Olivier Kassel
Karlsruhe, BW, Germany
Last Updated: 09/26/2026
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Found 11 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
The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation.
Journal: Scientific reports
Published: July 23, 2020
The LIM domain protein nTRIP6 acts as a co-repressor for the transcription factor MEF2C in myoblasts.
Journal: Scientific reports
Published: December 07, 2015
The E3 ubiquitin ligase Trim7 mediates c-Jun/AP-1 activation by Ras signalling.
Journal: Nature communications
Published: August 11, 2014
The LIM domain protein nTRIP6 recruits the mediator complex to AP-1-regulated promoters.
Journal: PloS one
Published: January 31, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026