Nicolas Simonis
Brussels, BRU 1050, Belgium
Last Updated: 09/26/2026
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Found 11 publications
An unusual presentation of de novo RAC3 variation in prenatal diagnosis.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: December 05, 2023
Systematic interactome mapping of acute lymphoblastic leukemia cancer gene products reveals EXT-1 tumor suppressor as a Notch1 and FBWX7 common interactor.
Journal: BMC cancer
Published: January 20, 2016
The transcription factor ERG recruits CCR4-NOT to control mRNA decay and mitotic progression.
Journal: Nature structural & molecular biology
Published: January 14, 2016
Predicting interactome network perturbations in human cancer: application to gene fusions in acute lymphoblastic leukemia.
Journal: Molecular biology of the cell
Published: October 03, 2014
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly.
Journal: Journal of medical genetics
Published: July 02, 2013
Protein interactions of the transcription factor Hoxa1.
Journal: BMC developmental biology
Published: October 16, 2012
Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus.
Journal: Journal of medical genetics
Published: October 09, 2012
Host-pathogen interactome mapping for HTLV-1 and -2 retroviruses.
Journal: Retrovirology
Published: October 13, 2011
Showing 1-11 of 11
Last Updated: 09/26/2026