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Dosage Counts: Correcting Trisomy-21-Related Phenotypes in Human Organoids and Xenografts.

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Studies in mice suggest that Olig2 gene dosage alters cerebral cortical interneuron development and contributes to trisomy-21/Down-syndrome-related intellectual disability. Xu et al. (2019) extend these studies through the remarkable use of… Click to show full abstract

Studies in mice suggest that Olig2 gene dosage alters cerebral cortical interneuron development and contributes to trisomy-21/Down-syndrome-related intellectual disability. Xu et al. (2019) extend these studies through the remarkable use of cerebral organoid and human iPSC/mouse brain chimera experimental systems that provide an opportunity for the development of novel therapeutics.

Keywords: trisomy related; correcting trisomy; related phenotypes; dosage counts; dosage; counts correcting

Journal Title: Cell stem cell
Year Published: 2019

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