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.
447 related articles for article (PubMed ID: 32142134)
1. Characteristic Features of FUS Inclusions in Spinal Motor Neurons of Sporadic Amyotrophic Lateral Sclerosis. Ikenaka K; Ishigaki S; Iguchi Y; Kawai K; Fujioka Y; Yokoi S; Abdelhamid RF; Nagano S; Mochizuki H; Katsuno M; Sobue G J Neuropathol Exp Neurol; 2020 Apr; 79(4):370-377. PubMed ID: 32142134 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. An autopsied case of sporadic adult-onset amyotrophic lateral sclerosis with FUS-positive basophilic inclusions. Matsuoka T; Fujii N; Kondo A; Iwaki A; Hokonohara T; Honda H; Sasaki K; Suzuki SO; Iwaki T Neuropathology; 2011 Feb; 31(1):71-6. PubMed ID: 20573033 [TBL] [Abstract][Full Text] [Related]
4. Atypical FTLD-FUS associated with ALS-TDP: a case report. Kobayashi Z; Arai T; Yokota O; Tsuchiya K; Hosokawa M; Oshima K; Niizato K; Akiyama H; Mizusawa H Neuropathology; 2013 Feb; 33(1):83-6. PubMed ID: 22640227 [TBL] [Abstract][Full Text] [Related]
5. Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations. Bäumer D; Hilton D; Paine SM; Turner MR; Lowe J; Talbot K; Ansorge O Neurology; 2010 Aug; 75(7):611-8. PubMed ID: 20668261 [TBL] [Abstract][Full Text] [Related]
6. Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis. Rademakers R; Stewart H; Dejesus-Hernandez M; Krieger C; Graff-Radford N; Fabros M; Briemberg H; Cashman N; Eisen A; Mackenzie IR Muscle Nerve; 2010 Aug; 42(2):170-6. PubMed ID: 20544928 [TBL] [Abstract][Full Text] [Related]
7. Aberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosis. Pokrishevsky E; Grad LI; Yousefi M; Wang J; Mackenzie IR; Cashman NR PLoS One; 2012; 7(4):e35050. PubMed ID: 22493728 [TBL] [Abstract][Full Text] [Related]
8. Combined fused in sarcoma-positive (FUS+) basophilic inclusion body disease and atypical tauopathy presenting with an amyotrophic lateral sclerosis/motor neurone disease (ALS/MND)-plus phenotype. Wharton SB; Verber NS; Wagner BE; Highley JR; Fillingham DJ; Waller R; Strand K; Ince PG; Shaw PJ Neuropathol Appl Neurobiol; 2019 Oct; 45(6):586-596. PubMed ID: 30659642 [TBL] [Abstract][Full Text] [Related]
9. Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis. Tada M; Doi H; Koyano S; Kubota S; Fukai R; Hashiguchi S; Hayashi N; Kawamoto Y; Kunii M; Tanaka K; Takahashi K; Ogawa Y; Iwata R; Yamanaka S; Takeuchi H; Tanaka F Am J Pathol; 2018 Feb; 188(2):507-514. PubMed ID: 29128563 [TBL] [Abstract][Full Text] [Related]
10. Requirements for stress granule recruitment of fused in sarcoma (FUS) and TAR DNA-binding protein of 43 kDa (TDP-43). Bentmann E; Neumann M; Tahirovic S; Rodde R; Dormann D; Haass C J Biol Chem; 2012 Jun; 287(27):23079-94. PubMed ID: 22563080 [TBL] [Abstract][Full Text] [Related]
11. Deficient RNA-editing enzyme ADAR2 in an amyotrophic lateral sclerosis patient with a FUS(P525L) mutation. Aizawa H; Hideyama T; Yamashita T; Kimura T; Suzuki N; Aoki M; Kwak S J Clin Neurosci; 2016 Oct; 32():128-9. PubMed ID: 27343041 [TBL] [Abstract][Full Text] [Related]
12. Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis. Kobayashi Z; Tsuchiya K; Arai T; Aoki M; Hasegawa M; Ishizu H; Akiyama H; Mizusawa H J Neurol Sci; 2010 Jun; 293(1-2):6-11. PubMed ID: 20409561 [TBL] [Abstract][Full Text] [Related]
13. FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations. Neumann M; Bentmann E; Dormann D; Jawaid A; DeJesus-Hernandez M; Ansorge O; Roeber S; Kretzschmar HA; Munoz DG; Kusaka H; Yokota O; Ang LC; Bilbao J; Rademakers R; Haass C; Mackenzie IR Brain; 2011 Sep; 134(Pt 9):2595-609. PubMed ID: 21856723 [TBL] [Abstract][Full Text] [Related]
14. FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation. Suzuki N; Kato S; Kato M; Warita H; Mizuno H; Kato M; Shimakura N; Akiyama H; Kobayashi Z; Konno H; Aoki M J Neuropathol Exp Neurol; 2012 Sep; 71(9):779-88. PubMed ID: 22878663 [TBL] [Abstract][Full Text] [Related]
15. Transportin 1 colocalization with Fused in Sarcoma (FUS) inclusions is not characteristic for amyotrophic lateral sclerosis-FUS confirming disrupted nuclear import of mutant FUS and distinguishing it from frontotemporal lobar degeneration with FUS inclusions. Troakes C; Hortobágyi T; Vance C; Al-Sarraj S; Rogelj B; Shaw CE Neuropathol Appl Neurobiol; 2013 Aug; 39(5):553-61. PubMed ID: 22934812 [TBL] [Abstract][Full Text] [Related]
16. Regionally different immunoreactivity for Smurf2 and pSmad2/3 in TDP-43-positive inclusions of amyotrophic lateral sclerosis. Nakamura M; Kaneko S; Wate R; Asayama S; Nakamura Y; Fujita K; Ito H; Kusaka H Neuropathol Appl Neurobiol; 2013 Feb; 39(2):144-56. PubMed ID: 22435645 [TBL] [Abstract][Full Text] [Related]
17. Linear Polyubiquitin Chain Modification of TDP-43-Positive Neuronal Cytoplasmic Inclusions in Amyotrophic Lateral Sclerosis. Nakayama Y; Tsuji K; Ayaki T; Mori M; Tokunaga F; Ito H J Neuropathol Exp Neurol; 2020 Mar; 79(3):256-265. PubMed ID: 31951008 [TBL] [Abstract][Full Text] [Related]
18. ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation. King A; Troakes C; Smith B; Nolan M; Curran O; Vance C; Shaw CE; Al-Sarraj S Acta Neuropathol Commun; 2015 Oct; 3():62. PubMed ID: 26452761 [TBL] [Abstract][Full Text] [Related]