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Michael A. Gitcho et al.
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Antonella Caccamo et al.
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Viktor I. Korolchuk et al.
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Mohammad Salajegheh et al.
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Conrad C. Weihl et al.
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Ai Kadokura et al.
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C. Schuberth et al.
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Jeong-Sun Ju et al.
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C. C. Weihl et al.
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An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene
Teresa Gidaro et al.
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Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice
Masaaki Komatsu et al.
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FoxO3 controls autophagy in skeletal muscle in vivo
Cristina Mammucari et al.
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Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease
Maria Filimonenko et al.
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Dissection of the autophagosome maturation process by a novel reporter protein, tandem fluorescent-tagged LC3
Shunsuke Kimura et al.
AUTOPHAGY (2007)
p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy
Serhiy Pankiv et al.
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Involvement of valosin-containing protein (VCP)/p97 in the formation and clearance of abnormal protein aggregates
Taeko Kobayashi et al.
GENES TO CELLS (2007)
Transgenic expression of inclusion body myopathy associated mutant p97/VCP causes weakness and ubiquitinated protein inclusions in mice
Conrad C. Weihl et al.
HUMAN MOLECULAR GENETICS (2007)
TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations
Manuela Neumann et al.
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Pathological consequences of VCP mutations on human striated muscle
Christian U. Huebbers et al.
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The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy
Philipp Christoph Janiesch et al.
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Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
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L. Guyant-Marechal et al.
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p97: The cell's molecular purgatory?
Dalia Halawani et al.
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Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
Taichi Hara et al.
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Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations
Mark S. Forman et al.
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Phosphatidylserine in addition to phosphatidylethanolamine is an in vitro target of the mammalian Atg8 modifiers, LC3, GABARAP, and GATE-16
Y Sou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Inclusion body myopathy-associated mutations in p97/VCP impair endoplasmic reticulum-associated degradation
CC Weihl et al.
HUMAN MOLECULAR GENETICS (2006)
Electron microscopy in neuromuscular disorders
C Fernandez et al.
ULTRASTRUCTURAL PATHOLOGY (2005)
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
G Skibinski et al.
NATURE GENETICS (2005)
Mutant valosin-containing protein causes a novel type of frontotemporal dementia
R Schröder et al.
ANNALS OF NEUROLOGY (2005)
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
GDJ Watts et al.
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Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway
S Dalal et al.
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RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis
C Wójcik et al.
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RW Kuncl et al.
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Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion
JMM Müller et al.
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Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone
N Laurin et al.
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The first molecular evidence that autophagy relates rimmed vacuole formation in chloroquine myopathy
T Suzuki et al.
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YH Ye et al.
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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease)
I Nishino et al.
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Y Sagiv et al.
EMBO JOURNAL (2000)