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D J Prockop

Showing results (161-170 of 266) with videos related to

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The Biochemical Journal|September 1, 1989
Structure of cDNA clones coding for human type II procollagen. The alpha 1(II) chain is more similar to the alpha 1(I) chain than two other alpha chains of fibrillar collagensC T Baldwin, A M Reginato, C Smith, et al.
The Journal of Biological Chemistry|June 25, 1983
Synthesis of a shortened pro-alpha 2(I) chain and decreased synthesis of pro-alpha 2(I) chains in a proband with osteogenesis imperfectaW J de Wet, T Pihlajaniemi, J Myers, et al.
The Journal of Biological Chemistry|July 15, 1990
Identical G+1 to A mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome. IV. An explanation for exon skipping some mutations and not othersH Kuivaniemi, S Kontusaari, G Tromp, et al.
Collagen and Related Research|October 1, 1984
Presence of translatable mRNA for pro alpha 2(I) chains in fibroblasts from a patient with osteogenesis imperfecta whose type I collagen does not contain alpha 2(I) chainsM L Chu, D Rowe, A C Nicholls, et al.
Human Mutation|January 1, 1993
Temperature sensitivity of aberrant RNA splicing with a mutation in the G+5 position of intron 37 of the gene for type III procollagen from a patient with Ehlers-Danlos syndrome type IVY Wu, H Kuivaniemi, G Tromp, et al.
The Journal of Clinical Investigation|February 1, 1993
Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineralR Pereira, J S Khillan, H J Helminen, et al.
The Journal of Biological Chemistry|June 21, 1996
Assembly in vitro of thin and thick fibrils of collagen II from recombinant procollagen II. The monomers in the tips of thick fibrils have the opposite orientation from monomers in the growing tips of collagen I fibrilsA Fertala, D F Holmes, K E Kadler, et al.
Genomics|July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresisP Ritvaniemi, J Hyland, J Ignatius, et al.
European Journal of Biochemistry|August 1, 1981
Comparison of the NH2-Terminal sequences of chick Type I preprocollagen chains synthesized in an nRNA-dependent reticulocyte lysateP N Graves, B R Olsen, P P Fietzek, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 26, 1998
Human COL9A1 and COL9A2 genes. Two genes of 90 and 15 kb code for similar polypeptides of the same collagen moleculeT Pihlajamaa, M M Vuoristo, S Annunen, et al.
Pageof 27

Showing results (161-170 of 266) with videos related to

Sort By:
Pageof 27
The Biochemical Journal|September 1, 1989
Structure of cDNA clones coding for human type II procollagen. The alpha 1(II) chain is more similar to the alpha 1(I) chain than two other alpha chains of fibrillar collagensC T Baldwin, A M Reginato, C Smith, et al.
The Journal of Biological Chemistry|June 25, 1983
Synthesis of a shortened pro-alpha 2(I) chain and decreased synthesis of pro-alpha 2(I) chains in a proband with osteogenesis imperfectaW J de Wet, T Pihlajaniemi, J Myers, et al.
The Journal of Biological Chemistry|July 15, 1990
Identical G+1 to A mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome. IV. An explanation for exon skipping some mutations and not othersH Kuivaniemi, S Kontusaari, G Tromp, et al.
Collagen and Related Research|October 1, 1984
Presence of translatable mRNA for pro alpha 2(I) chains in fibroblasts from a patient with osteogenesis imperfecta whose type I collagen does not contain alpha 2(I) chainsM L Chu, D Rowe, A C Nicholls, et al.
Human Mutation|January 1, 1993
Temperature sensitivity of aberrant RNA splicing with a mutation in the G+5 position of intron 37 of the gene for type III procollagen from a patient with Ehlers-Danlos syndrome type IVY Wu, H Kuivaniemi, G Tromp, et al.
The Journal of Clinical Investigation|February 1, 1993
Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineralR Pereira, J S Khillan, H J Helminen, et al.
The Journal of Biological Chemistry|June 21, 1996
Assembly in vitro of thin and thick fibrils of collagen II from recombinant procollagen II. The monomers in the tips of thick fibrils have the opposite orientation from monomers in the growing tips of collagen I fibrilsA Fertala, D F Holmes, K E Kadler, et al.
Genomics|July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresisP Ritvaniemi, J Hyland, J Ignatius, et al.
European Journal of Biochemistry|August 1, 1981
Comparison of the NH2-Terminal sequences of chick Type I preprocollagen chains synthesized in an nRNA-dependent reticulocyte lysateP N Graves, B R Olsen, P P Fietzek, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 26, 1998
Human COL9A1 and COL9A2 genes. Two genes of 90 and 15 kb code for similar polypeptides of the same collagen moleculeT Pihlajamaa, M M Vuoristo, S Annunen, et al.
Pageof 27