs) promote rat meniscal regeneration by being activated to express Indian hedgehog that enhances expression of type II collagenM Horie, H Choi, R H Lee, et al.

American Journal of Medical Genetics|November 7, 1998

Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.

Ciba Foundation Symposium|January 1, 1988

Expression of type I procollagen genesD J Prockop, K E Kadler, Y Hojima, et al.

American Journal of Human Genetics|January 1, 1993

A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.

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.

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Showing results (221-230 of 270) with videos related to

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Pageof 27

Osteoarthritis and Cartilage|July 4, 2012

Intra-articular injection of human mesenchymal stem cells (MSCs) promote rat meniscal regeneration by being activated to express Indian hedgehog that enhances expression of type II collagenM Horie, H Choi, R H Lee, et al.

American Journal of Medical Genetics|November 7, 1998

Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.

Ciba Foundation Symposium|January 1, 1988

Expression of type I procollagen genesD J Prockop, K E Kadler, Y Hojima, et al.

American Journal of Human Genetics|January 1, 1993

A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.

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.

Pageof 27