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DNA多态性与疾病关联研究

DNA polymorphism and the study of disease associations.

作者信息

Cooper D N, Clayton J F

机构信息

Haematology Department, King's College Hospital School of Medicine and Dentistry, London, UK.

出版信息

Hum Genet. 1988 Apr;78(4):299-312. doi: 10.1007/BF00291724.

Abstract

Recombinant DNA approaches to disease analysis may be as applicable to studies of disease association as they are to the analysis and diagnosis of single-gene defects. Population and/or family association analyses, using restriction fragment length polymorphisms around candidate genes as markers, have been employed to study conditions such as atherosclerosis and disease with an HLA-association. Progress made to date in disease-association studies using recombinant DNA methodology is reviewed, the rationale behind such studies is examined and associated problems and pitfalls discussed.

摘要

重组DNA技术在疾病分析中的应用,对于疾病关联性研究可能与对单基因缺陷的分析和诊断同样适用。利用候选基因周围的限制性片段长度多态性作为标记进行群体和/或家族关联性分析,已被用于研究诸如动脉粥样硬化以及与HLA相关的疾病等情况。本文回顾了迄今为止使用重组DNA方法在疾病关联性研究中取得的进展,探讨了此类研究背后的基本原理,并讨论了相关问题和陷阱。

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