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Tempol improves neuroinflammation and delays motor dysfunction in a mouse  model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text

Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic  lateral sclerosis
Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic lateral sclerosis

Cortical Circuit Dysfunction as a Potential Driver of Amyotrophic Lateral  Sclerosis
Cortical Circuit Dysfunction as a Potential Driver of Amyotrophic Lateral Sclerosis

AAV9-mediated gene delivery of MCT1 to oligodendrocytes does not provide a  therapeutic benefit in a mouse model of ALS: Molecular Therapy - Methods &  Clinical Development
AAV9-mediated gene delivery of MCT1 to oligodendrocytes does not provide a therapeutic benefit in a mouse model of ALS: Molecular Therapy - Methods & Clinical Development

MicroRNA-206 Delays ALS Progression and Promotes Regeneration of  Neuromuscular Synapses in Mice | Science
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science

Murine Models of Neurodegenerative Diseases - Maze Engineers
Murine Models of Neurodegenerative Diseases - Maze Engineers

Laboratory Models of ALS - The ALS Association
Laboratory Models of ALS - The ALS Association

Zuoshang Xu Lab - University of Massachusetts Chan Medical School
Zuoshang Xu Lab - University of Massachusetts Chan Medical School

Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews  Neuroscience
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience

Drug target validation in mouse models of ALS. (A) Comparison between... |  Download Scientific Diagram
Drug target validation in mouse models of ALS. (A) Comparison between... | Download Scientific Diagram

Opinion: more mouse models and more translation needed for ALS | Molecular  Neurodegeneration | Full Text
Opinion: more mouse models and more translation needed for ALS | Molecular Neurodegeneration | Full Text

Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS |  eNeuro
Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS | eNeuro

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions  characteristic of ALS and frontotemporal lobar degeneration | PNAS
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration | PNAS

File:ALS animal models.jpg - Wikimedia Commons
File:ALS animal models.jpg - Wikimedia Commons

Realizing the gains and losses in C9ORF72 ALS/FTD | Nature Neuroscience
Realizing the gains and losses in C9ORF72 ALS/FTD | Nature Neuroscience

SOD1-G93A Mouse Model - QPS Neuropharmacology
SOD1-G93A Mouse Model - QPS Neuropharmacology

Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs

Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse  model of Amyotrophic Lateral Sclerosis | Semantic Scholar
Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse model of Amyotrophic Lateral Sclerosis | Semantic Scholar

In ALS Animal Model, Engineered Neural Cells Delay Disease, Extend Life
In ALS Animal Model, Engineered Neural Cells Delay Disease, Extend Life

Motor neuron disease, TDP-43 pathology, and memory deficits in mice  expressing ALS–FTD-linked UBQLN2 mutations | PNAS
Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS

Amyotrophic lateral sclerosis (ALS):SOD1 mouse helps researchers identify  immune component
Amyotrophic lateral sclerosis (ALS):SOD1 mouse helps researchers identify immune component

IJMS | Free Full-Text | Brain Protease Activated Receptor 1 Pathway: A  Therapeutic Target in the Superoxide Dismutase 1 (SOD1) Mouse Model of Amyotrophic  Lateral Sclerosis
IJMS | Free Full-Text | Brain Protease Activated Receptor 1 Pathway: A Therapeutic Target in the Superoxide Dismutase 1 (SOD1) Mouse Model of Amyotrophic Lateral Sclerosis

Identification of novel neuroprotective molecule effective in ALS mouse  models | The University of Tokyo
Identification of novel neuroprotective molecule effective in ALS mouse models | The University of Tokyo

November 2015 Pathomechanistic model mice of sporadic ALS: Conditional  ADAR2 knockout mice AR2 | Experimental Animal Division (RIKEN BRC)
November 2015 Pathomechanistic model mice of sporadic ALS: Conditional ADAR2 knockout mice AR2 | Experimental Animal Division (RIKEN BRC)

A major step towards the cure of sporadic ALS | The University of Tokyo
A major step towards the cure of sporadic ALS | The University of Tokyo

Working with ALS Mice: Guidelines for Preclinical Testing and Colony  Management
Working with ALS Mice: Guidelines for Preclinical Testing and Colony Management