Cecile Delettre

Montpellier, France

Last Updated: 09/26/2026

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Found 29 publications

Sexual Dimorphism Is Associated With Corneal Nerve and Epithelial Alterations and Tear-Film Defects in Pax6 Haploinsufficiency Mouse Model.

Sexual Dimorphism Is Associated With Corneal Nerve and Epithelial Alterations and Tear-Film Defects in Pax6 Haploinsufficiency Mouse Model.

Journal: Investigative ophthalmology & visual science

Published: May 18, 2026

High-performance proteomics reveals immune, epithelial, and vascular dysregulation underlying lacrimal fluid defects in patients with aniridia.

High-performance proteomics reveals immune, epithelial, and vascular dysregulation underlying lacrimal fluid defects in patients with aniridia.

Journal: BMC ophthalmology

Published: September 30, 2025

EFA6A regulates retinal function through the control of photoreceptor cell activity and structure.

EFA6A regulates retinal function through the control of photoreceptor cell activity and structure.

Journal: iScience

Published: September 24, 2025

WFS1 gene delivery rescues visual function in a mouse model of Wolfram syndrome.

WFS1 gene delivery rescues visual function in a mouse model of Wolfram syndrome.

Journal: Acta neuropathologica communications

Published: August 21, 2025

Inherited mitochondrial dysfunction triggered by OPA1 mutation impacts the sensory innervation fibre identity, functionality and regenerative potential in the cornea.

Inherited mitochondrial dysfunction triggered by OPA1 mutation impacts the sensory innervation fibre identity, functionality and regenerative potential in the cornea.

Journal: Scientific reports

Published: April 26, 2024

AAV2/9-mediated gene transfer into murine lacrimal gland leads to a long-term targeted tear film modification.

AAV2/9-mediated gene transfer into murine lacrimal gland leads to a long-term targeted tear film modification.

Journal: Molecular therapy. Methods & clinical development

Published: June 07, 2022

Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?

Optic neuropathy linked to ACAD9 pathogenic variants: A potentially riboflavin-responsive disorder?

Journal: Mitochondrion

Published: April 06, 2021

Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations!

Journal: Annals of clinical and translational neurology

Published: May 04, 2019

Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy.

Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy.

Journal: The Journal of clinical investigation

Published: February 28, 2019

ER-mitochondria cross-talk is regulated by the Ca2+ sensor NCS1 and is impaired in Wolfram syndrome.

ER-mitochondria cross-talk is regulated by the Ca2+ sensor NCS1 and is impaired in Wolfram syndrome.

Journal: Science signaling

Published: October 25, 2018

Reply: The expanding neurological phenotype of DNM1L-related disorders.

Reply: The expanding neurological phenotype of DNM1L-related disorders.

Journal: Brain : a journal of neurology

Published: March 13, 2018

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Journal: Human genetics

Published: February 13, 2018

Showing 1-12 of 29

Last Updated: 09/26/2026