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Balancing serendipity and reproducibility: Pluripotent stem cells as experimental systems for intellectual and developmental disorders

Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) and their differentiation into neural lineages is a revolutionary experimental system for studying neurological disorders, including intellectual and developmental disabilities (IDDs). However, issues related to variability a...

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Detalles Bibliográficos
Autores principales: Anderson, Nickesha C., Chen, Pin-Fang, Meganathan, Kesavan, Afshar Saber, Wardiya, Petersen, Andrew J., Bhattacharyya, Anita, Kroll, Kristen L., Sahin, Mustafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190574/
https://www.ncbi.nlm.nih.gov/pubmed/33861989
http://dx.doi.org/10.1016/j.stemcr.2021.03.025
Descripción
Sumario:Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) and their differentiation into neural lineages is a revolutionary experimental system for studying neurological disorders, including intellectual and developmental disabilities (IDDs). However, issues related to variability and reproducibility have hindered translating preclinical findings into drug discovery. Here, we identify areas for improvement by conducting a comprehensive review of 58 research articles that utilized iPSC-derived neural cells to investigate genetically defined IDDs. Based upon these findings, we propose recommendations for best practices that can be adopted by research scientists as well as journal editors.