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Boosting the peripheral immune response in the skeletal muscles improved motor function in ALS transgenic mice - ScienceDirect
Boosting the peripheral immune response in the skeletal muscles improved motor function in ALS transgenic mice - ScienceDirect

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

Innate immune adaptor TRIF confers neuroprotection in ALS mice by eliminating abnormal glial cells | Asia Research News
Innate immune adaptor TRIF confers neuroprotection in ALS mice by eliminating abnormal glial cells | Asia Research News

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

A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model - ScienceDirect
A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model - ScienceDirect

IJMS | Free Full-Text | Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives
IJMS | Free Full-Text | Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives

Metabolic changes in an animal model of amyotrophic lateral sclerosis evaluated by [18F]-FDG positron emission tomography | Translational Neurodegeneration | Full Text
Metabolic changes in an animal model of amyotrophic lateral sclerosis evaluated by [18F]-FDG positron emission tomography | Translational Neurodegeneration | Full Text

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

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

CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background | Scientific Reports
CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background | Scientific Reports

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

Researchers Identify Potential New Approach for Improving Quality of Life for ALS Patients - Neuroscience News
Researchers Identify Potential New Approach for Improving Quality of Life for ALS Patients - Neuroscience News

Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model

Frontiers | The usage and advantages of several common amyotrophic lateral sclerosis animal models
Frontiers | The usage and advantages of several common amyotrophic lateral sclerosis animal models

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

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

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

Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy - ScienceDirect
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy - ScienceDirect

Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis
Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis

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

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

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