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 401
- 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
1 - 10 of 2895
- Impact of functional studies on exome sequence variant interpretation in early-onset cardiac conduction system diseases(2020)
Authors: Kenshi Hayashi, Ryota Teramoto, Akihiro Nomura, Yoshihiro Asano, Manu Beerens, Yasutaka Kurata, Isao Kobayashi, Noboru Fujino, Hiroshi Furusho, Kenji Sakata, et al.
Pages: 2116 - 2130 - Sclerosing bone dysplasias : leads toward novel osteoporosis treatments(2014)
Authors: Igor Fijalkowski, E Boudin, G Mortier, W Van Hul
Pages: 243 - 251 - Wars2 is a determinant of angiogenesis(2016)
Authors: Mao Wang, Patrick Sips, Ester Khin, Maxime Rotival, Ximing Sun, Rizwan Ahmed, Anissa Anindya Widjaja, Sebastian Schafer, Permeen Yusoff, Pervinder Kaur Choksi, et al.
- Selective glucocorticoid receptor modulation maintains bone mineral density in mice(2012)Volume: 50
Authors: S Thiele, E Tsourdi, Karolien De Bosscher, J Tuckermann, LC Hofbauer, M Rauner
Pages: S49 - S49 - Selective glucocorticoid receptor modulation maintains bone mineral density in mice(2012)
Authors: Sylvia Thiele, Nicole Ziegler, Elena Tsourdi, Karolien De Bosscher, Jan P Tuckermann, Lorenz C Hofbauer, Martina Rauner
Pages: 2242 - 2250 - New Activation Modus of STAT3 A TYROSINE-LESS REGION OF THE INTERLEUKIN-22 RECEPTOR RECRUITS STAT3 BY INTERACTING WITH ITS COILED-COIL DOMAIN(2009)
Authors: L Dumoutier, C de Meester, Jan Tavernier, JC Renauld
Pages: 26377 - 26384 - BRCA1 hypomethylation causes chemoresistance in high-risk neuroblastoma(2017)Volume: 64
Authors: A Hakkert, M Ebus, J Koster, Franki Speleman, R Versteeg, H Heyn, J Molenaar
Pages: S121 - S122 - Association of unbalanced translocation der(1;7) with germline GATA2 mutations(2021)
Authors: Emilia J. Kozyra, Gudrun Goehring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak, Valerie de Haas, Jan Stary, Henrik Hasle, Akiko Shimamura, et al.
Pages: 2441 - 2445 - A mechanistic classification of clinical phenotypes in neuroblastoma(2018)Volume: 65
Authors: S Ackermann, M Cartolano, B Hero, A Roderwieser, C Bartenhagen, C Rosswog, F Hertwig, T Simon, A Eggert, Franki Speleman, et al.
Pages: S87 - S88 - Oncogenic activation of FOXR1 by 11q23 intrachromosomal deletion-fusions in neuroblastoma(2012)
Authors: EE Santo, ME Ebus, J Koster, JH Schulte, A Lakeman, P van Sluis, J Vermeulen, D Gisselsson, I Øra, S Lindner, et al.
Pages: 1571 - 1581