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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 28, 2004
Contribution of the LRP5 gene to normal variation in peak BMD in womenDaniel L Koller, Shoji Ichikawa, Michelle L Johnson, et al.Oncotarget|May 7, 2015
FGF23 is elevated in multiple myeloma and increases heparanase expression by tumor cellsAttaya Suvannasankha, Douglas R Tompkins, Daniel F Edwards, et al.Bone|August 30, 2008
CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white menKang Chu, Daniel L Koller, Shoji Ichikawa, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 7, 2006
Human ALOX12, but not ALOX15, is associated with BMD in white men and womenShoji Ichikawa, Daniel L Koller, Michelle L Johnson, et al.The Journal of Clinical Endocrinology and Metabolism|February 19, 2010
Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American womenDaniel L Koller, Shoji Ichikawa, Dongbing Lai, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|May 29, 2008
Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white womenShoji Ichikawa, Daniel L Koller, Leah R Curry, et al.American Journal of Human Genetics|December 31, 2004
Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongationKenneth E White, Jose M Cabral, Siobhan I Davis, et al.BMC Genomics|July 1, 2026
Variant-specific RNA testing resolves variants of uncertain significance in exome testingAudrey K O'Neill, Grace E VanNoy, Brooklynn Gasser, et al.Human Mutation|April 14, 2025
Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes-ENG and ACVRL1Desiree DeMille, Jamie McDonald, Carmelo Bernabeu, et al.American Journal of Medical Genetics. Part A|April 2, 2010
Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutationsShoji Ichikawa, Geneviève Baujat, Aksel Seyahi, et al.Pageof 5