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Journal Abstract Search

1374 related items for PubMed ID: 30150420

  • 1. From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis.
    Alrafiah AR.
    In Vivo; 2018; 32(5):983-998. PubMed ID: 30150420
    [Abstract] [Full Text] [Related]

  • 2. Altered calcium dynamics and glutamate receptor properties in iPSC-derived motor neurons from ALS patients with C9orf72, FUS, SOD1 or TDP43 mutations.
    Bursch F, Kalmbach N, Naujock M, Staege S, Eggenschwiler R, Abo-Rady M, Japtok J, Guo W, Hensel N, Reinhardt P, Boeckers TM, Cantz T, Sterneckert J, Van Den Bosch L, Hermann A, Petri S, Wegner F.
    Hum Mol Genet; 2019 Sep 01; 28(17):2835-2850. PubMed ID: 31108504
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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 29; 108():200-206. PubMed ID: 34404558
    [Abstract] [Full Text] [Related]

  • 5. Oligodendrocytes contribute to motor neuron death in ALS via SOD1-dependent mechanism.
    Ferraiuolo L, Meyer K, Sherwood TW, Vick J, Likhite S, Frakes A, Miranda CJ, Braun L, Heath PR, Pineda R, Beattie CE, Shaw PJ, Askwith CC, McTigue D, Kaspar BK.
    Proc Natl Acad Sci U S A; 2016 Oct 18; 113(42):E6496-E6505. PubMed ID: 27688759
    [Abstract] [Full Text] [Related]

  • 6. Gene Therapy in Amyotrophic Lateral Sclerosis.
    Fang T, Je G, Pacut P, Keyhanian K, Gao J, Ghasemi M.
    Cells; 2022 Jun 29; 11(13):. PubMed ID: 35805149
    [Abstract] [Full Text] [Related]

  • 7. Stable transgenic C9orf72 zebrafish model key aspects of the ALS/FTD phenotype and reveal novel pathological features.
    Shaw MP, Higginbottom A, McGown A, Castelli LM, James E, Hautbergue GM, Shaw PJ, Ramesh TM.
    Acta Neuropathol Commun; 2018 Nov 19; 6(1):125. PubMed ID: 30454072
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. 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 08; 7(8):e1002214. PubMed ID: 21829392
    [Abstract] [Full Text] [Related]

  • 10. ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues.
    Bayer H, Lang K, Buck E, Higelin J, Barteczko L, Pasquarelli N, Sprissler J, Lucas T, Holzmann K, Demestre M, Lindenberg KS, Danzer KM, Boeckers T, Ludolph AC, Dupuis L, Weydt P, Witting A.
    Neurobiol Dis; 2017 Jan 08; 97(Pt A):36-45. PubMed ID: 27818323
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Genetic analysis of the SOD1 and C9ORF72 genes in Hungarian patients with amyotrophic lateral sclerosis.
    Tripolszki K, Csányi B, Nagy D, Ratti A, Tiloca C, Silani V, Kereszty É, Török N, Vécsei L, Engelhardt JI, Klivényi P, Nagy N, Széll M.
    Neurobiol Aging; 2017 May 08; 53():195.e1-195.e5. PubMed ID: 28222900
    [Abstract] [Full Text] [Related]

  • 13. A Systematic and Comprehensive Review on Disease-Causing Genes in Amyotrophic Lateral Sclerosis.
    Srinivasan E, Rajasekaran R.
    J Mol Neurosci; 2020 Nov 08; 70(11):1742-1770. PubMed ID: 32415434
    [Abstract] [Full Text] [Related]

  • 14. Genetic analysis of amyotrophic lateral sclerosis in the Slovenian population.
    Vrabec K, Koritnik B, Leonardis L, Dolenc-Grošelj L, Zidar J, Smith B, Vance C, Shaw C, Rogelj B, Glavač D, Ravnik-Glavač M.
    Neurobiol Aging; 2015 Mar 08; 36(3):1601.e17-20. PubMed ID: 25585530
    [Abstract] [Full Text] [Related]

  • 15. Dysregulation of AMPA receptor subunit expression in sporadic ALS post-mortem brain.
    Gregory JM, Livesey MR, McDade K, Selvaraj BT, Barton SK, Chandran S, Smith C.
    J Pathol; 2020 Jan 08; 250(1):67-78. PubMed ID: 31579943
    [Abstract] [Full Text] [Related]

  • 16. Genetics of amyotrophic lateral sclerosis: A review.
    Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL.
    J Neurol Sci; 2019 Apr 15; 399():217-226. PubMed ID: 30870681
    [Abstract] [Full Text] [Related]

  • 17. ALS-linked FUS exerts a gain of toxic function involving aberrant p38 MAPK activation.
    Sama RR, Fallini C, Gatto R, McKeon JE, Song Y, Rotunno MS, Penaranda S, Abdurakhmanov I, Landers JE, Morfini G, Brady ST, Bosco DA.
    Sci Rep; 2017 Mar 08; 7(1):115. PubMed ID: 28273913
    [Abstract] [Full Text] [Related]

  • 18. Genetic architecture of ALS in Sardinia.
    Borghero G, Pugliatti M, Marrosu F, Marrosu MG, Murru MR, Floris G, Cannas A, Parish LD, Occhineri P, Cau TB, Loi D, Ticca A, Traccis S, Manera U, Canosa A, Moglia C, Calvo A, Barberis M, Brunetti M, Pliner HA, Renton AE, Nalls MA, Traynor BJ, Restagno G, Chiò A, ITALSGEN and SARDINALS Consortia.
    Neurobiol Aging; 2014 Dec 08; 35(12):2882.e7-2882.e12. PubMed ID: 25123918
    [Abstract] [Full Text] [Related]

  • 19. Little Helpers or Mean Rogue-Role of Microglia in Animal Models of Amyotrophic Lateral Sclerosis.
    Cihankaya H, Theiss C, Matschke V.
    Int J Mol Sci; 2021 Jan 20; 22(3):. PubMed ID: 33498186
    [Abstract] [Full Text] [Related]

  • 20. Emerging understanding of the genotype-phenotype relationship in amyotrophic lateral sclerosis.
    Goutman SA, Chen KS, Paez-Colasante X, Feldman EL.
    Handb Clin Neurol; 2018 Jan 20; 148():603-623. PubMed ID: 29478603
    [Abstract] [Full Text] [Related]

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