Article
The CB1 receptor interacts with cereblon and drives cereblon deficiency-associated memory shortfalls.
EMBO molecular medicine - 1 Apr 2024
Costas-Insua Carlos, Hermoso-López Alba, Moreno Estefanía, Montero-Fernández Carlos, Álvaro-Blázquez Alicia, Maroto Irene B, Sánchez-Ruiz Andrea, Diez-Alarcia Rebeca, Blázquez Cristina, Morales Paula, Canela Enric I, Casadó Vicent, Urigüen Leyre, Perea Gertrudis, Bellocchio Luigi, Rodríguez-Crespo Ignacio, Guzmán Manuel
Abstract excerpt
Cereblon/CRBN is a substrate-recognition component of the Cullin4A-DDB1-Roc1 E3 ubiquitin ligase complex. Destabilizing mutations in the human CRBN gene cause a form of autosomal recessive non-syndromic intellectual disability (ARNSID) that is modelled by knocking-out the mouse Crbn gene. A reduction in excitatory neurotransmission has been proposed as an underlying mechanism of the disease. However, the precise...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
