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D J Prockop

Showing results (251-260 of 266) with videos related to

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The Journal of Biological Chemistry|April 15, 1994
Characterization of type I procollagen N-proteinase from fetal bovine tendon and skin. Purification of the 500-kilodalton form of the enzyme from bovine tendonY Hojima, M M Mörgelin, J Engel, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Blood|February 27, 2001
Clinical responses to bone marrow transplantation in children with severe osteogenesis imperfectaE M Horwitz, D J Prockop, P L Gordon, et al.
Nature Medicine|March 23, 1999
Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfectaE M Horwitz, D J Prockop, L A Fitzpatrick, et al.
The Journal of Biological Chemistry|July 31, 1999
Complete sequence of the 23-kilobase human COL9A3 gene. Detection of Gly-X-Y triplet deletions that represent neutral variantsP Paassilta, T Pihlajamaa, S Annunen, et al.
Spine|November 29, 2001
Premature vertebral endplate ossification and mild disc degeneration in mice after inactivation of one allele belonging to the Col2a1 gene for Type II collagenJ Sahlman, R Inkinen, T Hirvonen, et al.
Science (New York, N.Y.)|July 20, 1999
An allele of COL9A2 associated with intervertebral disc diseaseS Annunen, P Paassilta, J Lohiniva, et al.
Calcified Tissue International|May 28, 2005
Abnormal response to physical activity in femurs after heterozygous inactivation of one allele of the Col2a1 gene for type II collagen in miceJ Nieminen, J Sahlman, T Hirvonen, et al.
Development (Cambridge, England)|November 15, 2000
Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinasesI A Kramerova, N Kawaguchi, L I Fessler, et al.
American Journal of Human Genetics|July 27, 1999
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.
Pageof 27

Showing results (251-260 of 266) with videos related to

Sort By:
Pageof 27
The Journal of Biological Chemistry|April 15, 1994
Characterization of type I procollagen N-proteinase from fetal bovine tendon and skin. Purification of the 500-kilodalton form of the enzyme from bovine tendonY Hojima, M M Mörgelin, J Engel, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Blood|February 27, 2001
Clinical responses to bone marrow transplantation in children with severe osteogenesis imperfectaE M Horwitz, D J Prockop, P L Gordon, et al.
Nature Medicine|March 23, 1999
Transplantability and therapeutic effects of bone marrow-derived mesenchymal cells in children with osteogenesis imperfectaE M Horwitz, D J Prockop, L A Fitzpatrick, et al.
The Journal of Biological Chemistry|July 31, 1999
Complete sequence of the 23-kilobase human COL9A3 gene. Detection of Gly-X-Y triplet deletions that represent neutral variantsP Paassilta, T Pihlajamaa, S Annunen, et al.
Spine|November 29, 2001
Premature vertebral endplate ossification and mild disc degeneration in mice after inactivation of one allele belonging to the Col2a1 gene for Type II collagenJ Sahlman, R Inkinen, T Hirvonen, et al.
Science (New York, N.Y.)|July 20, 1999
An allele of COL9A2 associated with intervertebral disc diseaseS Annunen, P Paassilta, J Lohiniva, et al.
Calcified Tissue International|May 28, 2005
Abnormal response to physical activity in femurs after heterozygous inactivation of one allele of the Col2a1 gene for type II collagen in miceJ Nieminen, J Sahlman, T Hirvonen, et al.
Development (Cambridge, England)|November 15, 2000
Papilin in development; a pericellular protein with a homology to the ADAMTS metalloproteinasesI A Kramerova, N Kawaguchi, L I Fessler, et al.
American Journal of Human Genetics|July 27, 1999
Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase geneA Colige, A L Sieron, S W Li, et al.
Pageof 27