From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
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Safety, pharmacokinetic, and functional effects of the nogo-a monoclonal antibody in amyotrophic lateral sclerosis: a randomized, first-in-human clinical trialAxonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transportAberrant localization of FUS and TDP43 is associated with misfolding of SOD1 in amyotrophic lateral sclerosisSNP haplotype mapping in a small ALS familyPhenotype of transgenic mice carrying a very low copy number of the mutant human G93A superoxide dismutase-1 gene associated with amyotrophic lateral sclerosisMetallochaperones, an intracellular shuttle service for metal ions.Complex genetics of amyotrophic lateral sclerosis.A screen to identify cellular modulators of soluble levels of an amyotrophic lateral sclerosis (ALS)-causing mutant SOD1.A decade of CDK5.Potential therapeutic drugs and methods for the treatment of amyotrophic lateral sclerosis.Nicotinamide adenine dinucleotide phosphate oxidase in experimental liver fibrosis: GKT137831 as a novel potential therapeutic agent.Dynein mutations impair autophagic clearance of aggregate-prone proteins.Copper and zinc metallation status of copper-zinc superoxide dismutase from amyotrophic lateral sclerosis transgenic mice.Familial amyotrophic lateral sclerosis.Reduced oxidative damage in ALS by high-dose enteral melatonin treatment.Antisense therapy in neurologyMotor neuron trophic factors: therapeutic use in ALS?The Copper Metabolism MURR1 domain protein 1 (COMMD1) modulates the aggregation of misfolded protein species in a client-specific mannerReduction of axonal caliber does not alleviate motor neuron disease caused by mutant superoxide dismutase 1Caspase-1 and -3 are sequentially activated in motor neuron death in Cu,Zn superoxide dismutase-mediated familial amyotrophic lateral sclerosisProtein aggregation in motor neurone disorders.The genetics of motor neuron diseases.Motor neuron degeneration promotes neural progenitor cell proliferation, migration, and neurogenesis in the spinal cords of amyotrophic lateral sclerosis mice.Adaptive and maladaptive motor axonal sprouting in aging and motoneuron disease.Quantitative ultrastructural analysis of a single spinal cord demyelinated lesion predicts total lesion load, axonal loss, and neurological dysfunction in a murine model of multiple sclerosisAmyotrophic lateral sclerosis: contemporary concepts in etiopathogenesis and pharmacotherapy.Current clinical trials in amyotrophic lateral sclerosis.Regulation of motor neuron specification by phosphorylation of neurogenin 2Calpain-mediated signaling mechanisms in neuronal injury and neurodegenerationEffect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiers.Concomitant rheumatoid arthritis and amyotrophic lateral sclerosis: report of two new cases and review of literature.RNA-binding proteins with prion-like domains in ALS and FTLD-U.Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosis.Selective vulnerability of motoneuron and perturbed mitochondrial calcium homeostasis in amyotrophic lateral sclerosis: implications for motoneurons specific calcium dysregulation.A retrospective review of the progress in amyotrophic lateral sclerosis drug discovery over the last decade and a look at the latest strategies.Glycoprotein NMB: an Emerging Role in Neurodegenerative Disease.Minocycline and riluzole brain disposition: interactions with p-glycoprotein at the blood-brain barrier.Peripheral nerve avulsion injuries as experimental models for adult motoneuron degeneration.Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis.Foot pad skin biopsy in mouse models of hereditary neuropathy.
P2860
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P2860
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@ast
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@en
type
label
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@ast
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@en
prefLabel
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@ast
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.
@en
P1433
P1476
From Charcot to SOD1: mechanisms of selective motor neuron death in ALS
@en
P2093
D W Cleveland
P304
P356
10.1016/S0896-6273(00)81108-3
P407
P577
1999-11-01T00:00:00Z