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本文引用的文献

1
Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme.迟发性阿尔茨海默病风险与胰岛素降解酶变体之间的关联研究。
Am J Med Genet B Neuropsychiatr Genet. 2005 Jul 5;136B(1):62-8. doi: 10.1002/ajmg.b.30186.
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Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease.
Hum Mutat. 2005 Mar;25(3):270-7. doi: 10.1002/humu.20138.
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Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.迟发性阿尔茨海默病与甘油醛-3-磷酸脱氢酶(GAPD)基因家族多个成员的基因变异之间的关联。
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Tree scanning: a method for using haplotype trees in phenotype/genotype association studies.树形扫描:一种在表型/基因型关联研究中使用单倍型树的方法。
Genetics. 2005 Jan;169(1):441-53. doi: 10.1534/genetics.104.030080. Epub 2004 Sep 15.
5
Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease.α-T-连环蛋白在人类大脑中表达,并与Wnt信号通路相互作用,但与阿尔茨海默病中10号染色体的连锁无关。
Neuromolecular Med. 2004;5(2):133-46. doi: 10.1385/NMM:5:2:133.
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Molecular genetics of Alzheimer's disease.阿尔茨海默病的分子遗传学
Curr Psychiatry Rep. 2004 Apr;6(2):125-33. doi: 10.1007/s11920-004-0052-6.
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The three sorCS genes are differentially expressed and regulated by synaptic activity.三种sorCS基因的表达存在差异,并受突触活动调控。
J Neurochem. 2004 Mar;88(6):1470-6. doi: 10.1046/j.1471-4159.2004.02286.x.
8
Incipient Alzheimer's disease: microarray correlation analyses reveal major transcriptional and tumor suppressor responses.早期阿尔茨海默病:微阵列相关性分析揭示主要转录和肿瘤抑制反应。
Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):2173-8. doi: 10.1073/pnas.0308512100. Epub 2004 Feb 9.
9
Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.尿激酶型纤溶酶原激活剂基因的变异并不能解释10号染色体上迟发性阿尔茨海默病的连锁信号。
Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):29-37. doi: 10.1002/ajmg.b.20036.
10
A comparison of bayesian methods for haplotype reconstruction from population genotype data.基于群体基因型数据的单倍型重建贝叶斯方法比较。
Am J Hum Genet. 2003 Nov;73(5):1162-9. doi: 10.1086/379378. Epub 2003 Oct 20.

对10号染色体的扫描发现了一个与晚发性阿尔茨海默病有强烈关联的新基因座。

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

作者信息

Grupe Andrew, Li Yonghong, Rowland Charles, Nowotny Petra, Hinrichs Anthony L, Smemo Scott, Kauwe John S K, Maxwell Taylor J, Cherny Sara, Doil Lisa, Tacey Kristina, van Luchene Ryan, Myers Amanda, Wavrant-De Vrièze Fabienne, Kaleem Mona, Hollingworth Paul, Jehu Luke, Foy Catherine, Archer Nicola, Hamilton Gillian, Holmans Peter, Morris Chris M, Catanese Joseph, Sninsky John, White Thomas J, Powell John, Hardy John, O'Donovan Michael, Lovestone Simon, Jones Lesley, Morris John C, Thal Leon, Owen Michael, Williams Julie, Goate Alison

机构信息

Celera Diagnostics, Alameda, CA, USA.

出版信息

Am J Hum Genet. 2006 Jan;78(1):78-88. doi: 10.1086/498851. Epub 2005 Nov 15.

DOI:10.1086/498851
PMID:16385451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1380225/
Abstract

Strong evidence of linkage to late-onset Alzheimer disease (LOAD) has been observed on chromosome 10, which implicates a wide region and at least one disease-susceptibility locus. Although significant associations with several biological candidate genes on chromosome 10 have been reported, these findings have not been consistently replicated, and they remain controversial. We performed a chromosome 10-specific association study with 1,412 gene-based single-nucleotide polymorphisms (SNPs), to identify susceptibility genes for developing LOAD. The scan included SNPs in 677 of 1,270 known or predicted genes; each gene contained one or more markers, about half (48%) of which represented putative functional mutations. In general, the initial testing was performed in a white case-control sample from the St. Louis area, with 419 LOAD cases and 377 age-matched controls. Markers that showed significant association in the exploratory analysis were followed up in several other white case-control sample sets to confirm the initial association. Of the 1,397 markers tested in the exploratory sample, 69 reached significance (P < .05). Five of these markers replicated at P < .05 in the validation sample sets. One marker, rs498055, located in a gene homologous to RPS3A (LOC439999), was significantly associated with Alzheimer disease in four of six case-control series, with an allelic P value of .0001 for a meta-analysis of all six samples. One of the case-control samples with significant association to rs498055 was derived from the linkage sample (P = .0165). These results indicate that variants in the RPS3A homologue are associated with LOAD and implicate this gene, adjacent genes, or other functional variants (e.g., noncoding RNAs) in the pathogenesis of this disorder.

摘要

在10号染色体上已观察到与晚发型阿尔茨海默病(LOAD)连锁的有力证据,这涉及一个广泛区域和至少一个疾病易感基因座。尽管已报道了与10号染色体上几个生物学候选基因的显著关联,但这些发现并未得到一致重复,且仍存在争议。我们对1412个基于基因的单核苷酸多态性(SNP)进行了10号染色体特异性关联研究,以确定LOAD发病的易感基因。该扫描包括1270个已知或预测基因中的677个基因的SNP;每个基因包含一个或多个标记,其中约一半(48%)代表推定的功能突变。一般来说,初始检测是在来自圣路易斯地区的白人病例对照样本中进行的,有419例LOAD病例和377例年龄匹配的对照。在探索性分析中显示出显著关联的标记在其他几个白人病例对照样本集中进行了后续验证,以确认初始关联。在探索性样本中测试的1397个标记中,69个达到显著水平(P < 0.05)。其中5个标记在验证样本集中以P < 0.05的水平得到重复。一个标记rs498055,位于与RPS3A(LOC439999)同源的基因中,在六个病例对照系列中的四个中与阿尔茨海默病显著相关,对所有六个样本进行荟萃分析的等位基因P值为0.0001。与rs498055有显著关联的一个病例对照样本来自连锁样本(P = 0.0165)。这些结果表明,RPS3A同源物中的变体与LOAD相关,并提示该基因、相邻基因或其他功能变体(如非编码RNA)参与了该疾病的发病机制。