• 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

Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

作者信息

Soong B W, Lee Yi-Chung

机构信息

The Neurological Institute, Taipei Veterans General Hospital, Peitou District, Taipei, Taiwan.

出版信息

Hum Genet. 2005 Dec;118(3-4):543.

PMID:16521289
Abstract
摘要

相似文献

1
Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.基因符号:NOTCH3。疾病:伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
Hum Genet. 2005 Dec;118(3-4):543.
2
Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Hum Genet. 2005 Feb;116(3):242.
3
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病
Acta Neurol Taiwan. 2008 Dec;17(4):295-6.
4
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)中的Notch3突变,这是一种导致中风和血管性痴呆的孟德尔遗传病。
Ann N Y Acad Sci. 1997 Sep 26;826:213-7. doi: 10.1111/j.1749-6632.1997.tb48472.x.
5
[From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].[从基因到疾病;从Notch3到伴有皮质下梗死和白质脑病的大脑常染色体显性动脉病]
Ned Tijdschr Geneeskd. 2001 Feb 24;145(8):359-60.
6
[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].四个患有伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病的中国家系中的NOTCH3基因突变
Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80.
7
Gene symbol: NOTCH3. Disease: CADASIL.基因符号:NOTCH3。疾病:伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)
Hum Genet. 2005 Dec;118(3-4):535.
8
Gene symbol: NOTCH3. Disease: CADASIL.基因符号:NOTCH3。疾病:大脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL)
Hum Genet. 2005 Dec;118(3-4):534.
9
Role of subvoxel free fluid on diffusion parameters in brain tissue with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and its correlation with physical disability: histogram analysis of standard and fluid-attenuated MR diffusion.脑小血管内游离液体在伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病脑组织扩散参数中的作用及其与身体残疾的相关性:标准和液体衰减磁共振扩散直方图分析
AJNR Am J Neuroradiol. 2003 Jun-Jul;24(6):1083-9.
10
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病:中国人群NOTCH3基因的两个新突变
J Neurol Sci. 2006 Jul 15;246(1-2):111-5. doi: 10.1016/j.jns.2006.02.011. Epub 2006 Mar 31.