References
- Proc. Natl. Acad. Sci. U.S.A. 102:14132-14138(2005)
Recruitment of the p97 ATPase and ubiquitin ligases to the site of
retrotranslocation at the endoplasmic reticulum membrane.
Ye Y., Shibata Y., Kikkert M., van Voorden S., Wiertz E., Rapoport T.A.
- Nat. Genet. 36:377-381(2004)
Inclusion body myopathy associated with Paget disease of bone and
frontotemporal dementia is caused by mutant valosin-containing protein.
Watts G.D.J., Wymer J., Kovach M.J., Mehta S.G., Mumm S., Darvish D.,
Pestronk A., Whyte M.P., Kimonis V.E.
- Neurology 65:1304-1305(2005)
nclusion body myopathy and Paget disease is linked to a novel mutation
in the VCP gene.
Haubenberger D., Bittner R.E., Rauch-Shorny S., Zimprich F., Mannhalter
C., Wagner L., Mineva I., Vass K., Auff E., Zimprich A..