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    Results: 1 to 20 of 168

    1.

    The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.

    Weydt P, Soyal SM, Gellera C, Didonato S, Weidinger C, Oberkofler H, Landwehrmeyer GB, Patsch W.

    Mol Neurodegener. 2009 Jan 8;4:3.PMID: 19133136 [PubMed - in process]Related articlesFree article

    2.

    [Molecular genetics of Huntington's disease]

    Goto J, Masuda N, Watanabe M, Kanazawa I.

    Rinsho Shinkeigaku. 1995 Dec;35(12):1529-31. Japanese. PMID: 8752453 [PubMed - indexed for MEDLINE]Related articles

    3.

    Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration.

    Weydt P, Pineda VV, Torrence AE, Libby RT, Satterfield TF, Lazarowski ER, Gilbert ML, Morton GJ, Bammler TK, Strand AD, Cui L, Beyer RP, Easley CN, Smith AC, Krainc D, Luquet S, Sweet IR, Schwartz MW, La Spada AR.

    Cell Metab. 2006 Nov;4(5):349-62. Epub 2006 Oct 19.PMID: 17055784 [PubMed - indexed for MEDLINE]Related articles

    4.

    PGC-1alpha as modifier of onset age in Huntington disease.

    Taherzadeh-Fard E, Saft C, Andrich J, Wieczorek S, Arning L.

    Mol Neurodegener. 2009 Feb 6;4:10.PMID: 19200361 [PubMed - in process]Related articlesFree article

    5.

    Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.

    Cui L, Jeong H, Borovecki F, Parkhurst CN, Tanese N, Krainc D.

    Cell. 2006 Oct 6;127(1):59-69.PMID: 17018277 [PubMed - indexed for MEDLINE]Related articles

    6.

    Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds.

    Gayán J, Brocklebank D, Andresen JM, Alkorta-Aranburu G; US-Venezuela Collaborative Research Group, Zameel Cader M, Roberts SA, Cherny SS, Wexler NS, Cardon LR, Housman DE.

    Genet Epidemiol. 2008 Jul;32(5):445-53.PMID: 18481795 [PubMed - indexed for MEDLINE]Related articles

    7.

    A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study.

    Li JL, Hayden MR, Almqvist EW, Brinkman RR, Durr A, Dodé C, Morrison PJ, Suchowersky O, Ross CA, Margolis RL, Rosenblatt A, Gómez-Tortosa E, Cabrero DM, Novelletto A, Frontali M, Nance M, Trent RJ, McCusker E, Jones R, Paulsen JS, Harrison M, Zanko A, Abramson RK, Russ AL, Knowlton B, Djoussé L, Mysore JS, Tariot S, Gusella MF, Wheeler VC, Atwood LD, Cupples LA, Saint-Hilaire M, Cha JH, Hersch SM, Koroshetz WJ, Gusella JF, MacDonald ME, Myers RH.

    Am J Hum Genet. 2003 Sep;73(3):682-7. Epub 2003 Aug 1.PMID: 12900792 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.

    Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, Myers RH, Wheeler VC.

    Hum Mol Genet. 2009 Aug 15;18(16):3039-47. Epub 2009 May 23.PMID: 19465745 [PubMed - indexed for MEDLINE]Related articles

    9.

    DNA haplotype analysis of CAG repeat in Taiwanese Huntington's disease patients.

    Wang CK, Wu YR, Hwu WL, Chen CM, Ro LS, Chen ST, Gwinn-Hardy K, Yang CC, Wu RM, Chen TF, Wang HC, Chao MC, Chiu MJ, Lu CJ, Lee-Chen GJ.

    Eur Neurol. 2004;52(2):96-100. Epub 2004 Jul 22.PMID: 15273431 [PubMed - indexed for MEDLINE]Related articles

    10.

    Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study.

    Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gómez-Tortosa E, García CA, Suchowersky O, Klimek ML, Trent RJ, McCusker E, Novelletto A, Frontali M, Paulsen JS, Jones R, Ashizawa T, Lazzarini A, Wheeler VC, Prakash R, Xu G, Djoussé L, Mysore JS, Gillis T, Hakky M, Cupples LA, Saint-Hilaire MH, Cha JH, Hersch SM, Penney JB, Harrison MB, Perlman SL, Zanko A, Abramson RK, Lechich AJ, Duckett A, Marder K, Conneally PM, Gusella JF, MacDonald ME, Myers RH.

    BMC Med Genet. 2006 Aug 17;7:71.PMID: 16914060 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease.

    Arning L, Monté D, Hansen W, Wieczorek S, Jagiello P, Akkad DA, Andrich J, Kraus PH, Saft C, Epplen JT.

    J Mol Med. 2008 Apr;86(4):485-90. Epub 2008 Mar 8.PMID: 18327563 [PubMed - indexed for MEDLINE]Related articles

    12.

    Impaired PGC-1alpha function in muscle in Huntington's disease.

    Chaturvedi RK, Adhihetty P, Shukla S, Hennessy T, Calingasan N, Yang L, Starkov A, Kiaei M, Cannella M, Sassone J, Ciammola A, Squitieri F, Beal MF.

    Hum Mol Genet. 2009 Aug 15;18(16):3048-65. Epub 2009 May 21.PMID: 19460884 [PubMed - indexed for MEDLINE]Related articles

    13.

    Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysis.

    Dodé C, Dürr A, Pêcheux C, Mouret JF, Belal S, Bachner L, Agid Y, Kaplan JC, Brice A, Feingold J.

    C R Acad Sci III. 1993 Nov;316(11):1374-80.PMID: 8087617 [PubMed - indexed for MEDLINE]Related articles

    14.

    Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

    Djoussé L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, Gómez-Tortosa E, Mayo Cabrero D, Jones R, Zanko A, Nance M, Abramson RK, Suchowersky O, Paulsen JS, Harrison MB, Yang Q, Cupples LA, Mysore J, Gusella JF, MacDonald ME, Myers RH.

    Neurogenetics. 2004 Jun;5(2):109-14. Epub 2004 Mar 17.PMID: 15029481 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    4p16.3 haplotype modifying age at onset of Huntington disease.

    Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen JE, Sørensen SA, Hasholt L.

    Clin Genet. 2009 Mar;75(3):244-50.PMID: 19250382 [PubMed - indexed for MEDLINE]Related articles

    16.

    Ancient origin of the CAG expansion causing Huntington disease in a Spanish population.

    García-Planells J, Burguera JA, Solís P, Millán JM, Ginestar D, Palau F, Espinós C.

    Hum Mutat. 2005 May;25(5):453-9.PMID: 15832309 [PubMed - indexed for MEDLINE]Related articles

    17.

    Evidence of oxidant damage in Huntington's disease: translational strategies using antioxidants.

    Stack EC, Matson WR, Ferrante RJ.

    Ann N Y Acad Sci. 2008 Dec;1147:79-92. Review.PMID: 19076433 [PubMed - indexed for MEDLINE]Related articles

    18.

    Huntington's disease like-2: review and update.

    Margolis RL, Rudnicki DD, Holmes SE.

    Acta Neurol Taiwan. 2005 Mar;14(1):1-8. Review.PMID: 15835282 [PubMed - indexed for MEDLINE]Related articles

    19.

    Analysis of the 5' upstream sequence of the Huntington's disease (HD) gene shows six new rare alleles which are unrelated to the age at onset of HD.

    Coles R, Leggo J, Rubinsztein DC.

    J Med Genet. 1997 May;34(5):371-4.PMID: 9152833 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Mitochondrial structural and functional dynamics in Huntington's disease.

    Reddy PH, Mao P, Manczak M.

    Brain Res Rev. 2009 Jun;61(1):33-48. Epub 2009 Apr 24. Review.PMID: 19394359 [PubMed - indexed for MEDLINE]Related articles

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