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。Exercise ameliorates the detrimental effect of chloroquine on skeletal muscles in mice via restoring autophagy flux
Dan Jiang et al.
ACTA PHARMACOLOGICA SINICA (2014)
Rapamycin nanoparticles target defective autophagy in muscular dystrophy to enhance both strength and cardiac function
Kristin P. Bibee et al.
FASEB JOURNAL (2014)
Genetic Reduction of Mammalian Target of Rapamycin Ameliorates Alzheimer's Disease-Like Cognitive and Pathological Deficits by Restoring Hippocampal Gene Expression Signature
Antonella Caccamo et al.
JOURNAL OF NEUROSCIENCE (2014)
Efficacy and Safety of Sirolimus for Renal Angiomyolipoma in Patients with Tuberous Sclerosis Complex or Sporadic Lymphangioleiomyomatosis: A Systematic Review
Zhu-feng Peng et al.
JOURNAL OF UROLOGY (2014)
Successful Treatment of Subungual Fibromas of Tuberous SclerosisWith Topical Rapamycin
John G. Muzic et al.
JAMA DERMATOLOGY (2014)
Rapamycin-induced autophagy aggravates pathology and weakness in a mouse model of VCP-associated myopathy
James K. Ching et al.
AUTOPHAGY (2013)
mTOR dysfunction contributes to vacuolar pathology and weakness in valosin-containing protein associated inclusion body myopathy
James K. Ching et al.
HUMAN MOLECULAR GENETICS (2013)
A progressive translational mouse model of human valosin-containing protein disease: The VCPR155H/+ mouse
Angele Nalbandian et al.
MUSCLE & NERVE (2013)
INCLUSION BODY MYOPATHY WITH PAGET DISEASE OF BONE AND FRONTOTEMPORAL DEMENTIA ASSOCIATED WITH A NOVEL G156S MUTATION IN THE VCP GENE
Junji Komatsu et al.
MUSCLE & NERVE (2013)
mTOR Inhibition Alleviates Mitochondrial Disease in a Mouse Model of Leigh Syndrome
Simon C. Johnson et al.
SCIENCE (2013)
Autophagy in Lysosomal Myopathies
May Christine V. Malicdan et al.
BRAIN PATHOLOGY (2012)
Autophagy: A double-edged sword in Alzheimer's disease
Ying-Tsen Tung et al.
JOURNAL OF BIOSCIENCES (2012)
The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology
Angele Nalbandian et al.
PLOS ONE (2012)
Slow development of ALS-like spinal cord pathology in mutant valosin-containing protein gene knock-in mice
H. Z. Yin et al.
CELL DEATH & DISEASE (2012)
Autophagy as a new therapeutic target in Duchenne muscular dystrophy
C. De Palma et al.
CELL DEATH & DISEASE (2012)
Fighting neurodegeneration with rapamycin: mechanistic insights
Jordi Bove et al.
NATURE REVIEWS NEUROSCIENCE (2011)
Autophagy gone awry in neurodegenerative diseases
Esther Wong et al.
NATURE NEUROSCIENCE (2010)
Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: Novel clinical and genetic findings
Kishore R. Kumar et al.
NEUROMUSCULAR DISORDERS (2010)
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
Jane O. Johnson et al.
NEURON (2010)
VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease
Mallikarjun Badadani et al.
PLOS ONE (2010)
Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease
Jeong-Sun Ju et al.
JOURNAL OF CELL BIOLOGY (2009)
Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree
T. D. Miller et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (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)
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts
Jouni Vesa et al.
NEUROMUSCULAR DISORDERS (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)
Autophagy in the pathogenesis of disease
Beth Levine et al.
CELL (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)
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia
G. D. J. Watts et al.
CLINICAL GENETICS (2007)
Valosin-containing protein gene mutations -: Clinical and neuropathologic features
L. Guyant-Marechal et al.
NEUROLOGY (2006)
Central pore residues mediate the p97/VCP activity required for ERAD
Byron DeLaBarre et al.
MOLECULAR CELL (2006)
Extension of chronological life span in yeast by decreased TOR pathway signaling
RW Powers et al.
GENES & DEVELOPMENT (2006)
Regulation of yeast replicative life span by TOR and Sch9 in response to nutrients
M Kaeberlein et al.
SCIENCE (2005)
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
D Haubenberger et al.
NEUROLOGY (2005)
Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
VE Kimonis et al.
ALZHEIMER DISEASE & ASSOCIATED DISORDERS (2005)
Mutant valosin-containing protein causes a novel type of frontotemporal dementia
R Schröder et al.
ANNALS OF NEUROLOGY (2005)
A series of ubiquitin binding factors connects CDC48/p97 to substrate multiubiquitylation and proteasomal targeting
H Richly et al.
CELL (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)
RNA interference of valosin-containing protein (VCP/p97) reveals multiple cellular roles linked to ubiquitin/proteasome-dependent proteolysis
C Wójcik et al.
JOURNAL OF CELL SCIENCE (2004)
Cdc48p is required for the cell cycle commitment point at start via degradation of the G1-CDK inhibitor Far1p
XR Fu et al.
JOURNAL OF CELL BIOLOGY (2003)
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes
GDJ Watts et al.
NEUROMUSCULAR DISORDERS (2003)
Cdc48-Ufd1-NpI4: Stuck in the middle with Ub
NW Bays et al.
CURRENT BIOLOGY (2002)
The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol
YH Ye et al.
NATURE (2001)
Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: Hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia
MJ Kovach et al.
MOLECULAR GENETICS AND METABOLISM (2001)
Valosin-containing protein is a multiubiquitin chain targeting factor required in ubiquitin-proteasome degradation
RM Dai et al.
NATURE CELL BIOLOGY (2001)
Functional analysis of the trypanosomal AAA protein TbVCP with trans-dominant ATP hydrolysis mutants
JR Lamb et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone
VE Kimonis et al.
GENETICS IN MEDICINE (2000)
分享论文
