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Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21 被引量:4
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作者 Aarti Ruparelia Frances Wiseman +2 位作者 Olivia Sheppard Victor L.J.Tybulewicz Elizabeth M.C.Fisher 《The Journal of Biomedical Research》 CAS 2010年第2期87-99,共13页
Elizabeth Fisher and Victor collaboratively for many years on Tybulewicz have worked the Down syndrome mouse model project. Elizabeth Fisher's background is in molecular genetics and mouse models, with an interest in... Elizabeth Fisher and Victor collaboratively for many years on Tybulewicz have worked the Down syndrome mouse model project. Elizabeth Fisher's background is in molecular genetics and mouse models, with an interest in anueploidy. Victor Tybulewicz is an immunologist whose primary interest is in signal transduction from the antigen receptors of B and T cells. 展开更多
关键词 Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21
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Detailed Deletion Mapping of Chromosome 9p21-22 in Nasopharyngeal Carcinoma
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作者 阳剑波 张晓梅 +6 位作者 邓龙文 谭国林 周鸣 曾朝阳 曹莉 沈守荣 李桂源 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 2000年第3期8-11,共4页
Objective: To further refine the extent of deletion on chromosome 9p21-22 in nasopharyngeal carcinoma (NPC) and provide evidence for discovering new tumor suppressor gene. Methods: Loss of heterozygosity (LOH) on chro... Objective: To further refine the extent of deletion on chromosome 9p21-22 in nasopharyngeal carcinoma (NPC) and provide evidence for discovering new tumor suppressor gene. Methods: Loss of heterozygosity (LOH) on chromosome 9p21-22 was analyzed in 25 paired blood and tumor samples by using 11 high-density microsatellite polymorphic markers. Results: 17 of 25 cases (68.0%) showed LOH at one or more loci. Higher frequencies of LOH were found at four loci: D9S161 (35.0%), D9S1678 (31.5%), D9S263 (33.3%) and D9S1853 (33.3%), where 6 cases had a contiguous stretch of allelic loss. Conclusion: The minimal common region of deletion might be defined between D9S161 and D9S1853 (estimated about 2.7 cM in extent) at 9p21.1, suggesting that inactivation of one or more tumor suppressor genes located in this region may be an important step in NPC. 展开更多
关键词 Nasopharyngeal carcinoma chromosome 9p21-22 Loss of heterozygosity Tumor suppressor gene
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