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.
822 related articles for article (PubMed ID: 25912081)
21. Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations. Tradewell ML; Yu Z; Tibshirani M; Boulanger MC; Durham HD; Richard S Hum Mol Genet; 2012 Jan; 21(1):136-49. PubMed ID: 21965298 [TBL] [Abstract][Full Text] [Related]
22. ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons. Lenzi J; De Santis R; de Turris V; Morlando M; Laneve P; Calvo A; Caliendo V; Chiò A; Rosa A; Bozzoni I Dis Model Mech; 2015 Jul; 8(7):755-66. PubMed ID: 26035390 [TBL] [Abstract][Full Text] [Related]
23. [Generation of induced pluripotent stem cells from amyotrophic lateral sclerosis patientcarrying SOD1-V14M mutation]. Liu X; Chen J; Li X; Gao S; Deng M Zhonghua Yi Xue Za Zhi; 2014 Jul; 94(27):2143-7. PubMed ID: 25327864 [TBL] [Abstract][Full Text] [Related]
24. FUS ALS neurons activate major stress pathways and reduce translation as an early protective mechanism against neurodegeneration. Szewczyk B; Günther R; Japtok J; Frech MJ; Naumann M; Lee HO; Hermann A Cell Rep; 2023 Feb; 42(2):112025. PubMed ID: 36696267 [TBL] [Abstract][Full Text] [Related]
25. Aggregation of ALS-linked FUS mutant sequesters RNA binding proteins and impairs RNA granules formation. Takanashi K; Yamaguchi A Biochem Biophys Res Commun; 2014 Sep; 452(3):600-7. PubMed ID: 25173930 [TBL] [Abstract][Full Text] [Related]
26. lncRNA Sequencing Reveals Neurodegeneration-Associated FUS Mutations Alter Transcriptional Landscape of iPS Cells That Persists in Motor Neurons. Provasek VE; Kodavati M; Guo W; Wang H; Boldogh I; Van Den Bosch L; Britz G; Hegde ML Cells; 2023 Oct; 12(20):. PubMed ID: 37887305 [TBL] [Abstract][Full Text] [Related]
27. Motor neuron differentiation of iPSCs obtained from peripheral blood of a mutant TARDBP ALS patient. Bossolasco P; Sassone F; Gumina V; Peverelli S; Garzo M; Silani V Stem Cell Res; 2018 Jul; 30():61-68. PubMed ID: 29800782 [TBL] [Abstract][Full Text] [Related]
28. Induced pluripotent stem cell-derived motor neurons from amyotrophic lateral sclerosis (ALS) patients carrying different superoxide dismutase 1 mutations recapitulate pathological features of ALS. Liu WC; Liu N; Wang Y; Huang C; Li YF; Wang H; Li XG; Deng M Chin Med J (Engl); 2021 Oct; 134(20):2457-2464. PubMed ID: 34669638 [TBL] [Abstract][Full Text] [Related]
29. ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues. Bayer H; Lang K; Buck E; Higelin J; Barteczko L; Pasquarelli N; Sprissler J; Lucas T; Holzmann K; Demestre M; Lindenberg KS; Danzer KM; Boeckers T; Ludolph AC; Dupuis L; Weydt P; Witting A Neurobiol Dis; 2017 Jan; 97(Pt A):36-45. PubMed ID: 27818323 [TBL] [Abstract][Full Text] [Related]
30. Stress-Specific Spatiotemporal Responses of RNA-Binding Proteins in Human Stem-Cell-Derived Motor Neurons. Harley J; Patani R Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33172210 [TBL] [Abstract][Full Text] [Related]
31. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China. Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859 [TBL] [Abstract][Full Text] [Related]
33. ALS mutations of FUS suppress protein translation and disrupt the regulation of nonsense-mediated decay. Kamelgarn M; Chen J; Kuang L; Jin H; Kasarskis EJ; Zhu H Proc Natl Acad Sci U S A; 2018 Dec; 115(51):E11904-E11913. PubMed ID: 30455313 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. Impaired nuclear transport induced by juvenile ALS causing P525L mutation in NLS domain of FUS: A molecular mechanistic study. Basu S; Rajendra KC; Alagar S; Bahadur RP Biochim Biophys Acta Proteins Proteom; 2022 Apr; 1870(4):140766. PubMed ID: 35134572 [TBL] [Abstract][Full Text] [Related]
36. IFNγ protects motor neurons from oxidative stress via enhanced global protein synthesis in FUS-associated amyotrophic lateral sclerosis. Assoni AF; Guerrero EN; Wardenaar R; Oliveira D; Bakker PL; Alves LM; Carvalho VM; Okamoto OK; Zatz M; Foijer F Brain Pathol; 2024 Jan; 34(1):e13206. PubMed ID: 37582053 [TBL] [Abstract][Full Text] [Related]
37. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Kwiatkowski TJ; Bosco DA; Leclerc AL; Tamrazian E; Vanderburg CR; Russ C; Davis A; Gilchrist J; Kasarskis EJ; Munsat T; Valdmanis P; Rouleau GA; Hosler BA; Cortelli P; de Jong PJ; Yoshinaga Y; Haines JL; Pericak-Vance MA; Yan J; Ticozzi N; Siddique T; McKenna-Yasek D; Sapp PC; Horvitz HR; Landers JE; Brown RH Science; 2009 Feb; 323(5918):1205-8. PubMed ID: 19251627 [TBL] [Abstract][Full Text] [Related]
38. CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs. Wang L; Yi F; Fu L; Yang J; Wang S; Wang Z; Suzuki K; Sun L; Xu X; Yu Y; Qiao J; Belmonte JCI; Yang Z; Yuan Y; Qu J; Liu GH Protein Cell; 2017 May; 8(5):365-378. PubMed ID: 28401346 [TBL] [Abstract][Full Text] [Related]
39. FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders. Zhou B; Wang H; Cai Y; Wen H; Wang L; Zhu M; Chen Y; Yu Y; Lu X; Zhou M; Fang P; Li X; Hong D Brain Behav; 2020 Jun; 10(6):e01625. PubMed ID: 32307925 [TBL] [Abstract][Full Text] [Related]
40. Homozygous ALS-linked FUS P525L mutations cell- autonomously perturb transcriptome profile and chemoreceptor signaling in human iPSC microglia. Kerk SY; Bai Y; Smith J; Lalgudi P; Hunt C; Kuno J; Nuara J; Yang T; Lanza K; Chan N; Coppola A; Tang Q; Espert J; Jones H; Fannell C; Zambrowicz B; Chiao E Stem Cell Reports; 2022 Mar; 17(3):678-692. PubMed ID: 35120624 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]