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 NAD-Booster Nicotinamide Riboside Potently Stimulates Hematopoiesis through Increased Mitochondrial Clearance
Nicola Vannini et al.
CELL STEM CELL (2019)
Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer's disease
Evandro F. Fang et al.
NATURE NEUROSCIENCE (2019)
Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H2O2 emission during impaired oxidative phosphorylation
Meghan C. Hughes et al.
JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE (2019)
CRISPR Correction of Duchenne Muscular Dystrophy
Yi-Li Min et al.
ANNUAL REVIEW OF MEDICINE, VOL 70 (2019)
The RNA-Binding Protein PUM2 Impairs Mitochondrial Dynamics and Mitophagy During Aging
Davide D'Amico et al.
MOLECULAR CELL (2019)
The mitophagy activator urolithin A is safe and induces a molecular signature of improved mitochondrial and cellular health in humans
Penelope A. Andreux et al.
NATURE METABOLISM (2019)
Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation
Robert G. Barker et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2018)
Combined Therapies for Duchenne Muscular Dystrophy to Optimize Treatment Efficacy
Gonzalo Cordova et al.
FRONTIERS IN GENETICS (2018)
Resveratrol Decreases Oxidative Stress by Restoring Mitophagy and Improves the Pathophysiology of Dystrophin-Deficient mdx Mice
Rio Sebori et al.
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2018)
Repairing Mitochondrial Dysfunction in Disease
Vincenzo Sorrentino et al.
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 58 (2018)
Deficit in PINK1/PARKIN-mediated mitochondrial autophagy at late stages of dystrophic cardiomyopathy
Chifei Kang et al.
CARDIOVASCULAR RESEARCH (2018)
Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy
Maria C. Vila et al.
CELL DEATH AND DIFFERENTIATION (2017)
Mitochondrial biogenesis and clearance: a balancing act
Christina Ploumi et al.
FEBS JOURNAL (2017)
Safety assessment of Urolithin A, a metabolite produced by the human gut microbiota upon dietary intake of plant derived ellagitannins and ellagic acid
Jacqueline Heilman et al.
FOOD AND CHEMICAL TOXICOLOGY (2017)
Exercise in claudicants increase or decrease walking ability and the response relates to mitochondrial function
Michel van Schaardenburgh et al.
JOURNAL OF TRANSLATIONAL MEDICINE (2017)
Progress toward Gene Therapy for Duchenne Muscular Dystrophy
Joel R. Chamberlain et al.
MOLECULAR THERAPY (2017)
Enhancing mitochondrial proteostasis reduces amyloid-β proteotoxicity
Vincenzo Sorrentino et al.
NATURE (2017)
The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review
S. Ryder et al.
ORPHANET JOURNAL OF RARE DISEASES (2017)
Development of Exon Skipping Therapies for Duchenne Muscular Dystrophy: A Critical Review and a Perspective on the Outstanding Issues
Annemieke Aartsma-Rus et al.
NUCLEIC ACID THERAPEUTICS (2017)
Mitophagy-driven mitochondrial rejuvenation regulates stem cell fate
Alejandro Vazquez-Martin et al.
AGING-US (2016)
Autophagy regulates satellite cell ability to regenerate normal and dystrophic muscles
E. Fiacco et al.
CELL DEATH AND DIFFERENTIATION (2016)
Autophagy maintains stemness by preventing senescence
Laura Garcia-Prat et al.
NATURE (2016)
Urolithin A induces mitophagy and prolongs lifespan in C-elegans and increases muscle function in rodents
Dongryeol Ryu et al.
NATURE MEDICINE (2016)
NAD+ repletion improves mitochondrial and stem cell function and enhances life span in mice
Hongbo Zhang et al.
SCIENCE (2016)
NAD+ repletion improves muscle function in muscular dystrophy and counters global PARylation
Dongryeol Ryu et al.
SCIENCE TRANSLATIONAL MEDICINE (2016)
Satellite Cells in Muscular Dystrophy - Lot in Polarity
Natasha C. Chang et al.
TRENDS IN MOLECULAR MEDICINE (2016)
Targeting muscle stem cell intrinsic defects to treat Duchenne muscular dystrophy
Nicolas A. Dumont et al.
NPJ REGENERATIVE MEDICINE (2016)
New method to assess mitophagy flux by flow cytometry
Marta Mauro-Lizcano et al.
AUTOPHAGY (2015)
Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process
Nicolas Brouilly et al.
HUMAN MOLECULAR GENETICS (2015)
Coordination of mitophagy and mitochondrial biogenesis during ageing in C-elegans
Konstantinos Palikaras et al.
NATURE (2015)
Isolation of skeletal muscle stem cells by fluorescence-activated cell sorting
Ling Liu et al.
NATURE PROTOCOLS (2015)
Muscular dystrophy in the mdx mouse is a severe myopathy compounded by hypotrophy, hypertrophy and hyperplasia
William Duddy et al.
SKELETAL MUSCLE (2015)
PGC-1α modulates denervation-induced mitophagy in skeletal muscle
Anna Vainshtein et al.
SKELETAL MUSCLE (2015)
Metabolic Dysfunction and Altered Mitochondrial Dynamics in the Utrophin-Dystrophin Deficient Mouse Model of Duchenne Muscular Dystrophy
Meghna Pant et al.
PLOS ONE (2015)
Mitophagy Is Required for Acute Cardioprotection by Simvastatin
Allen M. Andres et al.
ANTIOXIDANTS & REDOX SIGNALING (2014)
Ubiquitin is phosphorylated by PINK1 to activate parkin
Fumika Koyano et al.
NATURE (2014)
Duchenne and Becker Muscular Dystrophies
Kevin M. Flanigan
NEUROLOGIC CLINICS (2014)
A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy
Jean K. Mah et al.
NEUROMUSCULAR DISORDERS (2014)
Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency
Emma Rybalka et al.
PLOS ONE (2014)
Mitophagy in hematopoietic stem cells The case for exploration
Aashish Joshi et al.
AUTOPHAGY (2013)
Defects in mitochondrial localization and ATP synthesis in the mdx mouse model of Duchenne muscular dystrophy are not alleviated by PDE5 inhibition
Justin M. Percival et al.
HUMAN MOLECULAR GENETICS (2013)
Autophagy as a new therapeutic target in Duchenne muscular dystrophy
C. De Palma et al.
CELL DEATH & DISEASE (2012)
Autophagy induction rescues muscular dystrophy
Paolo Grumati et al.
AUTOPHAGY (2011)
Resveratrol Ameliorates Muscular Pathology in the Dystrophic mdx Mouse, a Model for Duchenne Muscular Dystrophy
Yusuke S. Hori et al.
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS (2011)
Role of TRPC1 channel in skeletal muscle function
Nadege Zanou et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2010)
Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice
Alessandra Sacco et al.
CELL (2010)
Mechanisms of muscle weakness in muscular dystrophy
Jeffery A. Goldstein et al.
JOURNAL OF GENERAL PHYSIOLOGY (2010)
PGC-1α regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy
Christoph Handschin et al.
GENES & DEVELOPMENT (2007)
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression
Mario Pescatori et al.
FASEB JOURNAL (2007)
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration
M Bakay et al.
BRAIN (2006)
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
A Subramanian et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse
A Briguet et al.
NEUROMUSCULAR DISORDERS (2004)
Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle
JN Haslett et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
分享论文
