Modulation of lipid peroxidation and mitochondrial function improves neuropathology in Huntington's disease mice
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Mitochondrial Dysfunction in Cancer and Neurodegenerative Diseases: Spotlight on Fatty Acid Oxidation and Lipoperoxidation ProductsMouse models of polyglutamine diseases in therapeutic approaches: review and data table. Part II.Mitochondrial lipids in neurodegenerationIdentification of hepta-histidine as a candidate drug for Huntington's disease by in silico-in vitro- in vivo-integrated screens of chemical librariesThe aggregation and inheritance of damaged proteins determines cell fate during mitosis.Autophagy and mitochondrial alterations in human retinal pigment epithelial cells induced by ethanol: implications of 4-hydroxy-nonenal.Ferrostatins inhibit oxidative lipid damage and cell death in diverse disease modelsPhospholipase A2 - nexus of aging, oxidative stress, neuronal excitability, and functional decline of the aging nervous system? Insights from a snail model system of neuronal aging and age-associated memory impairmentOxidative stress in neurodegenerative diseases: mechanisms and therapeutic perspectivesInteraction of aldehydes derived from lipid peroxidation and membrane proteinsPotential biomarkers to follow the progression and treatment response of Huntington's disease.4-Hydroxy-2-nonenal, a reactive product of lipid peroxidation, and neurodegenerative diseases: a toxic combination illuminated by redox proteomics studiesAntioxidants in Huntington's disease.Lipid peroxidation triggers neurodegeneration: a redox proteomics view into the Alzheimer disease brain.Paradoxical cellular effects and biological role of the multifaceted compound nordihydroguaiaretic acid.Huntington's Disease: Pathogenic Mechanisms and Therapeutic Targets.Neurite transection produces cytosolic oxidation, which enhances plasmalemmal repair.Larrea tridentata: A novel source for anti-parasitic agents active against Entamoeba histolytica, Giardia lamblia and Naegleria fowleri.Effect of Quercetin in the 1-Methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine-Induced Mouse Model of Parkinson's Disease.Mitochondrial modulators improve lipid composition and attenuate memory deficits in experimental model of Huntington's disease.Rotenone Induces the Formation of 4-Hydroxynonenal Aggresomes. Role of ROS-Mediated Tubulin Hyperacetylation and Autophagic Flux Disruption.Postnatal melatonin treatment protects against affective disorders induced by early-life immune stimulation by reducing the microglia cell activation and oxidative stress.Remodeling of heterochromatin structure slows neuropathological progression and prolongs survival in an animal model of Huntington's disease.
P2860
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P2860
Modulation of lipid peroxidation and mitochondrial function improves neuropathology in Huntington's disease mice
description
2010 nî lūn-bûn
@nan
2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@ast
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@en
type
label
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@ast
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@en
prefLabel
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@ast
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@en
P2093
P2860
P1476
Modulation of lipid peroxidati ...... y in Huntington's disease mice
@en
P2093
Bela Kosaras
Junghee Lee
Kerry Cormier
Neil W Kowall
Rajiv R Ratan
Steve J Del Signore
P2860
P2888
P304
P356
10.1007/S00401-010-0788-5
P577
2010-12-16T00:00:00Z