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Showing results (211-220 of 234) with videos related to

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Human Mutation|May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutationsAileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 1, 2023
Mmp14 is required for matrisome homeostasis and circadian rhythm in fibroblastsChing-Yan Chloé Yeung, Richa Garva, Adam Pickard, et al.
The Journal of Clinical Endocrinology and Metabolism|July 8, 2016
Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix MineralizationNadja Fratzl-Zelman, Aileen M Barnes, MaryAnn Weis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2015
Hindlimb Skeletal Muscle Function and Skeletal Quality and Strength in +/G610C Mice With and Without Weight-Bearing ExerciseYoungjae Jeong, Stephanie M Carleton, Bettina A Gentry, et al.
Plos One|May 21, 2010
Generalized connective tissue disease in Crtap-/- mouseDustin Baldridge, Jennifer Lennington, MaryAnn Weis, et al.
Elife|May 26, 2021
Tendon and motor phenotypes in the <i>Crtap</i> mouse model of recessive osteogenesis imperfectaMatthew William Grol, Nele A Haelterman, Joohyun Lim, et al.
Plos Genetics|June 27, 2014
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaWayne A Cabral, Irina Perdivara, MaryAnn Weis, et al.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 2020
Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasiaWayne A Cabral, Nadja Fratzl-Zelman, MaryAnn Weis, et al.
Nature|January 18, 2019
HIF-1α metabolically controls collagen synthesis and modification in chondrocytesSteve Stegen, Kjell Laperre, Guy Eelen, et al.
Pageof 24

Showing results (211-220 of 234) with videos related to

Sort By:
Pageof 24
Human Mutation|May 29, 2013
Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutationsAileen M Barnes, Geraldine Duncan, Maryann Weis, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|November 1, 2023
Mmp14 is required for matrisome homeostasis and circadian rhythm in fibroblastsChing-Yan Chloé Yeung, Richa Garva, Adam Pickard, et al.
The Journal of Clinical Endocrinology and Metabolism|July 8, 2016
Non-Lethal Type VIII Osteogenesis Imperfecta Has Elevated Bone Matrix MineralizationNadja Fratzl-Zelman, Aileen M Barnes, MaryAnn Weis, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 2, 2015
Hindlimb Skeletal Muscle Function and Skeletal Quality and Strength in +/G610C Mice With and Without Weight-Bearing ExerciseYoungjae Jeong, Stephanie M Carleton, Bettina A Gentry, et al.
Plos One|May 21, 2010
Generalized connective tissue disease in Crtap-/- mouseDustin Baldridge, Jennifer Lennington, MaryAnn Weis, et al.
Elife|May 26, 2021
Tendon and motor phenotypes in the <i>Crtap</i> mouse model of recessive osteogenesis imperfectaMatthew William Grol, Nele A Haelterman, Joohyun Lim, et al.
Plos Genetics|June 27, 2014
Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfectaWayne A Cabral, Irina Perdivara, MaryAnn Weis, et al.
Nature Genetics|February 6, 2007
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfectaWayne A Cabral, Weizhong Chang, Aileen M Barnes, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 2020
Substitution of murine type I collagen A1 3-hydroxylation site alters matrix structure but does not recapitulate osteogenesis imperfecta bone dysplasiaWayne A Cabral, Nadja Fratzl-Zelman, MaryAnn Weis, et al.
Nature|January 18, 2019
HIF-1α metabolically controls collagen synthesis and modification in chondrocytesSteve Stegen, Kjell Laperre, Guy Eelen, et al.
Pageof 24