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
- Functional analysis of mice harboring a knockout or knockin of the alternatively spliced exon C of p120ctn
Authors: Tim Pieters
- Functional dissection of transcriptional regulation during normal and malignant T-cell development : an integrative (epi)genomic approach(2016)
Authors: Kaat Durinck
- Responsible implementation of expanded carrier screening (vol 24, pg e1, 2016)(2017)
Authors: Lidewij Henneman, Pascal Borry, Davit Chokoshvili, Martina C. Cornel, Carla G. van El, Francesca Forzano, Alison Hall, Heidi C. Howard, Sandra Janssens, Hulya Kayserili, et al.
Pages: 1291 - 1291 - Genetic control of bone mass(2016)
Authors: E Boudin, Igor Fijalkowski, G Hendrickx, W Van Hul
Pages: 13 - 23 - The role of extracellular modulators of canonical Wnt signaling in bone metabolism and diseases(2013)
Authors: E Boudin, Igor Fijalkowski, E Piters, W Van Hul
Pages: 220 - 240 - FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly(2013)
Authors: Nicolas Simonis, Isabelle Migeotte, Nelle Lambert, Camille Perazzolo, Deepthi C de Silva, Boyan Dimitrov, Claudine Heinrichs, Sandra Janssens, Bronwyn Kerr, Geert Mortier, et al.
Pages: 585 - 592 - Barber-Say syndrome in a father and daughter(2010)
Authors: Nathalie Roche, PHILIPPE HOUTMEYERS, Sandra Janssens, Phillip Blondeel
Pages: 2563 - 2568 - Hydrogen sulfide improves survival after cardiac arrest and cardiopulmonary resuscitation via a nitric oxide synthase 3-dependent mechanism in mice(2009)
Authors: Shizuka Minamishima, Masahiko Bougaki, Patrick Sips, Jia De Yu, Yoji Andrew Minamishima, John W Elrod, David J Lefer, Kenneth D Bloch, Fumito Ichinose
Pages: 888 - 896 - S-Nitrosoglutathione reductase improves cardiac dysfunction in a mouse model of sepsis(2012)Volume: 126
Authors: Patrick Sips, Lin Zou, Tomoya Irie, Rebecca Nguyen, Wei Chao, Masao Kaneki, Fumito Ichinose
Number of pages: 1 - Pinpointing molecular mechanisms of long non-coding RNAs : at the crossroads of biochemistry and genetics(2022)
Authors: Louis Delhaye