Cytokine Profiling in Patients with VCP-Associated Disease

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

(2012) SG Mehta et al.   CLINICAL GENETICS

Global Gene Profiling of VCP-associated Inclusion Body Myopathy

(2012) Angèle Nalbandian et al.   CTS-Clinical and Translational Science

TNF-α triggers rapid membrane insertion of Ca2+ permeable AMPA receptors into adult motor neurons and enhances their susceptibility to slow excitotoxic injury

(2012) Hong Z. Yin et al.   EXPERIMENTAL NEUROLOGY

Emerging functions of the VCP/p97 AAA-ATPase in the ubiquitin system

(2012) Hemmo Meyer et al.   NATURE CELL BIOLOGY

VCP/p97, Down-Regulated by microRNA-129-5p, Could Regulate the Progression of Hepatocellular Carcinoma

(2012) Yu Liu et al.   PLoS One

Stalled Proteasomes Are Directly Relieved by P97 Recruitment

(2011) Elada Isakov et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Valosin-containing protein mutation and Parkinson’s disease

(2011) Nora Chan et al.   PARKINSONISM & RELATED DISORDERS

p97/VCP at the intersection of the autophagy and the ubiquitin proteasome system

(2010) Jeong-Sun Ju et al.   Autophagy

Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone

(2010) Sara K. Custer et al.   HUMAN MOLECULAR GENETICS

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

(2010) Janel O. Johnson et al.   NEURON

Regulated Endoplasmic Reticulum-associated Degradation of a Polytopic Protein

(2009) Yukio Ikeda et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

(2009) Jouni Vesa et al.   NEUROMUSCULAR DISORDERS