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The Global ETD Search service is a free service for researchers
to find electronic theses and dissertations. This service is
provided by the
Networked Digital Library of Theses and Dissertations.
Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
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Showing 1 to 8 of 8 (0.086 seconds)Spelling suggestions: "subject:"osteoporosis -- 1genetic aspects."" "subject:"osteoporosis -- cogenetic aspects.""
| 1 |
Genetic determinants of osteoporosis in Cooley's anemiaYung, Ka-hung., 翁家紅. January 2004 (has links)
published_or_final_version / Medical Sciences / Master / Master of Medical Sciences
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| 2 |
Genetic linkage and association studies to identify candidate genes for bone mineral density variation in Southern ChineseCheung, Ching-lung., 張正龍. January 2007 (has links)
published_or_final_version / Medicine / Doctoral / Doctor of Philosophy
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| 3 |
The role of estrogen receptor alpha & beta polymorphisms in osteoporosisLai, Ming-hei., 賴銘曦. January 2007 (has links)
published_or_final_version / Medicine / Master / Master of Research in Medicine
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| 4 |
Identification of candidate genes for bone mineral density variation in Southern Chinese by integrating computational gene prioritization,linkage and association approachesLi, Hoi-yee., 李凱怡. January 2010 (has links)
published_or_final_version / Biochemistry / Doctoral / Doctor of Philosophy
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| 5 |
Probing the molecular mechanisms of how polymorphisms in Cerberus-likeresult in low bone mineral densityLee, B. C., Bob., 李卜駿. January 2007 (has links)
published_or_final_version / Biochemistry / Master / Master of Philosophy
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| 6 |
Genetic variation at the NPT2 locus : implications for hereditary hypophosphatemic rickets with hypercalciuria and osteoporosisJones, Andrew Owain. January 2000 (has links)
Recognising that NPT2 is the major Na/Pi cotransporter in the kidney, that hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is caused by a renal Pi leak and, that Npt2 knockout mice demonstrate a biochemical phenotype similar to that of patients with HHRH, we sought to determine whether NPT2 was a candidate gene for this disorder. Using single-strand conformation polymorphsim (SSCP) analysis and sequencing in six unrelated pedigrees with the disease, we found no disease-causing mutations. Two polymorphisms were identified in the gene and used as markers to examine segregation of NPT2 with the disease. HHRH did not segregate with the gene markers. In addition, the impact of NPT2 on bone mineral density (BMD) was examined by genotyping a population of 104 individuals for which BMD data was available, and determining whether there was an association between NPT2 genotype and bone density. No significant association was found between NPT2 genotype and BMD.
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| 7 |
Genetic variation at the NPT2 locus : implications for hereditary hypophosphatemic rickets with hypercalciuria and osteoporosisJones, Andrew Owain. January 2000 (has links)
No description available.
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| 8 |
Genome-wide association study of bone mineral density in ChineseXiao, Sumei., 肖蘇妹. January 2010 (has links)
published_or_final_version / Medicine / Doctoral / Doctor of Philosophy
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