• 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

Alzheimer's disease and possible gene interaction.

作者信息

St George-Hyslop P, McLachlan D C, Tsuda T, Rogaev E, Karlinsky H, Lippa C F, Pollen D

出版信息

Science. 1994 Jan 28;263(5146):537. doi: 10.1126/science.8290965.

DOI:10.1126/science.8290965
PMID:8290965
Abstract
摘要

相似文献

1
Alzheimer's disease and possible gene interaction.
Science. 1994 Jan 28;263(5146):537. doi: 10.1126/science.8290965.
2
Cell biology of the beta-amyloid precursor protein and the genetics of Alzheimer's disease.β-淀粉样前体蛋白的细胞生物学与阿尔茨海默病的遗传学
Cold Spring Harb Symp Quant Biol. 1996;61:587-96.
3
Alzheimer's disease: phenotypes and genotypes.
Funct Neurol. 1997 May-Aug;12(3-4):147-51.
4
[Familial Alzheimer's disease by beta-amyloid protein precursor (beta APP) mutations].[β-淀粉样蛋白前体（βAPP）突变所致家族性阿尔茨海默病]
Nihon Rinsho. 2004 Jan;62 Suppl:86-9.
5
[Advances in the study of Alzheimer's disease associated genes].
Zhonghua Yi Xue Za Zhi. 1999 Feb;79(2):158-60.
6
Apolipoprotein E genotype and Alzheimer's disease. Alzheimer's Disease Collaborative Group.载脂蛋白E基因型与阿尔茨海默病。阿尔茨海默病协作组。
Lancet. 1993 Sep 18;342(8873):737-8.
7
Genetic discoveries as the basis of personalized therapy: rosiglitazone treatment of Alzheimer's disease.基于基因发现的个性化治疗：罗格列酮治疗阿尔茨海默病
Pharmacogenomics J. 2006 Jul-Aug;6(4):222-4. doi: 10.1038/sj.tpj.6500383.
8
Apolipoprotein E genotype and neuropathological phenotype in two members of a German family with chromosome 14-linked early onset Alzheimer's disease.
Acta Neuropathol. 1995;90(3):257-65. doi: 10.1007/BF00296509.
9
Alzheimer's disease and genetic testing.阿尔茨海默病与基因检测。
Alzheimer Dis Assoc Disord. 1994;8(2):63-5; discussion 66-7.
10
[Current genetic linkages of Alzheimer's disease].
Duodecim. 1995;111(5):389-92.

引用本文的文献

1
Genetic Biomarkers on Age-Related Cognitive Decline.与年龄相关的认知衰退的基因生物标志物
Front Psychiatry. 2017 Nov 21;8:247. doi: 10.3389/fpsyt.2017.00247. eCollection 2017.
2
Optimizing the fragment complementation of APEX2 for detection of specific protein-protein interactions in live cells.优化 APEX2 的片段互补性，用于检测活细胞中特定的蛋白质-蛋白质相互作用。
Sci Rep. 2017 Sep 27;7(1):12039. doi: 10.1038/s41598-017-12365-9.
3
Panel of Genetic Variations as a Potential Non-invasive Biomarker for Early Diagnosis of Alzheimer's Disease.
基因变异面板作为阿尔茨海默病早期诊断的潜在非侵入性生物标志物。
Clin Psychopharmacol Neurosci. 2011 Aug;9(2):54-66. doi: 10.9758/cpn.2011.9.2.54. Epub 2011 Aug 31.
4
The genetics and neuropathology of Alzheimer's disease.阿尔茨海默病的遗传学和神经病理学。
Acta Neuropathol. 2012 Sep;124(3):305-23. doi: 10.1007/s00401-012-0996-2. Epub 2012 May 23.
5
Genetic studies in Alzheimer's disease.阿尔茨海默病的遗传学研究。
Dialogues Clin Neurosci. 2003 Mar;5(1):17-26. doi: 10.31887/DCNS.2003.5.1/yptang.
6
Fish-on-a-chip: a sensitive detection microfluidic system for Alzheimer's disease.鱼芯片：用于阿尔茨海默病的灵敏检测微流控系统。
J Biomed Sci. 2011 May 28;18(1):33. doi: 10.1186/1423-0127-18-33.
7
Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.荟萃分析证实CR1、CLU和PICALM为阿尔茨海默病风险基因座，并揭示了与APOE基因型的相互作用。
Arch Neurol. 2010 Dec;67(12):1473-84. doi: 10.1001/archneurol.2010.201. Epub 2010 Aug 9.
8
The role of cerebral amyloid beta accumulation in common forms of Alzheimer disease.脑淀粉样β蛋白积累在常见形式阿尔茨海默病中的作用。
J Clin Invest. 2005 May;115(5):1121-9. doi: 10.1172/JCI25100.
9
Similar promotion of Abeta1-42 fibrillogenesis by native apolipoprotein E epsilon3 and epsilon4 isoforms.天然载脂蛋白E ε3和ε4亚型对β淀粉样蛋白1-42纤维形成的类似促进作用。
J Neuroinflammation. 2004 Aug 16;1(1):15. doi: 10.1186/1742-2094-1-15.
10
The solved and unsolved mysteries of the genetics of early-onset Alzheimer's disease.早发性阿尔茨海默病遗传学的已解与未解之谜。
Neuromolecular Med. 2002;2(1):1-10. doi: 10.1385/NMM:2:1:01.