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本文引用的文献

1
DAPK1 variants are associated with Alzheimer's disease and allele-specific expression.死亡相关蛋白激酶1(DAPK1)变体与阿尔茨海默病及等位基因特异性表达相关。
Hum Mol Genet. 2006 Sep 1;15(17):2560-8. doi: 10.1093/hmg/ddl178. Epub 2006 Jul 17.
2
Ethnicity-dependent genetic association of ABCA2 with sporadic Alzheimer's disease.ABCA2与散发性阿尔茨海默病的种族依赖性基因关联。
Am J Med Genet B Neuropsychiatr Genet. 2006 Jul 5;141B(5):534-6. doi: 10.1002/ajmg.b.30345.
3
ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.ABCA2是早发性阿尔茨海默病的一个强大遗传风险因素。
Neurobiol Dis. 2005 Feb;18(1):119-25. doi: 10.1016/j.nbd.2004.09.011.
4
Molecular genetics of late-onset Alzheimer's disease.晚发性阿尔茨海默病的分子遗传学
Ann Hum Genet. 2004 Jul;68(Pt 4):381-404. doi: 10.1046/j.1529-8817.2004.00110.x.

9号染色体上的DAPK1和ABCA2单核苷酸多态性与阿尔茨海默病无关联。

No association of DAPK1 and ABCA2 SNPs on chromosome 9 with Alzheimer's disease.

作者信息

Minster Ryan L, DeKosky Steven T, Kamboh M Ilyas

机构信息

Department of Human Genetics, University of Pittsburgh, Pittsburgh, PA 15261, United States.

出版信息

Neurobiol Aging. 2009 Nov;30(11):1890-1. doi: 10.1016/j.neurobiolaging.2008.01.006. Epub 2008 Mar 11.

DOI:10.1016/j.neurobiolaging.2008.01.006
PMID:18336955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2763561/
Abstract

Recently genetic variation in the DAPK1 and ABCA2 genes has been reported to be associated with late- and early-onset Alzheimer's disease (AD), respectively. We examined the most significant two single-nucleotide polymorphisms (SNPs) in DAPK1 in a large case-control cohort of late-onset subjects and matched controls and one of the most significant SNPs in ABCA2 in a small set of early-onset subjects as well. We did not detect associations with AD for any variation.

摘要

最近有报道称,DAPK1和ABCA2基因的遗传变异分别与晚发型和早发型阿尔茨海默病(AD)相关。我们在一个大型晚发型病例对照队列及其匹配对照中检测了DAPK1中最显著的两个单核苷酸多态性(SNP),并在一小部分早发型受试者中检测了ABCA2中最显著的一个SNP。我们未检测到任何变异与AD有关联。