Frontiers | Circadian Rhythm Dysfunction Accelerates Disease Progression in a Mouse Model With Amyotrophic Lateral Sclerosis
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
Amyotrophic lateral sclerosis (ALS):SOD1 mouse helps researchers identify immune component
Boosting the peripheral immune response in the skeletal muscles improved motor function in ALS transgenic mice - ScienceDirect
Zuoshang Xu Lab - University of Massachusetts Chan Medical School
Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic lateral sclerosis
Human iPSC-derived neural progenitor cells secreting GDNF provide protection in rodent models of ALS and retinal degeneration - ScienceDirect
A major step towards the cure of sporadic ALS | The University of Tokyo
Working with ALS Mice: Guidelines for Preclinical Testing and Colony Management
IJMS | Free Full-Text | Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse Model
From Mouse Models to Human Disease: An Approach for Amyotrophic Lateral Sclerosis | In Vivo
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
Cortical Circuit Dysfunction as a Potential Driver of Amyotrophic Lateral Sclerosis
Murine Models of Neurodegenerative Diseases - Maze Engineers
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model
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
Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
November 2015 Pathomechanistic model mice of sporadic ALS: Conditional ADAR2 knockout mice AR2 | Experimental Animal Division (RIKEN BRC)
Amyotrophic Lateral Sclerosis: Marking the differences in motoneurons | eLife
Frontiers | Mouse Models of C9orf72 Hexanucleotide Repeat Expansion in Amyotrophic Lateral Sclerosis/ Frontotemporal Dementia
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse model of Amyotrophic Lateral Sclerosis | Semantic Scholar
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
File:ALS animal models.jpg - Wikimedia Commons
Laboratory Models of ALS - The ALS Association
