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
- Disentangling the complexity and diversity of glucocorticoid receptor signalingFrom1 Jan 2024 → TodayFunding: FWO research project (including WEAVE 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
- European Training Program to Understand, Diagnose and Treat Autosomal Dominant Retinal DiseasesFrom1 Jan 2024 → TodayFunding: Horizon Europe - Marie Skłodowska-Curie-actions
Publications
1 - 10 of 2887
- Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss(2009)
Authors: AN Mhatre, Sandra Janssens, MA Nardi, Y Li, AK Lalwani
Pages: 185 - 190 - Protein S-nitrosylation regulates Ca2+handling and myofilament Ca2+sensitivity in beta-adrenergic signaling(2013)Volume: 27
Authors: Tomoya Irie, Patrick Sips, Kentaro Tokuda, Fumito Ichinose
Number of pages: 1 - Pathophysiology of hypertension in the absence of nitric oxide/cyclic GMP signaling(2013)
Authors: Robrecht Thoonen, Patrick Sips, Kenneth D Bloch, Emmanuel S. Buys
Pages: 47 - 58 - Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfecta(2016)
Authors: L Hruskova, Igor Fijalkowski, W Van Hul, I Marik, G Mortier, P Martasek, I Mazura
Pages: 442 - 447 - Mutations in sFRP1 or sFRP4 are not a common cause of craniotubular hyperostosis(2013)
Authors: E Boudin, E Piters, Igor Fijalkowski, G Stevenheydens, E Steenackers, O Kuismin, JS Moilanen, G Mortier, W Van Hul
Pages: 292 - 295 - Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters(2014)
Authors: G Hendrickx, E Boudin, Igor Fijalkowski, TL Nielsen, M Andersen, K Brixen, W Van Hul
Pages: 57 - 65 - Genetic modification of hypertension by sGCU+03B1U+2081(2013)
Authors: Patrick Sips, Emmanuel S Buys
Pages: 312 - 318 - Nitrosylation of calcium-handling proteins in cardiac adrenergic signaling and hypertrophy(2015)
Authors: Tomoya Irie, Patrick Sips, Shinichi Kai, Kotaro Kida, Kohei Ikeda, Shuichi Hirai, Kasra Moazzami, Pawina Jiramongkolchai, Donald B Bloch, Paschalis-Thomas Doulias, et al.
Pages: 793 - 803 - Selective glucocorticoid receptor modulators(2010)
Authors: Karolien De Bosscher
Pages: 96 - 104 - Endogenous controls for miRNA analysis in renal cells and tissue(2016)Volume: 31
Authors: Michael Rudnicki, Ninella Schweibert, Anneleen Beckers, Stefan Schneeberger, Alfred Koenigsrainer, Georg Boehmig, Jo Vandesompele, Gert Mayer, Johannes Leierer
Pages: 169 - 170