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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Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

By Metzger Silke   Rong Juan   Nguyen Huu-Phuc   Cape Austin   Tomiuk Juergen   Soehn Anne S.   Propping Peter   Freudenberg-Hua Yun   Freudenberg Jan   Tong Liang   Li Shi-Hua   Li Xiao-Jiang   Riess Olaf  

Human Molecular Genetics, Vol. 17, Iss. 8, 2008-04 ,pp. : 1137-1146

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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Identical oligomeric and fibrillar structures captured from the brains of R6/2 and knock-in mouse models of Huntington's disease

By Sathasivam Kirupa   Lane Amin   Legleiter Justin   Warley Alice   Woodman Ben   Finkbeiner Steve   Paganetti Paolo   Muchowski Paul J.   Wilson Stuart   Bates Gillian P.  

Human Molecular Genetics, Vol. 19, Iss. 1, 2010-01 ,pp. : 65-78

Oxford University Press

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Huntingtin interacts with cystathionine -synthase

By Boutell J.M.   Wood J.D.   Harper P.S.   Jones A.L.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 371-378

Oxford University Press

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