DYRK1A roles in human neural progenitors
DYRK1A roles in human neural progenitors
About this item
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Publisher
Switzerland: Frontiers Media S.A
Journal title
Language
English
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Publisher
Switzerland: Frontiers Media S.A
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Scope and Contents
Contents
Mutations in
(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-specificity kinase (tyrosine and serine/threonine) that plays a key role in various cellular processes and is a critical r...
Alternative Titles
Full title
DYRK1A roles in human neural progenitors
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_007876060561448e8985e8f58b97b4ae
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_007876060561448e8985e8f58b97b4ae
Other Identifiers
ISSN
1662-453X,1662-4548
E-ISSN
1662-453X
DOI
10.3389/fnins.2025.1533253
