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Mitochondrial CardiomyopathiesNanoparticle-Based and Bioengineered Probes and Sensors to Detect Physiological and Pathological Biomarkers in Neural CellsSestrin2, a Regulator of Thermogenesis and Mitohormesis in Brown Adipose TissueMitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.Shotgun lipidomics in substantiating lipid peroxidation in redox biology: Methods and applicationsA novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis.Metabolic pathways regulated by TAp73 in response to oxidative stressA deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function.The role of mitochondrial ROS in antibacterial immunity.microRNA-mediated differential expression of TRMU, GTPBP3 and MTO1 in cell models of mitochondrial-DNA diseases.How to bake a brain: yeast as a model neuron.A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction.The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.Application of Bioactive Compounds from Scutellaria in Neurologic Disorders.Growth hormone secretagogues hexarelin and JMV2894 protect skeletal muscle from mitochondrial damages in a rat model of cisplatin-induced cachexia.Bioenergetic regulation of microglia.A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function.Oxidative Stress: Mechanistic Insights into Inherited Mitochondrial Disorders and Parkinson's Disease.Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.Neuroprotective and anti-inflammatory effects of morin in a murine model of Parkinson's disease.Nrf2-Inducers Counteract Neurodegeneration in Frataxin-Silenced Motor Neurons: Disclosing New Therapeutic Targets for Friedreich's Ataxia.Contribution of the tRNAIle 4317A>G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A>G mutation.N-acetylcysteine and vitamin E rescue animal longevity and cellular oxidative stress in pre-clinical models of mitochondrial complex I disease.KH176 Safeguards Mitochondrial Diseased Cells from Redox Stress-Induced Cell Death by Interacting with the Thioredoxin System/Peroxiredoxin Enzyme Machinery.Altered Redox Homeostasis in Branched-Chain Amino Acid Disorders, Organic Acidurias, and Homocystinuria.Randomized dose-escalation trial of elamipretide in adults with primary mitochondrial myopathy.Nitroxyl Modified Tobacco Mosaic Virus as a Metal-Free High-Relaxivity MRI and EPR Active Superoxide SensorCurrent and Emerging Treatment Modalities for Leber's Hereditary Optic Neuropathy: A Review of the Literature
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Oxidative stress in inherited mitochondrial diseases.
@en
type
label
Oxidative stress in inherited mitochondrial diseases.
@en
prefLabel
Oxidative stress in inherited mitochondrial diseases.
@en
P2860
P1476
Oxidative stress in inherited mitochondrial diseases.
@en
P2093
Genki Hayashi
Gino Cortopassi
P2860
P356
10.1016/J.FREERADBIOMED.2015.05.039
P577
2015-06-11T00:00:00Z