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L Ala-Kokko

Showing results (41-50 of 85) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasiaP Vandenberg, J S Khillan, D J Prockop, et al.
American Journal of Human Genetics|March 26, 1999
COL9A3: A third locus for multiple epiphyseal dysplasiaP Paassilta, J Lohiniva, S Annunen, et al.
Psychiatric Genetics|December 23, 1998
Human G(olf) gene polymorphisms and vulnerability to bipolar disorderW H Berrettini, J Vuoristo, T N Ferraro, et al.
Annals of the Rheumatic Diseases|December 3, 2003
Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosisN Noponen-Hietala, E Kyllönen, M Männikkö, et al.
The Journal of Biological Chemistry|August 5, 1991
Expression of a human cartilage procollagen gene (COL2A1) in mouse 3T3 cellsL Ala-Kokko, J Hyland, C Smith, et al.
Archives of Toxicology|January 1, 1996
Biochemical and morphological characterization of carbon tetrachloride-induced lung fibrosis in ratsP Pääkkö, S Anttila, R Sormunen, et al.
The Journal of Biological Chemistry|April 21, 1995
Tissue-specific expression of the gene for type I procollagen (COL1A1) in transgenic mice. Only 476 base pairs of the promoter are required if collagen genes are used as reportersB P Sokolov, L Ala-Kokko, R Dhulipala, et al.
American Journal of Human Genetics|July 1, 1993
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)J Körkkö, P Ritvaniemi, L Haataja, et al.
The Journal of Biological Chemistry|July 12, 2001
Sp3 represses the Sp1-mediated transactivation of the human COL2A1 gene in primary and de-differentiated chondrocytesC Ghayor, C Chadjichristos, J F Herrouin, 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.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1991
Expression of a partially deleted gene of human type II procollagen (COL2A1) in transgenic mice produces a chondrodysplasiaP Vandenberg, J S Khillan, D J Prockop, et al.
American Journal of Human Genetics|March 26, 1999
COL9A3: A third locus for multiple epiphyseal dysplasiaP Paassilta, J Lohiniva, S Annunen, et al.
Psychiatric Genetics|December 23, 1998
Human G(olf) gene polymorphisms and vulnerability to bipolar disorderW H Berrettini, J Vuoristo, T N Ferraro, et al.
Annals of the Rheumatic Diseases|December 3, 2003
Sequence variations in the collagen IX and XI genes are associated with degenerative lumbar spinal stenosisN Noponen-Hietala, E Kyllönen, M Männikkö, et al.
The Journal of Biological Chemistry|August 5, 1991
Expression of a human cartilage procollagen gene (COL2A1) in mouse 3T3 cellsL Ala-Kokko, J Hyland, C Smith, et al.
Archives of Toxicology|January 1, 1996
Biochemical and morphological characterization of carbon tetrachloride-induced lung fibrosis in ratsP Pääkkö, S Anttila, R Sormunen, et al.
The Journal of Biological Chemistry|April 21, 1995
Tissue-specific expression of the gene for type I procollagen (COL1A1) in transgenic mice. Only 476 base pairs of the promoter are required if collagen genes are used as reportersB P Sokolov, L Ala-Kokko, R Dhulipala, et al.
American Journal of Human Genetics|July 1, 1993
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)J Körkkö, P Ritvaniemi, L Haataja, et al.
The Journal of Biological Chemistry|July 12, 2001
Sp3 represses the Sp1-mediated transactivation of the human COL2A1 gene in primary and de-differentiated chondrocytesC Ghayor, C Chadjichristos, J F Herrouin, 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.
Pageof 9