About: ALS: a disease of motor neurons and their nonneuronal neighbors

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scientific article (publication date: 5 October 2006)

Attributes	Values
rdf:type	Item
description	article scientifique publié en 2006 (fr) artículu científicu espublizáu en 2006 (ast) 2006 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy) 2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в жовтні 2006 (uk) مقالة علمية (نشرت في 5-10-2006) (ar) wetenschappelijk artikel (gepubliceerd op 2006/10/05) (nl) im Oktober 2006 veröffentlichter wissenschaftlicher Artikel (de) scientific article (publication date: 5 October 2006) (en)
publication date	wds:Q29618000-8B6E215C-4F70-4D59-B84F-396285B57BBE
publication date	2006-10-05 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q29618000-B5D7EF13-F368-4F95-B674-7D429CF0B1A4
language of work or name	English
author name string	wds:Q29618000-55776D78-41EE-41F4-977E-6F1A9F370202 wds:Q29618000-675056DD-ADFC-46CD-B190-8C8E316327F1 wds:Q29618000-A36D8D39-6C8A-4C15-8C21-485FE3979796
OpenCitations bibliographic resource ID	wds:Q29618000-06015DE8-67AD-42E9-880B-89D7E06D47C7
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/848073
author name string	Boillée S Cleveland DW Vande Velde C
OpenCitations bibliographic resource ID	848073
rdfs:label	ALS: a disease of motor neurons and their nonneuronal neighbors (en) ALS: a disease of motor neurons and their nonneuronal neighbors (ast)
skos:prefLabel	ALS: a disease of motor neurons and their nonneuronal neighbors (en) ALS: a disease of motor neurons and their nonneuronal neighbors (ast)
name	ALS: a disease of motor neurons and their nonneuronal neighbors (en) ALS: a disease of motor neurons and their nonneuronal neighbors (ast)
title	wds:Q29618000-7AD97F7B-48DB-4F30-9510-12C46656D93E
title	ALS: a disease of motor neurons and their nonneuronal neighbors (en)
page(s)	wds:Q29618000-5BC51504-C601-442E-84E6-B53BA55F550E
page(s)	39-59
instance of	wds:Q29618000-C337F3AA-CE49-4186-877C-593F4F18339E wds:Q29618000-c5d631e6-4df7-4597-825c-22b3f9f8518a
instance of	review article scholarly article
main subject	wds:Q29618000-AA3C3502-973F-4699-A797-A5B5A01F906D
main subject	amyotrophic lateral sclerosis
PubMed ID	wds:Q29618000-5F9A88CB-7541-4359-9F13-485C76945076
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17015226
PubMed ID	17015226
published in	wds:Q29618000-E645E42D-FC90-4CE1-B12F-98B37937BE48
published in	Neuron
issue	wds:Q29618000-96BA5A09-FE65-473F-8D1C-7B299706F2EA
volume	wds:Q29618000-BDB8EAD0-9828-4A27-A0D0-998B2ED9C4EC
issue	1
volume	52
DOI	wds:Q29618000-805196B7-CBD2-4867-8F60-ACC0893C3628
DOI	http://dx.doi.org/10.1016/J.NEURON.2006.09.018
DOI	10.1016/J.NEURON.2006.09.018
ResearchGate publication ID	wds:Q29618000-7C89B323-FF50-4A94-9153-74A78D51EC82
ResearchGate publication ID	6780305
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q29618000
is cites work of	Endogenous regulatory T lymphocytes ameliorate amyotrophic lateral sclerosis in mice and correlate with disease progression in patients with amyotrophic lateral sclerosis Regulatory T-lymphocytes mediate amyotrophic lateral sclerosis progression and survival CD4+ T cells support glial neuroprotection, slow disease progression, and modify glial morphology in an animal model of inherited ALS. Deregulation of TDP-43 in amyotrophic lateral sclerosis triggers nuclear factor κB-mediated pathogenic pathways The Neuroinflammatory Response in ALS: The Roles of Microglia and T Cells ER stress in Alzheimer's disease: a novel neuronal trigger for inflammation and Alzheimer's pathology ER stress and unfolded protein response in amyotrophic lateral sclerosis T cell-microglial dialogue in Parkinson's disease and amyotrophic lateral sclerosis: are we listening? The "dying-back" phenomenon of motor neurons in ALS. Deficits in axonal transport precede ALS symptoms in vivo Revisiting oxidative damage in ALS: microglia, Nox, and mutant SOD1 Axonal transport deficits and degeneration can evolve independently in mouse models of amyotrophic lateral sclerosis. Riluzole exerts central and peripheral modulating effects in amyotrophic lateral sclerosis. Autophagy induction enhances TDP43 turnover and survival in neuronal ALS models. Transcranial magnetic stimulation and amyotrophic lateral sclerosis: pathophysiological insights Heat shock transcription factor 1 as a therapeutic target in neurodegenerative diseases Loss of ALS2/Alsin exacerbates motor dysfunction in a SOD1-expressing mouse ALS model by disturbing endolysosomal trafficking Genetics of motor neuron disorders: new insights into pathogenic mechanisms MicroRNA-206: a potential circulating biomarker candidate for amyotrophic lateral sclerosis Resveratrol improves motoneuron function and extends survival in SOD1(G93A) ALS mice. The changing scene of amyotrophic lateral sclerosis Isoprostanes and neuroprostanes as biomarkers of oxidative stress in neurodegenerative diseases Synergistic effects of GDNF and VEGF on lifespan and disease progression in a familial ALS rat model The prostaglandin E2 EP2 receptor accelerates disease progression and inflammation in a model of amyotrophic lateral sclerosis Glutamate transporters and the excitotoxic path to motor neuron degeneration in amyotrophic lateral sclerosis Exercise and amyotrophic lateral sclerosis Motoneuron survival is promoted by specific exercise in a mouse model of amyotrophic lateral sclerosis TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia Therapeutic potential of mood stabilizers lithium and valproic acid: beyond bipolar disorder Mutant TDP-43 and FUS cause age-dependent paralysis and neurodegeneration in C. elegans FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patients Molecular actions and therapeutic potential of lithium in preclinical and clinical studies of CNS disorders A fruitful endeavor: modeling ALS in the fruit fly Neuromuscular effects of G93A-SOD1 expression in zebrafish. A drosophila model for amyotrophic lateral sclerosis reveals motor neuron damage by human SOD1. Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouse. Species-dependent neuropathology in transgenic SOD1 pigs Differential Roles of M1 and M2 Microglia in Neurodegenerative Diseases Novel telomerase-increasing compound in mouse brain delays the onset of amyotrophic lateral sclerosis Neuron-specific expression of mutant superoxide dismutase is sufficient to induce amyotrophic lateral sclerosis in transgenic mice Role of the Sigma-1 receptor in Amyotrophic Lateral Sclerosis (ALS) Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis Reduction of circulating endothelial cells in peripheral blood of ALS patients

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