• 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

Absence of association between codon 129 and 219 polymorphisms of the prion protein gene and vascular dementia.

作者信息

Jeong Byung-Hoon, Na Hae-Ri, Bae Jae-Chun, Lee Kyung-Hee, Lee Yun-Jung, Kim Nam-Ho, Song Joon-Ho, Carp Richard I, Kim Yong-Sun

机构信息

Ilsong Institute of Life Science, Hallym University, Anyang, South Korea.

出版信息

Dement Geriatr Cogn Disord. 2007;24(2):86-90. doi: 10.1159/000103913. Epub 2007 Jun 14.

DOI:10.1159/000103913
PMID:17570906
Abstract

BACKGROUND

Polymorphisms of the prion protein gene (PRNP) are known to cause a strong susceptibility to the occurrence of prion diseases, such as Creutzfeldt-Jakob disease, and might be associated with other neurodegenerative disorders. However, an association between PRNP polymorphisms and vascular dementia (VaD) has not been reported thus far.

OBJECTIVE

To investigate whether the PRNP polymorphisms are associated with an increased risk for developing VaD in the Korean population.

METHODS

We compared the genotype, allele and haplotype frequencies of PRNP polymorphisms in 160 VaD patients with those in 236 healthy Koreans.

RESULTS AND CONCLUSION

Codon 129 (M129V) and 219 (Q219K) polymorphisms in Korean VaD patients were found in the open reading frame of PRNP. Our study shows that there is no significant difference in the genotype, allele and haplotype frequencies of PRNP codon 129 and 219 polymorphisms between Korean VaD patients and normal controls. This was the first genetic association study of the polymorphisms of PRNP with VaD.

摘要

相似文献

1
Absence of association between codon 129 and 219 polymorphisms of the prion protein gene and vascular dementia.
Dement Geriatr Cogn Disord. 2007;24(2):86-90. doi: 10.1159/000103913. Epub 2007 Jun 14.
2
Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.朊蛋白基因(PRNP)1368多态性与阿尔茨海默病或血管性痴呆之间无关联。
BMC Med Genet. 2009 Apr 8;10:32. doi: 10.1186/1471-2350-10-32.
3
Polymorphisms at codons 129 and 219 of the prion protein gene (PRNP) are not associated with sporadic Alzheimer's disease in the Korean population.朊蛋白基因(PRNP)第129和219密码子的多态性与韩国人群散发性阿尔茨海默病无关。
Eur J Neurol. 2007 Jun;14(6):621-6. doi: 10.1111/j.1468-1331.2007.01786.x.
4
No association of prion protein gene polymorphisms with Alzheimer's disease in Korean population.韩国人群中朊蛋白基因多态性与阿尔茨海默病无关联。
Exp Mol Med. 2006 Dec 31;38(6):727-31. doi: 10.1038/emm.2006.85.
5
Polymorphisms of the prion protein gene (PRNP) in a Korean population.韩国人群中朊病毒蛋白基因(PRNP)的多态性。
J Hum Genet. 2004;49(6):319-324. doi: 10.1007/s10038-004-0150-7. Epub 2004 May 18.
6
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.在一项大型德国病例对照研究中,PRNP基因5'非翻译区的M129V独立多态性与散发性克雅氏病存在显著关联。
J Med Genet. 2006 Oct;43(10):e53. doi: 10.1136/jmg.2006.040931.
7
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.朊蛋白基因和多配体蛋白聚糖基因中的多态性会增加克雅氏病的易感性。
Eur J Hum Genet. 2004 May;12(5):389-94. doi: 10.1038/sj.ejhg.5201161.
8
The M129V polymorphism of codon 129 in the prion gene (PRNP) in the Danish population.丹麦人群中朊病毒基因(PRNP)第129密码子的M129V多态性。
Eur J Epidemiol. 2008;23(1):23-7. doi: 10.1007/s10654-007-9197-z. Epub 2007 Nov 7.
9
PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.英国散发型和变异型克雅氏病中的 PRNP 变异突出了遗传风险因素和一种新的非同义多态性。
BMC Med Genet. 2009 Dec 26;10:146. doi: 10.1186/1471-2350-10-146.
10
Association of sporadic Creutzfeldt-Jakob disease with homozygous genotypes at PRNP codons 129 and 219 in the Korean population.韩国人群中散发性克雅氏病与PRNP密码子129和219处纯合基因型的关联。
Neurogenetics. 2005 Dec;6(4):229-32. doi: 10.1007/s10048-005-0016-y. Epub 2005 Oct 11.

引用本文的文献

1
Prion protein E219K polymorphism: from the discovery of the KANNO blood group to interventions for human prion disease.朊病毒蛋白E219K多态性:从神野血型的发现到人类朊病毒病的干预措施
Front Neurol. 2024 Jul 10;15:1392984. doi: 10.3389/fneur.2024.1392984. eCollection 2024.
2
Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases.(朊病毒)基因中突变的特征及其在神经退行性疾病中的可能作用。
Neuropsychiatr Dis Treat. 2018 Aug 14;14:2067-2085. doi: 10.2147/NDT.S165445. eCollection 2018.
3
Lack of association between PRNP 1368 polymorphism and Alzheimer's disease or vascular dementia.
朊蛋白基因(PRNP)1368多态性与阿尔茨海默病或血管性痴呆之间无关联。
BMC Med Genet. 2009 Apr 8;10:32. doi: 10.1186/1471-2350-10-32.