Christelle Etard
Karlsruhe, BW, Germany
Last Updated: 09/26/2026
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Found 18 publications
A simple and rapid shaking-based assay to genotype live, early developmental stage zebrafish embryos.
Journal: Laboratory animals
Published: August 14, 2025
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.
Journal: American journal of human genetics
Published: July 22, 2024
Novel MYH10 heterozygous variants associated to a syndrome combining mainly ptosis and ocular coloboma expand the MYH10 related phenotypes.
Journal: European journal of human genetics : EJHG
Published: February 16, 2024
Short internal open reading frames repress the translation of N-terminally truncated proteoforms.
Journal: EMBO reports
Published: February 13, 2024
Loss of the Bardet-Biedl protein Bbs1 alters photoreceptor outer segment protein and lipid composition.
Journal: Nature communications
Published: July 09, 2021
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress.
Journal: EMBO molecular medicine
Published: December 05, 2019
Mutation of a serine near the catalytic site of the choline acetyltransferase a gene almost completely abolishes motility of the zebrafish embryo.
Journal: PloS one
Published: July 16, 2018
Loss of zebrafish Smyd1a interferes with myofibrillar integrity without triggering the misfolded myosin response.
Journal: Biochemical and biophysical research communications
Published: December 20, 2017
A compact unc45b-promoter drives muscle-specific expression in zebrafish and mouse.
Journal: Genesis (New York, N.Y. : 2000)
Published: April 20, 2016
Whole transcriptome data analysis of zebrafish mutants affecting muscle development.
Journal: Data in brief
Published: March 09, 2016
Last Updated: 09/26/2026