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Cell Stem Cell
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December 7, 2019
Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells
Laura C Ortinau, Hamilton Wang, Kevin Lei, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 31, 2015
Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap(-/-) Mice, a Model of Recessive Osteogenesis Imperfecta
Ingo Grafe, Stefanie Alexander, Tao Yang, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
May 1, 2023
Activation of β-adrenergic receptor signaling prevents glucocorticoid-induced obesity and adipose tissue dysfunction in male mice
Manuel Gado, Annett Heinrich, Denise Wiedersich, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 10, 2011
Mutations in SERPINF1 cause osteogenesis imperfecta type VI
Erica P Homan, Frank Rauch, Ingo Grafe, et al.
Nature Medicine
|
May 6, 2014
Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta
Ingo Grafe, Tao Yang, Stefanie Alexander, et al.
Plos Genetics
|
January 28, 2014
Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues
Erica P Homan, Caressa Lietman, Ingo Grafe, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 17, 2017
Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone
Caressa D Lietman, Joohyun Lim, Ingo Grafe, et al.
The Journal of Clinical Investigation
|
February 3, 2022
Targeting TGF-β for treatment of osteogenesis imperfecta
I-Wen Song, Sandesh Cs Nagamani, Dianne Nguyen, et al.
Clinical Genetics
|
August 29, 2018
A multicenter study to evaluate pulmonary function in osteogenesis imperfecta
Allison Tam, Shan Chen, Evan Schauer, et al.
Human Molecular Genetics
|
June 7, 2020
A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance
Bridget M Stroup, Ronit Marom, Xiaohui Li, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Cell Stem Cell
|
December 7, 2019
Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells
Laura C Ortinau, Hamilton Wang, Kevin Lei, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 31, 2015
Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap(-/-) Mice, a Model of Recessive Osteogenesis Imperfecta
Ingo Grafe, Stefanie Alexander, Tao Yang, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
May 1, 2023
Activation of β-adrenergic receptor signaling prevents glucocorticoid-induced obesity and adipose tissue dysfunction in male mice
Manuel Gado, Annett Heinrich, Denise Wiedersich, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
August 10, 2011
Mutations in SERPINF1 cause osteogenesis imperfecta type VI
Erica P Homan, Frank Rauch, Ingo Grafe, et al.
Nature Medicine
|
May 6, 2014
Excessive transforming growth factor-β signaling is a common mechanism in osteogenesis imperfecta
Ingo Grafe, Tao Yang, Stefanie Alexander, et al.
Plos Genetics
|
January 28, 2014
Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues
Erica P Homan, Caressa Lietman, Ingo Grafe, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 17, 2017
Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone
Caressa D Lietman, Joohyun Lim, Ingo Grafe, et al.
The Journal of Clinical Investigation
|
February 3, 2022
Targeting TGF-β for treatment of osteogenesis imperfecta
I-Wen Song, Sandesh Cs Nagamani, Dianne Nguyen, et al.
Clinical Genetics
|
August 29, 2018
A multicenter study to evaluate pulmonary function in osteogenesis imperfecta
Allison Tam, Shan Chen, Evan Schauer, et al.
Human Molecular Genetics
|
June 7, 2020
A global Slc7a7 knockout mouse model demonstrates characteristic phenotypes of human lysinuric protein intolerance
Bridget M Stroup, Ronit Marom, Xiaohui Li, et al.
Page
of 3