• 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

相似文献

1
Parental sex effect in families with alcoholism.酗酒家庭中的父母性别效应。
Genet Epidemiol. 1999;17 Suppl 1:S409-13. doi: 10.1002/gepi.1370170769.
2
Sex-based linkage analysis of alcoholism.酗酒的性别连锁分析。
Genet Epidemiol. 1999;17 Suppl 1:S289-94. doi: 10.1002/gepi.1370170749.
3
A genome scan for parent-of-origin linkage effects in alcoholism.在酗酒症中进行亲代来源连锁效应的基因组扫描。
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S160. doi: 10.1186/1471-2156-6-S1-S160.
4
Parent-of-origin, imprinting, mitochondrial, and X-linked effects in traits related to alcohol dependence: presentation Group 18 of Genetic Analysis Workshop 14.酒精依赖相关性状中的亲本来源、印记、线粒体及X连锁效应:遗传分析研讨会14的第18组报告
Genet Epidemiol. 2005;29 Suppl 1:S125-32. doi: 10.1002/gepi.20121.
5
Genetic imprinting analysis for alcoholism genes using variance components approach.利用方差分量法进行酗酒基因的遗传印记分析。
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S161. doi: 10.1186/1471-2156-6-S1-S161.
6
Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families.在57个德国家庭样本中对双相情感障碍与18号染色体的连锁关系进行评估。
Mol Psychiatry. 1999 Jan;4(1):76-84. doi: 10.1038/sj.mp.4000454.
7
The analysis of parental origin of alleles may detect susceptibility loci for complex disorders.等位基因亲本来源的分析可能会检测出复杂疾病的易感基因座。
Hum Hered. 1999 Jul;49(4):197-204. doi: 10.1159/000022875.
8
Linkage of chromosome 1 markers to alcoholism-related phenotypes by sib pair linkage analysis of principal components.通过主成分的同胞对连锁分析将1号染色体标记与酒精中毒相关表型进行连锁分析。
Genet Epidemiol. 1999;17 Suppl 1:S271-6. doi: 10.1002/gepi.1370170746.
9
A genome-wide search for susceptibility genes linked to alcohol dependence.一项针对与酒精依赖相关的易感基因的全基因组搜索。
Genet Epidemiol. 1999;17 Suppl 1:S295-300. doi: 10.1002/gepi.1370170750.
10
Linkage of an alcoholism-related severity phenotype to chromosome 16.一种与酒精中毒相关的严重程度表型与16号染色体的连锁关系。
Alcohol Clin Exp Res. 1998 Dec;22(9):2035-42.

引用本文的文献

1
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index.新方法识别出SLC2A10和KCNK9基因中的单核苷酸多态性,并证明了亲本来源效应与体重指数之间的关联。
PLoS Genet. 2014 Jul 31;10(7):e1004508. doi: 10.1371/journal.pgen.1004508. eCollection 2014 Jul.
2
A unified framework integrating parent-of-origin effects for association study.整合亲源效应的关联研究统一框架。
PLoS One. 2013 Aug 26;8(8):e72208. doi: 10.1371/journal.pone.0072208. eCollection 2013.
3
A genome scan for parent-of-origin linkage effects in alcoholism.
在酗酒症中进行亲代来源连锁效应的基因组扫描。
BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S160. doi: 10.1186/1471-2156-6-S1-S160.

酗酒家庭中的父母性别效应。

Parental sex effect in families with alcoholism.

作者信息

Wyszynski D F, Panhuysen C I

机构信息

Department of Public Health, School of Medicine, University of Buenos Aires, Argentina.

出版信息

Genet Epidemiol. 1999;17 Suppl 1:S409-13. doi: 10.1002/gepi.1370170769.

DOI:10.1002/gepi.1370170769
PMID:10597471
Abstract

Parental sex effects have been shown to influence the inheritance of a number of complex disorders. In this paper we performed affected sib-pair analyses on 105 families with recurrent alcoholism to evaluate the effects that the parent of origin might have on this disorder. Three alternative classification schemes were used and the families were grouped as maternal, paternal, mixed, or unknown. Paternal effects were observed at D9S64, D16S475, and D16S2622, while maternal effects were expressed at FABP2, D8S280, D8S1715, and D8S1988. Except for D16S2622, none of these markers resulted in a significant p-value when all families were analyzed together. These results suggest that the parental sex should not be ignored and that a discriminatory analysis should always be performed.

摘要

亲代性别效应已被证明会影响多种复杂疾病的遗传。在本文中,我们对105个有复发性酒精中毒的家庭进行了患病同胞对分析,以评估亲代来源对这种疾病可能产生的影响。我们使用了三种不同的分类方案,将家庭分为母系、父系、混合或未知类型。在D9S64、D16S475和D16S2622位点观察到父系效应,而在FABP2、D8S280、D8S1715和D8S1988位点观察到母系效应。当对所有家庭进行综合分析时,除了D16S2622外,这些标记物均未产生显著的p值。这些结果表明,亲代性别不容忽视,应始终进行区分分析。