Humanising mice to enable modelling of neurodegenerative diseases | UCL Queen Square Institute of Neurology - UCL – University College London
![Metabolic changes in an animal model of amyotrophic lateral sclerosis evaluated by [18F]-FDG positron emission tomography | Translational Neurodegeneration | Full Text](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs40035-021-00246-1/MediaObjects/40035_2021_246_Fig1_HTML.png "Metabolic changes in an animal model of amyotrophic lateral sclerosis evaluated by [18F]-FDG positron emission tomography | Translational Neurodegeneration | Full Text")
Metabolic changes in an animal model of amyotrophic lateral sclerosis evaluated by [18F]-FDG positron emission tomography | Translational Neurodegeneration | Full Text
IJMS | Free Full-Text | Novel P2X7 Antagonist Ameliorates the Early Phase of ALS Disease and Decreases Inflammation and Autophagy in SOD1-G93A Mouse Model
Frontiers | Mouse Models of C9orf72 Hexanucleotide Repeat Expansion in Amyotrophic Lateral Sclerosis/ Frontotemporal Dementia
Innate immune adaptor TRIF confers neuroprotection in ALS mice by eliminating abnormal glial cells | Asia Research News
Frontiers | Neuroprotective Effects of Shenqi Fuzheng Injection in a Transgenic SOD1-G93A Mouse Model of Amyotrophic Lateral Sclerosis
IJMS | Free Full-Text | Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives
Rodent Amyotrophic Lateral Sclerosis (ALS) Model - Creative Biolabs
Identification of novel neuroprotective molecule effective in ALS mouse models | The University of Tokyo
Frontiers | The usage and advantages of several common amyotrophic lateral sclerosis animal models
Gut microbes tune inflammation and lifespan in a mouse model of amyotrophic lateral sclerosis
Murine Models of Neurodegenerative Diseases - Maze Engineers.
Opinion: more mouse models and more translation needed for ALS | Molecular Neurodegeneration | Full Text
Zuoshang Xu Lab - University of Massachusetts Chan Medical School
Rescuing potential of neurotrophic factors and miRNAs in preserving NMJ... | Download Scientific Diagram
Realizing the gains and losses in C9ORF72 ALS/FTD | Nature Neuroscience
Increasing MuSK Activity Delays Denervation and Improves Motor Function in ALS Mice - ScienceDirect
A New AAV10-U7-Mediated Gene Therapy Prolongs Survival and Restores Function in an ALS Mouse Model - ScienceDirect
Researchers Identify Potential New Approach for Improving Quality of Life for ALS Patients - Neuroscience News
Stage-dependent remodeling of projections to motor cortex in ALS mouse model revealed by a new variant retrograde-AAV9 | eLife
Full article: Amyotrophic lateral sclerosis and intestinal microbiota—toward establishing cause and effect
Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS–FTD-linked UBQLN2 mutations | PNAS
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model
Frontiers | Circadian Rhythm Dysfunction Accelerates Disease Progression in a Mouse Model With Amyotrophic Lateral Sclerosis
Modelling amyotrophic lateral sclerosis in rodents | Nature Reviews Neuroscience
Figure 3.1 from The neuromuscular transmission of the SOD 1 ( G 93 A ) mouse model of Amyotrophic Lateral Sclerosis | Semantic Scholar
MicroRNA-206 Delays ALS Progression and Promotes Regeneration of Neuromuscular Synapses in Mice | Science
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
