Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis
File:ALS animal models.jpg - Wikimedia Commons
Working with ALS Mice: Guidelines for Preclinical Testing and Colony Management
Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS
Loss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy - ScienceDirect
Full article: Amyotrophic lateral sclerosis and intestinal microbiota—toward establishing cause and effect
Multiple strategy with bone marrow cells to treat ALS - UABDivulga Barcelona Research & Innovation
Murine Models of Neurodegenerative Diseases - Maze Engineers
Drug target validation in mouse models of ALS. (A) Comparison between... | Download Scientific Diagram
A major step towards the cure of sporadic ALS | The University of Tokyo
IJMS | Free Full-Text | Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse Model
Opinion: more mouse models and more translation needed for ALS | Molecular Neurodegeneration | Full Text
Amyotrophic Lateral Sclerosis ALS models | Sylics - Research Solutions in Neuroscience
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
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
Neuromuscular Junction Dysfunction in Amyotrophic Lateral Sclerosis | SpringerLink
Frontiers | Circadian Rhythm Dysfunction Accelerates Disease Progression in a Mouse Model With Amyotrophic Lateral Sclerosis
Identification of novel neuroprotective molecule effective in ALS mouse models | The University of Tokyo
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration | PNAS
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic lateral sclerosis
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
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience
Amyotrophic lateral sclerosis (ALS):SOD1 mouse helps researchers identify immune component
