The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

Published:2005-12-01 Issue:2 Volume:15 Page:223-232
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Gloeckner Christian Johannes,Kinkl Norbert,Schumacher Annette,Braun Ralf J.,O'Neill Eric,Meitinger Thomas,Kolch Walter,Prokisch Holger,Ueffing Marius

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/2/223/1620061/ddi439.pdf

Reference43 articles.

1. Paisan-Ruiz, C., Jain, S., Evans, E.W., Gilks, W.P., Simon, J., van der Brug, M., de Munain, A.L., Aparicio, S., Gil, A.M., Khan, N. et al. (2004) Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron, 44, 595–600.

2. Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., Kachergus, J., Hulihan, M., Uitti, R.J., Calne, D.B. et al. (2004) Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron, 44, 601–607.

3. Farrer, M., Stone, J., Mata, I.F., Lincoln, S., Kachergus, J., Hulihan, M., Strain, K.J. and Maraganore, D.M. (2005) LRRK2 mutations in Parkinson disease. Neurology, 65, 738–740.

4. Gilks, W.P., Abou-Sleiman, P.M., Gandhi, S., Jain, S., Singleton, A., Lees, A.J., Shaw, K., Bhatia, K.P., Bonifati, V., Quinn, N.P. et al. (2005) A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet, 365, 415–416.

5. Toft, M., Mata, I.F., Kachergus, J.M., Ross, O.A. and Farrer, M.J. (2005) LRRK2 mutations and Parkinsonism. Lancet, 365, 1229–1230.

Cited by 429 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. Cryo-electron tomography reveals the microtubule-bound form of inactive LRRK2;2024-09-09

2. Cryo-electron tomography reveals the microtubule-bound form of inactive LRRK2;2024-09-09

3. Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease;Neurobiology of Disease;2024-09

4. Intramolecular feedback regulation of the LRRK2 Roc G domain by a LRRK2 kinase dependent mechanism;2024-08-28

5. Leucine-Rich Repeat Kinases;Annual Review of Biochemistry;2024-08-02

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