Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone

By Custer Sara K.   Neumann Manuela   Lu Hongbo   Wright Alexander C.   Taylor J. Paul  

Human Molecular Genetics, Vol. 19, Iss. 9, 2010-05 ,pp. : 1741-1755

Oxford University Press

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Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation

By Weihl Conrad C.   Dalal Seema   Pestronk Alan   Hanson Phyllis I.  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 189-199

Oxford University Press

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Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice

By Weihl Conrad C.   Miller Sara E.   Hanson Phyllis I.   Pestronk Alan  

Human Molecular Genetics, Vol. 16, Iss. 8, 2007-04 ,pp. : 919-928

Oxford University Press

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The polyglutamine neurodegenerative protein ataxin-3 binds polyubiquitylated proteins and has ubiquitin protease activity

By Burnett Barrington   Li Fusheng  

Human Molecular Genetics, Vol. 12, Iss. 23, 2003-12 ,pp. : 3195-3205

Oxford University Press

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Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy

By Yi Ling   Donsante Anthony   Kennerson Marina L.   Mercer Julian F.B.   Garbern James Y.   Kaler Stephen G.  

Human Molecular Genetics, Vol. 21, Iss. 8, 2012-04 ,pp. : 1794-1807

Oxford University Press

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