SmgGDS, a new piece in the thoracic aortic aneurysm and dissection puzzle

Por Renard, Marjolijn
Publicado no J Thorac Dis (2018)

FBN1: The Disease-Causing Gene for Marfan Syndrome and Other Genetic Disorders

Por Sakai, Lynn Y., Keene, Douglas R., Renard, Marjolijn, De Backer, Julie
Publicado no Gene (2016)

Genes in Thoracic Aortic Aneurysms and Dissections – Do they Matter?: Translation and Integration of Research and Modern Genetic Techniques into Daily Clinical Practice

Por De Backer, Julie, Renard, Marjolijn, Campens, Laurence, François, Katrien, Callewaert, Bert, Coucke, Paul, De Paepe, Anne
Publicado no Aorta (Stamford) (2013)

Gene panel sequencing in heritable thoracic aortic disorders and related entities – results of comprehensive testing in a cohort of 264 patients

Por Campens, Laurence, Callewaert, Bert, Muiño Mosquera, Laura, Renard, Marjolijn, Symoens, Sofie, De Paepe, Anne, Coucke, Paul, De Backer, Julie
Publicado no Orphanet J Rare Dis (2015)

Sex, pregnancy and aortic disease in Marfan syndrome

Por Renard, Marjolijn, Muiño-Mosquera, Laura, Manalo, Elise C., Tufa, Sara, Carlson, Eric J., Keene, Douglas R., De Backer, Julie, Sakai, Lynn Y.
Publicado no PLoS One (2017)

Correction: Sex, pregnancy and aortic disease in Marfan syndrome

Por Renard, Marjolijn, Muiño-Mosquera, Laura, Manalo, Elise C., Tufa, Sara, Carlson, Eric J., Keene, Douglas R., Backer, Julie De, Sakai, Lynn Y.
Publicado no PLoS One (2018)

MEK1/2 Inhibition in Murine Heart and Aorta After Oral Administration of Refametinib Supplemented Drinking Water

Por Steijns, Felke, Bracke, Nathalie, Renard, Marjolijn, De Backer, Julie, Sips, Patrick, Debunne, Nathan, Wynendaele, Evelien, Verbeke, Frederick, De Spiegeleer, Bart, Campens, Laurence
Publicado no Front Pharmacol (2020)

Ambulatory Electrocardiographic Monitoring and Ectopic Beat Detection in Conscious Mice

Por Steijns, Felke, Tóth, Máté I., Demolder, Anthony, Larsen, Lars E., Desloovere, Jana, Renard, Marjolijn, Raedt, Robrecht, Segers, Patrick, De Backer, Julie, Sips, Patrick
Publicado no Sensors (Basel) (2020)

Characterization of a distinct lethal arteriopathy syndrome in twenty-two infants associated with an identical, novel mutation in FBLN4 gene, confirms fibulin-4 as a critical deter...

Por Kappanayil, Mahesh, Nampoothiri, Sheela, Kannan, Rajesh, Renard, Marjolijn, Coucke, Paul, Malfait, Fransiska, Menon, Swapna, Ravindran, Hiran K, Kurup, Renu, Faiyaz-Ul-Haque, Muhammad, Kumar, Krishna, De Paepe, Anne
Publicado em 2012

New insights into the pathogenesis of autosomal dominant cutis laxa with report of five ELN mutations

Por Callewaert, Bert, Renard, Marjolijn, Hucthagowder, Vishwanathan, Albrecht, Beate, Hausser, Ingrid, Blair, Edward, Dias, Cristina, Albino, Alice, Wachi, Hiroshi, Sato, Fumiaki, Mecham, Robert P., Loeys, Bart, Coucke, Paul J., De Paepe, Anne, Urban, Zsolt
Publicado em 2011

Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice

Por Renard, Marjolijn, Vanhauwaert, Suzanne, Vanhomwegen, Marine, Rihani, Ali, Vandamme, Niels, Goossens, Steven, Berx, Geert, Van Vlierberghe, Pieter, Haigh, Jody J., Decaesteker, Bieke, Van Laere, Jolien, Lambertz, Irina, Speleman, Frank, Vandesompele, Jo, Willaert, Andy
Publicado no Sci Rep (2018)

Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity

Por Hadj-Rabia, Smail, Callewaert, Bert L, Bourrat, Emmanuelle, Kempers, Marlies, Plomp, Astrid S, Layet, Valerie, Bartholdi, Deborah, Renard, Marjolijn, Backer, Julie De, Malfait, Fransiska, Vanakker, Olivier M, Coucke, Paul J, De Paepe, Anne M, Bodemer, Christine
Publicado em 2013

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD

Por Renard, Marjolijn, Callewaert, Bert, Baetens, Machteld, Campens, Laurence, MacDermot, Kay, Fryns, Jean-Pierre, Bonduelle, Maryse, Dietz, Hal, Gaspar, Isabel Mendes, Cavaco, Diogo, Stattin, Eva-Lena, Schrander-Stumpel, Constance, Coucke, Paul, Loeys, Bart, De Paepe, Anne, De Backer, Julie
Publicado em 2011

Absence of Cardiovascular Manifestations in a Haploinsufficient Tgfbr1 Mouse Model

Por Renard, Marjolijn, Trachet, Bram, Casteleyn, Christophe, Campens, Laurence, Cornillie, Pieter, Callewaert, Bert, Deleye, Steven, Vandeghinste, Bert, van Heijningen, Paula M., Dietz, Harry, De Vos, Filip, Essers, Jeroen, Staelens, Steven, Segers, Patrick, Loeys, Bart, Coucke, Paul, De Paepe, Anne, De Backer, Julie
Publicado em 2014

Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency

Por Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L
Publicado em 2010

Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection

Por Renard, Marjolijn, Francis, Catherine, Ghosh, Rajarshi, Scott, Alan F., Witmer, P. Dane, Adès, Lesley C., Andelfinger, Gregor U., Arnaud, Pauline, Boileau, Catherine, Callewaert, Bert L., Guo, Dongchuan, Hanna, Nadine, Lindsay, Mark E., Morisaki, Hiroko, Morisaki, Takayuki, Pachter, Nicholas, Robert, Leema, Van Laer, Lut, Dietz, Harry C., Loeys, Bart L., Milewicz, Dianna M., Backer, Julie De
Publicado no J Am Coll Cardiol (2018)

Variants in ADRB1 and CYP2C9: Association with Response to Atenolol and Losartan in Marfan Syndrome

Por Van Driest, Sara L., Sleeper, Lynn A., Gelb, Bruce D., Morris, Shaine A., Dietz, Harry C., Forbus, Geoffrey A., Goldmuntz, Elizabeth, Hoskoppal, Arvind, James, Jeanne, Lee, Teresa M., Levine, Jami C., Li, Jennifer S., Loeys, Bart L., Markham, Larry W., Meester, Josephina A. N., Mital, Seema, Mosley, Jonathan D., Olson, Aaron K., Renard, Marjolijn, Shaffer, Christian M., Sharkey, Angela, Young, Luciana, Lacro, Ronald V., Roden, Dan M.
Publicado no J Pediatr (2020)

In-Frame Mutations in Exon 1 of SKI Cause Dominant Shprintzen-Goldberg Syndrome

Por Carmignac, Virginie, Thevenon, Julien, Adès, Lesley, Callewaert, Bert, Julia, Sophie, Thauvin-Robinet, Christel, Gueneau, Lucie, Courcet, Jean-Benoit, Lopez, Estelle, Holman, Katherine, Renard, Marjolijn, Plauchu, Henri, Plessis, Ghislaine, De Backer, Julie, Child, Anne, Arno, Gavin, Duplomb, Laurence, Callier, Patrick, Aral, Bernard, Vabres, Pierre, Gigot, Nadège, Arbustini, Eloisa, Grasso, Maurizia, Robinson, Peter N., Goizet, Cyril, Baumann, Clarisse, Di Rocco, Maja, Sanchez Del Pozo, Jaime, Huet, Frédéric, Jondeau, Guillaume, Collod-Beroud, Gwenaëlle, Beroud, Christophe, Amiel, Jeanne, Cormier-Daire, Valérie, Rivière, Jean-Baptiste, Boileau, Catherine, De Paepe, Anne, Faivre, Laurence
Publicado em 2012