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Aileen M Barnes

Showing results (1-10 of 34) with videos related to

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Cell and Tissue Research|October 29, 2009
Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfectaJoan C Marini, Wayne A Cabral, Aileen M Barnes
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 27, 2004
Netrin-1 and semaphorin 3A promote or inhibit cortical axon branching, respectively, by reorganization of the cytoskeletonErik W Dent, Aileen M Barnes, Fangjun Tang, et al.
Cell Cycle (Georgetown, Tex.)|July 17, 2007
Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone developmentJoan C Marini, Wayne A Cabral, Aileen M Barnes, et al.
Nature Reviews. Endocrinology|June 15, 2011
New perspectives on osteogenesis imperfectaAntonella Forlino, Wayne A Cabral, Aileen M Barnes, et al.
Human Molecular Genetics|October 23, 2009
Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complexWeizhong Chang, Aileen M Barnes, Wayne A Cabral, et al.
Disease Models & Mechanisms|May 16, 2022
Dissecting the phenotypic variability of osteogenesis imperfectaNadia Garibaldi, Roberta Besio, Raymond Dalgleish, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 8, 2022
Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular PathogenesisHeeseog Kang, Smriti Aryal Ac, Aileen M Barnes, et al.
Cells|April 11, 2025
<i>CRTAP</i>-Null Osteoblasts Have Increased Proliferation, Protein Secretion, and Skeletal Morphogenesis Gene Expression with Downregulation of Cellular AdhesionAileen M Barnes, Apratim Mitra, Marianne M Knue, et al.
Human Mutation|June 22, 2012
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrixAileen M Barnes, Wayne A Cabral, MaryAnn Weis, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2014
Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expressionAdi Reich, Alison S Bae, Aileen M Barnes, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Cell and Tissue Research|October 29, 2009
Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfectaJoan C Marini, Wayne A Cabral, Aileen M Barnes
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 27, 2004
Netrin-1 and semaphorin 3A promote or inhibit cortical axon branching, respectively, by reorganization of the cytoskeletonErik W Dent, Aileen M Barnes, Fangjun Tang, et al.
Cell Cycle (Georgetown, Tex.)|July 17, 2007
Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone developmentJoan C Marini, Wayne A Cabral, Aileen M Barnes, et al.
Nature Reviews. Endocrinology|June 15, 2011
New perspectives on osteogenesis imperfectaAntonella Forlino, Wayne A Cabral, Aileen M Barnes, et al.
Human Molecular Genetics|October 23, 2009
Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complexWeizhong Chang, Aileen M Barnes, Wayne A Cabral, et al.
Disease Models & Mechanisms|May 16, 2022
Dissecting the phenotypic variability of osteogenesis imperfectaNadia Garibaldi, Roberta Besio, Raymond Dalgleish, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 8, 2022
Antagonism Between PEDF and TGF-β Contributes to Type VI Osteogenesis Imperfecta Bone and Vascular PathogenesisHeeseog Kang, Smriti Aryal Ac, Aileen M Barnes, et al.
Cells|April 11, 2025
<i>CRTAP</i>-Null Osteoblasts Have Increased Proliferation, Protein Secretion, and Skeletal Morphogenesis Gene Expression with Downregulation of Cellular AdhesionAileen M Barnes, Apratim Mitra, Marianne M Knue, et al.
Human Mutation|June 22, 2012
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrixAileen M Barnes, Wayne A Cabral, MaryAnn Weis, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2014
Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expressionAdi Reich, Alison S Bae, Aileen M Barnes, et al.
Pageof 4