Sandrine Humbert

Paris, France

Last Updated: 09/26/2026

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Found 48 publications

Abnormal cortical development sets the stage in Huntington disease.

Abnormal cortical development sets the stage in Huntington disease.

Journal: Journal of Huntington's disease
Published: February 27, 2026

Structure of the Huntingtin F-actin complex reveals its role in cytoskeleton organization.

Structure of the Huntingtin F-actin complex reveals its role in cytoskeleton organization.

Journal: Science advances
Published: September 19, 2025

CAG repeat mosaicism is gene specific in spinocerebellar ataxias.

CAG repeat mosaicism is gene specific in spinocerebellar ataxias.

Journal: American journal of human genetics
Published: September 28, 2023

Treating early transient neuronal defects in a mouse model of Huntington's disease delays the signs of the disease in adulthood

Treating early transient neuronal defects in a mouse model of Huntington's disease delays the signs of the disease in adulthood

Journal: Medecine sciences : M/S
Published: April 24, 2023

Treating early postnatal circuit defect delays Huntington's disease onset and pathology in mice.

Treating early postnatal circuit defect delays Huntington's disease onset and pathology in mice.

Journal: Science (New York, N.Y.)
Published: September 22, 2022

Customization of the translational complex regulates mRNA-specific translation to control CNS regeneration.

Customization of the translational complex regulates mRNA-specific translation to control CNS regeneration.

Journal: Neuron
Published: August 18, 2022

Huntingtin regulates calcium fluxes in skeletal muscle.

Huntingtin regulates calcium fluxes in skeletal muscle.

Journal: The Journal of general physiology
Published: April 12, 2022

Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus.

Calcineurin and huntingtin form a calcium-sensing machinery that directs neurotrophic signals to the nucleus.

Journal: Science advances
Published: January 05, 2022

Huntingtin coordinates dendritic spine morphology and function through cofilin-mediated control of the actin cytoskeleton.

Huntingtin coordinates dendritic spine morphology and function through cofilin-mediated control of the actin cytoskeleton.

Journal: Cell reports
Published: November 04, 2021

A pathogenic proteolysis-resistant huntingtin isoform induced by an antisense oligonucleotide maintains huntingtin function.

A pathogenic proteolysis-resistant huntingtin isoform induced by an antisense oligonucleotide maintains huntingtin function.

Journal: JCI insight
Published: August 12, 2021

Longitudinal multimodal MRI characterization of a knock-in mouse model of Huntington's disease reveals early gray and white matter alterations.

Longitudinal multimodal MRI characterization of a knock-in mouse model of Huntington's disease reveals early gray and white matter alterations.

Journal: Human molecular genetics
Published: July 23, 2021

Developmental defects in Huntington's disease show that axonal growth and microtubule reorganization require NUMA1.

Developmental defects in Huntington's disease show that axonal growth and microtubule reorganization require NUMA1.

Journal: Neuron
Published: April 14, 2021
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Last Updated: 09/26/2026