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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Polycystin-2 is regulated by endoplasmic reticulum-associated degradation

By Liang Genqing   Li Qiang   Tang Yan   Kokame Koichi   Kikuchi Tadashi   Wu Guanqing   Chen Xing-Zhen  

Human Molecular Genetics, Vol. 17, Iss. 8, 2008-04 ,pp. : 1109-1119

Oxford University Press

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Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)

By Fujita Eriko   Kouroku Yoriko   Kumagai Hiromichi   Misutani Akifumi   Matsuda Chie   Hayashi Yukiko K.   Momoi Takashi  

Human Molecular Genetics, Vol. 16, Iss. 6, 2007-03 ,pp. : 618-629

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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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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