Boosting the peripheral immune response in the skeletal muscles improved motor function in ALS transgenic mice - ScienceDirect
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience
Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration | PNAS
DOK7 gene therapy enhances motor activity and life span in ALS model mice | EMBO Molecular Medicine
ALS-like phenotypes of HB9:Cre–Tardbp lx/ mice. A, top, time scale of... | Download Scientific Diagram
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
Researchers Identify Potential New Approach for Improving Quality of Life for ALS Patients - Neuroscience News
Amyotrophic Lateral Sclerosis: Marking the differences in motoneurons | eLife
Amyotrophic Lateral Sclerosis disease - QPS Austria
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
Microendoscopy detects altered muscular contractile dynamics in a mouse model of amyotrophic lateral sclerosis | Scientific Reports
Increasing MuSK Activity Delays Denervation and Improves Motor Function in ALS Mice - ScienceDirect
A major step towards the cure of sporadic ALS | The University of Tokyo
Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS
Could CRISPR help develop a cure for ALS? Read our blog
ALS Association Greater New York | New Jersey | Long Island | Hudson Valley
Realizing the gains and losses in C9ORF72 ALS/FTD | Nature Neuroscience
Zuoshang Xu Lab - University of Massachusetts Chan Medical School
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model
Drug target validation in mouse models of ALS. (A) Comparison between... | Download Scientific Diagram
Opposite Synaptic Alterations at the Neuromuscular Junction in an ALS Mouse Model: When Motor Units Matter | Journal of Neuroscience
Optimised and Rapid Pre-clinical Screening in the SOD1G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis (ALS) | PLOS ONE
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration | PNAS
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
Protective role of the gut microbiota in a mouse model of amyotrophic lateral sclerosis - YouTube
