Organisation
Department of Biomolecular Medicine
Department
Current researchers
1 - 10 of 245 results
- Kris Gevaert (Responsible)
- Karolien Aelbrecht (Member)
- Christophe Ampe (Member)
- Jasper Anckaert (Member)
- Milton Boaheng Antwi (Member)
- Andrea Argentini (Member)
- Caroline Asselman (Member)
- Francisco Avila Cobos (Member)
- Lynn Backers (Member)
- Miriam Bauwens (Member)
Projects
1 - 10 of 400
- Identification of molecular mechanisms involved in Osteogenesis ImperfectaFrom1 Oct 2024 → TodayFunding: BOF - doctoral mandates
- Validation of Actionable Genomic ABerrations in a paediatric Oncology Network for Doctorate studentsFrom1 May 2024 → TodayFunding: BOF - doctoral mandates
- Identification of modifier genes responsible for the phenotypic variability in Osteogenesis Imperfecta (OI)- patients using zebrafish modelsFrom14 Feb 2024 → TodayFunding: BOF - doctoral mandates
- Facility : Patiënt-afgeleide xenograft modellen – UGent;From1 Feb 2024 → TodayFunding: BOF - research organisations
- The role of upstream open reading frames (uORFs) in retinal health, disease and therapyFrom1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
- Perturbation of extracellular matrix (ECM)-degrading cellulair devices by means of photoporation-directed nanobody delivery in immune cells and cancer cells.From1 Jan 2024 → TodayFunding: BOF - projects
- Probing the proteome structure in living cellsFrom1 Jan 2024 → TodayFunding: BOF - projects
- A SIOPEN pragmatic clinical trial to MOnitor NeuroblastomA relapse with LIquid biopsy Sensitive AnalysisFrom1 Jan 2024 → TodayFunding: HORIZON.2.1 - Health
- Disentangling the complexity and diversity of glucocorticoid receptor signalingFrom1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
- European Training Program to Understand, Diagnose and Treat Autosomal Dominant Retinal DiseasesFrom1 Jan 2024 → TodayFunding: Horizon Europe - Marie Skłodowska-Curie-actions
Publications
2201 - 2210 of 2887
- HTSplotter : an end-to-end data processing, analysis and visualisation tool for chemical and genetic in vitro perturbation screening(2024)
Authors: Carolina de Carvalho Nunes, Jasper Anckaert, Fanny De Vloed, Jolien De Wyn, Kaat Durinck, Jo Vandesompele, Franki Speleman, Vanessa Vermeirssen
- Revealing the transitory and local effect of zebularine on development and on proteome dynamics of Salix purpurea(2024)
Authors: Andrea Pagano, Carolina Gomes, Evy Timmerman, Paweł Sulima, Jerzy Andrzej Przyborowski, Dariusz Kruszka, Francis Impens, Jorge Almiro Pinto Paiva
- Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes(2008)
Authors: HC MEFFORD, AJ SHARP, C BAKER, A ITSARA, ZS JIANG, Karen Buysse, SW HUANG, VK MALONEY, JA CROLLA, D BARALLE, et al.
Pages: 1685 - ALK positively regulates MYCN activity through repression of HBP1 expression(2019)
Authors: Shana Claeys, Geertrui Denecker, Kaat Durinck, Bieke Decaesteker, Liselot Mus, Siebe Loontiens, Suzanne Vanhauwaert, Kristina Althoff, Caroline Wigerup, Daniel Bexell, et al.
Pages: 2690 - 2705 - Searching for liquid RNA biomarkers for esophageal adenocarcinoma(2019)
Authors: Kathleen Schoofs, Annouck Philippron, Philippe Nafteux, Lieven Depypere, Piet Pattyn, Jo Vandesompele, Katleen De Preter
Number of pages: 1 - cDNA and targeted RNA sequencing to unravel hidden genetic defects in PID patients with only one-disease related variant in genes with recessive inheritance(2019)
Authors: Lynn Backers, Marieke De Bruyne, Filomeen Haerynck
Number of pages: 1 - A case of dendritic cell, monocyte, B and NK lymphoid deficiency (DCML)(2014)Volume: 34
Authors: Melissa Dullaers, Tessa Kerre, Frauke Coppieters, Dorine Sichien, Nancy De Cabooter, Veronique Debacker, Reinhart Speeckaert, Paul Coucke, Elias Debaere, Filomeen Haerynck, et al.
Pages: S239 - S240 - A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation(2019)
Authors: Simon Tavernier, V Athanasopoulos, PATRICK VERLOO, G Behrens, Jens Staal, Delfien Bogaert, Leslie Naesens, Marieke De Bruyne, Sofie Van Gassen, Eef Parthoens, et al.
- The extracellular RNA quality control (exRNAQC) study : controlling pre-analytical variables of RNA sequencing in blood-based precision medicine(2018)
Authors: Francisco Avila Cobos, Anneleen Decock, Katleen De Preter, Bert Dhondt, Olivier De Wever, Bram De Wilde, Celine Everaert, Carolina Fierro, Hetty Helsmoortel, An Hendrix, et al.
Number of pages: 1 - Missing heritability in Bloom syndrome : first report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene(2020)
Authors: Lynn Backers, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, Kathleen Claes
Number of pages: 1