46 resultaten gevonden
Publicaties Silke Peeters | Silke Peeters | Universiteit Antwerpen
Silke Peeters onbezoldigd medewerker 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…
Publicaties Gustavo Egea | Gustavo Egea | Universiteit Antwerpen
Gustavo Egea onbezoldigd gastprofessor Publicaties Gustavo Egea Sex-and age-dependent neurovascular abnormalities linked to neuroinflammation lead to exacerbated post-ischemic brain injury in Marfan syndrome mice Bron Redox Biology - ISSN 2213-2317-83 (2025) p. 1-23 Auteur(s) Gemma Manich, Belen Per…
Publications Gustavo Egea | Gustavo Egea | University of Antwerp
Gustavo Egea unpaid guest prof. Publications Gustavo Egea Sex-and age-dependent neurovascular abnormalities linked to neuroinflammation lead to exacerbated post-ischemic brain injury in Marfan syndrome mice Source Redox Biology - ISSN 2213-2317-83 (2025) p. 1-23 Author(s) Gemma Manich, Belen Perez, …
Publications Silke Peeters | Silke Peeters | University of Antwerp
Silke Peeters unpaid staff 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, Bart Loeys …
Publicaties Josephina Meester | Josephina Meester | Universiteit Antwerpen
Josephina Meester docent - postdoc mandaat FWO Publicaties Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Bron Genome medicine - ISSN 1756-994X-16:…
Publicaties Lotte Van Den Heuvel | Lotte Van Den Heuvel | Universiteit Antwerpen
Lotte Van Den Heuvel onbezoldigd medewerker Publicaties Lotte Van Den Heuvel 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…
Publications Lotte Van Den Heuvel | Lotte Van Den Heuvel | University of Antwerp
Lotte Van Den Heuvel unpaid staff Publications Lotte Van Den Heuvel 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. Couck…
Publications Josephina Meester | Josephina Meester | University of Antwerp
Josephina Meester assistant professor - postdoc researcher FWO Publications Josephina Meester Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine -…
Onderzoek Lotte Van Den Heuvel | Lotte Van Den Heuvel | Universiteit Antwerpen
Lotte Van Den Heuvel onbezoldigd medewerker Onderzoek Lotte Van Den Heuvel Onderzoeksgroep Medische Genetica (MEDGEN) Ontdekking van genetische modifiers die de fenotypische cardiovasculaire variabiliteit in Marfan syndroom verklaren voor meer geïndividualiseerde behandelingen. 01/11/2019 - 31/10/2…
Research Lotte Van Den Heuvel | Lotte Van Den Heuvel | University of Antwerp
Lotte Van Den Heuvel unpaid staff Research Lotte Van Den Heuvel Research team Medical Genetics (MEDGEN) Discovery of genetic modifiers of the phenotypical cardiovascular variability in Marfan syndrome to pave the road to individualized treatment protocols. 01/11/2019 - 31/10/2024 Abstract Marfan syn…
Onderzoek Silke Peeters | Silke Peeters | Universiteit Antwerpen
Silke Peeters onbezoldigd medewerker 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- e…
Research Silke Peeters | Silke Peeters | University of Antwerp
Silke Peeters unpaid staff 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 IPSC-chon…
Publications Lucia Buccioli | Lucia Buccioli | University of Antwerp
Lucia Buccioli predoc researcher FWO Publications Lucia Buccioli 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) Ir…
Publications Irene Valdivia Callejon | Irene Valdivia Callejon | University of Antwerp
Irene Valdivia Callejon predoc researcher FWO Publications Irene Valdivia Callejon 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.…
Publicaties Lucia Buccioli | Lucia Buccioli | Universiteit Antwerpen
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…
Publicaties Irene Valdivia Callejon | Irene Valdivia Callejon | Universiteit Antwerpen
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 …
Publications Wendy Dewals | Wendy Dewals | University of Antwerp
Wendy Dewals unpaid staff Publications Wendy Dewals Arterial aneurysm and dissection : toward the evolving phenotype of Tatton-Brown-Rahman syndrome Source Journal of medical genetics - ISSN 0022-2593-61:9 (2024) p. 870-877 Author(s) Vicken Totten, Gisela Teixido-Tura, Fermina Lopez-Grondona, Paula …
Publicaties Wendy Dewals | Wendy Dewals | Universiteit Antwerpen
Wendy Dewals onbezoldigd medewerker Publicaties Wendy Dewals Arterial aneurysm and dissection : toward the evolving phenotype of Tatton-Brown-Rahman syndrome Bron Journal of medical genetics - ISSN 0022-2593-61:9 (2024) p. 870-877 Auteur(s) Vicken Totten, Gisela Teixido-Tura, Fermina Lopez-Grondona,…
Publications Aline Verstraeten | Aline Verstraeten | University of Antwerp
Aline Verstraeten associate research professor Publications Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Source Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Author…
Publications Ilse Luyckx | Ilse Luyckx | University of Antwerp
Ilse Luyckx senior researcher Publications Ilse Luyckx Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals Source Journal of medical genetics - ISSN 0022-2593-62:3 (2025) p. 199-205 Author(s) Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A. Boswell-Patterson, Ingrid M.B.H…
Publications Jolien Schippers | Jolien Schippers | University of Antwerp
Jolien Schippers Publications Jolien Schippers An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Source Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Author(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van …
Publicaties Aline Verstraeten | Aline Verstraeten | Universiteit Antwerpen
Aline Verstraeten hoofddocent Publicaties Aline Verstraeten The complex heritability in thoracic aortic aneurysm and dissection : from clinical insights to stem cell disease modelling Bron Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, 2025,233 p. Auteur(s) Joe Davis Velche…
Publicaties Jolien Schippers | Jolien Schippers | Universiteit Antwerpen
Jolien Schippers Publicaties Jolien Schippers An NGS-based approach for precise and footprint-free CRISPR-based gene editing in human stem cells Bron Methods: a companion to methods in enzymology - ISSN 1046-2023-241 (2025) p. 33-42 Auteur(s) Bert Vandendriessche, Jolien Huyghebaert, Kirsten Van Ros…
Publicaties Ilse Luyckx | Ilse Luyckx | Universiteit Antwerpen
Ilse Luyckx senior onderzoeker Publicaties Ilse Luyckx Sexual dimorphism in SMAD3 pathogenic variant-harbouring individuals Bron Journal of medical genetics - ISSN 0022-2593-62:3 (2025) p. 199-205 Auteur(s) Julie Richer, Joe Davis Velchev, Sharan Goobie, Christie A. Boswell-Patterson, Ingrid M.B.H. …
Publications Lut Van Laer | Lut Van Laer | University of Antwerp
Lut Van Laer associate professor Publications Lut Van Laer Interpretation and classification of FBN1 variants associated with Marfan syndrome : consensus recommendations from the Clinical Genome Resource's FBN1 variant curation expert panel Source Genome medicine - ISSN 1756-994X-16:1 (2024) p. 1-14…