Mitochondrial dysfunction in genetic animal models of Parkinson's disease
about
After the banquet: mitochondrial biogenesis, mitophagy, and cell survivalCircadian dysfunction may be a key component of the non-motor symptoms of Parkinson's disease: insights from a transgenic mouse modelAdaptive cellular stress pathways as therapeutic targets of dietary phytochemicals: focus on the nervous systemVPS35, the Retromer Complex and Parkinson's Disease.A time to reap, a time to sow: mitophagy and biogenesis in cardiac pathophysiologyImpairment of mitochondria in adult mouse brain overexpressing predominantly full-length, N-terminally acetylated human α-synucleinMitochondrial Dysfunction and α-Synuclein Synaptic Pathology in Parkinson's Disease: Who's on First?Photobiomodulation Suppresses Alpha-Synuclein-Induced Toxicity in an AAV-Based Rat Genetic Model of Parkinson's Disease.Physiological phenotype and vulnerability in Parkinson's diseaseAltered Mitochondrial Respiration and Other Features of Mitochondrial Function in Parkin-Mutant Fibroblasts from Parkinson's Disease Patients.High-dose thiamine as initial treatment for Parkinson's diseaseBrain iron homeostasis: from molecular mechanisms to clinical significance and therapeutic opportunitiesLRRK2 and vesicle trafficking.Autophagy: a critical regulator of cellular metabolism and homeostasis.Autophagy: a crucial moderator of redox balance, inflammation, and apoptosis in lung disease.Iron in neurodegenerative disorders of protein misfolding: a case of prion disorders and Parkinson's disease.The impact of autophagy on cell death modalities.Mitochondrial control of cell bioenergetics in Parkinson's disease.Sirtuins as modifiers of Parkinson's disease pathology.Metabolic Dysfunction in Parkinson's Disease: Bioenergetics, Redox Homeostasis and Central Carbon Metabolism.Autophagy: An Integral Component of the Mammalian Stress Response.Selective and Mechanically Robust Sensors for Electrochemical Measurements of Real-Time Hydrogen Peroxide Dynamics in Vivo.Neuroprotective effect of α-mangostin on mitochondrial dysfunction and α-synuclein aggregation in rotenone-induced model of Parkinson's disease in differentiated SH-SY5Y cells.Trehalose Inhibits A53T Mutant α-Synuclein Overexpression and Neurotoxicity in Transduced PC12 Cells.Treadmill Exercise Attenuates α-Synuclein Levels by Promoting Mitochondrial Function and Autophagy Possibly via SIRT1 in the Chronic MPTP/P-Induced Mouse Model of Parkinson's Disease.Circadian Dysfunction in Parkinson's Disease
P2860
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P2860
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@ast
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@en
type
label
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@ast
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@en
prefLabel
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@ast
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@en
P2860
P356
P1476
Mitochondrial dysfunction in genetic animal models of Parkinson's disease
@en
P2093
Darren J Moore
P2860
P304
P356
10.1089/ARS.2011.4200
P577
2011-10-04T00:00:00Z