DYRK1A roles in human neural progenitors

IntroductionMutations in dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) represent one of the most prevalent monogenic causes of neurodevelopmental disorders (NDDs), often associated with intellectual developmental disorder and autism spectrum disorder. DYRK1A encodes a dual-s...

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Bibliographic Details
Main Authors: Jeremie Courraud, Angélique Quartier, Nathalie Drouot, Irene Zapata-Bodalo, Johan Gilet, Alexandra Benchoua, Jean-Louis Mandel, Amélie Piton
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2025.1533253/full