Onderzoeker
Marjolijn Renard
- Disciplines:Epigenetica, Klinische genetica en moleculaire diagnostiek, Immunogenetica, Genetica
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 okt 2018 → 1 nov 2019 - Vakgroep Civiele Techniek (Departement)
Lid
Vanaf1 okt 2010 → 28 feb 2013 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 okt 2006 → 30 sep 2018
Publicaties
1 - 10 van 55
- Unraveling the role of TGFβ signaling in thoracic aortic aneurysm and dissection using Fbn1 mutant mouse models(2023)
Auteurs: Violette Deleeuw, Eric Carlson, Marjolijn Renard, Keith D. Zientek, Phillip A. Wilmarth, Ashok P. Reddy, Elise C. Manalo, Sara F. Tufa, Douglas R. Keene, Margie Olbinado, et al.
Pagina's: 17 - 33 - MEK1/2 inhibition in murine heart and aorta after oral administration of refametinib supplemented drinking water(2020)
Auteurs: Felke Steijns, Nathalie Bracke, Marjolijn Renard, Julie De Backer, Patrick Sips, Nathan Debunne, Evelien Wynendaele, Frederick Verbeke, Bart De Spiegeleer, Laurence Campens
- Spontaneous right ventricular pseudoaneurysms and increased arrhythmogenicity in a mouse model of Marfan syndrome(2020)
Auteurs: Felke Steijns, Marjolijn Renard, Marine Vanhomwegen, Petra Vermassen, Jana Desloovere, Robrecht Raedt, Lars Emil Larsen, Máté István Tóth, Julie De Backer, Patrick Sips
- Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects(2020)
Auteurs: Joyce Burger, Aude Beyens, Marjolijn Renard, Sander Barnhoorn, Christophe Casteleyn, Dieter Reinhardt, Benedicte Descamps, Christian Vanhove, Ingrid van der Pluijm, Jeroen Essers, et al.
Pagina's: 1476 - 1488 - Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice(2018)
Auteurs: Marjolijn Renard, Suzanne Vanhauwaert, Ali Rihani, Niels Vandamme, Pieter Van Vlierberghe, Jody J Haigh, Bieke Decaesteker, Irina Lambertz
- Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline(2018)
Auteurs: Felke Steijns, Tjorven Audenaert, Ilse Meerschaut, Wouter Steyaert, Bert Callewaert, Marjolijn Renard
- SmgGDS, a new piece in the thoracic aortic aneurysm and dissection puzzle(2018)
Auteurs: Marjolijn Renard
Pagina's: S4133 - S4136 - Intrinsic cardiomyopathy in Marfan syndrome: results from in- and ex-vivo studies of the Fbn1C1039G/+ model and longitudinal findings in humans(2015)
Auteurs: Laurence Campens, Marjolijn Renard, Bram Trachet, Laura Muiño Mosquera, Lynn Sakai
Pagina's: 256 - 263 - Marfan syndrome and related heritable thoracic aortic aneurysms and dissections(2015)
Auteurs: Marjolijn Renard, Laurence Campens, Laura Muiño Mosquera, Bert Callewaert, Yskert von Kodolitsch
Pagina's: 4061 - 4075 - Gene panel sequencing in heritable thoracic aortic disorders and related entities: results of comprehensive testing in a cohort of 264 patients(2015)
Auteurs: Laurence Campens, Bert Callewaert, Laura Muiño Mosquera, Marjolijn Renard