288 related articles for article (PubMed ID: 25888396)
41. Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS.
Ito D; Suzuki N
Neurology; 2011 Oct; 77(17):1636-43. PubMed ID: 21956718
[TBL] [Abstract][Full Text] [Related]
42. Rab1-dependent ER-Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS.
Soo KY; Halloran M; Sundaramoorthy V; Parakh S; Toth RP; Southam KA; McLean CA; Lock P; King A; Farg MA; Atkin JD
Acta Neuropathol; 2015 Nov; 130(5):679-97. PubMed ID: 26298469
[TBL] [Abstract][Full Text] [Related]
43. Amyotrophic lateral sclerosis-linked FUS/TLS alters stress granule assembly and dynamics.
Baron DM; Kaushansky LJ; Ward CL; Sama RR; Chian RJ; Boggio KJ; Quaresma AJ; Nickerson JA; Bosco DA
Mol Neurodegener; 2013 Aug; 8():30. PubMed ID: 24090136
[TBL] [Abstract][Full Text] [Related]
44. ALS-associated mutations in TDP-43 increase its stability and promote TDP-43 complexes with FUS/TLS.
Ling SC; Albuquerque CP; Han JS; Lagier-Tourenne C; Tokunaga S; Zhou H; Cleveland DW
Proc Natl Acad Sci U S A; 2010 Jul; 107(30):13318-23. PubMed ID: 20624952
[TBL] [Abstract][Full Text] [Related]
45. TDP-43 or FUS-induced misfolded human wild-type SOD1 can propagate intercellularly in a prion-like fashion.
Pokrishevsky E; Grad LI; Cashman NR
Sci Rep; 2016 Mar; 6():22155. PubMed ID: 26926802
[TBL] [Abstract][Full Text] [Related]
46. Exome sequencing to identify de novo mutations in sporadic ALS trios.
Chesi A; Staahl BT; Jovičić A; Couthouis J; Fasolino M; Raphael AR; Yamazaki T; Elias L; Polak M; Kelly C; Williams KL; Fifita JA; Maragakis NJ; Nicholson GA; King OD; Reed R; Crabtree GR; Blair IP; Glass JD; Gitler AD
Nat Neurosci; 2013 Jul; 16(7):851-5. PubMed ID: 23708140
[TBL] [Abstract][Full Text] [Related]
47. Pathogenesis of FUS-associated ALS and FTD: insights from rodent models.
Nolan M; Talbot K; Ansorge O
Acta Neuropathol Commun; 2016 Sep; 4(1):99. PubMed ID: 27600654
[TBL] [Abstract][Full Text] [Related]
48. Stress granules in neurodegeneration--lessons learnt from TAR DNA binding protein of 43 kDa and fused in sarcoma.
Bentmann E; Haass C; Dormann D
FEBS J; 2013 Sep; 280(18):4348-70. PubMed ID: 23587065
[TBL] [Abstract][Full Text] [Related]
49. 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]
50. Recruitment into stress granules prevents irreversible aggregation of FUS protein mislocalized to the cytoplasm.
Shelkovnikova TA; Robinson HK; Connor-Robson N; Buchman VL
Cell Cycle; 2013 Oct; 12(19):3194-202. PubMed ID: 24013423
[TBL] [Abstract][Full Text] [Related]
51. ALS-Related Mutant FUS Protein Is Mislocalized to Cytoplasm and Is Recruited into Stress Granules of Fibroblasts from Asymptomatic FUS P525L Mutation Carriers.
Lo Bello M; Di Fini F; Notaro A; Spataro R; Conforti FL; La Bella V
Neurodegener Dis; 2017; 17(6):292-303. PubMed ID: 29035885
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. Molecular basis of amyotrophic lateral sclerosis.
Liscic RM; Breljak D
Prog Neuropsychopharmacol Biol Psychiatry; 2011 Mar; 35(2):370-2. PubMed ID: 20655970
[TBL] [Abstract][Full Text] [Related]
54. Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations.
Feuillette S; Delarue M; Riou G; Gaffuri AL; Wu J; Lenkei Z; Boyer O; Frébourg T; Campion D; Lecourtois M
J Mol Neurosci; 2017 May; 62(1):114-122. PubMed ID: 28429234
[TBL] [Abstract][Full Text] [Related]
55. RNA-Binding Proteins in Amyotrophic Lateral Sclerosis.
Zhao M; Kim JR; van Bruggen R; Park J
Mol Cells; 2018 Sep; 41(9):818-829. PubMed ID: 30157547
[TBL] [Abstract][Full Text] [Related]
56. Shared Molecular Mechanisms in Alzheimer's Disease and Amyotrophic Lateral Sclerosis: Neurofilament-Dependent Transport of sAPP, FUS, TDP-43 and SOD1, with Endoplasmic Reticulum-Like Tubules.
Muresan V; Ladescu Muresan Z
Neurodegener Dis; 2016; 16(1-2):55-61. PubMed ID: 26605911
[TBL] [Abstract][Full Text] [Related]
57. Rethinking ALS: the FUS about TDP-43.
Lagier-Tourenne C; Cleveland DW
Cell; 2009 Mar; 136(6):1001-4. PubMed ID: 19303844
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.
Da Cruz S; Cleveland DW
Curr Opin Neurobiol; 2011 Dec; 21(6):904-19. PubMed ID: 21813273
[TBL] [Abstract][Full Text] [Related]
60. ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import.
Dormann D; Rodde R; Edbauer D; Bentmann E; Fischer I; Hruscha A; Than ME; Mackenzie IR; Capell A; Schmid B; Neumann M; Haass C
EMBO J; 2010 Aug; 29(16):2841-57. PubMed ID: 20606625
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
