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。Secondary coenzyme Q10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts
David Cotan et al.
FASEB JOURNAL (2011)
The use of individual patient's fibroblasts in the search for personalized treatment of nuclear encoded OXPHOS diseases
Ann Saada
MOLECULAR GENETICS AND METABOLISM (2011)
Regulation of autophagy by ROS: physiology and pathology
Ruth Scherz-Shouval et al.
TRENDS IN BIOCHEMICAL SCIENCES (2011)
MELAS and L-arginine therapy: pathophysiology of stroke-like episodes
Yasutoshi Koga et al.
MITOCHONDRIAL RESEARCH IN TRANSLATIONAL MEDICINE (2010)
COENZYME Q AND MITOCHONDRIAL DISEASE
Catarina M. Quinzii et al.
DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2010)
Mitochondrial diseases and the role of the yeast models
Teresa Rinaldi et al.
FEMS YEAST RESEARCH (2010)
Yeast Models of Human Mitochondrial Diseases
Antoni Barrientos
IUBMB LIFE (2010)
Treatment of mitochondrial electron transport chain disorders: A review of clinical trials over the past decade
Douglas S. Kerr
MOLECULAR GENETICS AND METABOLISM (2010)
Coenzyme Q(10) is frequently reduced in muscle of patients with mitochondrial myopathy
Sabrina Sacconi et al.
NEUROMUSCULAR DISORDERS (2010)
Treatment Options for Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome
Kristin M. Santa
PHARMACOTHERAPY (2010)
Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes Basic Concepts, Clinical Phenotype, and Therapeutic Management of MELAS Syndrome
Douglas M. Sproule et al.
YEAR IN NEUROLOGY 2008 (2008)
Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency
Giovanni Montini et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Yeast as a model of human mitochondrial tRNA base substitutions: Investigation of the molecular basis of respiratory defects
Arianna Montanari et al.
RNA (2008)
Mitochondrial disorders
Massimo Zeviani et al.
CURRENT OPINION IN NEUROLOGY (2007)
Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation
J. Finsterer
ACTA NEUROLOGICA SCANDINAVICA (2007)
Selective degradation of mitochondria by mitophagy
Insil Kim et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2007)
Cell and animal models of mtDNA biology: progress and prospects
Shaharyar M. Khan et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
ROS, mitochondria and the regulation of autophagy
Ruth Scherz-Shouval et al.
TRENDS IN CELL BIOLOGY (2007)
Human coenzyme Q(10) deficiency
Catarina M. Quinzii et al.
NEUROCHEMICAL RESEARCH (2007)
Mitochondrial function and toxicity: Role of the B vitamin family on mitochondrial energy metabolism
Flore Depeint et al.
CHEMICO-BIOLOGICAL INTERACTIONS (2006)
Diabetes-associated mitochondrial DNA mutation A3243G impairs cellular metabolic pathways necessary for beta cell function
P. B. M. de Andrade et al.
DIABETOLOGIA (2006)
A mutation in para-hydroxybenzoate-polyprenyl transferase (COQ2) causes primary coenzyme Q10 deficiency
C Quinzii et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome - A review of treatment options
Fernando Scaglia et al.
CNS DRUGS (2006)
Approaches to the treatment of Mitochondrial Diseases - Invited review
Salvatore DiMauro et al.
MUSCLE & NERVE (2006)
Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutation
RSJ Tafrechi et al.
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2005)
Mitochondrial tRNA 3 ' end metabolism and human disease
L Levinger et al.
NUCLEIC ACIDS RESEARCH (2004)
Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: A single-step approach
RK Bai et al.
CLINICAL CHEMISTRY (2004)
Codon-specific translational defect caused by a wobble modification deficiency in mutant tRNA from a human mitochondrial disease
Y Kirino et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters
CD Gajewski et al.
MOLECULAR BIOLOGY OF THE CELL (2003)
Nutritional cofactor treatment in mitochondrial disorders
B Marriage et al.
JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION (2003)
The yeast counterparts of human 'MELAS' mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu
M Feuermann et al.
EMBO REPORTS (2003)
A practical approach to the diagnosis and management of MELAS: Case report and review
M Thambisetty et al.
NEUROLOGIST (2002)
A colony color method identifies the vulnerability of mitochondria to oxidative damage
G Kim et al.
MUTAGENESIS (2002)
Intracellular distribution of the fluorescent dye nonyl acridine orange responds to the mitochondrial membrane potential: implications for assays of cardiolipin and mitochondrial mass
J Jacobson et al.
JOURNAL OF NEUROCHEMISTRY (2002)
Effect of coenzyme Q10 supplementation on mitochondrial function after myocardial ischemia reperfusion
JA Crestanello et al.
JOURNAL OF SURGICAL RESEARCH (2002)
Treatment of mitochondrial cytopathies
DR Gold et al.
SEMINARS IN NEUROLOGY (2001)
分享论文
