Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA

Published:1998-10 Issue:2 Volume:20 Page:198-202
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Reddy P. Hemachandra,Williams Maya,Charles Vinod,Garrett Lisa,Pike-Buchanan Lisa,Whetsell William O.,Miller Georgina,Tagle Danilo A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1098_198.pdf

Reference30 articles.

1. Vonsattel, J.P. et al. Neuropathological classification of Huntington's disease. J. Neuropathol. Exp. Neurol. 44, 559– 577 (1985).

2. Folstein, S.E. Huntington's Disease (Johns Hopkins University Press, Baltimore, 1990).

3. Hedreen, J.C., Peyser, C.E., Folstein, S.E. & Ross, C.A. Neuronal loss in layers V and VI of cerebral cortex in Huntington's disease. Neurosci. Lett. 133, 257– 261 (1991).

4. Spargo, E., Everall, I.P. & Lantos, P.L. Neuronal loss in the hippocampus in Huntington's disease: a comparison with HIV infection. J. Neurol. Neurosurg. Psychiatry 56, 487–491 ( 1993).

5. The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971–983 (1993).

Cited by 339 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Advantages and differences among various animal models of Huntington’s disease;Ageing and Neurodegenerative Diseases;2024-08-10

2. In vivo CRISPR base editing for treatment of Huntington’s disease;2024-07-07

3. Revisiting the Mitochondrial Function and Communication in Neurodegenerative Diseases;Current Pharmaceutical Design;2024-04

4. Contribution of Glial Cells to Polyglutamine Diseases: Observations from Patients and Mouse Models;Neurotherapeutics;2023-01

5. Single-nuclei transcriptome analysis of Huntington disease iPSC and mouse astrocytes implicates maturation and functional deficits;iScience;2023-01

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3