Article
CDKL5 phosphorylates neuronal ELAVL proteins to promote mRNA binding, protein synthesis and visual cortex development
2026-04-07
Abstract excerpt
Loss-of-function mutations in the X-linked CDKL5 gene lead to a severe neurodevelopmental disorder characterized by early-onset epilepsy, known as CDKL5 Deficiency Disorder (CDD). Despite its clinical significance, the physiological substrates of the serine/threonine kinase CDKL5 and its roles in neuronal development remain poorly understood. To address this, we performed quantitative phosphoproteomics analysis in...
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Identifiers and source
- Literature Corpus work
- db3f726a-d853-5b17-bb6a-7d9034675bc5
- DOI
- 10.64898/2026.04.07.716766
