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F Bateman

Showing results (111-120 of 203) with videos related to

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Human Mutation|March 17, 2004
Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assemblyJohn F Bateman, Susanna Freddi, Robyn McNeil, et al.
The Journal of Biological Chemistry|July 4, 2003
Complexes of matrilin-1 and biglycan or decorin connect collagen VI microfibrils to both collagen II and aggrecanCharlotte Wiberg, Andreas R Klatt, Raimund Wagener, et al.
The Journal of Biological Chemistry|August 30, 1996
Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened alpha2(I) chains show differential incorporation into the bone and skin extracellular matrixS Mundlos, D Chan, Y M Weng, et al.
Proteomics|December 14, 2006
Proteomic analysis of mouse growth plate cartilageDaniele Belluoccio, Richard Wilson, David J Thornton, et al.
Plos One|January 10, 2013
WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytesUwe Hansen, Justin M Allen, Rachel White, et al.
The Journal of Biological Chemistry|July 5, 1989
A frameshift mutation results in a truncated nonfunctional carboxyl-terminal pro alpha 1(I) propeptide of type I collagen in osteogenesis imperfectaJ F Bateman, S R Lamande, H H Dahl, et al.
Stem Cell Research|May 24, 2020
Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editingJinia Lilianty, Yudha Nur Patria, Edouard G Stanley, et al.
The EMBO Journal|June 1, 1989
A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos syndrome type VIID Weil, M D'Alessio, F Ramirez, et al.
The American Journal of Pathology|December 26, 2001
A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic miceO Jacenko, D Chan, A Franklin, et al.
Brain Research|September 12, 2000
UNCL, the mammalian homologue of UNC-50, is an inner nuclear membrane RNA-binding proteinJ Fitzgerald, D Kennedy, N Viseshakul, et al.
Pageof 21

Showing results (111-120 of 203) with videos related to

Sort By:
Pageof 21
Human Mutation|March 17, 2004
Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assemblyJohn F Bateman, Susanna Freddi, Robyn McNeil, et al.
The Journal of Biological Chemistry|July 4, 2003
Complexes of matrilin-1 and biglycan or decorin connect collagen VI microfibrils to both collagen II and aggrecanCharlotte Wiberg, Andreas R Klatt, Raimund Wagener, et al.
The Journal of Biological Chemistry|August 30, 1996
Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened alpha2(I) chains show differential incorporation into the bone and skin extracellular matrixS Mundlos, D Chan, Y M Weng, et al.
Proteomics|December 14, 2006
Proteomic analysis of mouse growth plate cartilageDaniele Belluoccio, Richard Wilson, David J Thornton, et al.
Plos One|January 10, 2013
WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytesUwe Hansen, Justin M Allen, Rachel White, et al.
The Journal of Biological Chemistry|July 5, 1989
A frameshift mutation results in a truncated nonfunctional carboxyl-terminal pro alpha 1(I) propeptide of type I collagen in osteogenesis imperfectaJ F Bateman, S R Lamande, H H Dahl, et al.
Stem Cell Research|May 24, 2020
Generation of a heterozygous COL2A1 (p.R989C) spondyloepiphyseal dysplasia congenita mutation iPSC line, MCRIi001-B, using CRISPR/Cas9 gene editingJinia Lilianty, Yudha Nur Patria, Edouard G Stanley, et al.
The EMBO Journal|June 1, 1989
A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos syndrome type VIID Weil, M D'Alessio, F Ramirez, et al.
The American Journal of Pathology|December 26, 2001
A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic miceO Jacenko, D Chan, A Franklin, et al.
Brain Research|September 12, 2000
UNCL, the mammalian homologue of UNC-50, is an inner nuclear membrane RNA-binding proteinJ Fitzgerald, D Kennedy, N Viseshakul, et al.
Pageof 21