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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

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

Figure 4 from Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies. | Semantic Scholar
Figure 4 from Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies. | Semantic Scholar

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

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

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

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

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

New ALS mouse models more closely mimic the human disease | The Robert Packard Center for ALS Research at Johns Hopkins
New ALS mouse models more closely mimic the human disease | The Robert Packard Center for ALS Research at Johns Hopkins

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

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

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

Microendoscopy detects altered muscular contractile dynamics in a mouse model of amyotrophic lateral sclerosis | Scientific Reports
Microendoscopy detects altered muscular contractile dynamics in a mouse model of amyotrophic lateral sclerosis | Scientific Reports

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

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration | PNAS
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration | PNAS

Multiple strategy with bone marrow cells to treat ALS - UABDivulga Barcelona Research & Innovation
Multiple strategy with bone marrow cells to treat ALS - UABDivulga Barcelona Research & Innovation

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

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

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

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

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

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

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

Amyotrophic Lateral Sclerosis: Marking the differences in motoneurons | eLife
Amyotrophic Lateral Sclerosis: Marking the differences in motoneurons | eLife

Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London

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

ALS Gene Therapy SynCav1 Found to Extend Survival in Mouse Model | Experimental Therapy Also Delayed Disease Onset, Regardless of Cause | ALS News Today
ALS Gene Therapy SynCav1 Found to Extend Survival in Mouse Model | Experimental Therapy Also Delayed Disease Onset, Regardless of Cause | ALS News Today

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