Expressing hNF-LE397Kresults in abnormal gaiting in a transgenic model of CMT2E
Author:
Publisher
Wiley
Subject
Behavioral Neuroscience,Neurology,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1601-183X.2012.00771.x/fullpdf
Reference23 articles.
1. Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease: nonsense mutation probably causes a recessive phenotype.;Abe;J Hum Genet,2009
2. Charcot-Marie-Tooth disease: a clinico-genetic confrontation.;Barisic;Ann Hum Genet,2008
3. New movements in neurofilament transport, turnover and disease.;Barry;Exp Cell Res,2007
4. HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.;d’Ydewalle;Nat Med,2011
5. Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.;De Jonghe;Ann Neurol,2001
Cited by 7 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. Neurofilaments in health and Charcot-Marie-Tooth disease;Frontiers in Cell and Developmental Biology;2023-12-18
2. Targeting SARM1 improves autophagic stress-induced axonal neuropathy;Autophagy;2023-08-18
3. Muscle spindle alterations precede onset of sensorimotor deficits in Charcot-Marie-Tooth type 2E;Genes, Brain and Behavior;2016-10-11
4. Tentonin 3/TMEM150c Confers Distinct Mechanosensitive Currents in Dorsal-Root Ganglion Neurons with Proprioceptive Function;Neuron;2016-07
5. Identification of mutations in theMYO9Agene in patients with congenital myasthenic syndrome;Brain;2016-06-03
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