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D J Prockop

Showing results (211-220 of 266) with videos related to

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Matrix (Stuttgart, Germany)|December 1, 1991
Completion of the last half of the structure of the human gene for the Pro alpha 1 (I) chain of type I procollagen (COL1A1)A Westerhausen, C D Constantinou, M Pack, et al.
The Journal of Biological Chemistry|November 21, 1998
Recombinant procollagen II: Deletion of D period segments identifies sequences that are required for helix stabilization and generates a temperature-sensitive N-proteinase cleavage siteW V Arnold, A Fertala, A L Sieron, et al.
The Biochemical Journal|February 15, 1994
Synthesis of recombinant human procollagen II in a stably transfected tumour cell line (HT1080)A Fertala, A L Sieron, A Ganguly, et al.
The Journal of Biological Chemistry|November 10, 1984
Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutationT Pihlajaniemi, L A Dickson, F M Pope, et al.
The Biochemical Journal|June 15, 1995
Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1)L Ala-Kokko, A P Kvist, M Metsäranta, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 23, 2001
Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)S W Li, M Takanosu, M Arita, et al.
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.
Pageof 27

Showing results (211-220 of 266) with videos related to

Sort By:
Pageof 27
Matrix (Stuttgart, Germany)|December 1, 1991
Completion of the last half of the structure of the human gene for the Pro alpha 1 (I) chain of type I procollagen (COL1A1)A Westerhausen, C D Constantinou, M Pack, et al.
The Journal of Biological Chemistry|November 21, 1998
Recombinant procollagen II: Deletion of D period segments identifies sequences that are required for helix stabilization and generates a temperature-sensitive N-proteinase cleavage siteW V Arnold, A Fertala, A L Sieron, et al.
The Biochemical Journal|February 15, 1994
Synthesis of recombinant human procollagen II in a stably transfected tumour cell line (HT1080)A Fertala, A L Sieron, A Ganguly, et al.
The Journal of Biological Chemistry|November 10, 1984
Osteogenesis imperfecta: cloning of a pro-alpha 2(I) collagen gene with a frameshift mutationT Pihlajaniemi, L A Dickson, F M Pope, et al.
The Biochemical Journal|June 15, 1995
Conservation of the sizes of 53 introns and over 100 intronic sequences for the binding of common transcription factors in the human and mouse genes for type II procollagen (COL2A1)L Ala-Kokko, A P Kvist, M Metsäranta, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 23, 2001
Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)S W Li, M Takanosu, M Arita, et al.
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.
Pageof 27