Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).
about
Idebenone protects against retinal damage and loss of vision in a mouse model of Leber's hereditary optic neuropathyLow-level light therapy of the eye and brainThe CREB/CRE transcriptional pathway: protection against oxidative stress-mediated neuronal cell deathProfiling of oxidative stress in patients with inborn errors of metabolism.Müller cell reactivity in response to photoreceptor degeneration in rats with defective polycystin-2.LHON: Mitochondrial Mutations and More.Rotenone Susceptibility Phenotype in Olfactory Derived Patient Cells as a Model of Idiopathic Parkinson's DiseaseOgg1 null mice exhibit age-associated loss of the nigrostriatal pathway and increased sensitivity to MPTP.Mouse mtDNA mutant model of Leber hereditary optic neuropathy.Mitochondrial complex I inhibition is not required for dopaminergic neuron death induced by rotenone, MPP+, or paraquat.Neuroprotective effects of near-infrared light in an in vivo model of mitochondrial optic neuropathy.Inherited mitochondrial optic neuropathies.Müller glial cells in retinal disease.Oxidative damage to macromolecules in human Parkinson disease and the rotenone model.GABA and Glutamate Uptake and Metabolism in Retinal Glial (Müller) Cells.Mitochondrial dysfunction in central nervous system white matter disorders.Mitochondrial optic neuropathy: In vivo model of neurodegeneration and neuroprotective strategies.Therapeutic strategies for Leber's hereditary optic neuropathy: A current update.Rotenone-induced death of RGC-5 cells is caspase independent, involves the JNK and p38 pathways and is attenuated by specific green tea flavonoids.bFGF-mediated redox activation of the PI3K/Akt pathway in retinal photoreceptor cells.Neuroprotective effects of memantine in a mouse model of retinal degeneration induced by rotenone.Rotenone Induces the Formation of 4-Hydroxynonenal Aggresomes. Role of ROS-Mediated Tubulin Hyperacetylation and Autophagic Flux Disruption.Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease.Oxidative stress in Chinese patients with Leber's hereditary optic neuropathy.Administration of memantine and imipramine alters mitochondrial respiratory chain and creatine kinase activities in rat brain.
P2860
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P2860
Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Partial mitochondrial complex ...... itary Optic Neuropathy (LHON).
@en
Partial mitochondrial complex ...... er Hereditary Optic Neuropathy
@nl
type
label
Partial mitochondrial complex ...... itary Optic Neuropathy (LHON).
@en
Partial mitochondrial complex ...... er Hereditary Optic Neuropathy
@nl
prefLabel
Partial mitochondrial complex ...... itary Optic Neuropathy (LHON).
@en
Partial mitochondrial complex ...... er Hereditary Optic Neuropathy
@nl
P2093
P1476
Partial mitochondrial complex ...... itary Optic Neuropathy (LHON).
@en
P2093
Barry Derham
Carlo Ferrarese
John P M Wood
Lucio Tremolizzo
Neville N Osborne
P304
P356
10.1016/J.NBD.2006.07.016
P577
2006-09-07T00:00:00Z