Yoann Saillour

Paris, 75014, France

Last Updated: 09/26/2026

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Found 21 publications

Bidirectional interaction between protocadherin 8 and the transcription factor Dbx1 regulates cerebral cortex development.

Bidirectional interaction between protocadherin 8 and the transcription factor Dbx1 regulates cerebral cortex development.

Journal: Development (Cambridge, England)
Published: June 07, 2025

Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis.

Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis.

Journal: Development (Cambridge, England)
Published: October 15, 2024

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism.

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism.

Journal: The Journal of clinical investigation
Published: July 07, 2023

Repurposing of the multiciliation gene regulatory network in fate specification of Cajal-Retzius neurons.

Repurposing of the multiciliation gene regulatory network in fate specification of Cajal-Retzius neurons.

Journal: Developmental cell
Published: November 23, 2022

Single-cell transcriptomics of the early developing mouse cerebral cortex disentangle the spatial and temporal components of neuronal fate acquisition.

Single-cell transcriptomics of the early developing mouse cerebral cortex disentangle the spatial and temporal components of neuronal fate acquisition.

Journal: Development (Cambridge, England)
Published: November 28, 2020

Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy.

Severe and progressive neuronal loss in myelomeningocele begins before 16 weeks of pregnancy.

Journal: American journal of obstetrics and gynecology
Published: October 13, 2019

Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex.

Evolutionary Gain of Dbx1 Expression Drives Subplate Identity in the Cerebral Cortex.

Journal: Cell reports
Published: April 24, 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

Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development.

Ciliogenesis and cell cycle alterations contribute to KIF2A-related malformations of cortical development.

Journal: Human molecular genetics
Published: July 31, 2017

The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity.

The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience
Published: December 09, 2016

Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia.

Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia.

Journal: Nature genetics
Published: April 01, 2016

Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.

Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.

Journal: Human molecular genetics
Published: September 25, 2015
Showing 1-12 of 21

Last Updated: 09/26/2026