Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease

By Calkins Marcus J.   Manczak Maria   Mao Peizhong   Shirendeb Ulziibat   Reddy P. Hemachandra  

Human Molecular Genetics, Vol. 20, Iss. 23, 2011-12 ,pp. : 4515-4529

Oxford University Press

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Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

By Shirendeb Ulziibat   Reddy Arubala P.   Manczak Maria   Calkins Marcus J.   Mao Peizhong   Tagle Danilo A.   Hemachandra Reddy P.  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1438-1455

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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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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The Huntington's disease mutation impairs Huntingtin's role in the transport of NF-B from the synapse to the nucleus

By Marcora Edoardo   Kennedy Mary B.  

Human Molecular Genetics, Vol. 19, Iss. 22, 2010-11 ,pp. : 4373-4384

Oxford University Press

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