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J F Bateman

Showing results (51-60 of 97) with videos related to

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The Biochemical Journal|September 15, 1994
A 5' splice site mutation affecting the pre-mRNA splicing of two upstream exons in the collagen COL1A1 gene. Exon 8 skipping and altered definition of exon 7 generates truncated pro alpha 1(I) chains with a non-collagenous insertion destabilizing the triple helixJ F Bateman, D Chan, I Moeller, et al.
Cell Structure and Function|July 8, 2000
Mammalian skeletogenesis and extracellular matrix: what can we learn from knockout mice?A Aszódi, J F Bateman, E Gustafsson, et al.
The Journal of Biological Chemistry|March 25, 1986
Induction of procollagen processing in fibroblast cultures by neutral polymersJ F Bateman, W G Cole, J J Pillow, et al.
Human Mutation|February 6, 1998
A type III collagen Gly559 to Arg helix mutation in Ehler's-Danlos syndrome type IVJ F Bateman, A A Chiodo, Y M Weng, et al.
The Biochemical Journal|December 15, 1986
Collagen defects in lethal perinatal osteogenesis imperfectaJ F Bateman, D Chan, T Mascara, et al.
The Journal of Biological Chemistry|January 27, 1995
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilageD Chan, W G Cole, C W Chow, et al.
The Journal of Clinical Investigation|April 29, 1998
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasiaD Chan, Y M Weng, H K Graham, et al.
The Journal of Biological Chemistry|August 25, 1988
Substitution of arginine for glycine 664 in the collagen alpha 1(I) chain in lethal perinatal osteogenesis imperfecta. Demonstration of the peptide defect by in vitro expression of the mutant cDNAJ F Bateman, S R Lamande, H H Dahl, et al.
The Journal of Biological Chemistry|May 25, 1987
Lethal perinatal osteogenesis imperfecta due to the substitution of arginine for glycine at residue 391 of the alpha 1(I) chain of type I collagenJ F Bateman, D Chan, I D Walker, et al.
The Journal of Biological Chemistry|April 25, 1986
Deletion of 24 amino acids from the pro-alpha 1(I) chain of type I procollagen in a patient with the Ehlers-Danlos syndrome type VIIW G Cole, D Chan, G W Chambers, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
The Biochemical Journal|September 15, 1994
A 5' splice site mutation affecting the pre-mRNA splicing of two upstream exons in the collagen COL1A1 gene. Exon 8 skipping and altered definition of exon 7 generates truncated pro alpha 1(I) chains with a non-collagenous insertion destabilizing the triple helixJ F Bateman, D Chan, I Moeller, et al.
Cell Structure and Function|July 8, 2000
Mammalian skeletogenesis and extracellular matrix: what can we learn from knockout mice?A Aszódi, J F Bateman, E Gustafsson, et al.
The Journal of Biological Chemistry|March 25, 1986
Induction of procollagen processing in fibroblast cultures by neutral polymersJ F Bateman, W G Cole, J J Pillow, et al.
Human Mutation|February 6, 1998
A type III collagen Gly559 to Arg helix mutation in Ehler's-Danlos syndrome type IVJ F Bateman, A A Chiodo, Y M Weng, et al.
The Biochemical Journal|December 15, 1986
Collagen defects in lethal perinatal osteogenesis imperfectaJ F Bateman, D Chan, T Mascara, et al.
The Journal of Biological Chemistry|January 27, 1995
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilageD Chan, W G Cole, C W Chow, et al.
The Journal of Clinical Investigation|April 29, 1998
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasiaD Chan, Y M Weng, H K Graham, et al.
The Journal of Biological Chemistry|August 25, 1988
Substitution of arginine for glycine 664 in the collagen alpha 1(I) chain in lethal perinatal osteogenesis imperfecta. Demonstration of the peptide defect by in vitro expression of the mutant cDNAJ F Bateman, S R Lamande, H H Dahl, et al.
The Journal of Biological Chemistry|May 25, 1987
Lethal perinatal osteogenesis imperfecta due to the substitution of arginine for glycine at residue 391 of the alpha 1(I) chain of type I collagenJ F Bateman, D Chan, I D Walker, et al.
The Journal of Biological Chemistry|April 25, 1986
Deletion of 24 amino acids from the pro-alpha 1(I) chain of type I procollagen in a patient with the Ehlers-Danlos syndrome type VIIW G Cole, D Chan, G W Chambers, et al.
Pageof 10