Abstract
Among motor neuron diseases, spinal muscular atrophy type 1 and amyotrophic lateral sclerosis are very aggressive diseases with no cure. With the breakthrough of human induced pluripotent stem cells, iPS, researchers have now at their disposal a powerful tool to generate human motor neurons in culture and study the pathological defects in patient cells. In this review, we will see which tools for the study of patients motoneurons were developed from iPS cells and the different cellular models that were generated. We will also see how these models were validated and current research to identify new therapeutic leads.
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CITATION STYLE
Bohl, D. (2016). Les cellules neuronales dérivées des cellules souches pluripotentes induites humaines: Modélisation des maladies du motoneurone. Biologie Aujourd’hui, 210(1), 27–36. https://doi.org/10.1051/jbio/2016004
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