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    題名: Monitoring of congenital adrenal hyperplasia by microbore HPLC-electrospray ionization tandem mass spectrometry of dried blood spots
    作者: Lai, CC;Tsai, CH;Tsai, FJ;Wu, JY;Lin, WD;Lee, CC
    貢獻者: 附設醫院基因醫學部;China Med Coll Hosp, Dept Med Genet & Med Res, Taichung 404, Taiwan
    日期: 2002
    上傳時間: 2010-09-24 14:45:38 (UTC+8)
    出版者: AMER ASSOC CLINICAL CHEMISTRY
    摘要: Objectives/Hypothesis: An important tumor suppressor gene, p53, plays a role in the regulation of cell progression and prevention of carcinogenesis. Mutated p53 is related to cell progression and malignancy. We aimed to evaluate the association between nasopharyngeal carcinoma and p53 polymorphism. Study Design: Case control study. Methods: All individuals were divided into two groups: nasopharyngeal carcinoma (n = 50) and non-nasopharyngeal carcinoma groups (n = 59). Their p53 codon 72 polymorphisms (arginine [Arg] homozygotes, heterozygotes, proline [Pro] homozygotes) were detected by polymerase chain reaction. Associations between nasopharyngeal carcinoma and p53 polymorphism were evaluated. Results: Distributions of various p53 polymorphisms significantly differed between the two groups. We noted a dominant presentation of Pro homozygotes in the nasopharyngeal carcinoma population over that in the non-nasopharyngeal carcinoma population. Proportions of Pro homozygotes and heterozygotes and Arg homozygotes were 32%, 28%, and 40% in the nasopharyngeal carcinoma population and were 13.5%, 44.1%, and 42.4% in the non-nasopharyngeal carcinoma population, respectively. Conclusions: An association exists between nasopharyngeal carcinoma and p53 codon 72 polymorphism. The p53 Pro homozygotes are to a higher risk of development of nasopharyngeal carcinoma.
    關聯: CLINICAL CHEMISTRY 48(2):354-356
    顯示於類別:[台中附設醫院] 期刊論文

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