Mutant valosin-containing protein causes a novel type of frontotemporal dementia-Reference-Cited by-同舟云学术

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

Published:2005-02-24 Issue:3 Volume:57 Page:457-461
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Schröder Rolf,Watts Giles D. J.,Mehta Sarju G.,Evert Bernd O.,Broich Petra,Fließbach Klaus,Pauls Katharina,Hans Volkmar H.,Kimonis Virginia,Thal Dietmar R.

Funder

Deutsche Forschungsgemeinschaft

BONFOR

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference20 articles.

1. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein;Watts;Nat Genet,2004

2. Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly;Hetzer;Nat Cell Biol,2001

3. Syntaxin 5 is a common component of the NSF- and p97-mediated reassembly pathways of Golgi cisternae from mitotic Golgi fragments in vitro;Rabouille;Cell,1998

4. p47 is a cofactor for p97-mediated membrane fusion;Kondo;Nature,1997

5. A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways;Meyer;EMBO J,2000

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