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Journal Abstract Search

173 related items for PubMed ID: 24525128

  • 1. Study of cholesterol metabolism in Huntington's disease.
    Leoni V, Caccia C.
    Biochem Biophys Res Commun; 2014 Apr 11; 446(3):697-701. PubMed ID: 24525128
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  • 3. CYP46A1 gene therapy deciphers the role of brain cholesterol metabolism in Huntington's disease.
    Kacher R, Lamazière A, Heck N, Kappes V, Mounier C, Despres G, Dembitskaya Y, Perrin E, Christaller W, Sasidharan Nair S, Messent V, Cartier N, Vanhoutte P, Venance L, Saudou F, Néri C, Caboche J, Betuing S.
    Brain; 2019 Aug 01; 142(8):2432-2450. PubMed ID: 31286142
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  • 5. Mass Spectrometry Analysis of Wild-Type and Knock-in Q140/Q140 Huntington's Disease Mouse Brains Reveals Changes in Glycerophospholipids Including Alterations in Phosphatidic Acid and Lyso-Phosphatidic Acid.
    Vodicka P, Mo S, Tousley A, Green KM, Sapp E, Iuliano M, Sadri-Vakili G, Shaffer SA, Aronin N, DiFiglia M, Kegel-Gleason KB.
    J Huntingtons Dis; 2015 Aug 01; 4(2):187-201. PubMed ID: 26397899
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  • 6. Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease.
    Valencia A, Reeves PB, Sapp E, Li X, Alexander J, Kegel KB, Chase K, Aronin N, DiFiglia M.
    J Neurosci Res; 2010 Jan 01; 88(1):179-90. PubMed ID: 19642201
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  • 7. Whole body cholesterol metabolism is impaired in Huntington's disease.
    Leoni V, Mariotti C, Nanetti L, Salvatore E, Squitieri F, Bentivoglio AR, Bandettini di Poggio M, Piacentini S, Monza D, Valenza M, Cattaneo E, Di Donato S.
    Neurosci Lett; 2011 May 02; 494(3):245-9. PubMed ID: 21406216
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  • 8. [Huntington disease. A review].
    Bonilla E.
    Invest Clin; 2000 Jun 02; 41(2):117-41. PubMed ID: 10961047
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  • 12. Mechanisms of copper ion mediated Huntington's disease progression.
    Fox JH, Kama JA, Lieberman G, Chopra R, Dorsey K, Chopra V, Volitakis I, Cherny RA, Bush AI, Hersch S.
    PLoS One; 2007 Mar 28; 2(3):e334. PubMed ID: 17396163
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  • 13. CYP46A1 protects against NMDA-mediated excitotoxicity in Huntington's disease: Analysis of lipid raft content.
    Boussicault L, Kacher R, Lamazière A, Vanhoutte P, Caboche J, Betuing S, Potier MC.
    Biochimie; 2018 Oct 28; 153():70-79. PubMed ID: 30107216
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  • 14. Increased Steady-State Mutant Huntingtin mRNA in Huntington's Disease Brain.
    Liu W, Chaurette J, Pfister EL, Kennington LA, Chase KO, Bullock J, Vonsattel JP, Faull RL, Macdonald D, DiFiglia M, Zamore PD, Aronin N.
    J Huntingtons Dis; 2013 Oct 28; 2(4):491-500. PubMed ID: 25062733
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  • 17. Dopamine enhances motor and neuropathological consequences of polyglutamine expanded huntingtin.
    Cyr M, Sotnikova TD, Gainetdinov RR, Caron MG.
    FASEB J; 2006 Dec 28; 20(14):2541-3. PubMed ID: 17065224
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  • 18. Sensitive biochemical aggregate detection reveals aggregation onset before symptom development in cellular and murine models of Huntington's disease.
    Weiss A, Klein C, Woodman B, Sathasivam K, Bibel M, Régulier E, Bates GP, Paganetti P.
    J Neurochem; 2008 Feb 28; 104(3):846-58. PubMed ID: 17986219
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  • 19. Huntington disease and the huntingtin protein.
    Zheng Z, Diamond MI.
    Prog Mol Biol Transl Sci; 2012 Feb 28; 107():189-214. PubMed ID: 22482451
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