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John F Bateman

Showing results (81-90 of 91) with videos related to

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Plos Genetics|September 7, 2013
Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndromeKerry A Miller, Casey J Ah-Cann, Megan F Welfare, et al.
Nature Genetics|October 4, 2011
Mutations in TRPV4 cause an inherited arthropathy of hands and feetShireen R Lamandé, Yuan Yuan, Irma L Gresshoff, et al.
Plos Genetics|October 17, 2009
Targeted induction of endoplasmic reticulum stress induces cartilage pathologyM Helen Rajpar, Ben McDermott, Louise Kung, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 14, 2012
Depletion of annexin A5, annexin A6, and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 responseIvan Grskovic, Anna Kutsch, Christian Frie, et al.
Plos Biology|February 15, 2007
Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and functionKwok Yeung Tsang, Danny Chan, Deborah Cheslett, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2023
Modeling human skeletal development using human pluripotent stem cellsShireen R Lamandé, Elizabeth S Ng, Trevor L Cameron, et al.
Bone|July 17, 2018
Identification of TGFβ-related genes regulated in murine osteoarthritis and chondrocyte hypertrophy by comparison of multiple microarray datasetsLaurie M G de Kroon, Guus G H van den Akker, Bent Brachvogel, et al.
Annals of the Rheumatic Diseases|September 23, 2020
Identification of the skeletal progenitor cells forming osteophytes in osteoarthritisAnke J Roelofs, Karolina Kania, Alexandra J Rafipay, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Plos Genetics|September 7, 2013
Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndromeKerry A Miller, Casey J Ah-Cann, Megan F Welfare, et al.
Nature Genetics|October 4, 2011
Mutations in TRPV4 cause an inherited arthropathy of hands and feetShireen R Lamandé, Yuan Yuan, Irma L Gresshoff, et al.
Plos Genetics|October 17, 2009
Targeted induction of endoplasmic reticulum stress induces cartilage pathologyM Helen Rajpar, Ben McDermott, Louise Kung, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 14, 2012
Depletion of annexin A5, annexin A6, and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 responseIvan Grskovic, Anna Kutsch, Christian Frie, et al.
Plos Biology|February 15, 2007
Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and functionKwok Yeung Tsang, Danny Chan, Deborah Cheslett, et al.
Annals of Neurology|October 1, 2008
Collagen VI glycine mutations: perturbed assembly and a spectrum of clinical severityRishika A Pace, Rachel A Peat, Naomi L Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 2023
Modeling human skeletal development using human pluripotent stem cellsShireen R Lamandé, Elizabeth S Ng, Trevor L Cameron, et al.
Bone|July 17, 2018
Identification of TGFβ-related genes regulated in murine osteoarthritis and chondrocyte hypertrophy by comparison of multiple microarray datasetsLaurie M G de Kroon, Guus G H van den Akker, Bent Brachvogel, et al.
Annals of the Rheumatic Diseases|September 23, 2020
Identification of the skeletal progenitor cells forming osteophytes in osteoarthritisAnke J Roelofs, Karolina Kania, Alexandra J Rafipay, et al.
Annals of Neurology|September 22, 2007
Molecular consequences of dominant Bethlem myopathy collagen VI mutationsNaomi L Baker, Matthias Mörgelin, Rishika A Pace, et al.
Pageof 10