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Mitochondrial gene therapy augments mitochondrial physiology in a Parkinson's disease cell model.Linezolid-induced optic neuropathy: a mitochondrial disorder?Maternal protein restriction leads to early life alterations in the expression of key molecules involved in the aging process in rat offspringRecombinant human mitochondrial transcription factor A stimulates mitochondrial biogenesis and ATP synthesis, improves motor function after MPTP, reduces oxidative stress and increases survival after endotoxinRecombinant mitochondrial transcription factor A with N-terminal mitochondrial transduction domain increases respiration and mitochondrial gene expression.A critical role of Fas-associated protein with death domain phosphorylation in intracellular reactive oxygen species homeostasis and aging.Packaging of single DNA molecules by the yeast mitochondrial protein Abf2pGenetic ablation of calcium-independent phospholipase A2gamma leads to alterations in mitochondrial lipid metabolism and function resulting in a deficient mitochondrial bioenergetic phenotypeSOD2, the principal scavenger of mitochondrial superoxide, is dispensable for embryogenesis and imaginal tissue development but essential for adult survivalRole of human DNA glycosylase Nei-like 2 (NEIL2) and single strand break repair protein polynucleotide kinase 3'-phosphatase in maintenance of mitochondrial genome.Polysaccharides from Enteromorpha prolifera Improve Glucose Metabolism in Diabetic Rats.SOD2 protects neurons from injury in cell culture and animal models of diabetic neuropathyCombination of alpha lipoic acid and superoxide dismutase leads to physiological and symptomatic improvements in diabetic neuropathyMitochondrial protein import and human health and disease.The mitochondrial genome, a growing interest inside an organelle.Mitochondrial DNA oxidative damage and repair in aging and Alzheimer's disease.Peroxisome-proliferator-activated receptors regulate redox signaling in the cardiovascular systemA Clinical Trial about a Food Supplement Containing α-Lipoic Acid on Oxidative Stress Markers in Type 2 Diabetic PatientsA matter of life and death: cardiac myocyte apoptosis and regeneration.VDAC3 has differing mitochondrial functions in two types of striated muscles.The emerging role of immune dysfunction in mitochondrial diseases as a paradigm for understanding immunometabolism.R(+)-Thioctic Acid Effects on Oxidative Stress and Peripheral Neuropathy in Type II Diabetic Patients: Preliminary Results by Electron Paramagnetic Resonance and Electroneurography.Mitochondrial dysfunction reduces yeast replicative lifespan by elevating RAS-dependent ROS production by the ER-localized NADPH oxidase Yno1.The potential mechanism of mitochondrial dysfunction in septic cardiomyopathy.Characterization of Drosophila ATPsynC mutants as a new model of mitochondrial ATP synthase disorders
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Animal models for mitochondrial disease.
@ast
Animal models for mitochondrial disease.
@en
Animal models for mitochondrial disease.
@nl
type
label
Animal models for mitochondrial disease.
@ast
Animal models for mitochondrial disease.
@en
Animal models for mitochondrial disease.
@nl
prefLabel
Animal models for mitochondrial disease.
@ast
Animal models for mitochondrial disease.
@en
Animal models for mitochondrial disease.
@nl
P1476
Animal models for mitochondrial disease.
@en
P2093
Douglas C Wallace
P356
10.1385/1-59259-284-8:003
P407
P577
2002-01-01T00:00:00Z