• 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

Abnormal gene product identified in Huntington's disease lymphocytes and brain.

作者信息

Ide K, Nukina N, Masuda N, Goto J, Kanazawa I

机构信息

Department of Neurology, Faculty of Medicine University of Tokyo, Japan.

出版信息

Biochem Biophys Res Commun. 1995 Apr 26;209(3):1119-25. doi: 10.1006/bbrc.1995.1613.

DOI:10.1006/bbrc.1995.1613
PMID:7733967
Abstract

Huntington's disease(HD) is associated with expansion of an unstable CAG repeat. Using antibodies against the synthetic peptide corresponding to the sequence of HD gene IT15, we have identified the HD gene product in normal lymphocytes as a approximately 350kDa protein by immunoblot analysis. Moreover, when a modified SDS-PAGE using a low concentration of methylenbisacrylamide was run longer, abnormal immunoreactive bands larger than normal ones were found exclusively in HD samples. These results demonstrate the existence of the expanded CAG repeat gene product and open a possibility that the expanded polyglutamine stretch may really participate in the pathological process of the CAG repeat diseases.

摘要

相似文献

1
Abnormal gene product identified in Huntington's disease lymphocytes and brain.
Biochem Biophys Res Commun. 1995 Apr 26;209(3):1119-25. doi: 10.1006/bbrc.1995.1613.
2
[Huntington's disease: trinucleotide disease or polyglutamine disease?].[亨廷顿舞蹈症:三核苷酸疾病还是多聚谷氨酰胺疾病?]
Rinsho Shinkeigaku. 1995 Dec;35(12):1540-1.
3
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian species.几种哺乳动物物种中亨廷顿舞蹈病基因(IT15)的CAG三联体重复区域的序列分析。
Ann Genet. 1996;39(2):81-6.
4
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain.在遗传性齿状核红核苍白球路易体萎缩症(DRPLA)患者大脑中鉴定出的异常基因产物。
Nat Genet. 1995 May;10(1):99-103. doi: 10.1038/ng0595-99.
5
A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes.一种针对三核苷酸重复序列的新型聚合酶链反应(PCR)检测方法,该三核苷酸重复序列在亨廷顿病染色体上不稳定且会发生扩增。
Mol Cell Probes. 1993 Jun;7(3):235-9. doi: 10.1006/mcpr.1993.1034.
6
Trinucleotide repeat length and rate of progression of Huntington's disease.亨廷顿舞蹈症的三核苷酸重复序列长度与疾病进展速率
Ann Neurol. 1994 Oct;36(4):630-5. doi: 10.1002/ana.410360412.
7
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.亨廷顿舞蹈病中三核苷酸重复序列扩增与表型变异的关系。
Nat Genet. 1993 Aug;4(4):393-7. doi: 10.1038/ng0893-393.
8
Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.亨廷顿舞蹈病新突变的分子分析:中间等位基因与起源性别效应
Nat Genet. 1993 Oct;5(2):174-9. doi: 10.1038/ng1093-174.
9
[Importance of the number of trinucleotide repeat expansions in the clinical manifestations of Huntington's chorea].[三核苷酸重复扩增数目在亨廷顿舞蹈病临床表现中的重要性]
Srp Arh Celok Lek. 1998 Mar-Apr;126(3-4):77-82.
10
[Gene analysis of Huntington's disease].
Nihon Shinkei Seishin Yakurigaku Zasshi. 1995 Oct;15(5):419-24.

引用本文的文献

1
Proteotoxicity and Neurodegenerative Diseases.蛋白毒性与神经退行性疾病。
Int J Mol Sci. 2020 Aug 6;21(16):5646. doi: 10.3390/ijms21165646.
2
Differential vulnerability of neurons in Huntington's disease: the role of cell type-specific features.亨廷顿病中神经元的差异易损性:细胞类型特异性特征的作用。
J Neurochem. 2010 Jun;113(5):1073-91. doi: 10.1111/j.1471-4159.2010.06672.x. Epub 2010 Mar 17.
3
Full-length huntingtin levels modulate body weight by influencing insulin-like growth factor 1 expression.全长亨廷顿蛋白水平通过影响胰岛素样生长因子 1 的表达来调节体重。
Hum Mol Genet. 2010 Apr 15;19(8):1528-38. doi: 10.1093/hmg/ddq026. Epub 2010 Jan 22.
4
Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease.人类血液的全基因组表达谱分析揭示了亨廷顿舞蹈病的生物标志物。
Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):11023-8. doi: 10.1073/pnas.0504921102. Epub 2005 Jul 25.
5
Huntington's disease and dentatorubral-pallidoluysian atrophy: proteins, pathogenesis and pathology.亨廷顿舞蹈症与齿状核红核苍白球路易体萎缩症:蛋白质、发病机制与病理学
Brain Pathol. 1997 Jul;7(3):1003-16. doi: 10.1111/j.1750-3639.1997.tb00898.x.