Regional and cellular gene expression changes in human Huntington's disease brain

By Hodges Angela   Strand Andrew D.   Aragaki Aaron K.   Kuhn Alexandre   Sengstag Thierry   Hughes Gareth   Elliston Lyn A.   Hartog Cathy   Goldstein Darlene R.   Thu Doris   Hollingsworth Zane R.   Collin Francois   Synek Beth   Holmans Peter A.   Young Anne B.   Wexler Nancy S.   Delorenzi Mauro   Kooperberg Charles   Augood Sarah J.   Faull Richard L.M.   Olson James M.  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 965-977

Oxford University Press

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Suppression of autophagy in skeletal muscle uncovers the accumulation of ubiquitinated proteins and their potential role in muscle damage in Pompe disease

By Raben Nina   Hill Victoria   Shea Lauren   Takikita Shoichi   Baum Rebecca   Mizushima Noboru   Ralston Evelyn   Plotz Paul  

Human Molecular Genetics, Vol. 17, Iss. 24, 2008-12 ,pp. : 3897-3908

Oxford University Press

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

By Chaturvedi Rajnish K.   Adhihetty Peter   Shukla Shubha   Hennessy Thomas   Calingasan Noel   Yang Lichuan   Starkov Anatoly   Kiaei Mahmoud   Cannella Milena   Sassone Jenny   Ciammola Andrea   Squitieri Fernando   Beal M. Flint  

Human Molecular Genetics, Vol. 18, Iss. 16, 2009-08 ,pp. : 3048-3065

Oxford University Press

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Increased huntingtin protein length reduces the number of polyglutamine-induced gene expression changes in mouse models of Huntington's disease

By Chan Edmond Y.W.  

Human Molecular Genetics, Vol. 11, Iss. 17, 2002-06 ,pp. : 1939-1951

Oxford University Press

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Polyglutamine and transcription: gene expression changes shared by DRPLA and Huntington's disease mouse models reveal context-independent effects

By Borchelt D.R.  

Human Molecular Genetics, Vol. 11, Iss. 17, 2002-06 ,pp. : 1927-1937

Oxford University Press

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