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D J Prockop

Showing results (201-210 of 266) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
cDNA cloning and expression of bovine procollagen I N-proteinase: a new member of the superfamily of zinc-metalloproteinases with binding sites for cells and other matrix componentsA Colige, S W Li, A L Sieron, et al.
Molecular Psychiatry|October 14, 2000
Sequence and genomic organization of the human G-protein Golfalpha gene (GNAL) on chromosome 18p11, a susceptibility region for bipolar disorder and schizophreniaJ T Vuoristo, W H Berrettini, J Overhauser, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1997
Mass spectrometric gene diagnosis of one-base substitution from polymerase chain reaction amplified human DNAT Tsuneyoshi, K Ishikawa, Y Koga, et al.
Biochemistry|October 25, 1983
Nucleotide sequences of complementary deoxyribonucleic acids for the pro alpha 1 chain of human type I procollagen. Statistical evaluation of structures that are conserved during evolutionM P Bernard, M L Chu, J C Myers, et al.
American Journal of Medical Genetics|June 14, 1996
A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindredC J Williams, A Ganguly, E Considine, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1984
Nuclease S1 mapping of a homozygous mutation in the carboxyl-propeptide-coding region of the pro alpha 2(I) collagen gene in a patient with osteogenesis imperfectaL A Dickson, T Pihlajaniemi, S Deak, et al.
The Journal of Biological Chemistry|May 6, 1994
Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytesP Freisinger, L Ala-Kokko, D LeGuellec, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Large introns in the 3' end of the gene for the pro alpha 1 (IV) chain of human basement membrane collagenR Soininen, L Tikka, L Chow, et al.
Human Mutation|January 1, 1997
Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrentJ Körkkö, H Kuivaniemi, P Paassilta, et al.
The Biochemical Journal|January 15, 1989
Increased expression of the gene for the pro alpha 1(IV) chain of basement-membrane procollagen in cultured skin fibroblasts from two variants of osteogenesis imperfectaT Pihlajaniemi, J McKeon, S Gay, et al.
Pageof 27

Showing results (201-210 of 266) with videos related to

Sort By:
Pageof 27
Proceedings of the National Academy of Sciences of the United States of America|March 18, 1997
cDNA cloning and expression of bovine procollagen I N-proteinase: a new member of the superfamily of zinc-metalloproteinases with binding sites for cells and other matrix componentsA Colige, S W Li, A L Sieron, et al.
Molecular Psychiatry|October 14, 2000
Sequence and genomic organization of the human G-protein Golfalpha gene (GNAL) on chromosome 18p11, a susceptibility region for bipolar disorder and schizophreniaJ T Vuoristo, W H Berrettini, J Overhauser, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1997
Mass spectrometric gene diagnosis of one-base substitution from polymerase chain reaction amplified human DNAT Tsuneyoshi, K Ishikawa, Y Koga, et al.
Biochemistry|October 25, 1983
Nucleotide sequences of complementary deoxyribonucleic acids for the pro alpha 1 chain of human type I procollagen. Statistical evaluation of structures that are conserved during evolutionM P Bernard, M L Chu, J C Myers, et al.
American Journal of Medical Genetics|June 14, 1996
A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindredC J Williams, A Ganguly, E Considine, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1984
Nuclease S1 mapping of a homozygous mutation in the carboxyl-propeptide-coding region of the pro alpha 2(I) collagen gene in a patient with osteogenesis imperfectaL A Dickson, T Pihlajaniemi, S Deak, et al.
The Journal of Biological Chemistry|May 6, 1994
Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytesP Freisinger, L Ala-Kokko, D LeGuellec, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1986
Large introns in the 3' end of the gene for the pro alpha 1 (IV) chain of human basement membrane collagenR Soininen, L Tikka, L Chow, et al.
Human Mutation|January 1, 1997
Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrentJ Körkkö, H Kuivaniemi, P Paassilta, et al.
The Biochemical Journal|January 15, 1989
Increased expression of the gene for the pro alpha 1(IV) chain of basement-membrane procollagen in cultured skin fibroblasts from two variants of osteogenesis imperfectaT Pihlajaniemi, J McKeon, S Gay, et al.
Pageof 27