Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS
File:ALS animal models.jpg - Wikimedia Commons
Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS | eNeuro
Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse model of Amyotrophic Lateral Sclerosis | 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
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis | In Vivo
ALS Animal Models - Disease Models | Target ALS
November 2015 Pathomechanistic model mice of sporadic ALS: Conditional ADAR2 knockout mice AR2 | Experimental Animal Division (RIKEN BRC)
Frontiers | Mouse Models of C9orf72 Hexanucleotide Repeat Expansion in Amyotrophic Lateral Sclerosis/ Frontotemporal Dementia
Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic lateral sclerosis
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration | PNAS
Drug target validation in mouse models of ALS. (A) Comparison between... | Download Scientific Diagram
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
In ALS Animal Model, Engineered Neural Cells Delay Disease, Extend Life
Neuroprotective effects of siRNAp11 in the SOD1-G93A mouse model of... | Download Scientific Diagram
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model - ScienceDirect
Working with ALS Mice: Guidelines for Preclinical Testing and Colony Management
Amyotrophic Lateral Sclerosis: Marking the differences in motoneurons | eLife
