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。Prevalence of Nuclear and Mitochondrial DNA Mutations Related to Adult Mitochondrial Disease
Grainne S. Gorman et al.
ANNALS OF NEUROLOGY (2015)
A Periodic Diet that Mimics Fasting Promotes Multi-System Regeneration, Enhanced Cognitive Performance, and Healthspan
Sebastian Brandhorst et al.
CELL METABOLISM (2015)
WIPI proteins: essential PtdIns3P effectors at the nascent autophagosome
Tassula Proikas-Cezanne et al.
JOURNAL OF CELL SCIENCE (2015)
Mitochondrial Diseases Part III: Therapeutic interventions in mouse models of OXPHOS deficiencies
Susana Peralta et al.
MITOCHONDRION (2015)
MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases
Masami Hashimoto et al.
MOLECULAR THERAPY (2015)
Expanding roles for AMPK in skeletal muscle plasticity
Remi Mounier et al.
TRENDS IN ENDOCRINOLOGY AND METABOLISM (2015)
NAD+-Dependent Activation of Sirt1 Corrects the Phenotype in a Mouse Model of Mitochondrial Disease
Raffaele Cerutti et al.
CELL METABOLISM (2014)
Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3
Nahid A. Khan et al.
EMBO MOLECULAR MEDICINE (2014)
Mitochondrially targeted ZFNs for selective degradation of pathogenic mitochondrial genomes bearing large-scale deletions or point mutations
Payam A. Gammage et al.
EMBO MOLECULAR MEDICINE (2014)
Gene Therapy Using a Liver-targeted AAV Vector Restores Nucleoside and Nucleotide Homeostasis in a Murine Model of MNGIE
Javier Torres-Torronteras et al.
MOLECULAR THERAPY (2014)
Metformin Protects Skeletal Muscle from Cardiotoxin Induced Degeneration
Francesca Langone et al.
PLOS ONE (2014)
AMPKα1 Regulates Macrophage Skewing at the Time of Resolution of Inflammation during Skeletal Muscle Regeneration
Remi Mounier et al.
CELL METABOLISM (2013)
Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs
Sandra R. Bacman et al.
NATURE MEDICINE (2013)
COX10 Mutations Resulting in Complex Multisystem Mitochondrial Disease That Remains Stable Into Adulthood
Robert D. S. Pitceathly et al.
JAMA NEUROLOGY (2013)
Chronic AICAR-induced AMP-kinase activation regulates adipocyte lipolysis in a time-dependent and fat depot-specific manner in rats
Mandeep P. Gaidhu et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2012)
CoQ10 deficiencies and MNGIE: Two treatable mitochondrial disorders
Michio Hirano et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2012)
The NAD+ Precursor Nicotinamide Riboside Enhances Oxidative Metabolism and Protects against High-Fat Diet-Induced Obesity
Caries Canto et al.
CELL METABOLISM (2012)
MASTR directs MyoD-dependent satellite cell differentiation during skeletal muscle regeneration
Mayssa H. Mokalled et al.
GENES & DEVELOPMENT (2012)
Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice
Shuichi Yatsuga et al.
HUMAN MOLECULAR GENETICS (2012)
Increased mitochondrial biogenesis in muscle improves aging phenotypes in the mtDNA mutator mouse
Lloye M. Dillon et al.
HUMAN MOLECULAR GENETICS (2012)
A defect in the mitochondrial complex III, but not complex IV, triggers early ROS-dependent damage in defined brain regions
Francisca Diaz et al.
HUMAN MOLECULAR GENETICS (2012)
AMPK promotes skeletal muscle autophagy through activation of forkhead FoxO3a and interaction with Ulk1
Anthony M. J. Sanchez et al.
JOURNAL OF CELLULAR BIOCHEMISTRY (2012)
Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity
Ursula Fuenfschilling et al.
NATURE (2012)
Human mitochondrial DNA: roles of inherited and somatic mutations
Eric A. Schon et al.
NATURE REVIEWS GENETICS (2012)
Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse
Lloye M. Dillon et al.
PLOS ONE (2012)
Metabolic remodeling agents show beneficial effects in the dystrophin-deficient mdx mouse model
Vanessa E. Jahnke et al.
SKELETAL MUSCLE (2012)
Regulation of PGC-1α, a nodal regulator of mitochondrial biogenesis
Pablo J. Fernandez-Marcos et al.
AMERICAN JOURNAL OF CLINICAL NUTRITION (2011)
In Vivo Correction of COX Deficiency by Activation of the AMPK/PGC-1α Axis
Carlo Viscomi et al.
CELL METABOLISM (2011)
The AMPK signalling pathway coordinates cell growth, autophagy and metabolism
Maria M. Mihaylova et al.
NATURE CELL BIOLOGY (2011)
Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy
Daniel F. Egan et al.
SCIENCE (2011)
Mitochondrial Energetics and Therapeutics
Douglas C. Wallace et al.
ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE (2010)
Mammalian Atg18 (WIPI2) localizes to omegasome-anchored phagophores and positively regulates LC3 lipidation
Hannah E. J. Polson et al.
AUTOPHAGY (2010)
The Association of AMPK with ULK1 Regulates Autophagy
Jong Woo Lee et al.
PLOS ONE (2010)
Targeting the Core of Transcription
D. Grahame Hardie
SCIENCE (2010)
PGC-1α/β induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders
Sarika Srivastava et al.
HUMAN MOLECULAR GENETICS (2009)
Prolonged AICAR-induced AMP-kinase activation promotes energy dissipation in white adipocytes: novel mechanisms integrating HSL and ATGL
Mandeep P. Gaidhu et al.
JOURNAL OF LIPID RESEARCH (2009)
被撤回的出版物: Increased muscle PGC-1 alpha expression protects from sarcopenia and metabolic disease during aging(Retracted article. See vol.113,pg.E8502,2016)
Tina Wenz et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Nuclear Control of Respiratory Chain Expression by Nuclear Respiratory Factors and PGC-1-Related Coactivator
Richard C. Scarpulla
MITOCHONDRIA AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISORDERS (2008)
Mitochondrial disorders in the nervous system
Salvatore DiMauro et al.
ANNUAL REVIEW OF NEUROSCIENCE (2008)
AMPK and PPARδ Agonists are exercise mimetics
Vihang A. Narkar et al.
CELL (2008)
Intravenous AICAR administration reduces hepatic glucose output and inhibits whole body lipolysis in type 2 diabetic patients
H. Boon et al.
DIABETOLOGIA (2008)
Acadesine, an adenosine-regulating agent with the potential for widespread indications
Brian G. Drew et al.
EXPERT OPINION ON PHARMACOTHERAPY (2008)
Activation of peroxisome proliferator-activated receptor pathway stimulates the mitochondrial respiratory chain and can correct deficiencies in patients' cells lacking its components
Jean Bastin et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
Analyzing real-time PCR data by the comparative C-T method
Thomas D. Schmittgen et al.
NATURE PROTOCOLS (2008)
Electrophoresis techniques to investigate defects in oxidative phosphorylation
Maria Antonietta Calvaruso et al.
METHODS (2008)
5-aminoimidazole-4-carboxamide 1-β-D-ribofuranoside acutely stimulates skeletal muscle 2-deoxyglucose uptake in healthy men
Daniel J. Cuthbertson et al.
DIABETES (2007)
AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α
Sibylle Jaeger et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation
JF Chen et al.
NATURE GENETICS (2006)
Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency
F Diaz et al.
HUMAN MOLECULAR GENETICS (2005)
Effects of α-AMPK knockout on exercise-induced gene activation in mouse skeletal muscle
SB Jorgensen et al.
FASEB JOURNAL (2005)
Transgenic mice that express Cre recombinase under control of a skeletal muscle-specific promoter from mef2c
AB Heidt et al.
GENESIS (2005)
Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse
A Flierl et al.
GENE THERAPY (2005)
Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1
SL Williams et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene
MJH Coenen et al.
ANNALS OF NEUROLOGY (2004)
Regulation of muscle fiber type and running endurance by PPARδ
YX Wang et al.
PLOS BIOLOGY (2004)
Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency
H Antonicka et al.
HUMAN MOLECULAR GENETICS (2003)
Serial analysis of gene expression in the skeletal muscle of endurance athletes compared to sedentary men
M Yoshioka et al.
FASEB JOURNAL (2003)
mef2c is activated directly by myogenic basic helix-loop-helix proteins during skeletal muscle development in vivo
E Dodou et al.
MECHANISMS OF DEVELOPMENT (2003)
Thyroid hormone regulates oxidative phosphorylation in the cerebral cortex and striatum of neonatal rats
B Martinez et al.
JOURNAL OF NEUROCHEMISTRY (2001)
A mutation in the human heme A:farnesyltransferase gene (COX10) causes cytochrome c oxidase deficiency
I Valnot et al.
HUMAN MOLECULAR GENETICS (2000)