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R Eyre

Showing results (191-200 of 234) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 1, 1993
The effect of short term treatment with alendronate on vertebral density and biochemical markers of bone remodeling in early postmenopausal womenS T Harris, B J Gertz, H K Genant, et al.
American Journal of Medical Genetics. Part A|June 5, 2019
The α2 chain of type IX collagen is essential for type IX collagen biosynthesisKarthika Balasubramanian, MaryAnn Weis, David R Eyre, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 2024
Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfectaAlexander Kot, Cora Chun, Jorge H Martin, et al.
The New England Journal of Medicine|June 15, 1995
Long-term treatment of osteopetrosis with recombinant human interferon gammaL L Key, R M Rodriguiz, S M Willi, et al.
American Journal of Human Genetics|March 2, 2010
Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfectaHelena E Christiansen, Ulrike Schwarze, Shawna M Pyott, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 2006
Sp1 family of transcription factors regulates the human alpha2 (XI) collagen gene (COL11A2) in Saos-2 osteoblastic cellsTomohiro Goto, Yoshito Matsui, Russell J Fernandes, et al.
Journal of Medical Genetics|April 4, 2000
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorderG R Mortier, M Weis, L Nuytinck, et al.
Clinical & Experimental Metastasis|March 29, 2018
EACR-MRS conference on Seed and Soil: In Vivo Models of MetastasisI Teles Alves, N Cohen, P G Ersan, et al.
The New England Journal of Medicine|January 22, 2010
Lack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingAileen M Barnes, Erin M Carter, Wayne A Cabral, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 24

Showing results (191-200 of 234) with videos related to

Sort By:
Pageof 24
The Journal of Clinical Endocrinology and Metabolism|June 1, 1993
The effect of short term treatment with alendronate on vertebral density and biochemical markers of bone remodeling in early postmenopausal womenS T Harris, B J Gertz, H K Genant, et al.
American Journal of Medical Genetics. Part A|June 5, 2019
The α2 chain of type IX collagen is essential for type IX collagen biosynthesisKarthika Balasubramanian, MaryAnn Weis, David R Eyre, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 1, 2024
Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome-osteogenesis imperfectaAlexander Kot, Cora Chun, Jorge H Martin, et al.
The New England Journal of Medicine|June 15, 1995
Long-term treatment of osteopetrosis with recombinant human interferon gammaL L Key, R M Rodriguiz, S M Willi, et al.
American Journal of Human Genetics|March 2, 2010
Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfectaHelena E Christiansen, Ulrike Schwarze, Shawna M Pyott, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 1, 2006
Sp1 family of transcription factors regulates the human alpha2 (XI) collagen gene (COL11A2) in Saos-2 osteoblastic cellsTomohiro Goto, Yoshito Matsui, Russell J Fernandes, et al.
Journal of Medical Genetics|April 4, 2000
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorderG R Mortier, M Weis, L Nuytinck, et al.
Clinical & Experimental Metastasis|March 29, 2018
EACR-MRS conference on Seed and Soil: In Vivo Models of MetastasisI Teles Alves, N Cohen, P G Ersan, et al.
The New England Journal of Medicine|January 22, 2010
Lack of cyclophilin B in osteogenesis imperfecta with normal collagen foldingAileen M Barnes, Erin M Carter, Wayne A Cabral, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathyC G Bönnemann, G F Cox, F Shapiro, et al.
Pageof 24