about
Misfolded CuZnSOD and amyotrophic lateral sclerosisALS-associated mutant SOD1G93A causes mitochondrial vacuolation by expansion of the intermembrane space and by involvement of SOD1 aggregation and peroxisomesThe complex molecular biology of amyotrophic lateral sclerosis (ALS)Ablation of the Ferroptosis Inhibitor Glutathione Peroxidase 4 in Neurons Results in Rapid Motor Neuron Degeneration and Paralysis.Induction by beta-bungarotoxin of apoptosis in cultured hippocampal neurons is mediated by Ca(2+)-dependent formation of reactive oxygen species.Sporadic amyotrophic lateral sclerosis: a hypothesis of persistent (non-lytic) enteroviral infection.The crucial role of caspase-9 in the disease progression of a transgenic ALS mouse model.Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathologyDorfin prevents cell death by reducing mitochondrial localizing mutant superoxide dismutase 1 in a neuronal cell model of familial amyotrophic lateral sclerosis.Influence of methylene blue on microglia-induced inflammation and motor neuron degeneration in the SOD1(G93A) model for ALS.Spinal cord endoplasmic reticulum stress associated with a microsomal accumulation of mutant superoxide dismutase-1 in an ALS modelProtein kinase Cepsilon binds peripherin and induces its aggregation, which is accompanied by apoptosis of neuroblastoma cells.Lack of a synergistic effect of a non-viral ALS gene therapy based on BDNF and a TTC fusion molecule.Neurodegeneration: what is it and where are we?Motor neuron trophic factors: therapeutic use in ALS?Molecular and cellular pathways of neurodegeneration in motor neurone diseaseMultidisciplinary Interventions in Motor Neuron Disease.Lipid peroxidation, oxidative stress genes and dietary factors in breast cancer protection: a hypothesisAmyotrophic lateral sclerosis: a consensus viewpoint on designing and implementing a clinical trial.Molecular targets for neuroprotection.Mitochondria in amyotrophic lateral sclerosis: a trigger and a target.Amyotrophic lateral sclerosis: all roads lead to Rome.Skeletal muscle in motor neuron diseases: therapeutic target and delivery route for potential treatments.TDP-43 and ubiquitinated cytoplasmic aggregates in sporadic ALS are low frequency and widely distributed in the lower motor neuron columns independent of disease spread.Characterization of early pathogenesis in the SOD1(G93A) mouse model of ALS: part I, background and methods.Mechanisms for activating Cu- and Zn-containing superoxide dismutase in the absence of the CCS Cu chaperone.Species-dependent neuropathology in transgenic SOD1 pigs.Review: The role of mitochondria in the pathogenesis of amyotrophic lateral sclerosis.Emerging drugs for amyotrophic lateral sclerosis.How can we improve clinical trials in amyotrophic lateral sclerosis?Vitamin D as a potential therapy in amyotrophic lateral sclerosis.Pericytes Extend Survival of ALS SOD1 Mice and Induce the Expression of Antioxidant Enzymes in the Murine Model and in IPSCs Derived Neuronal Cells from an ALS Patient.Computing disease-linked SOD1 mutations: deciphering protein stability and patient-phenotype relations.Hypoxia causes autophagic stress and derangement of metabolic adaptation in a cell model of amyotrophic lateral sclerosis.Huperzine A provides neuroprotection against several cell death inducers using in vitro model systems of motor neuron cell death.Mitochondrial damage modulates alternative splicing in neuronal cells: implications for neurodegeneration.Characterization of the caspase cascade in a cell culture model of SOD1-related familial amyotrophic lateral sclerosis: expression, activation and therapeutic effects of inhibition.The arachidonic acid 5-lipoxygenase inhibitor nordihydroguaiaretic acid inhibits tumor necrosis factor alpha activation of microglia and extends survival of G93A-SOD1 transgenic mice.Implications of white matter damage in amyotrophic lateral sclerosis (Review).Is amyotrophic lateral sclerosis a mitochondrial channelopathy?
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Programmed cell death in amyotrophic lateral sclerosis
@ast
Programmed cell death in amyotrophic lateral sclerosis
@en
Programmed cell death in amyotrophic lateral sclerosis
@nl
type
label
Programmed cell death in amyotrophic lateral sclerosis
@ast
Programmed cell death in amyotrophic lateral sclerosis
@en
Programmed cell death in amyotrophic lateral sclerosis
@nl
prefLabel
Programmed cell death in amyotrophic lateral sclerosis
@ast
Programmed cell death in amyotrophic lateral sclerosis
@en
Programmed cell death in amyotrophic lateral sclerosis
@nl
P2860
P356
P1476
Programmed cell death in amyotrophic lateral sclerosis
@en
P2093
Christelle Guégan
P2860
P304
P356
10.1172/JCI200317610
P407
P577
2003-01-01T00:00:00Z