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Persistent neuronal stress signalling underlies Angelman syndrome phenotypes

Confidence95·multiple reportsImportance97NP-EVT-20261021-A60B264

Nature, Published online: 21 October 2026; doi:10.1038/s41586-026-11165-4 Genetic and proteomic analyses in human neurons and mouse models of Angelman syndrome (AS) show that loss of the ubiquitin ligase UBE3A leads to an overabundance of asparagine synthetase, and that this is linked with many AS phenotypes.

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Persistent neuronal stress signalling underlies Angelman syndrome phenotypes
Jason J. Yi · 10/21/2026, 12:00:00 AM
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