197 related articles for article (PubMed ID: 23545117)
1. Genome wide array analysis indicates that an amyotrophic lateral sclerosis mutation of FUS causes an early increase of CAMK2N2 in vitro.
Convertini P; Zhang J; de la Grange P; Hayward LJ; Zhu H; Stamm S
Biochim Biophys Acta; 2013 Aug; 1832(8):1129-35. PubMed ID: 23545117
[TBL] [Abstract][Full Text] [Related]
2. ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation.
Zhou Y; Liu S; Liu G; Oztürk A; Hicks GG
PLoS Genet; 2013 Oct; 9(10):e1003895. PubMed ID: 24204307
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Self-assembled FUS binds active chromatin and regulates gene transcription.
Yang L; Gal J; Chen J; Zhu H
Proc Natl Acad Sci U S A; 2014 Dec; 111(50):17809-14. PubMed ID: 25453086
[TBL] [Abstract][Full Text] [Related]
5. Directly converted patient-specific induced neurons mirror the neuropathology of FUS with disrupted nuclear localization in amyotrophic lateral sclerosis.
Lim SM; Choi WJ; Oh KW; Xue Y; Choi JY; Kim SH; Nahm M; Kim YE; Lee J; Noh MY; Lee S; Hwang S; Ki CS; Fu XD; Kim SH
Mol Neurodegener; 2016 Jan; 11():8. PubMed ID: 26795035
[TBL] [Abstract][Full Text] [Related]
6. Nuclear localization sequence of FUS and induction of stress granules by ALS mutants.
Gal J; Zhang J; Kwinter DM; Zhai J; Jia H; Jia J; Zhu H
Neurobiol Aging; 2011 Dec; 32(12):2323.e27-40. PubMed ID: 20674093
[TBL] [Abstract][Full Text] [Related]
7. Mutations in the 3' untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis.
Sabatelli M; Moncada A; Conte A; Lattante S; Marangi G; Luigetti M; Lucchini M; Mirabella M; Romano A; Del Grande A; Bisogni G; Doronzio PN; Rossini PM; Zollino M
Hum Mol Genet; 2013 Dec; 22(23):4748-55. PubMed ID: 23847048
[TBL] [Abstract][Full Text] [Related]
8. Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis.
Tyzack GE; Luisier R; Taha DM; Neeves J; Modic M; Mitchell JS; Meyer I; Greensmith L; Newcombe J; Ule J; Luscombe NM; Patani R
Brain; 2019 Sep; 142(9):2572-2580. PubMed ID: 31368485
[TBL] [Abstract][Full Text] [Related]
9. FUS interacts with nuclear matrix-associated protein SAFB1 as well as Matrin3 to regulate splicing and ligand-mediated transcription.
Yamaguchi A; Takanashi K
Sci Rep; 2016 Oct; 6():35195. PubMed ID: 27731383
[TBL] [Abstract][Full Text] [Related]
10. Mislocated FUS is sufficient for gain-of-toxic-function amyotrophic lateral sclerosis phenotypes in mice.
Shiihashi G; Ito D; Yagi T; Nihei Y; Ebine T; Suzuki N
Brain; 2016 Sep; 139(Pt 9):2380-94. PubMed ID: 27368346
[TBL] [Abstract][Full Text] [Related]
11. Amyotrophic Lateral Sclerosis associated FUS mutation shortens mitochondria and induces neurotoxicity.
Nakaya T; Maragkakis M
Sci Rep; 2018 Oct; 8(1):15575. PubMed ID: 30349096
[TBL] [Abstract][Full Text] [Related]
12. Extensive splicing changes in an ALS/FTD transgenic mouse model overexpressing cytoplasmic fused in sarcoma.
Ito D; Taguchi R; Deguchi M; Ogasawara H; Inoue E
Sci Rep; 2020 Mar; 10(1):4857. PubMed ID: 32184412
[TBL] [Abstract][Full Text] [Related]
13. RNA-binding ability of FUS regulates neurodegeneration, cytoplasmic mislocalization and incorporation into stress granules associated with FUS carrying ALS-linked mutations.
Daigle JG; Lanson NA; Smith RB; Casci I; Maltare A; Monaghan J; Nichols CD; Kryndushkin D; Shewmaker F; Pandey UB
Hum Mol Genet; 2013 Mar; 22(6):1193-205. PubMed ID: 23257289
[TBL] [Abstract][Full Text] [Related]
14. Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq.
van Blitterswijk M; Wang ET; Friedman BA; Keagle PJ; Lowe P; Leclerc AL; van den Berg LH; Housman DE; Veldink JH; Landers JE
PLoS One; 2013; 8(4):e60788. PubMed ID: 23577159
[TBL] [Abstract][Full Text] [Related]
15. Intracellular localization and splicing regulation of FUS/TLS are variably affected by amyotrophic lateral sclerosis-linked mutations.
Kino Y; Washizu C; Aquilanti E; Okuno M; Kurosawa M; Yamada M; Doi H; Nukina N
Nucleic Acids Res; 2011 Apr; 39(7):2781-98. PubMed ID: 21109527
[TBL] [Abstract][Full Text] [Related]
16. Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules.
Bosco DA; Lemay N; Ko HK; Zhou H; Burke C; Kwiatkowski TJ; Sapp P; McKenna-Yasek D; Brown RH; Hayward LJ
Hum Mol Genet; 2010 Nov; 19(21):4160-75. PubMed ID: 20699327
[TBL] [Abstract][Full Text] [Related]
17. Subcellular localization and RNAs determine FUS architecture in different cellular compartments.
Yang L; Zhang J; Kamelgarn M; Niu C; Gal J; Gong W; Zhu H
Hum Mol Genet; 2015 Sep; 24(18):5174-83. PubMed ID: 26123490
[TBL] [Abstract][Full Text] [Related]
18. Mechanism of karyopherin-β2 binding and nuclear import of ALS variants FUS(P525L) and FUS(R495X).
Gonzalez A; Mannen T; Çağatay T; Fujiwara A; Matsumura H; Niesman AB; Brautigam CA; Chook YM; Yoshizawa T
Sci Rep; 2021 Feb; 11(1):3754. PubMed ID: 33580145
[TBL] [Abstract][Full Text] [Related]
19. Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
Belzil VV; St-Onge J; Daoud H; Desjarlais A; Bouchard JP; Dupré N; Camu W; Dion PA; Rouleau GA
J Hum Genet; 2011 Mar; 56(3):247-9. PubMed ID: 21160488
[TBL] [Abstract][Full Text] [Related]
20. ALS mutations in TLS/FUS disrupt target gene expression.
Coady TH; Manley JL
Genes Dev; 2015 Aug; 29(16):1696-706. PubMed ID: 26251528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]