相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy
Peter Reilich et al.
NEUROMUSCULAR DISORDERS (2010)
Identification of polyubiquitin binding proteins involved in NF-κB signaling using protein arrays
Beau J. Fenner et al.
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS (2009)
Myofibrillar Myopathies: A Clinical and Myopathological Guide
Rolf Schroeder et al.
BRAIN PATHOLOGY (2009)
The Arp2/3 Activator WASH Controls the Fission of Endosomes through a Large Multiprotein Complex
Emmanuel Derivery et al.
DEVELOPMENTAL CELL (2009)
TCEB1 promotes invasion of prostate cancer cells
Sanni E. Jalava et al.
INTERNATIONAL JOURNAL OF CANCER (2009)
Ubiquilin and p97/VCP bind erasin, forming a complex involved in ERAD
Precious J. Lim et al.
JOURNAL OF CELL BIOLOGY (2009)
A NOVEL MUTATION IN THE VCP GENE (G157R) IN A GERMAN FAMILY WITH INCLUSION-BODY MYOPATHY WITH PAGET DISEASE OF BONE AND FRONTOTEMPORAL DEMENTIA
Atbin Djamshidian et al.
MUSCLE & NERVE (2009)
Consequences of mutations within the C terminus of the FHL1 gene
B. Schoser et al.
NEUROLOGY (2009)
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia
Tanya Stojkovic et al.
NEUROMUSCULAR DISORDERS (2009)
Proteomics of MUC1-containing lipid rafts from plasma membranes and exosomes of human breast carcinoma cells MCF-7
Simon Staubach et al.
PROTEOMICS (2009)
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
Virginia. E. Kimonis et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Electrotransfer of proteins in an environmentally friendly methanol-free transfer buffer
Marco A. Villanueva
ANALYTICAL BIOCHEMISTRY (2008)
UBXD7 binds multiple ubiquitin ligases and implicates p97 in HIF1α turnover
Gabriela Alexandru et al.
CELL (2008)
A concerted action of HNF4α and HNF1α links hepatitis B virus replication to hepatocyte differentiation
Maria Quasdorff et al.
CELLULAR MICROBIOLOGY (2008)
Impaired Protein Aggregate Handling and Clearance Underlie the Pathogenesis of p97/VCP-associated Disease
Jeong-Sun Ju et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms
Sara Salinas et al.
LANCET NEUROLOGY (2008)
HDAC6 at the intersection of autophagy, the ubiquitin-proteasome system and neurodegeneration
Udai Bhan Pandey et al.
AUTOPHAGY (2007)
Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis
Steven A. Greenberg et al.
MUSCLE & NERVE (2007)
STATc is a key regulator of the transcriptional response to hyperosmotic shock
Jianbo Na et al.
BMC GENOMICS (2007)
Pathological consequences of VCP mutations on human striated muscle
Christian U. Huebbers et al.
BRAIN (2007)
Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
Paul N. Valdmanis et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease
Huu Phuc Nguyen et al.
HUMAN MOLECULAR GENETICS (2006)
p97: The cell's molecular purgatory?
Dalia Halawani et al.
MOLECULAR CELL (2006)
An arginine/lysine-rich motif is crucial for VCP/p97-mediated modulation of ataxin-3 fibrillogenesis
A Boeddrich et al.
EMBO JOURNAL (2006)
Traffic accidents: Molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias
C Soderblom et al.
PHARMACOLOGY & THERAPEUTICS (2006)
High-resolution array comparative genomic hybridization of chromosome arm 8q:: Evaluation of genetic progression markers for prostate cancer
M van Duin et al.
GENES CHROMOSOMES & CANCER (2005)
Multiprotein complexes that link dislocation, ubiquitination, and extraction of misfolded proteins from the endoplasmic reticulum membrane
BN Lilley et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies
CS Clemen et al.
FEBS LETTERS (2005)
VEGF-PLCγ1 pathway controls cardiac contractility in the embryonic heart
W Rottbauer et al.
GENES & DEVELOPMENT (2005)
Protein structure prediction servers at university college london
K Bryson et al.
NUCLEIC ACIDS RESEARCH (2005)
The genome of the social amoeba Dictyostelium discoideum
L Eichinger et al.
NATURE (2005)
Mutant valosin-containing protein causes a novel type of frontotemporal dementia
R Schröder et al.
ANNALS OF NEUROLOGY (2005)
RNA interference of VCP/p97 increases Mallory body formation
L Nan et al.
EXPERIMENTAL AND MOLECULAR PATHOLOGY (2005)
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
GDJ Watts et al.
NATURE GENETICS (2004)
Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway
S Dalal et al.
MOLECULAR BIOLOGY OF THE CELL (2004)
A membrane protein complex mediates retro-translocation from the ER lumen into the cytosol
YH Ye et al.
NATURE (2004)
RAD21 and KIAA0196 at 8q24 are amplified and overexpressed in prostate cancer
KP Porkka et al.
GENES CHROMOSOMES & CANCER (2004)
The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stress
Y Kawaguchi et al.
CELL (2003)
Advances in the hereditary spastic paraplegias
JK Fink
EXPERIMENTAL NEUROLOGY (2003)
DNA damage modulates nucleolar interaction of the Werner protein with the AAA ATPase p97/VCP
JJ Partridge et al.
MOLECULAR BIOLOGY OF THE CELL (2003)
Complete structure of p97/valosin-containing protein reveals communication between nucleotide domains
B DeLaBarre et al.
NATURE STRUCTURAL BIOLOGY (2003)
Selective striatal neuronal loss in a YAC128 mouse model of Huntington disease
EJ Slow et al.
HUMAN MOLECULAR GENETICS (2003)
Vacuole-creating protein in neurodegenerative diseases in humans
Y Mizuno et al.
NEUROSCIENCE LETTERS (2003)
Transgenic rat model of Huntington's disease
S von Hörsten et al.
HUMAN MOLECULAR GENETICS (2003)
Oligomerization, F-actin interaction, and membrane association of the ubiquitous mammalian coronin 3 are mediated by its carboxyl terminus
Z Spoerl et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Functional ATPase activity of p97/valosin-containing protein (VCP) is required for the quality control of endoplasmic reticulum in neuronally differentiated mammalian PC12 cells
T Kobayashi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Conformational changes of the multifunction p97 AAA ATPase during its ATPase cycle
I Rouiller et al.
NATURE STRUCTURAL BIOLOGY (2002)
AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation
E Rabinovich et al.
MOLECULAR AND CELLULAR BIOLOGY (2002)
The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol
YH Ye et al.
NATURE (2001)
Distinct AAA-ATPase p97 complexes function in discrete steps of nuclear assembly
M Hetzer et al.
NATURE CELL BIOLOGY (2001)
VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration
M Hirabayashi et al.
CELL DEATH AND DIFFERENTIATION (2001)
SNARE proteins are highly enriched in lipid rafts in PC12 cells: Implications for the spatial control of exocytosis
LH Chamberlain et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2001)
Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
S Vielhaber et al.
BRAIN (2000)
A complex of mammalian Ufd1 and Npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways
HH Meyer et al.
EMBO JOURNAL (2000)
The PSIPRED protein structure prediction server
LJ McGuffin et al.
BIOINFORMATICS (2000)
分享论文
