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Organisation
Department of Biomolecular Medicine
Department
Main organisation:Faculty of Medicine and Health Sciences
Lifecycle:1 Oct 2018 → Today
Organisation profile:The Department of Biomolecular Medicine is part of the Faculty of Medicine and Health Sciences. Its research is centered around the area of biomolecular medicine.
Keywords:biomoleculaire geneeskunde
Disciplines:Molecular and cell biology
Current researchers
81 - 90 of 313 results
- Arthur Declercq (Member)
- Anneleen Decock (Member)
- Kylian Decroix (Member)
- Philippe Decruyenaere (Member)
- Sven Degroeve (Member)
- Emma Delanote (Member)
- Violette Deleeuw (Member)
- Nina Demeulemeester (Member)
- Lisa Demoen (Member)
- Hans Demol (Member)
Projects
81 - 90 of 533
- Enrichment of extracellular vesicles for discovery of biomarkers for early cancer diagnosisFrom1 Jan 2024 → TodayFunding: BOF - projects
- Exploring the feasability of the implementation of preconceptional expanded carrier screening by general practitioners and gynecologists.From1 Jan 2024 → TodayFunding: BOF - projects
- Clinical and pathophysiological characteristics of ectopic calcification: from bench to bedsideFrom1 Jan 2024 → TodayFunding: BOF - projects
- An integrated translational platform to gain insights in and improve diagnosis and management of the Ehlers-Danlos Syndromes.From1 Jan 2024 → TodayFunding: BOF - projects
- Evaluation of the role of Myhre syndrome associated SMAD4 variants in neurodevelopment and fibrosisFrom1 Jan 2024 → 31 Dec 2024Funding: BOF - projects
- Analysis of human protein complexes in lysosomal pathologiesFrom1 Jan 2024 → TodayFunding: BOF - projects
- Characterization and targeting of the function of the HNRNPC RNA binding protein in T-cell leukemiaFrom1 Jan 2024 → TodayFunding: FWO research project (including WEAVE projects)
- Evaluation of non-coding elements as novel therapeutic targetsFrom1 Jan 2024 → 31 Dec 2024Funding: BOF - projects
- European Training Program to Understand, Diagnose and Treat Autosomal Dominant Retinal DiseasesFrom1 Jan 2024 → TodayFunding: BOF - projects, HORIZON.1.2 - Marie Skłodowska-Curie-actions (MSCA)
- Shortcutting the diagnostic odyssey for rare diseases.From1 Jan 2024 → 31 Dec 2024Funding: BOF - projects
Publications
1 - 10 of 3986
- Loss of function of RIMS2 causes a syndromic congenital cone-rod synaptic disease with neurodevelopmental and pancreatic involvement(2020)Published in: AMERICAN JOURNAL OF HUMAN GENETICSISSN: 1537-6605Issue: 6Volume: 106Pages: 859 - 871
- Structure and antagonism of the receptor complex mediated by human TSLP in allergy and asthma(2017)Published in: NATURE COMMUNICATIONSISSN: 2041-1723Volume: 8
- Ectopic microRNA-150-5p transcription sensitizes glucocorticoid therapy response in MM1S multiple myeloma cells but fails to overcome hormone therapy resistance in MM1R cells(2014)Published in: PLOS ONEISSN: 1932-6203Issue: 12Volume: 9
- A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics : the case of NPC1 deficiency(2017)Published in: SCIENTIFIC REPORTSISSN: 2045-2322Volume: 7
- Genome-wide copy number variation scan identifies complement component C4 as novel susceptibility gene for Crohn's disease(2016)Published in: INFLAMMATORY BOWEL DISEASESISSN: 1078-0998Issue: 3Volume: 22Pages: 505 - 515
- MicroRNA profiling reveals a role for microRNA-218-5p in the pathogenesis of chronic obstructive pulmonary disease(2017)Published in: AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINEISSN: 1073-449XIssue: 1Volume: 195Pages: 43 - 56
- The mTOR and PP2A pathways regulate PHD2 phosphorylation to fine-tune HIF1α levels and colorectal cancer cell survival under hypoxia(2017)Published in: CELL REPORTSISSN: 2211-1247Issue: 7Volume: 18Pages: 1699 - 1712
- Evaluation of a marker independent isolation method for circulating tumor cells in esophageal adenocarcinoma(2021)Published in: PLOS ONEISSN: 1932-6203Issue: 5Volume: 16
- High-density mapping of the MHC identifies a shared role for HLA-DRB1⋆01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis(2015)Published in: NATURE GENETICSISSN: 1546-1718Issue: 2Volume: 47Pages: 172 - 179
- Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders(2021)Published in: GENOME MEDICINEISSN: 1756-994XIssue: 1Volume: 13