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 402
- Discovery of genetic modifiers of the phenotypical cardiovascular variability in Marfan syndrome to pave the road to individualized treatment protocols.From1 Nov 2024 → TodayFunding: BOF - doctoral mandates
- 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)
Publications
11 - 20 of 2896
- Constitutive membrane binding of the multi-site docking protein Gab1 in JAK2-V617F expressing cells(2015)Volume: 76
Authors: Hannes Bongartz, Wiebke Hessenkemper, Alexandra Wolf, Rene Eulenfeld, Philip C Simister, Iris Behrmann, Jan Tavernier, Stephan M Feller, Claude Haan, Fred Schaper
Pages: 80 - 80 - High efficiency targeting of IFN-U+03B1 activity: possible applications in fighting tumours and infections(2015)
Authors: Gilles Uzé, Jan Tavernier
Pages: 179 - 182 - Peroxiredoxin-controlled G-CSF signalling at the endoplasmic reticulum-early endosome interface(2011)
Authors: Karishma Palande, Onno Roovers, Judith Gits, Carola Verwijmeren, Yoshihito Iuchi, Junichi Fujii, Benjamin G Neel, Robert Karisch, Jan Tavernier, Ivo P Touw
Pages: 3695 - 3705 - Identification of BIRC6 as a novel intervention target for neuroblastoma therapy(2012)
Authors: Fieke Lamers, Linda Schild, Jan Koster, Franki Speleman, Ingrid Øra, Ellen M Westerhout, Peter van Sluis, Rogier Versteeg, Huib N Caron, Jan J Molenaar
- Functional characterization of naturally occurring pathogenic mutations in the human leptin receptor(2008)
Authors: Wendy Kimber, Frank Peelman, Xavier Prieur, Theresia Wangensteen, Stephen O'Rahilly, Jan Tavernier, I. Sadaf Farooq
Pages: 6043 - 6052 - An assessment of air as a source of DNA contamination encountered when performing PCR(2009)
Authors: N Witt, G Rodger, Jo Vandesompele, V Benes, A Zumla, GA Rook, JF Huggett
Pages: 236 - 240 - Dermatosparaxis (EhlersU+2013Danlos type VIIC): prenatal diagnosis following a previous pregnancy with unexpected skull fractures at delivery(2013)
Authors: Joyce Solomons, Paul Coucke, Sofie Symoens, Marta C Cohen, F Michael Pope, Bart E Wagner, Glenda Sobey, Rebecca Black, Deirdre Cilliers
Pages: 1122 - 1125 - Association between Kniest dysplasia and chondrosarcoma in a child(2015)
Authors: Audrey Hochart, Anne Dieux, Paul Coucke, Damien Fron, Pierre Fayoux, Pierre Labalette, Nathalie Boutry, Fabienne Escande, Sébastien Aubert, Florence Renaud, et al.
Pages: 3204 - 3208 - Study of the role of type V collagen in heritable connective tissue diseases(2012)
Authors: Sofie Symoens
- Omics assisted N-terminal proteoform and protein expression profiling on methionine aminopeptidase 1 (MetAP1) deletion(2018)
Authors: Veronique Jonckheere, Daria Fijalkowska, Petra Van Damme
Pages: 694 - 708