Organisation
Department of Biomolecular Medicine
Department
Current researchers
21 - 30 of 245 results
- Lisa Caboor (Member)
- Sam Calis (Member)
- Toon Callens (Member)
- Bert Callewaert (Member)
- Nico Callewaert (Member)
- Marjolein Carron (Member)
- Kathleen Claes (Member)
- Tine Claeys (Member)
- Dorien Clarisse (Member)
- Marlies Colman (Member)
Projects
21 - 30 of 400
- Beurs Emmanuel van der Schueren (EvdS) Carolien Van Damme: "Scrutinizing the role of GJC1 as replicative stress resistor in MYCN driven neuroblastoma"From1 Nov 2023 → TodayFunding: Nonprofit institution or equivalents
- Capturing the ubiquitination and protein interaction landscape of the central regulator of nodulation TOO MUCH LOVE in soybeanFrom1 Nov 2023 → TodayFunding: FWO fellowships
- Study of novel bivalent ligands targeting glucocorticoid and mineralocorticoid receptor heterodimers: towards an improved glucocorticoid-based multiple myeloma therapy"From1 Nov 2023 → TodayFunding: Nonprofit institution or equivalents
- Role of the ultraconserved IRXA cluster in North Carolina Macular Dystrophy, a retinal enhanceropathyFrom1 Nov 2023 → TodayFunding: FWO fellowships
- Integrative interactome and protein modification analysis of HNF4α in sepsisFrom1 Nov 2023 → TodayFunding: FWO fellowships
- Safety first: optimizing artificial oocyte creation through diploid cell haploidizationFrom1 Nov 2023 → TodayFunding: FWO fellowships
- Unipept Next: A differential, multi-omics, highly flexible UnipeptFrom1 Nov 2023 → TodayFunding: BOF - postdoctoral mandates
- A diaPASEF powered computational deep dive into the myotonic dystrophy type 1 liquid biopsy proteomeFrom1 Nov 2023 → TodayFunding: FWO Strategic Basic Research Grant
- Plasma cfRNA biomarker tail genes for cancer screening and monitoringFrom15 Oct 2023 → TodayFunding: IOF - technology concept exploration
- Design of a novel antisense oligonucleotide therapy for inherited blindnessFrom15 Oct 2023 → TodayFunding: IOF - technology validation in lab
Publications
1 - 10 of 2885
- 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