777 related articles for article (PubMed ID: 21965298)
1. 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]
2. The effect of PRMT1-mediated arginine methylation on the subcellular localization, stress granules, and detergent-insoluble aggregates of FUS/TLS.
Yamaguchi A; Kitajo K
PLoS One; 2012; 7(11):e49267. PubMed ID: 23152885
[TBL] [Abstract][Full Text] [Related]
3. Cytoplasmic sequestration of FUS/TLS associated with ALS alters histone marks through loss of nuclear protein arginine methyltransferase 1.
Tibshirani M; Tradewell ML; Mattina KR; Minotti S; Yang W; Zhou H; Strong MJ; Hayward LJ; Durham HD
Hum Mol Genet; 2015 Feb; 24(3):773-86. PubMed ID: 25274782
[TBL] [Abstract][Full Text] [Related]
4. Protein arginine methyltransferase 1 and 8 interact with FUS to modify its sub-cellular distribution and toxicity in vitro and in vivo.
Scaramuzzino C; Monaghan J; Milioto C; Lanson NA; Maltare A; Aggarwal T; Casci I; Fackelmayer FO; Pennuto M; Pandey UB
PLoS One; 2013; 8(4):e61576. PubMed ID: 23620769
[TBL] [Abstract][Full Text] [Related]
5. The hnRNP RALY regulates PRMT1 expression and interacts with the ALS-linked protein FUS: implication for reciprocal cellular localization.
Gasperini L; Rossi A; Cornella N; Peroni D; Zuccotti P; Potrich V; Quattrone A; Macchi P
Mol Biol Cell; 2018 Dec; 29(26):3067-3081. PubMed ID: 30354839
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS.
Suárez-Calvet M; Neumann M; Arzberger T; Abou-Ajram C; Funk E; Hartmann H; Edbauer D; Kremmer E; Göbl C; Resch M; Bourgeois B; Madl T; Reber S; Jutzi D; Ruepp MD; Mackenzie IR; Ansorge O; Dormann D; Haass C
Acta Neuropathol; 2016 Apr; 131(4):587-604. PubMed ID: 26895297
[TBL] [Abstract][Full Text] [Related]
8. Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.
Dormann D; Madl T; Valori CF; Bentmann E; Tahirovic S; Abou-Ajram C; Kremmer E; Ansorge O; Mackenzie IR; Neumann M; Haass C
EMBO J; 2012 Nov; 31(22):4258-75. PubMed ID: 22968170
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Treatment with a Global Methyltransferase Inhibitor Induces the Intranuclear Aggregation of ALS-Linked FUS Mutant In Vitro.
Fujii S; Takanashi K; Kitajo K; Yamaguchi A
Neurochem Res; 2016 Apr; 41(4):826-35. PubMed ID: 26603295
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Sequestration of PRMT1 and Nd1-L mRNA into ALS-linked FUS mutant R521C-positive aggregates contributes to neurite degeneration upon oxidative stress.
Jun MH; Ryu HH; Jun YW; Liu T; Li Y; Lim CS; Lee YS; Kaang BK; Jang DJ; Lee JA
Sci Rep; 2017 Jan; 7():40474. PubMed ID: 28094300
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.
Groen EJ; Fumoto K; Blokhuis AM; Engelen-Lee J; Zhou Y; van den Heuvel DM; Koppers M; van Diggelen F; van Heest J; Demmers JA; Kirby J; Shaw PJ; Aronica E; Spliet WG; Veldink JH; van den Berg LH; Pasterkamp RJ
Hum Mol Genet; 2013 Sep; 22(18):3690-704. PubMed ID: 23681068
[TBL] [Abstract][Full Text] [Related]
16. A complex of C9ORF72 and p62 uses arginine methylation to eliminate stress granules by autophagy.
Chitiprolu M; Jagow C; Tremblay V; Bondy-Chorney E; Paris G; Savard A; Palidwor G; Barry FA; Zinman L; Keith J; Rogaeva E; Robertson J; Lavallée-Adam M; Woulfe J; Couture JF; Côté J; Gibbings D
Nat Commun; 2018 Jul; 9(1):2794. PubMed ID: 30022074
[TBL] [Abstract][Full Text] [Related]
17. TLS and PRMT1 synergistically coactivate transcription at the survivin promoter through TLS arginine methylation.
Du K; Arai S; Kawamura T; Matsushita A; Kurokawa R
Biochem Biophys Res Commun; 2011 Jan; 404(4):991-6. PubMed ID: 21187067
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]