Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
Identification of novel neuroprotective molecule effective in ALS mouse models | The University of Tokyo
Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS
Relative changes in body weight, clinical score and survival in ALS... | Download Scientific Diagram
Increasing MuSK Activity Delays Denervation and Improves Motor Function in ALS Mice - ScienceDirect
Drug target validation in mouse models of ALS. (A) Comparison between... | Download Scientific Diagram
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
A major step towards the cure of sporadic ALS | The University of Tokyo
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
Development of ALS-like phenotype and pathology in the hSOD1T116X... | Download Scientific Diagram
Neurimmune's anti-SOD1 antibody shows promise in ALS mouse studies | Fierce Biotech
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
Full article: Amyotrophic lateral sclerosis and intestinal microbiota—toward establishing cause and effect
IJMS | Free Full-Text | Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse Model
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
Multiple strategy with bone marrow cells to treat ALS - UABDivulga Barcelona Research & Innovation
Working with ALS Mice: Guidelines for Preclinical Testing and Colony Management
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration | PNAS
Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience
Stage-dependent remodeling of projections to motor cortex in ALS mouse model revealed by a new variant retrograde-AAV9 | eLife
Opinion: more mouse models and more translation needed for ALS | Molecular Neurodegeneration | Full Text
Capturing Symptoms of ALS in Mice♢ - Journal of Biological Chemistry
Researchers Identify Potential New Approach for Improving Quality of Life for ALS Patients - Neuroscience News
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
Motor neuronal protection by l-arginine prolongs survival of mutant SOD1 (G93A) ALS mice - ScienceDirect
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration | PNAS
