https://scholars.lib.ntu.edu.tw/handle/123456789/538657
標題: | Association between Ataxia Telangiectasia Mutated gene polymorphisms and childhood leukemia in Taiwan | 作者: | Wang C.-H. Wu K.-H. YUNG-LI YANG Peng C.-T. Tsai F.-J. Lin D.-T. Chiu C.-F. Lin C.-C. Bau D.-T. |
關鍵字: | Ataxia telangiectasia mutated; Childhood leukemia; Polymorphism | 公開日期: | 2011 | 出版社: | Chinese Physiological Society | 卷: | 54 | 期: | 6 | 起(迄)頁: | 413-418 | 來源出版物: | Chinese Journal of Physiology | 摘要: | The ataxia telangiectasia mutated (ATM) gene plays a major role in repairing the double-strand breaks and maintaining the genome stability. In this case-control study, associations of seven ATM single-nucleotide polymorphisms (rs600931, rs189037, rs652311, rs624366, rs228589, rs227092 and rs227060) with risks in childhood leukemia in a Taiwanese population were investigated. Two hundred and sixty-six patients with childhood leukemia and 266 age-matched healthy controls recruited were genotyped and analyzed. The P-values of the distributions of the genotypic frequencies in the seven ATM polymorphisms were 0.8925, 0.2835, 0.5772, 0.8731, 0.3641, 0.9181 and 0.5071, respectively. The Pvalues of the distributions of the allelic frequencies in the seven ATM polymorphisms were 0.6158, 0.1179, 0.6971, 0.7944, 0.1887, 0.6605 and 0.2747, respectively. Although the results did not indicate that ATM polymorphism is directly associated with childhood leukemia, the gene-gene and gene-environment interactions of ATM with other factors is worthy of further investigation in the future. ? 2011 by The Chinese Physiological Society and Airiti Press Inc. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84455194028&doi=10.4077%2fCJP.2011.AMM106&partnerID=40&md5=34cf3824c99174de51c6fd92d7ae2484 https://scholars.lib.ntu.edu.tw/handle/123456789/538657 |
ISSN: | 0304-4920 | DOI: | 10.4077/CJP.2011.AMM106 | SDG/關鍵字: | adult; article; ataxia telangiectasia mutated gene; child; child health; childhood leukemia; controlled study; disease association; female; gene expression regulation; gene frequency; gene function; gene location; genetic association; genetic risk; genetic susceptibility; genetic variability; genotype environment interaction; human; major clinical study; male; mutational analysis; mutator gene; school child; single nucleotide polymorphism; Taiwan |
顯示於: | 醫學系 |
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