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The Journal of Clinical Investigation|December 1, 1995
Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidismS H Pearce, D Trump, C Wooding, et al.Nature Genetics|December 30, 1999
Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisA E Hughes, S H Ralston, J Marken, et al.Cancer Letters|May 12, 2000
Immunohistochemical analysis of polycyclic aromatic hydrocarbon-DNA adducts in breast tumor tissueR M Santella, M D Gammon, Y J Zhang, et al.Human Molecular Genetics|December 14, 2001
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel geneE Cleiren, O Bénichou, E Van Hul, et al.The New England Journal of Medicine|March 27, 1980
Successful bone-marrow transplantation for infantile malignant osteopetrosisP F Coccia, W Krivit, J Cervenka, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 5, 2000
Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasiaK N Fedde, L Blair, J Silverstein, et al.Journal of Dental Research|February 27, 2015
Periodontal Defects in the A116T Knock-in Murine Model of OdontohypophosphatasiaB L Foster, C R Sheen, N E Hatch, et al.The Journal of Clinical Investigation|May 29, 1998
Insulin-like growth factor system abnormalities in hepatitis C-associated osteosclerosis. Potential insights into increasing bone mass in adultsS Khosla, A A Hassoun, B K Baker, et al.European Journal of Human Genetics : EJHG|October 22, 1998
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4qM Devoto, K Shimoya, J Caminis, et al.The Journal of Clinical Endocrinology and Metabolism|October 13, 1998
Mutational analysis of PHEX gene in X-linked hypophosphatemiaP H Dixon, P T Christie, C Wooding, et al.Pageof 36