Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Leah R. Curry"'
Autor:
Xiaoling Xuei, Siu L. Hui, Howard J. Edenberg, Leah R. Curry, Daniel L. Koller, Tatiana Foroud, Michael J. Econs, Dongbing Lai, Shoji Ichikawa, Munro Peacock
Publikováno v:
Calcified Tissue International. 84:97-102
Phenotypic variation in bone mineral density (BMD) among healthy adults is influenced by both genetic and environmental factors. Genetic sequence variations in the adenylate cyclase 10 (ADCY10) gene, which is also called soluble adenylate cyclase, ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a7fd1a8aff13f81f59bd5c122632a42
https://doi.org/10.1007/s00223-008-9200-z
https://doi.org/10.1007/s00223-008-9200-z
Autor:
Siu Hui, Xiaoling Xuei, Munro Peacock, Tatiana Foroud, Michael J. Econs, Daniel L. Koller, Leah R. Curry, Dongbing Lai, Shoji Ichikawa, Howard J. Edenberg
Publikováno v:
Osteoporosis International. 19:637-643
Animal studies suggest that arachidonate 5-lipoxygenase (encoded by ALOX5) may be a genetic determinant of bone mineral density. We tested this hypothesis in a sample of healthy men and women and did not find consistent evidence for an association be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a43d5d306aff5090c5b0f9eff200711
https://doi.org/10.1007/s00198-007-0484-z
https://doi.org/10.1007/s00198-007-0484-z
Autor:
Elizabeth W. Pugh, Tatiana Foroud, Siu L. Hui, Kimberly F. Doheny, Daniel L. Koller, Howard J. Edenberg, Xiaoling Xuei, Leah R. Curry, Michael J. Econs, Dongbing Lai, Shoji Ichikawa, Ya Yu Tsai, Munro Peacock
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23(10)
Osteoporosis is a complex disease with both genetic and environmental risk factors. A major determinant of osteoporotic fractures is peak BMD obtained during young adulthood. We previously reported linkage of chromosome 1q (LOD = 4.3) with variation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76b695c4dc2a75819781a9d72e6ab9a6
https://pubmed.ncbi.nlm.nih.gov/18505370
https://pubmed.ncbi.nlm.nih.gov/18505370
Autor:
Anthony M. Austin, Howard J. Edenberg, Siu L. Hui, Tatiana Foroud, Michael J. Econs, Daniel L. Koller, Munro Peacock, Dongbing Lai, Leah R. Curry, Shoji Ichikawa, Xiaoling Xuei, Richard Snyder, Kang Chu
Publikováno v:
Bone. 43(6)
Mutations in the chloride channel 7 gene (CLCN7) cause osteopetrosis, and polymorphisms of CLCN7 in the non-disease allele are associated with penetrance of the autosomal dominant osteopetrosis (ADO) phenotype. Studies have also shown an association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5bdfd55709901c25227e6af2e823fd1
https://pubmed.ncbi.nlm.nih.gov/18755304
https://pubmed.ncbi.nlm.nih.gov/18755304
Autor:
Michelle L. Johnson, Michael J. Econs, Selina A. Estwick, Leah R. Curry, Andrea H. Sorenson, Elizabeth A. Traxler, Shoji Ichikawa, Erik A. Imel
Publikováno v:
Bone. 43(4)
X-linked hypophosphatemic rickets (XLH) is a dominantly inherited disorder characterized by renal phosphate wasting, aberrant vitamin D metabolism, and abnormal bone mineralization. XLH is caused by inactivating mutations in PHEX (phosphate-regulatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0d99800b2c059afb5c4aa32ab75aa43
https://pubmed.ncbi.nlm.nih.gov/18625346
https://pubmed.ncbi.nlm.nih.gov/18625346