Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington’s disease

By Schapira A.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1829-1845

Oxford University Press

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Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis

By Kennedy Laura  

Human Molecular Genetics, Vol. 12, Iss. 24, 2003-12 ,pp. : 3359-3367

Oxford University Press

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Decreased expression of striatal signaling genes in a mouse model of Huntington’s disease

By Luthi-Carter Ruth   Strand Andrew   Peters Nikki L.   Solano Steven M.   Hollingsworth Zane R.   Menon Anil S.   Frey Ariel S.   Spektor Boris S.   Penney Ellen B.   Schilling Gabriele   Ross Christopher A.   Borchelt David R.   Tapscott Stephen J.   Young Anne B.   Cha Jang-Ho J.   Olson James M.  

Human Molecular Genetics, Vol. 9, Iss. 9, 2000-05 ,pp. : 1259-1271

Oxford University Press

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Neurological abnormalities in a knock-in mouse model of Huntington’s disease

By Detloff P.J.  

Human Molecular Genetics, Vol. 10, Iss. 2, 2001-01 ,pp. : 137-144

Oxford University Press

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Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington’s disease (HD) transgenic mice and HD patients

By Wanker E.E.  

Human Molecular Genetics, Vol. 10, Iss. 21, 2001-10 ,pp. : 2425-2435

Oxford University Press

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