ALS/FTLD: experimental models and reality-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

ALS/FTLD: experimental models and reality

Published:2017-01-05 Issue:2 Volume:133 Page:177-196
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Tan Rachel H.,Ke Yazi D.,Ittner Lars M.,Halliday Glenda M.

Funder

National Health and Medical Research Council

Australian Research Council

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-016-1666-6.pdf

Reference137 articles.

1. Ahmed Z, Bigio EH, Budka H, Dickson DW, Ferrer I, Ghetti B, Giaccone G, Hatanpaa KJ, Holton JL, Josephs KA, Powers J, Spina S, Takahashi H, White CL 3rd, Revesz T, Kovacs GG (2013) Globular glial tauopathies (GGT): consensus recommendations. Acta Neuropathol 126:537–544. doi: 10.1007/s00401-013-1171-0

2. Allen B, Ingram E, Takao M, Smith MJ, Jakes R, Virdee K, Yoshida H, Holzer M, Craxton M, Emson PC, Atzori C, Migheli A, Crowther RA, Ghetti B, Spillantini MG, Goedert M (2002) Abundant tau filaments and nonapoptotic neurodegeneration in transgenic mice expressing human P301S tau protein. J Neurosci 22:9340–9351

3. Almeida S, Zhang ZJ, Coppola G, Mao WJ, Futai K, Karydas A, Geschwind MD, Tartaglia MC, Gao FY, Gianni D, Sena-Esteves M, Geschwind DH, Miller BL, Farese RV, Gao FB (2012) Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects (vol 2, pg 789, 2012). Cell Rep 2:1471. doi: 10.1016/j.celrep.2012.11.006

4. Ash PEA, Bieniek KF, Gendron TF, Caulfield T, Lin WL, DeJesus-Hernandez M, van Blitterswijk MM, Jansen-West K, Paul JW, Rademakers R, Boylan KB, Dickson DW, Petrucelli L (2013) Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. Neuron 77:639–646. doi: 10.1016/j.neuron.2013.02.004

5. Babin PJ, Goizet C, Raldua D (2014) Zebrafish models of human motor neuron diseases: advantages and limitations. Prog Neurobiol 118:36–58. doi: 10.1016/j.pneurobio.2014.03.001

Cited by 81 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. Rebalancing the motor circuit restores movement in a Caenorhabditis elegans model for TDP-43 toxicity;Cell Reports;2024-05

2. Den Rauch riechen, bevor man das Feuer sieht – die oligosymptomatische Prodromalphase neurodegenerativer Erkrankungen;Der Nervenarzt;2024-04-17

3. ALS-Associated TDP-43 Dysfunction Compromises UPF1-Dependent mRNA Metabolism Pathways Including Alternative Polyadenylation and 3’UTR Length;2024-02-02

4. IκB kinase phosphorylates cytoplasmic TDP-43 and promotes its proteasome degradation;Journal of Cell Biology;2024-01-10

5. Simple models to understand complex disease: 10 years of progress from Caenorhabditis elegans models of amyotrophic lateral sclerosis and frontotemporal lobar degeneration;Frontiers in Neuroscience;2024-01-04

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