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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

290 related items for PubMed ID: 20566711

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  • 3. AKT-sensitive or insensitive pathways of toxicity in glial cells and neurons in Drosophila models of Huntington's disease.
    Liévens JC, Iché M, Laval M, Faivre-Sarrailh C, Birman S.
    Hum Mol Genet; 2008 Mar 15; 17(6):882-94. PubMed ID: 18065778
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  • 4. Impairment of the Glial Phagolysosomal System Drives Prion-Like Propagation in a Drosophila Model of Huntington's Disease.
    Davis GH, Zaya A, Pearce MMP.
    J Neurosci; 2024 May 15; 44(20):. PubMed ID: 38589228
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  • 5. Methylene Blue Partially Rescues Heart Defects in a Drosophila Model of Huntington's Disease.
    Heidari R, Monnier V, Martin E, Tricoire H.
    J Huntingtons Dis; 2015 May 15; 4(2):173-86. PubMed ID: 26397898
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  • 14. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism.
    Seong IS, Ivanova E, Lee JM, Choo YS, Fossale E, Anderson M, Gusella JF, Laramie JM, Myers RH, Lesort M, MacDonald ME.
    Hum Mol Genet; 2005 Oct 01; 14(19):2871-80. PubMed ID: 16115812
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  • 15. Prion-like transmission of neuronal huntingtin aggregates to phagocytic glia in the Drosophila brain.
    Pearce MMP, Spartz EJ, Hong W, Luo L, Kopito RR.
    Nat Commun; 2015 Apr 13; 6():6768. PubMed ID: 25866135
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  • 18. Human glia can both induce and rescue aspects of disease phenotype in Huntington disease.
    Benraiss A, Wang S, Herrlinger S, Li X, Chandler-Militello D, Mauceri J, Burm HB, Toner M, Osipovitch M, Jim Xu Q, Ding F, Wang F, Kang N, Kang J, Curtin PC, Brunner D, Windrem MS, Munoz-Sanjuan I, Nedergaard M, Goldman SA.
    Nat Commun; 2016 Jun 07; 7():11758. PubMed ID: 27273432
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  • 20. Cell-intrinsic glial pathology is conserved across human and murine models of Huntington's disease.
    Benraiss A, Mariani JN, Osipovitch M, Cornwell A, Windrem MS, Villanueva CB, Chandler-Militello D, Goldman SA.
    Cell Rep; 2021 Jul 06; 36(1):109308. PubMed ID: 34233199
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