Onderzoeker
Elke Bogaert
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 feb 2019 → Heden
Projecten
1 - 1 of 1
- Uitbreiding van het TDP-43 proteinopathie spectrum van de zenuw naar de spier: een cellulaire, biofysische en muti-omics studie.Vanaf1 jan 2024 → HedenFinanciering: FWO Onderzoeksproject (incl. WEAVE projecten)
Publicaties
1 - 10 van 21
- Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder(2024)
Auteurs: Maria del Rocio Pérez Baca, Maria Palomares, Michiel Vanhooydonck, Eva D'haene, Lies Vantomme, Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñáur, Itsaso Losantos-García, Björn Menten, et al.
Aantal pagina's: 1 - Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder(2024)
Auteurs: Maria del Rocio Pérez Baca, Maria Palomares, Michiel Vanhooydonck, Eva D'haene, Eva Z. Jacobs, Lies Vantomme, Fernando Santos-Simarro, Roser Lleuger-Pujol, Sixto García-Miñaúr, Itsaso Losantos-García, et al.
Aantal pagina's: 1 - Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability(2024)
Auteurs: Maria del Rocio Pérez Baca, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Sadegheh Haghshenas, Aidin Foroutan, Michael A Levy, Jennifer Kerkhof, et al.
Pagina's: 509 - 528 - Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism : possible implication for Alzheimer's disease(2023)
Auteurs: M Denechaud, Sarah Geurs, T Comptdaer, S Bégard, A Garcia-Núñez, LA Pechereau, T Bouillet, Y Vermeiren, PP De Deyn, R Perbet, et al.
- Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders(2023)
Auteurs: Nika Schuermans, Hannah Verdin, Jody Ghijsels, Madeleine Hellemans, Elke Debackere, Elke Bogaert, Sofie Symoens, Leslie Naesens, Elien Lecomte, David Crosiers, et al.
- SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability(2023)
Auteurs: Elke Bogaert, Aurore Garde, Thierry Gautier, Kathleen Rooney, Yannis Duffourd, Pontus LeBlanc, Emma Van Reempts, Frederic Tran Mau-Them, Ingrid M. Wentzensen, Kit Sing Au, et al.
Pagina's: 790 - 808 - Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3(2022)Volume: 30
Auteurs: Nika Schuermans, Salima El Chehadeh, Dimitri Hemelsoet, Elke Bogaert, Elke Debackere, Pascale Hilbert, Nike Van Doninck, Marie-Caroline Taquet, Toon Rosseel, Griet De Clercq, et al.
Pagina's: 80 - 80 - A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene(2022)
Auteurs: Maria del Rocio Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Bart Dermaut, Aidin Foroutan, Jennifer Kerkhof, et al.
Aantal pagina's: 1 - A zebrafish model for C9orf72 ALS reveals RNA toxicity as a pathogenic mechanism(2018)
Auteurs: B Swinnen, A Bento-Abreu, TF Gendron, S Boeynaems, Elke Bogaert, R Nuyts, M Timmers, W Scheveneels, N Hersmus, J Wang, et al.
Pagina's: 427 - 443 - FUS-induced neurotoxicity in Drosophila is prevented by downregulating nucleocytoplasmic transport proteins(2018)
Auteurs: J Steyaert, W Scheveneels, J Vanneste, P Van Damme, W Robberecht, P Callaerts, Elke Bogaert, L Van Den Bosch
Pagina's: 4103 - 4116