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D J Prockop

Showing results (241-250 of 266) with videos related to

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The Biochemical Journal|May 1, 1995
Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationshipsJ Bonaventure, L Cohen-Solal, P Ritvaniemi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1998
Marrow stromal cells as a source of progenitor cells for nonhematopoietic tissues in transgenic mice with a phenotype of osteogenesis imperfectaR F Pereira, M D O'Hara, A V Laptev, et al.
Neurology|December 1, 1993
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patientsH Kuivaniemi, D J Prockop, Y Wu, et al.
Osteoarthritis and Cartilage|March 10, 2001
More knee joint osteoarthritis (OA) in mice after inactivation of one allele of type II procollagen gene but less OA after lifelong voluntary wheel running exerciseT Lapveteläinen, M Hyttinen, J Lindblom, et al.
The Biochemical Journal|April 4, 2001
Transgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterilityS W Li, M Arita, A Fertala, et al.
The Journal of Clinical Investigation|June 1, 1993
Sequencing of cDNA from 50 unrelated patients reveals that mutations in the triple-helical domain of type III procollagen are an infrequent cause of aortic aneurysmsG Tromp, Y Wu, D J Prockop, et al.
Gene|September 26, 1996
Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)I C Scott, R Halila, J M Jenkins, et al.
British Journal of Cancer|November 8, 2007
A potential role for Dkk-1 in the pathogenesis of osteosarcoma predicts novel diagnostic and treatment strategiesN Lee, A J Smolarz, S Olson, et al.
American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.
American Journal of Human Genetics|November 1, 1989
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen geneR G Knowlton, E J Weaver, A F Struyk, et al.
Pageof 27

Showing results (241-250 of 266) with videos related to

Sort By:
Pageof 27
The Biochemical Journal|May 1, 1995
Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationshipsJ Bonaventure, L Cohen-Solal, P Ritvaniemi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1998
Marrow stromal cells as a source of progenitor cells for nonhematopoietic tissues in transgenic mice with a phenotype of osteogenesis imperfectaR F Pereira, M D O'Hara, A V Laptev, et al.
Neurology|December 1, 1993
Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patientsH Kuivaniemi, D J Prockop, Y Wu, et al.
Osteoarthritis and Cartilage|March 10, 2001
More knee joint osteoarthritis (OA) in mice after inactivation of one allele of type II procollagen gene but less OA after lifelong voluntary wheel running exerciseT Lapveteläinen, M Hyttinen, J Lindblom, et al.
The Biochemical Journal|April 4, 2001
Transgenic mice with inactive alleles for procollagen N-proteinase (ADAMTS-2) develop fragile skin and male sterilityS W Li, M Arita, A Fertala, et al.
The Journal of Clinical Investigation|June 1, 1993
Sequencing of cDNA from 50 unrelated patients reveals that mutations in the triple-helical domain of type III procollagen are an infrequent cause of aortic aneurysmsG Tromp, Y Wu, D J Prockop, et al.
Gene|September 26, 1996
Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)I C Scott, R Halila, J M Jenkins, et al.
British Journal of Cancer|November 8, 2007
A potential role for Dkk-1 in the pathogenesis of osteosarcoma predicts novel diagnostic and treatment strategiesN Lee, A J Smolarz, S Olson, et al.
American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.
American Journal of Human Genetics|November 1, 1989
Genetic linkage analysis of hereditary arthro-ophthalmopathy (Stickler syndrome) and the type II procollagen geneR G Knowlton, E J Weaver, A F Struyk, et al.
Pageof 27