about
Dysregulated axonal RNA translation in amyotrophic lateral sclerosisMeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female ratsMutant PFN1 causes ALS phenotypes and progressive motor neuron degeneration in mice by a gain of toxicity.Modelling amyotrophic lateral sclerosis: progress and possibilitiesCompartment-dependent mitochondrial alterations in experimental ALS, the effects of mitophagy and mitochondriogenesisALS skeletal muscle shows enhanced TGF-β signaling, fibrosis and induction of fibro/adipogenic progenitor markers.Macrophage-mediated inflammation and glial response in the skeletal muscle of a rat model of familial amyotrophic lateral sclerosis (ALS)Early Cognitive/Social Deficits and Late Motor Phenotype in Conditional Wild-Type TDP-43 Transgenic Mice.New Insights on the Mechanisms of Disease Course Variability in ALS from Mutant SOD1 Mouse Models.Advances in the Development of Disease-Modifying Treatments for Amyotrophic Lateral Sclerosis.Drugs in clinical development for the treatment of amyotrophic lateral sclerosis.Impact of high iron intake on cognition and neurodegeneration in humans and in animal models: a systematic review.Bridging the gap: large animal models in neurodegenerative research.ALS/FTLD: experimental models and reality.Altered Intracellular Milieu of ADAR2-Deficient Motor Neurons in Amyotrophic Lateral SclerosisAntisense Oligonucleotides: Translation from Mouse Models to Human Neurodegenerative Diseases.Motoneuron Disease: Basic Science.TDP-43 in the spectrum of MND-FTLD pathologies.Fine-Tuning ER Stress Signal Transducers to Treat Amyotrophic Lateral Sclerosis.The Dual Role of Microglia in ALS: Mechanisms and Therapeutic Approaches.An amyotrophic lateral sclerosis-linked mutation in GLE1 alters the cellular pool of human Gle1 functional isoforms.Inflammatory and non-inflammatory monocytes as novel prognostic biomarkers of survival in SOD1G93A mouse model of Amyotrophic Lateral Sclerosis.NLRP3 Inflammasome Activation in a Transgenic Amyotrophic Lateral Sclerosis Model.Disruption of calcitonin gene-related peptide signaling accelerates muscle denervation and dampens cytotoxic neuroinflammation in SOD1 mutant mice.TDP-43 gains function due to perturbed autoregulation in a Tardbp knock-in mouse model of ALS-FTD.Temporospatial Analysis and New Players in the Immunology of Amyotrophic Lateral Sclerosis.Profile of Arachidonic Acid-Derived Inflammatory Markers and Its Modulation by Nitro-Oleic Acid in an Inherited Model of Amyotrophic Lateral Sclerosis.Kir4.1-Dependent Astrocyte-Fast Motor Neuron Interactions Are Required for Peak Strength.RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis.Safety and efficacy of human embryonic stem cell-derived astrocytes following intrathecal transplantation in SOD1G93A and NSG animal models.
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Rodent Models of Amyotrophic Lateral Sclerosis
@ast
Rodent Models of Amyotrophic Lateral Sclerosis
@en
type
label
Rodent Models of Amyotrophic Lateral Sclerosis
@ast
Rodent Models of Amyotrophic Lateral Sclerosis
@en
prefLabel
Rodent Models of Amyotrophic Lateral Sclerosis
@ast
Rodent Models of Amyotrophic Lateral Sclerosis
@en
P2860
P1476
Rodent Models of Amyotrophic Lateral Sclerosis
@en
P2093
Jeffrey D Rothstein
Thomas Philips
P2860
P304
P356
10.1002/0471141755.PH0567S69
P577
2015-06-01T00:00:00Z