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The American Review of Respiratory Disease
|
May 1, 1989
Malotilate prevents accumulation of type III pN-collagen, type IV collagen, and laminin in carbon tetrachloride-induced pulmonary fibrosis in rats
P Pääkkö, R Sormunen, L Risteli, et al.
Nature Genetics
|
November 1, 1992
A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI
J Hyland, L Ala-Kokko, P Royce, et al.
The Biochemical Journal
|
July 1, 1992
Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse
M Vikkula, M Metsäranta, A C Syvänen, et al.
The Biochemical Journal
|
May 15, 1987
Gene expression of type I, III and IV collagens in hepatic fibrosis induced by dimethylnitrosamine in the rat
L Ala-Kokko, T Pihlajaniemi, J C Myers, et al.
Genomics
|
April 1, 1993
A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasia
M Vikkula, P Ritvaniemi, A F Vuorio, et al.
The British Journal of Dermatology
|
November 1, 1990
Effect of long-term PUVA treatment of psoriasis on the collagen and elastin gene expression and growth of skin fibroblasts in vitro
A Oikarinen, L Ala-Kokko, M Tamminen, 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 electrophoresis
P Ritvaniemi, J Hyland, J Ignatius, et al.
Circulation
|
February 18, 1997
Origin of extracellular matrix synthesis during coronary repair
Y Shi, J E O'Brien, L Ala-Kokko, 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 molecule
T Pihlajamaa, M M Vuoristo, S Annunen, et al.
American Journal of Human Genetics
|
March 7, 1998
Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations
J Körkkö, L Ala-Kokko, A De Paepe, et al.
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Search research articles
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Showing results (31-40 of 85) with videos related to
Sort By:
Page
of 9
The American Review of Respiratory Disease
|
May 1, 1989
Malotilate prevents accumulation of type III pN-collagen, type IV collagen, and laminin in carbon tetrachloride-induced pulmonary fibrosis in rats
P Pääkkö, R Sormunen, L Risteli, et al.
Nature Genetics
|
November 1, 1992
A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI
J Hyland, L Ala-Kokko, P Royce, et al.
The Biochemical Journal
|
July 1, 1992
Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse
M Vikkula, M Metsäranta, A C Syvänen, et al.
The Biochemical Journal
|
May 15, 1987
Gene expression of type I, III and IV collagens in hepatic fibrosis induced by dimethylnitrosamine in the rat
L Ala-Kokko, T Pihlajaniemi, J C Myers, et al.
Genomics
|
April 1, 1993
A mutation in the amino-terminal end of the triple helix of type II collagen causing severe osteochondrodysplasia
M Vikkula, P Ritvaniemi, A F Vuorio, et al.
The British Journal of Dermatology
|
November 1, 1990
Effect of long-term PUVA treatment of psoriasis on the collagen and elastin gene expression and growth of skin fibroblasts in vitro
A Oikarinen, L Ala-Kokko, M Tamminen, 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 electrophoresis
P Ritvaniemi, J Hyland, J Ignatius, et al.
Circulation
|
February 18, 1997
Origin of extracellular matrix synthesis during coronary repair
Y Shi, J E O'Brien, L Ala-Kokko, 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 molecule
T Pihlajamaa, M M Vuoristo, S Annunen, et al.
American Journal of Human Genetics
|
March 7, 1998
Analysis of the COL1A1 and COL1A2 genes by PCR amplification and scanning by conformation-sensitive gel electrophoresis identifies only COL1A1 mutations in 15 patients with osteogenesis imperfecta type I: identification of common sequences of null-allele mutations
J Körkkö, L Ala-Kokko, A De Paepe, et al.
Page
of 9