Valerie Martinelli
Gosselies, WAL 6041, Belgium
Last Updated: 09/26/2026
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Found 8 publications
Alteration of actin cytoskeletal organisation in fetal akinesia deformation sequence.
Journal: Scientific reports
Published: June 15, 2023
Inhibition of HIV-1 gene transcription by KAP1 in myeloid lineage.
Journal: Scientific reports
Published: June 05, 2020
Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts.
Journal: Scientific reports
Published: June 02, 2020
Targeted CRM1-inhibition perturbs leukemogenic NUP214 fusion proteins and exerts anti-cancer effects in leukemia cell lines with NUP214 rearrangements.
Journal: Oncotarget
Published: May 23, 2020
Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence.
Journal: PLoS genetics
Published: August 20, 2018
Localisation of Nup153 and SENP1 to nuclear pore complexes is required for 53BP1-mediated DNA double-strand break repair.
Journal: Journal of cell science
Published: October 10, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026