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.
7. 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]
8. 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]
9. 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]
10. Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis. Verbeeck C; Deng Q; Dejesus-Hernandez M; Taylor G; Ceballos-Diaz C; Kocerha J; Golde T; Das P; Rademakers R; Dickson DW; Kukar T Mol Neurodegener; 2012 Oct; 7():53. PubMed ID: 23046583 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. 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]
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. 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]
17. Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation. Tateishi T; Hokonohara T; Yamasaki R; Miura S; Kikuchi H; Iwaki A; Tashiro H; Furuya H; Nagara Y; Ohyagi Y; Nukina N; Iwaki T; Fukumaki Y; Kira J Acta Neuropathol; 2010 Mar; 119(3):355-64. PubMed ID: 19967541 [TBL] [Abstract][Full Text] [Related]
18. [Clinical and pathological characteristics of FUS/TLS-associated amyotrophic lateral sclerosis (ALS)]. Murayama S Rinsho Shinkeigaku; 2010 Nov; 50(11):948-50. PubMed ID: 21921522 [TBL] [Abstract][Full Text] [Related]
19. Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations. Neumann M; Valori CF; Ansorge O; Kretzschmar HA; Munoz DG; Kusaka H; Yokota O; Ishihara K; Ang LC; Bilbao JM; Mackenzie IR Acta Neuropathol; 2012 Nov; 124(5):705-16. PubMed ID: 22842875 [TBL] [Abstract][Full Text] [Related]
20. Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease. Ito H; Fujita K; Nakamura M; Wate R; Kaneko S; Sasaki S; Yamane K; Suzuki N; Aoki M; Shibata N; Togashi S; Kawata A; Mochizuki Y; Mizutani T; Maruyama H; Hirano A; Takahashi R; Kawakami H; Kusaka H Acta Neuropathol; 2011 Apr; 121(4):555-7. PubMed ID: 21327942 [No Abstract] [Full Text] [Related] [Next] [New Search]