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 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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mTOR dysfunction contributes to vacuolar pathology and weakness in valosin-containing protein associated inclusion body myopathy

By Ching James K.   Elizabeth Sarita V.   Ju Jeong-Sun   Lusk Caleb   Pittman Sara K.   Weihl Conrad C.  

Human Molecular Genetics, Vol. 22, Iss. 6, 2013-03 ,pp. : 1167-1179

Oxford University Press

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Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity

By Sunada Y.  

Human Molecular Genetics, Vol. 10, Iss. 3, 2001-02 ,pp. : 173-178

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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