Amrit Estivalet
Overview
Explore the profile of Amrit Estivalet including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
165
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0
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Recent Articles
1.
Calvet C, Peineau T, Benamer N, Cornille M, Lelli A, Plion B, et al.
iScience
. 2022 Dec;
25(12):105628.
PMID: 36483015
Hearing depends on fast and sustained calcium-dependent synaptic vesicle fusion at the ribbon synapses of cochlear inner hair cells (IHCs). The implication of the canonical neuronal SNARE complex in this...
2.
Zeitz C, Mejecase C, Michiels C, Condroyer C, Wohlschlegel J, Foussard M, et al.
Int J Mol Sci
. 2021 Aug;
22(15).
PMID: 34360642
The purpose of this work was to identify the gene defect underlying a relatively mild rod-cone dystrophy (RCD), lacking disease-causing variants in known genes implicated in inherited retinal disorders (IRD),...
3.
Trouillet A, Dubus E, Degardin J, Estivalet A, Ivkovic I, Godefroy D, et al.
Sci Rep
. 2018 Feb;
8(1):1968.
PMID: 29386551
Usher syndrome type 1 (USH1) is a major cause of inherited deafness and blindness in humans. The eye disorder is often referred to as retinitis pigmentosa, which is characterized by...
4.
Schietroma C, Parain K, Estivalet A, Aghaie A, de Monvel J, Picaud S, et al.
J Cell Biol
. 2017 May;
216(6):1849-1864.
PMID: 28495838
Usher syndrome type 1 (USH1) causes combined hearing and sight defects, but how mutations in USH1 genes lead to retinal dystrophy in patients remains elusive. The USH1 protein complex is...
5.
Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice
Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, et al.
J Cell Biol
. 2012 Oct;
199(2):381-99.
PMID: 23045546
The mechanisms underlying retinal dystrophy in Usher syndrome type I (USH1) remain unknown because mutant mice lacking any of the USH1 proteins-myosin VIIa, harmonin, cadherin-23, protocadherin-15, sans-do not display retinal...