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John F Bateman

Showing results (41-50 of 94) with videos related to

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Arthritis and Rheumatism|February 5, 2010
Premature arthritis is a distinct type II collagen phenotypePeter Kannu, John F Bateman, Susan Randle, et al.
Journal of Proteome Research|January 23, 2016
Novel Elements of the Chondrocyte Stress Response Identified Using an in Vitro Model of Mouse Cartilage DegradationRichard Wilson, Suzanne B Golub, Lynn Rowley, et al.
Molecular Biology of the Cell|April 10, 2009
Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protectionYoshihito Ishida, Akitsugu Yamamoto, Akira Kitamura, et al.
Human Molecular Genetics|November 26, 2004
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophyNaomi L Baker, Matthias Mörgelin, Rachel Peat, et al.
Stem Cell Research|May 15, 2019
The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC lineSara Howden, Hani Hosseini Far, Ali Motazedian, et al.
Stem Cell Research|December 30, 2019
Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editingYudha Nur Patria, Jinia Lilianty, Andrew G Elefanty, et al.
American Journal of Human Genetics|February 29, 2008
Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasiaJacqueline T Tan, Friederike Kremer, Susanna Freddi, et al.
Molecular & Cellular Proteomics : MCP|March 2, 2010
Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomicsRichard Wilson, Anders F Diseberg, Lavinia Gordon, et al.
Plos One|October 22, 2013
bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1Kerry A Miller, Christopher T Gordon, Megan F Welfare, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 24, 2007
Bulldog dwarfism in Dexter cattle is caused by mutations in ACANJulie A L Cavanagh, Imke Tammen, Peter A Windsor, et al.
Pageof 10

Showing results (41-50 of 94) with videos related to

Sort By:
Pageof 10
Arthritis and Rheumatism|February 5, 2010
Premature arthritis is a distinct type II collagen phenotypePeter Kannu, John F Bateman, Susan Randle, et al.
Journal of Proteome Research|January 23, 2016
Novel Elements of the Chondrocyte Stress Response Identified Using an in Vitro Model of Mouse Cartilage DegradationRichard Wilson, Suzanne B Golub, Lynn Rowley, et al.
Molecular Biology of the Cell|April 10, 2009
Autophagic elimination of misfolded procollagen aggregates in the endoplasmic reticulum as a means of cell protectionYoshihito Ishida, Akitsugu Yamamoto, Akira Kitamura, et al.
Human Molecular Genetics|November 26, 2004
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophyNaomi L Baker, Matthias Mörgelin, Rachel Peat, et al.
Stem Cell Research|May 15, 2019
The use of simultaneous reprogramming and gene correction to generate an osteogenesis imperfecta patient COL1A1 c. 3936 G>T iPSC line and an isogenic control iPSC lineSara Howden, Hani Hosseini Far, Ali Motazedian, et al.
Stem Cell Research|December 30, 2019
Generation of a SOX9-tdTomato reporter human iPSC line, MCRIi001-A-2, using CRISPR/Cas9 editingYudha Nur Patria, Jinia Lilianty, Andrew G Elefanty, et al.
American Journal of Human Genetics|February 29, 2008
Competency for nonsense-mediated reduction in collagen X mRNA is specified by the 3' UTR and corresponds to the position of mutations in Schmid metaphyseal chondrodysplasiaJacqueline T Tan, Friederike Kremer, Susanna Freddi, et al.
Molecular & Cellular Proteomics : MCP|March 2, 2010
Comprehensive profiling of cartilage extracellular matrix formation and maturation using sequential extraction and label-free quantitative proteomicsRichard Wilson, Anders F Diseberg, Lavinia Gordon, et al.
Plos One|October 22, 2013
bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1Kerry A Miller, Christopher T Gordon, Megan F Welfare, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 24, 2007
Bulldog dwarfism in Dexter cattle is caused by mutations in ACANJulie A L Cavanagh, Imke Tammen, Peter A Windsor, et al.
Pageof 10