These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
809 related articles for article (PubMed ID: 21856723)
21. Autophagy regulates amyotrophic lateral sclerosis-linked fused in sarcoma-positive stress granules in neurons. Ryu HH; Jun MH; Min KJ; Jang DJ; Lee YS; Kim HK; Lee JA Neurobiol Aging; 2014 Dec; 35(12):2822-2831. PubMed ID: 25216585 [TBL] [Abstract][Full Text] [Related]
23. The presence of heterogeneous nuclear ribonucleoproteins in frontotemporal lobar degeneration with FUS-positive inclusions. Gami-Patel P; Bandopadhyay R; Brelstaff J; Revesz T; Lashley T Neurobiol Aging; 2016 Oct; 46():192-203. PubMed ID: 27500866 [TBL] [Abstract][Full Text] [Related]
24. Aggregation of FET Proteins as a Pathological Change in Amyotrophic Lateral Sclerosis. Furukawa Y; Tokuda E Adv Exp Med Biol; 2017; 925():1-12. PubMed ID: 27311318 [TBL] [Abstract][Full Text] [Related]
34. TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration. Lagier-Tourenne C; Polymenidou M; Cleveland DW Hum Mol Genet; 2010 Apr; 19(R1):R46-64. PubMed ID: 20400460 [TBL] [Abstract][Full Text] [Related]
35. Characterization and expression analysis in the developing embryonic brain of the porcine FET family: FUS, EWS, and TAF15. Blechingberg J; Holm IE; Nielsen AL Gene; 2012 Feb; 493(1):27-35. PubMed ID: 22143032 [TBL] [Abstract][Full Text] [Related]
36. Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS. Ito D; Seki M; Tsunoda Y; Uchiyama H; Suzuki N Ann Neurol; 2011 Jan; 69(1):152-62. PubMed ID: 21280085 [TBL] [Abstract][Full Text] [Related]
37. FUS pathology in basophilic inclusion body disease. Munoz DG; Neumann M; Kusaka H; Yokota O; Ishihara K; Terada S; Kuroda S; Mackenzie IR Acta Neuropathol; 2009 Nov; 118(5):617-27. PubMed ID: 19830439 [TBL] [Abstract][Full Text] [Related]
38. Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation. Mackenzie IR; Ansorge O; Strong M; Bilbao J; Zinman L; Ang LC; Baker M; Stewart H; Eisen A; Rademakers R; Neumann M Acta Neuropathol; 2011 Jul; 122(1):87-98. PubMed ID: 21604077 [TBL] [Abstract][Full Text] [Related]
39. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Deng HX; Zhai H; Bigio EH; Yan J; Fecto F; Ajroud K; Mishra M; Ajroud-Driss S; Heller S; Sufit R; Siddique N; Mugnaini E; Siddique T Ann Neurol; 2010 Jun; 67(6):739-48. PubMed ID: 20517935 [TBL] [Abstract][Full Text] [Related]
40. Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal aging. Japtok J; Lojewski X; Naumann M; Klingenstein M; Reinhardt P; Sterneckert J; Putz S; Demestre M; Boeckers TM; Ludolph AC; Liebau S; Storch A; Hermann A Neurobiol Dis; 2015 Oct; 82():420-429. PubMed ID: 26253605 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]