Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease

By Kim Jinho   Moody Jennifer P.   Edgerly Christina K.   Bordiuk Olivia L.   Cormier Kerry   Smith Karen   Beal M. Flint   Ferrante Robert J.  

Human Molecular Genetics, Vol. 19, Iss. 20, 2010-10 ,pp. : 3919-3935

Oxford University Press

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Abnormal interaction between the mitochondrial fission protein Drp1 and hyperphosphorylated tau in Alzheimer's disease neurons: implications for mitochondrial dysfunction and neuronal damage

By Manczak Maria   Reddy P. Hemachandra  

Human Molecular Genetics, Vol. 21, Iss. 11, 2012-06 ,pp. : 2538-2547

Oxford University Press

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Mutant huntingtin's interaction with mitochondrial protein Drp1 impairs mitochondrial biogenesis and causes defective axonal transport and synaptic degeneration in Huntington's disease

By Shirendeb Ulziibat P.   Calkins Marcus J.   Manczak Maria   Anekonda Vishwanath   Dufour Brett   McBride Jodi L.   Mao Peizhong   Reddy P. Hemachandra  

Human Molecular Genetics, Vol. 21, Iss. 2, 2012-01 ,pp. : 406-420

Oxford University Press

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Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease

By Van Raamsdonk Jeremy M.   Murphy Zoe   Slow Elizabeth J.   Leavitt Blair R.   Hayden Michael R.  

Human Molecular Genetics, Vol. 14, Iss. 24, 2005-12 ,pp. : 3823-3835

Oxford University Press

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Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease

By Yang Y-Z.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1555-1567

Oxford University Press

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