Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism

By Charbonnier F.  

Human Molecular Genetics, Vol. 7, Iss. 11, 1998-11 ,pp. : 1825-1829

Oxford University Press

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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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Drosophila FMRP regulates microtubule network formation and axonal transport of mitochondria

By Yao Aiyu   Jin Shan   Li Xinhai   Liu Zhihua   Ma Xuehua   Tang Jing   Zhang Yong Q.  

Human Molecular Genetics, Vol. 20, Iss. 1, 2011-01 ,pp. : 51-63

Oxford University Press

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Mutation in saposin D domain of sphingolipid activator protein gene causes urinary system defects and cerebellar Purkinje cell degeneration with accumulation of hydroxy fatty acid-containing ceramide in mouse

By Matsuda Junko  

Human Molecular Genetics, Vol. 13, Iss. 21, 2004-11 ,pp. : 2709-2723

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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