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R Eyre

Showing results (221-230 of 234) with videos related to

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Plos Genetics|April 28, 2016
Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl HydroxylationMelissa E Heard, Roberta Besio, MaryAnn Weis, et al.
The New England Journal of Medicine|December 29, 2006
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfectaAileen M Barnes, Weizhong Chang, Roy Morello, et al.
Bone Research|June 15, 2026
Murine model of high bone mass osteogenesis imperfecta exhibits bone matrix hyper-mineralization, misaligned mineral crystals, and altered osteoblast differentiationAileen M Barnes, M Helen Rajpar, Joseph E Perosky, et al.
Human Molecular Genetics|February 2, 2011
Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypesShawna M Pyott, Ulrike Schwarze, Helena E Christiansen, et al.
Plos Genetics|July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis ImperfectaWayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
Nature Medicine|February 27, 2019
Gain-of-function mutation of microRNA-140 in human skeletal dysplasiaGiedre Grigelioniene, Hiroshi I Suzuki, Fulya Taylan, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2018
Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathiesCharlotte Gistelinck, Ronald Y Kwon, Fransiska Malfait, et al.
Cell|October 24, 2006
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfectaRoy Morello, Terry K Bertin, Yuqing Chen, et al.
Osteoarthritis and Cartilage|April 13, 2002
Fibroblast growth factor-18 is a trophic factor for mature chondrocytes and their progenitorsJ L Ellsworth, J Berry, T Bukowski, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Pageof 24

Showing results (221-230 of 234) with videos related to

Sort By:
Pageof 24
Plos Genetics|April 28, 2016
Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl HydroxylationMelissa E Heard, Roberta Besio, MaryAnn Weis, et al.
The New England Journal of Medicine|December 29, 2006
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfectaAileen M Barnes, Weizhong Chang, Roy Morello, et al.
Bone Research|June 15, 2026
Murine model of high bone mass osteogenesis imperfecta exhibits bone matrix hyper-mineralization, misaligned mineral crystals, and altered osteoblast differentiationAileen M Barnes, M Helen Rajpar, Joseph E Perosky, et al.
Human Molecular Genetics|February 2, 2011
Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypesShawna M Pyott, Ulrike Schwarze, Helena E Christiansen, et al.
Plos Genetics|July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis ImperfectaWayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
Nature Medicine|February 27, 2019
Gain-of-function mutation of microRNA-140 in human skeletal dysplasiaGiedre Grigelioniene, Hiroshi I Suzuki, Fulya Taylan, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2018
Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathiesCharlotte Gistelinck, Ronald Y Kwon, Fransiska Malfait, et al.
Cell|October 24, 2006
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfectaRoy Morello, Terry K Bertin, Yuqing Chen, et al.
Osteoarthritis and Cartilage|April 13, 2002
Fibroblast growth factor-18 is a trophic factor for mature chondrocytes and their progenitorsJ L Ellsworth, J Berry, T Bukowski, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Pageof 24