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The Journal of Biological Chemistry|November 25, 1989

Substitution of serine for alpha 1(I)-glycine 844 in a severe variant of osteogenesis imperfecta minimally destabilizes the triple helix of type I procollagen. The effects of glycine substitutions on thermal stability are either position of amino acid specificM Pack, C D Constantinou, K Kalia, et al.

The Journal of Biological Chemistry|July 25, 1986

Defects in the processing of procollagen to collagen are demonstrable in cultured fibroblasts from patients with the Ehlers-Danlos and osteogenesis imperfecta syndromesR R Minor, M Sippola-Thiele, J McKeon, et al.

Diabetes Research (Edinburgh, Scotland)|May 1, 1990

Streptozotocin-diabetes but not galactose-feeding increases the serum concentration of type IV collagen antigens in ratsT Danne, R Poulsom, D Schuppan, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998

Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats--similarities to astrocyte graftsS A Azizi, D Stokes, B J Augelli, et al.

Human Mutation|January 1, 1996

Direct sequencing of PCR products derived from cDNAs for the pro alpha 1 and pro alpha 2 chains of type I procollagen as a screening method to detect mutations in patients with osteogenesis imperfectaJ Zhuang, G Tromp, H Kuivaniemi, et al.

The Biochemical Journal|June 1, 1989

Structure of cDNA clones coding for the entire prepro alpha 1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferencesL Ala-Kokko, S Kontusaari, C T Baldwin, et al.

Hepatology (Baltimore, Md.)|July 1, 1992

Hepatic fibrosis in rats produced by carbon tetrachloride and dimethylnitrosamine: observations suggesting immunoassays of serum for the 7S fragment of type IV collagen are a more sensitive index of liver damage than immunoassays for the NH2-terminal propeptide of type III procollagenL Ala-Kokko, V Günzler, J B Hoek, et al.

Collagen and Related Research|July 1, 1982

Separation of human pro alpha 1 (I) and pro alpha 2 (I) procollagen chains by reverse phase high performance liquid chromatographyM Van der Rest, C A Stolle, D J Prockop, et al.

Journal of Cellular Biochemistry|October 28, 1999

Donor variation in the growth properties and osteogenic potential of human marrow stromal cellsD G Phinney, G Kopen, W Righter, et al.

American Journal of Human Genetics|September 1, 1992

Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic motherS Kontusaari, G Tromp, H Kuivaniemi, et al.

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Showing results (171-180 of 292) with videos related to

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The Journal of Biological Chemistry|November 25, 1989

Substitution of serine for alpha 1(I)-glycine 844 in a severe variant of osteogenesis imperfecta minimally destabilizes the triple helix of type I procollagen. The effects of glycine substitutions on thermal stability are either position of amino acid specificM Pack, C D Constantinou, K Kalia, et al.

The Journal of Biological Chemistry|July 25, 1986

Defects in the processing of procollagen to collagen are demonstrable in cultured fibroblasts from patients with the Ehlers-Danlos and osteogenesis imperfecta syndromesR R Minor, M Sippola-Thiele, J McKeon, et al.

Diabetes Research (Edinburgh, Scotland)|May 1, 1990

Streptozotocin-diabetes but not galactose-feeding increases the serum concentration of type IV collagen antigens in ratsT Danne, R Poulsom, D Schuppan, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 9, 1998

Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats--similarities to astrocyte graftsS A Azizi, D Stokes, B J Augelli, et al.

Human Mutation|January 1, 1996

Direct sequencing of PCR products derived from cDNAs for the pro alpha 1 and pro alpha 2 chains of type I procollagen as a screening method to detect mutations in patients with osteogenesis imperfectaJ Zhuang, G Tromp, H Kuivaniemi, et al.

The Biochemical Journal|June 1, 1989

Structure of cDNA clones coding for the entire prepro alpha 1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferencesL Ala-Kokko, S Kontusaari, C T Baldwin, et al.

Hepatology (Baltimore, Md.)|July 1, 1992

Hepatic fibrosis in rats produced by carbon tetrachloride and dimethylnitrosamine: observations suggesting immunoassays of serum for the 7S fragment of type IV collagen are a more sensitive index of liver damage than immunoassays for the NH2-terminal propeptide of type III procollagenL Ala-Kokko, V Günzler, J B Hoek, et al.

Collagen and Related Research|July 1, 1982

Separation of human pro alpha 1 (I) and pro alpha 2 (I) procollagen chains by reverse phase high performance liquid chromatographyM Van der Rest, C A Stolle, D J Prockop, et al.

Journal of Cellular Biochemistry|October 28, 1999

Donor variation in the growth properties and osteogenic potential of human marrow stromal cellsD G Phinney, G Kopen, W Righter, et al.

American Journal of Human Genetics|September 1, 1992

Substitution of aspartate for glycine 1018 in the type III procollagen (COL3A1) gene causes type IV Ehlers-Danlos syndrome: the mutated allele is present in most blood leukocytes of the asymptomatic and mosaic motherS Kontusaari, G Tromp, H Kuivaniemi, et al.

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