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Wayne A Cabral

Showing results (41-50 of 48) with videos related to

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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.
The Journal of Biological Chemistry|May 20, 2008
Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebratesShawn M Sweeney, Joseph P Orgel, Andrzej Fertala, et al.
The New England Journal of Medicine|December 29, 2006
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfectaAileen M Barnes, Weizhong Chang, Roy Morello, et al.
Plos Genetics|July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis ImperfectaWayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Nature|January 7, 2021
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in miceLuke W Koblan, Michael R Erdos, Christopher Wilson, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
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.
The Journal of Biological Chemistry|May 20, 2008
Candidate cell and matrix interaction domains on the collagen fibril, the predominant protein of vertebratesShawn M Sweeney, Joseph P Orgel, Andrzej Fertala, et al.
The New England Journal of Medicine|December 29, 2006
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfectaAileen M Barnes, Weizhong Chang, Roy Morello, et al.
Plos Genetics|July 22, 2016
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis ImperfectaWayne A Cabral, Masaki Ishikawa, Matthias Garten, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Nature|January 7, 2021
In vivo base editing rescues Hutchinson-Gilford progeria syndrome in miceLuke W Koblan, Michael R Erdos, Christopher Wilson, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
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