Pierre Billuart

Paris, 75014, France

Last Updated: 09/26/2026

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Found 39 publications

Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures.

Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures.

Journal: International journal of molecular sciences

Published: November 22, 2022

Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.

Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.

Journal: Biomedicines

Published: October 23, 2022

Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization.

Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization.

Journal: Biological psychiatry

Published: June 30, 2022

Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1.

Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1.

Journal: Cells

Published: February 25, 2022

Astrocytes close the mouse critical period for visual plasticity.

Astrocytes close the mouse critical period for visual plasticity.

Journal: Science (New York, N.Y.)

Published: November 01, 2020

A role for astrocytes in intellectual disabilities?

A role for astrocytes in intellectual disabilities?

Journal: Medecine sciences : M/S

Published: October 07, 2020

A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans.

A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3' end processing is associated with intellectual disability in humans.

Journal: Nucleic acids research

Published: January 30, 2020

ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual Disability.

ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual Disability.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: February 27, 2019

Do Astrocytes Play a Role in Intellectual Disabilities?

Do Astrocytes Play a Role in Intellectual Disabilities?

Journal: Trends in neurosciences

Published: February 25, 2019

The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migration.

The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migration.

Journal: Glia

Published: August 31, 2018

Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.

Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.

Journal: Gene

Published: July 31, 2018

IL-38 Ameliorates Skin Inflammation and Limits IL-17 Production from γδ T Cells.

IL-38 Ameliorates Skin Inflammation and Limits IL-17 Production from γδ T Cells.

Journal: Cell reports

Published: July 02, 2018

Showing 1-12 of 39

Last Updated: 09/26/2026