Silke Peeters postdoc researcher FWO Publications Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Source Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Author(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, B…

Silke Peeters postdoc mandaat FWO Publicaties Silke Peeters An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Bron Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Auteur(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J. Coucke, Bart Lo…

Gustavo Egea onbezoldigd gastprofessor Publicaties Gustavo Egea Navigating toward gene therapy in Marfan syndrome : a hope for halting aortic aneurysm Bron Molecular Therapy. Methods & Clinical Development - ISSN 2329-0501-32:1 (2024) p. 1-2 Auteur(s) Gustavo Egea Citatielink Hyperuricaemia does not…

Josephina Meester assistant professor - postdoc researcher FWO Publications Josephina Meester An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Source Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Author(s) Lotte Van Den Heuvel, Silke Peeters, Joseph…

Silke Peeters postdoc mandaat FWO Onderzoek Silke Peeters Onderzoeksgroep Medische Genetica (MEDGEN) Expertise Ons onderzoek is gericht op de opheldering van de genetische mechanismen die genetische afwijkingen en erfelijke bindweefselaandoeningen veroorzaken, met de nadruk op cardiovasculaire- en s…

Silke Peeters postdoc researcher FWO Research Silke Peeters Research team Medical Genetics (MEDGEN) Expertise Our research is focused on the elucidation of the genetic mechanisms causing congenital anomalies and heritable connective tissue disorders with focus on cardiovascular -and growth disorders…

Josephina Meester docent - postdoc mandaat FWO Publicaties Josephina Meester An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome Bron Drug discovery today - ISSN 1359-6446-29:7 (2024) p. 1-12 Auteur(s) Lotte Van Den Heuvel, Silke Peeters, Josephina Meester, Paul J…

Wendy Dewals onbezoldigd medewerker Publicaties Wendy Dewals Management of aortic disease in children with FBN1-related Marfan syndrome : a joint statement from the paediatric subgroup of the European Reference Network of Vascular Diseases (VASCERN, Heritable Thoracic Aortic Disease working group) a…

Lucia Buccioli predoc mandaat FWO Publicaties Lucia Buccioli Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Auteur(s) Irene Va…

Irene Valdivia Callejon predoc mandaat FWO Publicaties Irene Valdivia Callejon Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 …

Melanie Perik unpaid staff Publications Melanie Perik From silence to surge : illuminating the stealthy threat of aneurysms and dissections with the aid of cell models and insights into the genetic architecture Source Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2024,269 …

Bart Loeys full research professor Publications Bart Loeys Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin Source Stem cell research - ISSN 1873-5061-81 (2024) p. 1-6 Author(s) Hanne Boen, Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Aleksa…

Bart Loeys gewoon hoogleraar Publicaties Bart Loeys Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin Bron Stem cell research - ISSN 1873-5061-81 (2024) p. 1-6 Auteur(s) Hanne Boen, Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Aleksandra Nija…

Melanie Perik onbezoldigd medewerker Publicaties Melanie Perik From silence to surge : illuminating the stealthy threat of aneurysms and dissections with the aid of cell models and insights into the genetic architecture Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 20…

Bart Loeys full research professor Research Bart Loeys Research team Medical Genetics (MEDGEN) Elucidating the TGFß paradox in aortic aneurysmal disease: unveiling the role of endothelial cells and nitric oxide. 01/11/2024 - 31/10/2025 Abstract Impaired TGFß signaling is a defining feature of thor…

Bart Loeys gewoon hoogleraar Onderzoek Bart Loeys Onderzoeksgroep Medische Genetica (MEDGEN) Opheldering van de TGFß paradox in aorta aneurysmata: de rol van endotheel cellen en stikstofoxide. 01/11/2024 - 31/10/2025 Abstract Verstoorde TGFß signalisatie is betrokken in aandoeningen met thoracale …

Ilse Luyckx senior researcher Publications Ilse Luyckx Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Source International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Author(s) Irene Valdiv…

Aline Verstraeten associate research professor Publications Aline Verstraeten From silence to surge : illuminating the stealthy threat of aneurysms and dissections with the aid of cell models and insights into the genetic architecture Source Antwerp, University of Antwerp, Faculty of Medicine and He…

Aline Verstraeten hoofddocent Publicaties Aline Verstraeten From silence to surge : illuminating the stealthy threat of aneurysms and dissections with the aid of cell models and insights into the genetic architecture Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2024,…

Ilse Luyckx senior onderzoeker Publicaties Ilse Luyckx Investigation of strategies to block downstream effectors of AT1R-mediated signalling to prevent aneurysm formation in Marfan syndrome Bron International journal of molecular sciences - ISSN 1661-6596-25:9 (2024) p. 1-12 Auteur(s) Irene Valdivia…

Laura Rabaut Publicaties Laura Rabaut Generation of four distinct isogenic cell lines with truncating variants in I-band or A-band titin Bron Stem cell research - ISSN 1873-5061-81 (2024) p. 1-6 Auteur(s) Hanne Boen, Bert Vandendriessche, Jolien Schippers, Laura Rabaut, Aleksandra Nijak, Peter Ponsa…

Jolien Schippers Publicaties Jolien Schippers Analysis of Wilms' tumor protein 1 specific TCR repertoire in AML patients uncovers higher diversity in patients in remission than in relapsed Bron Annals of hematology - ISSN 0939-5555- (2024) p. Auteur(s) Sofie Gielis, Donovan Flumens, Sanne van der He…

Jarl Bastianen Publicaties Jarl Bastianen Phenotypic spectrum of the first Belgian MYBPC3 founder : a large multi-exon deletion with a varying phenotype Bron Frontiers in genetics - ISSN 1664-8021-15 (2024) p. 1-15 Auteur(s) Hanne Boen, Maaike Alaerts, Lut Van Laer, Johan Saenen, Inge Goovaerts, Jar…

Lut Van Laer hoofddocent Onderzoek Lut Van Laer Onderzoeksgroep Medische Genetica (MEDGEN) Expertise Mijn expertise situeert zich in cardiogenetica, meer bepaald in moleculaire cardiogenetica. Cardiogenetica omvat de volgende aandoeningen: thoracaal aorta aneurysma en dissectie, primaire elektrische…

Merlijn Nemegeer doctoral scholarship holder Research Merlijn Nemegeer Research team Medical Genetics (MEDGEN) The role of the COL4A2 NC1-domain in cerebrovascular and aneurysmal disorders: a functional approach. 01/10/2021 - 30/09/2025 Abstract COL4A1- and COL4A2-related disorders cause a broad spe…