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611 related items for PubMed ID: 21829392

  • 1. FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis.
    Kabashi E, Bercier V, Lissouba A, Liao M, Brustein E, Rouleau GA, Drapeau P.
    PLoS Genet; 2011 Aug; 7(8):e1002214. PubMed ID: 21829392
    [Abstract] [Full Text] [Related]

  • 2. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
    Millecamps S, Salachas F, Cazeneuve C, Gordon P, Bricka B, Camuzat A, Guillot-Noël L, Russaouen O, Bruneteau G, Pradat PF, Le Forestier N, Vandenberghe N, Danel-Brunaud V, Guy N, Thauvin-Robinet C, Lacomblez L, Couratier P, Hannequin D, Seilhean D, Le Ber I, Corcia P, Camu W, Brice A, Rouleau G, LeGuern E, Meininger V.
    J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002
    [Abstract] [Full Text] [Related]

  • 3. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS.
    Tsai CP, Soong BW, Lin KP, Tu PH, Lin JL, Lee YC.
    Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325
    [Abstract] [Full Text] [Related]

  • 4. 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 Mar; 7(4):e35050. PubMed ID: 22493728
    [Abstract] [Full Text] [Related]

  • 5. SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience.
    Brown JA, Min J, Staropoli JF, Collin E, Bi S, Feng X, Barone R, Cao Y, O'Malley L, Xin W, Mullen TE, Sims KB.
    Amyotroph Lateral Scler; 2012 Feb; 13(2):217-22. PubMed ID: 22292843
    [Abstract] [Full Text] [Related]

  • 6. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China.
    Hou L, Jiao B, Xiao T, Zhou L, Zhou Z, Du J, Yan X, Wang J, Tang B, Shen L.
    Sci Rep; 2016 Sep 08; 6():32478. PubMed ID: 27604643
    [Abstract] [Full Text] [Related]

  • 7. 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 08; 67(6):739-48. PubMed ID: 20517935
    [Abstract] [Full Text] [Related]

  • 8. 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 08; 49(4):258-63. PubMed ID: 22499346
    [Abstract] [Full Text] [Related]

  • 9. 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 08; 130(5):679-97. PubMed ID: 26298469
    [Abstract] [Full Text] [Related]

  • 10. TARDBP and FUS mutations associated with amyotrophic lateral sclerosis: summary and update.
    Lattante S, Rouleau GA, Kabashi E.
    Hum Mutat; 2013 Jun 08; 34(6):812-26. PubMed ID: 23559573
    [Abstract] [Full Text] [Related]

  • 11. De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.
    DeJesus-Hernandez M, Kocerha J, Finch N, Crook R, Baker M, Desaro P, Johnston A, Rutherford N, Wojtas A, Kennelly K, Wszolek ZK, Graff-Radford N, Boylan K, Rademakers R.
    Hum Mutat; 2010 May 08; 31(5):E1377-89. PubMed ID: 20232451
    [Abstract] [Full Text] [Related]

  • 12. Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo.
    Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, Bourgouin P, Rochefort D, Bel Hadj S, Durham HD, Vande Velde C, Rouleau GA, Drapeau P.
    Hum Mol Genet; 2010 Feb 15; 19(4):671-83. PubMed ID: 19959528
    [Abstract] [Full Text] [Related]

  • 13. Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.
    Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH.
    Neurobiol Aging; 2012 May 15; 33(5):1017.e17-23. PubMed ID: 22244934
    [Abstract] [Full Text] [Related]

  • 14. Co-aggregation of RNA binding proteins in ALS spinal motor neurons: evidence of a common pathogenic mechanism.
    Keller BA, Volkening K, Droppelmann CA, Ang LC, Rademakers R, Strong MJ.
    Acta Neuropathol; 2012 Nov 15; 124(5):733-47. PubMed ID: 22941224
    [Abstract] [Full Text] [Related]

  • 15. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.
    Bertolin C, D'Ascenzo C, Querin G, Gaiani A, Boaretto F, Salvoro C, Vazza G, Angelini C, Cagnin A, Pegoraro E, Sorarù G, Mostacciuolo ML.
    Neurobiol Aging; 2014 May 15; 35(5):1212.e7-1212.e10. PubMed ID: 24325798
    [Abstract] [Full Text] [Related]

  • 16. Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
    Edgar S, Ellis M, Abdul-Aziz NA, Goh KJ, Shahrizaila N, Kennerson ML, Ahmad-Annuar A.
    Neurobiol Aging; 2021 Dec 15; 108():200-206. PubMed ID: 34404558
    [Abstract] [Full Text] [Related]

  • 17. 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 15; 42(2):170-6. PubMed ID: 20544928
    [Abstract] [Full Text] [Related]

  • 18. Identification of novel FUS and TARDBP gene mutations in Chinese amyotrophic lateral sclerosis patients with HRM analysis.
    Wang F, Fu S, Lei J, Wu H, Shi S, Chen K, Hu J, Xu X.
    Aging (Albany NY); 2020 Nov 05; 12(22):22859-22868. PubMed ID: 33159016
    [Abstract] [Full Text] [Related]

  • 19. Amyotrophic lateral sclerosis patients with various gene mutations show diverse motor phenotypes and survival in China.
    Jiang Q, Lin J, Wei Q, Yang T, Hou Y, Zhang L, Ou R, Xiao Y, Wang S, Zheng X, Li C, Shang H.
    J Med Genet; 2024 Aug 29; 61(9):839-846. PubMed ID: 38886047
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 6():22155. PubMed ID: 26926802
    [Abstract] [Full Text] [Related]

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