• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

FXYD6 基因与汉族人群精神分裂症无关。

No association between the FXYD6 gene and schizophrenia in the Chinese Han population.

机构信息

Bio-X Center, Shanghai Jiao Tong University, 1954 Huashan Road, Shanghai 200030, PR China.

出版信息

J Psychiatr Res. 2010 Apr;44(6):409-12. doi: 10.1016/j.jpsychires.2009.10.009. Epub 2010 Feb 9.

DOI:10.1016/j.jpsychires.2009.10.009
PMID:20149392
Abstract

Choudhury et al. identified FXYD6 as a susceptible gene for schizophrenia in the London and Aberdeen populations. We genotyped D11S1998 and 8 SNPs (rs869789, rs11216567, rs10790212, rs876797, rs4938445, rs497768, rs11216598, rs11605223) in a Chinese sample consisting of 1514 schizophrenia patients and 1514 healthy controls. We also compared the expression levels of FXYD6 in lymphocytes in 86 schizophrenia patients and 94 controls. No association was detected either in D11S1998 or the 8 SNPs. No difference was found in expression level between patients and controls. Our study suggests that FXYD6 does not play a role in schizophrenia in the Chinese Han population.

摘要

Choudhury 等人在伦敦和阿伯丁人群中发现 FXYD6 是精神分裂症的易感基因。我们对一个由 1514 名精神分裂症患者和 1514 名健康对照组成的中国样本进行了 D11S1998 和 8 个 SNP(rs869789、rs11216567、rs10790212、rs876797、rs4938445、rs497768、rs11216598、rs11605223)的基因分型。我们还比较了 86 名精神分裂症患者和 94 名对照者淋巴细胞中 FXYD6 的表达水平。在 D11S1998 或 8 个 SNP 中均未检测到相关性。患者和对照组之间的表达水平没有差异。我们的研究表明,FXYD6 在中国汉族人群中与精神分裂症无关。

相似文献

1
No association between the FXYD6 gene and schizophrenia in the Chinese Han population.FXYD6 基因与汉族人群精神分裂症无关。
J Psychiatr Res. 2010 Apr;44(6):409-12. doi: 10.1016/j.jpsychires.2009.10.009. Epub 2010 Feb 9.
2
[A family-based association study of FXYD6 gene polymorphisms and schizophrenia].[FXYD6基因多态性与精神分裂症的家系关联研究]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Oct;28(5):539-42. doi: 10.3760/cma.j.issn.1003-9406.2011.05.015.
3
A genetic association study of the FXYD domain containing ion transport regulator 6 (FXYD6) gene, encoding phosphohippolin, in susceptibility to schizophrenia in a Japanese population.一项针对编码磷酸海马蛋白的含FXYD结构域离子转运调节因子6(FXYD6)基因与日本人群精神分裂症易感性的基因关联研究。
Neurosci Lett. 2008 Jun 13;438(1):70-5. doi: 10.1016/j.neulet.2008.04.010. Epub 2008 Apr 9.
4
A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia.一项针对两个不同样本中11号染色体q22 - 24区域的基因关联研究表明,编码磷酸海马素的FXYD6基因与精神分裂症易感性有关。
Am J Hum Genet. 2007 Apr;80(4):664-72. doi: 10.1086/513475. Epub 2007 Mar 1.
5
Association analysis of the RGS4 gene in Han Chinese and Scottish populations with schizophrenia.汉族和苏格兰人群中RGS4基因与精神分裂症的关联分析。
Genes Brain Behav. 2005 Oct;4(7):444-8. doi: 10.1111/j.1601-183X.2005.00167.x.
6
A novel replicated association between FXYD6 gene and schizophrenia.FXYD6 基因与精神分裂症的新型复制关联。
Biochem Biophys Res Commun. 2011 Feb 4;405(1):118-21. doi: 10.1016/j.bbrc.2011.01.005. Epub 2011 Jan 7.
7
FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population.FoxP2 与中国汉族人群的精神分裂症和重度抑郁症显著相关。
World J Biol Psychiatry. 2013 Mar;14(2):146-50. doi: 10.3109/15622975.2011.615860. Epub 2012 Mar 9.
8
An association study between PPP1R1B gene and schizophrenia in the Chinese population.中国人群中PPP1R1B基因与精神分裂症的关联研究。
Prog Neuropsychopharmacol Biol Psychiatry. 2007 Aug 15;31(6):1303-6. doi: 10.1016/j.pnpbp.2007.05.014. Epub 2007 Jun 7.
9
Polymorphisms of myelin-associated glycoprotein gene are associated with schizophrenia in the Chinese Han population.髓磷脂相关糖蛋白基因多态性与中国汉族人群的精神分裂症相关。
Neurosci Lett. 2005 Nov 18;388(3):126-31. doi: 10.1016/j.neulet.2005.06.051.
10
Association of plasma homocysteine and methylenetetrahydrofolate reductase C677T gene variant with schizophrenia: A Chinese Han population-based case-control study.血浆同型半胱氨酸及亚甲基四氢叶酸还原酶C677T基因变异与精神分裂症的关联:一项基于中国汉族人群的病例对照研究。
Psychiatry Res. 2009 Aug 15;168(3):205-8. doi: 10.1016/j.psychres.2008.05.009. Epub 2009 Jun 28.

引用本文的文献

1
Association Study Between Polymorphic Loci in Cholesterol Metabolism Pathway and Gallstone in the Tibetan Population.藏族人群胆固醇代谢途径多态性位点与胆结石的关联研究
Front Genet. 2022 May 16;13:902553. doi: 10.3389/fgene.2022.902553. eCollection 2022.
2
CalPen (Calculator of Penetrance), a web-based tool to estimate penetrance in complex genetic disorders.CalPen(外显率计算器),一个用于估计复杂遗传疾病外显率的网络工具。
PLoS One. 2020 Jan 29;15(1):e0228156. doi: 10.1371/journal.pone.0228156. eCollection 2020.