Motor Neuron diseases
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Characterizations
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RELATED DISEASE MODELS
discover our disease models
Neuro developmental disorders
We offer an extensive library of synaptopathy and genetic epilepsy iPSC lines. Our excitatory and inhibitory iNeurons with functional assays deliver reliable, high‑quality preclinical efficacy insights.
Read more »
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Motor Neuron diseases
Our human motor neuron–muscle co‑culture system models neuromuscular junctions and ALS‑related phenotypes, enabling precise evaluation of disease mechanisms and therapeutic effects in vitro.
Read more »
Neuro degenerative diseases
With expertise in Parkinson’s disease and dopaminergic iNeurons, we provide validated assays that reveal neurodegenerative mechanisms and support robust preclinical therapeutic assessment.
Read more »
Other Neurological disorders
Our validated human iNeuron models, functional activity assays, and in‑house CRISPR engineering enable tailored disease models that meet diverse research needs across neurological indications.
Read more »
-
Neuro developmental disorders
We offer an extensive library of synaptopathy and genetic epilepsy iPSC lines. Our excitatory and inhibitory iNeurons with functional assays deliver reliable, high‑quality preclinical efficacy insights.
Read more »
-
Motor Neuron diseases
Our human motor neuron–muscle co‑culture system models neuromuscular junctions and ALS‑related phenotypes, enabling precise evaluation of disease mechanisms and therapeutic effects in vitro.
Read more »
-
Neuro degenerative diseases
With expertise in Parkinson’s disease and dopaminergic iNeurons, we provide validated assays that reveal neurodegenerative mechanisms and support robust preclinical therapeutic assessment.
Read more »
-
Neuro developmental disorders
We offer an extensive library of synaptopathy and genetic epilepsy iPSC lines. Our excitatory and inhibitory iNeurons with functional assays deliver reliable, high‑quality preclinical efficacy insights.
Read more »
-
Motor Neuron diseases
Our human motor neuron–muscle co‑culture system models neuromuscular junctions and ALS‑related phenotypes, enabling precise evaluation of disease mechanisms and therapeutic effects in vitro.
Read more »
