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 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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Ataxin-3 binds VCP/p97 and regulates retrotranslocation of ERAD substrates

By Zhong Xiaoyan   Pittman Randall N.  

Human Molecular Genetics, Vol. 15, Iss. 16, 2006-08 ,pp. : 2409-2420

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

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Immunocytochemical Localization of the Menkes Copper Transport Protein (ATP7A) to the Trans -Golgi Network

By Dierick Herman A.   Adam Ayla N.   Escara-Wilke June F.   Glover Thomas W.  

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