Andrea Lelli

Paris, France

Last Updated: 09/26/2026

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Found 10 publications

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Compensatory Interplay Between Clarin-1 and Clarin-2 Deafness-Associated Proteins Governs Phenotypic Variability in Hearing.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: October 30, 2025

Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.

Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 20, 2023

The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses.

The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses.

Journal: iScience

Published: March 10, 2022

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.

Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 24, 2020

Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.

Clarin-2 is essential for hearing by maintaining stereocilia integrity and function.

Journal: EMBO molecular medicine

Published: January 09, 2019

CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.

CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.

Journal: EMBO molecular medicine

Published: November 01, 2017

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G.

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: August 25, 2017

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth.

Journal: The Journal of cell biology

Published: September 02, 2015

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.

EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.

Journal: Orphanet journal of rare diseases

Published: January 14, 2014

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice.

Journal: The Journal of cell biology

Published: October 10, 2012

Showing 1-10 of 10

Last Updated: 09/26/2026