• 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

Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy.

作者信息

Bandmann O, Wenning G K, Quinn N P, Harding A E

出版信息

J Neurol Neurosurg Psychiatry. 1995 Nov;59(5):557. doi: 10.1136/jnnp.59.5.557.

DOI:10.1136/jnnp.59.5.557
PMID:8530951
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1073729/
Abstract
摘要

相似文献

1
Arg296 to Cys296 polymorphism in exon 6 of cytochrome P-450-2D6 (CYP2D6) is not associated with multiple system atrophy.细胞色素P-450-2D6（CYP2D6）第6外显子中从精氨酸296到半胱氨酸296的多态性与多系统萎缩无关。
J Neurol Neurosurg Psychiatry. 1995 Nov;59(5):557. doi: 10.1136/jnnp.59.5.557.
2
DNA haplotype-dependent differences in the amino acid sequence of debrisoquine 4-hydroxylase (CYP2D6): evidence for two major allozymes in extensive metabolisers.
Hum Genet. 1994 Oct;94(4):401-6. doi: 10.1007/BF00201601.
3
A polymorphic CfoI site in exon 6 of the human cytochrome P450 CYP2D6 gene detected by the polymerase chain reaction.通过聚合酶链反应检测到的人类细胞色素P450 CYP2D6基因外显子6中的一个多态性CfoI位点。
Hum Genet. 1993 Jul;91(6):616-7. doi: 10.1007/BF00205091.
4
A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease.一种与帕金森病相关的新型细胞色素P-450IID6突变基因。
J Biochem. 1993 Aug;114(2):263-6. doi: 10.1093/oxfordjournals.jbchem.a124164.
5
A novel cytochrome P-450IID6 (CYPIID6) mutant gene associated with multiple system atrophy.一种与多系统萎缩相关的新型细胞色素P-450IID6（CYPIID6）突变基因。
J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):263-4. doi: 10.1136/jnnp.58.2.263.
6
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.多系统萎缩中细胞色素P450 2D6-异喹胍羟化酶基因多态性
Mov Disord. 1995 May;10(3):277-8. doi: 10.1002/mds.870100307.
7
Familial Parkinson's disease and polymorphism at the CYP2D6 locus.家族性帕金森病与细胞色素P450 2D6基因座的多态性
J Neurol Neurosurg Psychiatry. 1994 Jul;57(7):871-2. doi: 10.1136/jnnp.57.7.871.
8
[Genetic polymorphism of drug metabolizing enzymes].[药物代谢酶的基因多态性]
Seikagaku. 1997 Oct;69(10):1196-9.
9
Gene-environment interaction in parkinson's disease. The case of CYP2D6 gene polymorphism.帕金森病中的基因-环境相互作用。CYP2D6基因多态性情况。
Adv Neurol. 1996;69:61-72.
10
"It's the genes, stupid". Molecular bases and clinical consequences of genetic cytochrome P450 2D6 polymorphism.“是基因，笨蛋”。细胞色素P450 2D6基因多态性的分子基础及临床后果
Life Sci. 1995;56(26):2285-98. doi: 10.1016/0024-3205(95)00223-s.

引用本文的文献

1
Multiple system atrophy: genetic or epigenetic?多系统萎缩：遗传因素还是表观遗传因素？
Exp Neurobiol. 2014 Dec;23(4):277-91. doi: 10.5607/en.2014.23.4.277. Epub 2014 Dec 12.
2
Genetic players in multiple system atrophy: unfolding the nature of the beast.多种系统萎缩中的遗传因素：揭示疾病本质。
Neurobiol Aging. 2011 Oct;32(10):1924.e5-14. doi: 10.1016/j.neurobiolaging.2011.04.001. Epub 2011 May 24.
3
Quantitative PCR-based screening of alpha-synuclein multiplication in multiple system atrophy.基于定量PCR的多系统萎缩中α-突触核蛋白倍增的筛查
Parkinsonism Relat Disord. 2007 Aug;13(6):340-2. doi: 10.1016/j.parkreldis.2006.12.005. Epub 2007 Feb 8.
4
Epidemiological evidence on multiple system atrophy.多系统萎缩的流行病学证据。
J Neural Transm (Vienna). 2005 Dec;112(12):1605-12. doi: 10.1007/s00702-005-0380-7.
5
Multiple system atrophy: cellular and molecular pathology.多系统萎缩：细胞与分子病理学
Mol Pathol. 2001 Dec;54(6):419-26.

本文引用的文献

1
A polymorphic CfoI site in exon 6 of the human cytochrome P450 CYP2D6 gene detected by the polymerase chain reaction.通过聚合酶链反应检测到的人类细胞色素P450 CYP2D6基因外显子6中的一个多态性CfoI位点。
Hum Genet. 1993 Jul;91(6):616-7. doi: 10.1007/BF00205091.
2
Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease.
Am J Med Genet. 1993 Oct 15;48(3):166-8. doi: 10.1002/ajmg.1320480311.
3
A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease.一种与帕金森病相关的新型细胞色素P-450IID6突变基因。
J Biochem. 1993 Aug;114(2):263-6. doi: 10.1093/oxfordjournals.jbchem.a124164.
4
A novel cytochrome P-450IID6 (CYPIID6) mutant gene associated with multiple system atrophy.一种与多系统萎缩相关的新型细胞色素P-450IID6（CYPIID6）突变基因。
J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):263-4. doi: 10.1136/jnnp.58.2.263.
5
CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy.多系统萎缩中细胞色素P450 2D6-异喹胍羟化酶基因多态性
Mov Disord. 1995 May;10(3):277-8. doi: 10.1002/mds.870100307.
6
Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease.异喹胍羟化酶基因多态性与帕金森病易感性
Lancet. 1992 Jun 6;339(8806):1375-7. doi: 10.1016/0140-6736(92)91196-f.
7
Mutant debrisoquine hydroxylation genes in Parkinson's disease.
Lancet. 1992 Apr 25;339(8800):1017-8. doi: 10.1016/0140-6736(92)90537-d.