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Gaucher’s Disease

Gaucher’s Disease Gaucher’s disease (GD), the most common lysomal storage disorder, is caused by lysosomal hydrolase glucocerebrosidase activity deficiency due to a mutation of the GBA gene. Generation of genetically modified animals that recapitulate GD symptoms in...

Spinal Muscular Atrophy

Spinal Muscular Atrophy Spinal muscular atrophy (SMA) is a rare autosomal recessive motor neurodegenerative disease and is the leading genetic cause of death among infants and toddlers. PsychoGenics has behaviorally characterized several mouse models of SMA.  ...

Rett Syndrome

Rett Syndrome View Fullscreen Amyotrophic Lateral SclerosisAlzheimer’s Disease and Frontotemporal DementiaASD and Neurodevelopment DisordersFragile X (FMR1 Mouse Model)Huntington′s DiseaseBrain & Spine Injury ModelsMuscular DystrophyParkinson′s DiseaseRett...

Parkinson′s Disease

Parkinson′s Disease Asyn Fibrils This is a presentation describing the Asyn Fibrils capabilities at PsychoGenics. Read More Line 61 This is a presentation describing the Line 61 capabilities at PsychoGenics. Read More Parkinson’s Disease: Validated Non-Genetic Animal...

Muscular Dystrophy

Muscular Dystrophy Duchenne muscular dystrophy (DMD) is an X-linked genetic disorder characterized by progressive muscle degeneration caused by the absence of dystrophin, a protein connecting the muscle fiber cytoskeleton to the extracellular matrix through the cell...