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Cancer Cell|September 10, 2014
Notch activation as a driver of osteogenic sarcomaJianning Tao, Ming-Ming Jiang, Lichun Jiang, et al.
Human Molecular Genetics|August 10, 2012
Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosisPhilippe M Campeau, James T Lu, Gautam Sule, et al.
The Journal of Clinical Investigation|December 29, 2020
Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiationZixue Jin, Jordan Kho, Brian Dawson, et al.
Human Molecular Genetics|November 5, 2021
Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndromeKeren Machol, Urszula Polak, Monika Weisz-Hubshman, 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 ImperfectaIngo Grafe, Stefanie Alexander, Tao Yang, et al.
Molecular Genetics and Metabolism|July 30, 2018
Arginase overexpression in neurons and its effect on traumatic brain injurySimran Madan, Bettina Kron, Zixue Jin, et al.
Human Molecular Genetics|September 12, 2015
Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiencyLindsay C Burrage, Qin Sun, Sarah H Elsea, et al.
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