Combined intramuscular and intraspinal transplant of bone marrow cells improves neuromuscular function in the SOD1G93A mice | Stem Cell Research & Therapy | Full Text
ALS-Linked SOD1 Mutants Enhance Neurite Outgrowth and Branching in Adult Motor Neurons
Optimised and Rapid Pre-clinical Screening in the SOD1G93A Transgenic Mouse Model of Amyotrophic Lateral Sclerosis (ALS) | PLOS ONE
General behavior of SOD1 G93A mice. (A) Body weight variations in... | Download Scientific Diagram
A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis | Science Translational Medicine
SOD1-G93A transgenic Mouse Models - QPS Neuropharmacology
Downregulating carnitine palmitoyl transferase 1 affects disease progression in the SOD1 G93A mouse model of ALS | Communications Biology
Frontiers | Human Motor Neurons With SOD1-G93A Mutation Generated From CRISPR/Cas9 Gene-Edited iPSCs Develop Pathological Features of Amyotrophic Lateral Sclerosis
Tempol improves neuroinflammation and delays motor dysfunction in a mouse model (SOD1G93A) of ALS | Journal of Neuroinflammation | Full Text
Targeting Extracellular Cyclophilin A Reduces Neuroinflammation and Extends Survival in a Mouse Model of Amyotrophic Lateral Sclerosis | Journal of Neuroscience
Simvastatin accelerated motoneurons death in SOD1G93A mice through inhibiting Rab7-mediated maturation of late autophagic vacuoles | Cell Death & Disease
Overexpression of MT-I in SOD1 G93A mice normalizes copper... | Download Scientific Diagram
Multimodal Actions of Neural Stem Cells in a Mouse Model of ALS: A Meta-Analysis | Science Translational Medicine
Overexpression of MT-I in SOD1 G93A mice ameliorates ALS-like... | Download Scientific Diagram
Parkin is a disease modifier in the mutant SOD1 mouse model of ALS | EMBO Molecular Medicine
Increasing MuSK Activity Delays Denervation and Improves Motor Function in ALS Mice - ScienceDirect
Amyotrophic Lateral Sclerosis disease - QPS Austria
Preliminary Observation about Alteration of Proteins and Their Potential Functions in Spinal Cord of SOD1 G93A Transgenic Mice
004435 - SOD1-G93A Strain Details
Neuron-Specific Expression of Mutant Superoxide Dismutase Is Sufficient to Induce Amyotrophic Lateral Sclerosis in Transgenic Mice | Journal of Neuroscience
002726 - SOD1-G93A Strain Details
Motor neuronal protection by l-arginine prolongs survival of mutant SOD1 ( G93A) ALS mice - ScienceDirect
Distinct roles for motor neuron autophagy early and late in the SOD1G93A mouse model of ALS | PNAS
SOD1-G93A transgenic Mouse Models - QPS Neuropharmacology
Molecular Chaperone Mediated Late-Stage Neuroprotection in the SOD1G93A Mouse Model of Amyotrophic Lateral Sclerosis | PLOS ONE
Molecules | Free Full-Text | A Novel Anti-Inflammatory d-Peptide Inhibits Disease Phenotype Progression in an ALS Mouse Model | HTML
