Laetitia Cobret
Rue Charles Sadron
Orleans, 45071, France
Orleans, 45071, France
Last Updated: 09/26/2026
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Found 10 publications
Pathogenic missense variants of CSNK2B associated with Poirier-Bienvenu neurodevelopmental disorder impact differently on CK2 holoenzyme formation.
Journal: Biological chemistry
Published: December 20, 2024
Missense mutation in the activation segment of the kinase CK2 models Okur-Chung neurodevelopmental disorder and alters the hippocampal glutamatergic synapse.
Journal: Molecular psychiatry
Published: October 20, 2023
BRET Analysis of GPCR Dimers in Neurons and Non-Neuronal Cells: Evidence for Inactive, Agonist, and Constitutive Conformations.
Journal: International journal of molecular sciences
Published: September 03, 2021
The NLRP3 p.A441V Mutation in NLRP3-AID Pathogenesis: Functional Consequences, Phenotype-Genotype Correlations and Evidence for a Recurrent Mutational Event.
Journal: ACR open rheumatology
Published: November 29, 2019
Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria.
Journal: The Journal of investigative dermatology
Published: March 05, 2019
Physical interaction between neurofibromin and serotonin 5-HT6 receptor promotes receptor constitutive activity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: October 30, 2016
Targeting the cis-dimerization of LINGO-1 with low MW compounds affects its downstream signalling.
Journal: British journal of pharmacology
Published: March 06, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026