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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 21, 2013
Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis
Katrin Gruenwald, Patrizio Castagnola, Roberta Besio, et al.
Spine
|
February 7, 1998
Consensus summary on the diagnosis and treatment of osteoporosis
G B Andersson, M P Bostrom, D R Eyre, et al.
Arthritis and Rheumatism
|
February 1, 1995
Changes in cartilage composition and physical properties due to stromelysin degradation
L J Bonassar, E H Frank, J C Murray, et al.
Human Molecular Genetics
|
November 5, 2021
Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome
Keren Machol, Urszula Polak, Monika Weisz-Hubshman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 1, 1996
Sublingual testosterone replacement improves muscle mass and strength, decreases bone resorption, and increases bone formation markers in hypogonadal men--a clinical research center study
C Wang, D R Eyre, R Clark, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 23, 2021
Localized chondro-ossification underlies joint dysfunction and motor deficits in the <i>Fkbp10</i> mouse model of osteogenesis imperfecta
Joohyun Lim, Caressa Lietman, Matthew W Grol, et al.
British Journal of Cancer
|
January 8, 2009
Incidence and survival of childhood bone cancer in northern England and the West Midlands, 1981-2002
R Eyre, R G Feltbower, E Mubwandarikwa, et al.
American Journal of Human Genetics
|
November 2, 2010
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene
Stuart W Tompson, Carlos A Bacino, Nicole P Safina, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 20, 2016
Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome
Charlotte Gistelinck, Paul Eckhard Witten, Ann Huysseune, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 6, 2019
COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing
Aileen M Barnes, Aarthi Ashok, Elena N Makareeva, et al.
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of 24
Search research articles
Search
Showing results (201-210 of 234) with videos related to
Sort By:
Page
of 24
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 21, 2013
Sc65 is a novel endoplasmic reticulum protein that regulates bone mass homeostasis
Katrin Gruenwald, Patrizio Castagnola, Roberta Besio, et al.
Spine
|
February 7, 1998
Consensus summary on the diagnosis and treatment of osteoporosis
G B Andersson, M P Bostrom, D R Eyre, et al.
Arthritis and Rheumatism
|
February 1, 1995
Changes in cartilage composition and physical properties due to stromelysin degradation
L J Bonassar, E H Frank, J C Murray, et al.
Human Molecular Genetics
|
November 5, 2021
Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome
Keren Machol, Urszula Polak, Monika Weisz-Hubshman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 1, 1996
Sublingual testosterone replacement improves muscle mass and strength, decreases bone resorption, and increases bone formation markers in hypogonadal men--a clinical research center study
C Wang, D R Eyre, R Clark, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 23, 2021
Localized chondro-ossification underlies joint dysfunction and motor deficits in the <i>Fkbp10</i> mouse model of osteogenesis imperfecta
Joohyun Lim, Caressa Lietman, Matthew W Grol, et al.
British Journal of Cancer
|
January 8, 2009
Incidence and survival of childhood bone cancer in northern England and the West Midlands, 1981-2002
R Eyre, R G Feltbower, E Mubwandarikwa, et al.
American Journal of Human Genetics
|
November 2, 2010
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene
Stuart W Tompson, Carlos A Bacino, Nicole P Safina, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 20, 2016
Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome
Charlotte Gistelinck, Paul Eckhard Witten, Ann Huysseune, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 6, 2019
COL1A1 C-propeptide mutations cause ER mislocalization of procollagen and impair C-terminal procollagen processing
Aileen M Barnes, Aarthi Ashok, Elena N Makareeva, et al.
Page
of 24