Researcher
Paul Coucke
- Disciplines:Genetically modified animals
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → Today - Department of Pediatrics and medical genetics (Department)
Member
From1 Oct 2002 → 30 Sep 2018
Projects
1 - 10 of 12
- Identification of molecular mechanisms involved in Osteogenesis ImperfectaFrom1 Oct 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
- Nuclear Transfer for female-related infertility and mitochondrial diseasesFrom1 Oct 2023 → TodayFunding: FWO Applied Biomedical Research (TBM)
- Unravelling the mitochondrial DNA reversion phenomenonFrom1 Nov 2022 → TodayFunding: FWO fellowships
- Cofunding core facility - Core Zebrafish Facility Ghent (Core ZFG)From1 Jul 2022 → TodayFunding: BOF - research organisations
- Comparison of editing, complementing or replacement of defective RNA molecules as a novel treatment method to overcome early embryonic developmental arrestFrom1 Oct 2021 → 14 Sep 2023Funding: FWO junior postdoctoral fellowship
- An integrated translational platform to improve the management and outcome of rare heritable connective tissue diseaseFrom1 Jan 2021 → TodayFunding: BOF - projects
- Research equipment for behavior analysis in zebrafish disease models.From1 Dec 2020 → 30 Nov 2022Funding: BOF - scientific equipment program
- Identification of modifier genes underlying the phenotypic variability in the ‘Brittle Bone Disease’, using zebrafish models and patient-derived induced pluripotent stem cellsFrom1 Oct 2019 → TodayFunding: BOF - projects
- Genetic analysis in consanguineous families from Palestine : a focus on Cystic Fibrosis and Osteogenesis ImperfectaFrom1 Oct 2015 → 30 Sep 2019Funding: BOF - Doctoral projects
Publications
31 - 40 of 56
- Fibroblasts in soft tissue mineralization display an osteogenic gene expression pattern but do not transform into mature osteoblasts(2016)
Authors: Matthias Van Gils, Eva De Vilder, Mohammad Hosen, Paul Coucke, Olivier LeSaux, Anne De Paepe, Olivier Vanakker
Number of pages: 1 - Identification of von Willebrand disease type 1 in a patient with EhlersU+2013Danlos syndrome classic type(2016)
Authors: HW Ott, S Perkhofer, Paul Coucke, Anne De Paepe, M Spannagl
Pages: e309 - e311 - Association between Kniest dysplasia and chondrosarcoma in a child(2015)
Authors: Audrey Hochart, Anne Dieux, Paul Coucke, Damien Fron, Pierre Fayoux, Pierre Labalette, Nathalie Boutry, Fabienne Escande, Sébastien Aubert, Florence Renaud, et al.
Pages: 3204 - 3208 - Altered cytoskeletal organization characterized lethal but not surviving Brtl(+/-) mice: insight on phenotypic variability in osteogenesis imperfecta(2015)
Authors: Laura Bianchi, Assunta Gagliardi, Silvia Maruelli, Roberta Besio, Claudia Landi, Roberta Gioia, Kenneth M. Kozloff, Basma M. Khoury, Paul Coucke, Sofie Symoens, et al.
Pages: 6118 - 6133 - Whole exome sequencing as a novel tool for the detection of modifier genes in Pseudoxanthoma elasticum(2015)Volume: 23
Authors: Eva De Vilder, Filip Van Nieuwerburgh, Dieter Deforce, Ludovic Martin, Georges Lefthériotis, Paul Coucke, Anne De Paepe, Olivier Vanakker
Pages: 106 - 107 - Type III collagen is important for collagen fibrillogenesis and for dermal and cardiovascular development(2015)Volume: 23
Authors: Sanne D'hondt, Brecht Guillemyn, Sofie Symoens, Wendy Toussaint, Leen Vanhoutte, Riet De Rycke, Paul Coucke, Bart Lambrecht, Patrick Segers, Anne De Paepe, et al.
Pages: 110 - 110 - A case of dendritic cell, monocyte, B and NK lymphoid deficiency (DCML)(2014)Volume: 34
Authors: Melissa Dullaers, Tessa Kerre, Frauke Coppieters, Dorine Sichien, Nancy De Cabooter, Veronique Debacker, Reinhart Speeckaert, Paul Coucke, Elias Debaere, Filomeen Haerynck, et al.
Pages: S239 - S240 - Arterial tortuosity syndrome(2014)
Authors: Bert Callewaert, Anne De Paepe, Paul Coucke, RA Pagon, MP Adam, HH Ardinger
Number of pages: 1 - Focal segmental glomerulosclerosis in a child with Marfan syndrome and novel fibrillin gene mutation(2014)Volume: 29
Authors: Ashraf Bakr, Mohammad Al-haggar, Riham Eid, Yahya Wahba, Paul Coucke, Mona Hafez, Amr Sarhan, Ayman Hammad, Ahmed Alrefay, Atef Almougy, et al.
Pages: 1825 - 1825 - Dermatosparaxis (EhlersU+2013Danlos type VIIC): prenatal diagnosis following a previous pregnancy with unexpected skull fractures at delivery(2013)
Authors: Joyce Solomons, Paul Coucke, Sofie Symoens, Marta C Cohen, F Michael Pope, Bart E Wagner, Glenda Sobey, Rebecca Black, Deirdre Cilliers
Pages: 1122 - 1125