Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis. - Wikidata - awgldk - TriplyDB

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q39823079

about

Microglia centered pathogenesis in ALS: insights in cell interconnectivity Corticospinal-specific HCN expression in mouse motor cortex: I(h)-dependent synaptic integration as a candidate microcircuit mechanism involved in motor control Epigenetic regulation of motor neuron cell death through DNA methylation.A versatile water-soluble chelating and radical scavenging platform.Extraocular motoneurons of the adult rat show higher levels of vascular endothelial growth factor and its receptor Flk-1 than other cranial motoneurons.The wobbler mouse, an ALS animal model.Acute stimulation of transplanted neurons improves motoneuron survival, axon growth, and muscle reinnervation.Animal models for metabolic, neuromuscular and ophthalmological rare diseases.Corticostriatal connectivity and its role in disease Role of energy metabolic deficits and oxidative stress in excitotoxic spinal motor neuron degeneration in vivo.Motor Alterations Induced by Chronic 4-Aminopyridine Infusion in the Spinal Cord In vivo: Role of Glutamate and GABA Receptors Delayed administration of VEGF rescues spinal motor neurons from death with a short effective time frame in excitotoxic experimental models in vivo.Effect of intra-cisternal application of kainic acid on the spinal cord and locomotor activity in rats.Glycoursodeoxycholic acid reduces matrix metalloproteinase-9 and caspase-9 activation in a cellular model of superoxide dismutase-1 neurodegeneration.Quercetin prevents spinal motor neuron degeneration induced by chronic excitotoxic stimulus by a sirtuin 1-dependent mechanism.Mouse models of neurodegenerative disease: preclinical imaging and neurovascular component.

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P2860

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

http://www.wikidata.org/entity/Q39823079

description

2009 nî lūn-bûn

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2009年の論文

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年学术文章

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2009年學術文章

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2009年學術文章

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2009年學術文章

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name

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

@en

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

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type

label

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

@en

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

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prefLabel

Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

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Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

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Molecular Neurodegeneration

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Experimental models for the study of neurodegeneration in amyotrophic lateral sclerosis.

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P2093

Luis B Tovar-Y-Romo

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Luz Diana Santa-Cruz

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Ricardo Tapia

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P2860

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

SOD1 mutations disrupt redox-sensitive Rac regulation of NADPH oxidase in a familial ALS model

Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition

Unstable mutants in the peripheral endosomal membrane component ALS2 cause early-onset motor neuron disease

Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model

Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease

Determination and analysis of the 2 A-structure of copper, zinc superoxide dismutase

Glutamate uptake

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

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scholarly article

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10.1186/1750-1326-4-31

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4

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2009-07-20T00:00:00Z

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19619317

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amyotrophic lateral sclerosis

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2720968

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