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Journal Abstract Search

875 related items for PubMed ID: 27604643

  • 21. 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
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  • 22. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
    Yan J, Deng HX, Siddique N, Fecto F, Chen W, Yang Y, Liu E, Donkervoort S, Zheng JG, Shi Y, Ahmeti KB, Brooks B, Engel WK, Siddique T.
    Neurology; 2010 Aug 31; 75(9):807-14. PubMed ID: 20668259
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  • 24. High frequency of the TARDBP p.M337 V mutation among south-eastern Chinese patients with familial amyotrophic lateral sclerosis.
    Xu GR, Hu W, Zhan LL, Wang C, Xu LQ, Lin MT, Chen WJ, Wang N, Zhang QJ.
    BMC Neurol; 2018 Apr 05; 18(1):35. PubMed ID: 29621978
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  • 25. A de novo missense mutation of the FUS gene in a "true" sporadic ALS case.
    Chiò A, Calvo A, Moglia C, Ossola I, Brunetti M, Sbaiz L, Lai SL, Abramzon Y, Traynor BJ, Restagno G.
    Neurobiol Aging; 2011 Mar 05; 32(3):553.e23-6. PubMed ID: 20598774
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  • 26. The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.
    Damme PV, Goris A, Race V, Hersmus N, Dubois B, Bosch LV, Matthijs G, Robberecht W.
    Eur J Neurol; 2010 May 05; 17(5):754-6. PubMed ID: 19922450
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  • 27. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis.
    Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T.
    Ann Neurol; 2010 Jun 05; 67(6):739-48. PubMed ID: 20517935
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  • 28. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S, Boillée S, Le Ber I, Seilhean D, Teyssou E, Giraudeau M, Moigneu C, Vandenberghe N, Danel-Brunaud V, Corcia P, Pradat PF, Le Forestier N, Lacomblez L, Bruneteau G, Camu W, Brice A, Cazeneuve C, Leguern E, Meininger V, Salachas F.
    J Med Genet; 2012 Apr 05; 49(4):258-63. PubMed ID: 22499346
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  • 31. Novel Pathogenic Variants Leading to Sporadic Amyotrophic Lateral Sclerosis in Greek Patients.
    Ivantsik O, John A, Kydonopoulou K, Mitropoulos K, Gerou S, Ali BR, Patrinos GP.
    Genes (Basel); 2024 Feb 28; 15(3):. PubMed ID: 38540370
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  • 35. C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.
    Drepper C, Herrmann T, Wessig C, Beck M, Sendtner M.
    Neurobiol Aging; 2011 Mar 28; 32(3):548.e1-4. PubMed ID: 20018407
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  • 36. Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.
    Hatano Y, Ishihara T, Onodera O.
    BMC Bioinformatics; 2023 May 19; 24(1):206. PubMed ID: 37208601
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  • 37. The distinct manifestation of young-onset amyotrophic lateral sclerosis in China.
    Lin J, Chen W, Huang P, Xie Y, Zheng M, Yao X.
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb 19; 22(1-2):30-37. PubMed ID: 32729724
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  • 38. 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 Feb 19; 7(4):e35050. PubMed ID: 22493728
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  • 40. 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 19; 42(2):170-6. PubMed ID: 20544928
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