Search Results - Séverine Leclerc
- Showing 1 - 7 results of 7
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Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease by Christoph Preuß, M. Capredon, Florian Wünnemann, Philippe Chétaille, Andrea Prince, Béatrice Godard, Séverine Leclerc, Nara Sobreira, Hua Ling, Philip Awadalla, Maryse Thibeault, Paul Khairy, Mark E. Samuels, Grégor Andelfinger
Published 2016Artigo -
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Specialized endothelial tip cells guide neuroretina vascularization and blood-retina-barrier formation by Georgia Zarkada, Joel P. Howard, Xue Xiao, Hyojin Park, Mathilde Bizou, Séverine Leclerc, Steffen E. Künzel, Blanche Boisseau, Jinyu Li, Gaël Cagnone, Jean Sébastien Joyal, Grégor Andelfinger, Anne Eichmann, Alexandre Dubrac
Published 2021Artigo -
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Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories by Marisol Lavertu-Jolin, Bidisha Chattopadhyaya, Pegah Chehrazi, Denise Carrier, Florian Wünnemann, Séverine Leclerc, Félix Dumouchel, Derek N. Robertson, Hicham Affia, Kamal Saba, Vijaya Gopal, Anant B. Patel, Grégor Andelfinger, Graciela Piñeyro, Graziella Di Cristo
Published 2023Artigo -
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Clearance of defective muscle stem cells by senolytics restores myogenesis in myotonic dystrophy type 1 by Talita C. Conte, Gilberto Duran-Bishop, Zakaria Orfi, Inès Mokhtari, Alyson Deprez, Isabelle Côté, Thomas Molina, Kim Taeyeon, Lydia Tellier, Marie‐Pier Roussel, Damien Maggiorani, Basma Benabdallah, Séverine Leclerc, Lara Feulner, Ornella Pellerito, Jean Mathieu, Grégor Andelfinger, Cynthia Gagnon, Christian Beauséjour, Serge McGraw, Élise Duchesne, Nicolas A. Dumont
Published 2023Artigo -
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Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm by Philippe Chétaille, Christoph Preuß, Silja Burkhard, Jean-Marc Côté, Christine Houde, Julie Castilloux, Jessica Piché, Natacha Gosset, Séverine Leclerc, Florian Wünnemann, Maryse Thibeault, Carmen Gagnon, Antonella Galli, Elizabeth Tuck, Gilles R.X. Hickson, Nour El Amine, Inès Boufaied, Emmanuelle Lemyre, Pascal de Santa Barbara, Sandrine Faure, Anders Jonzon, Michel Cameron, Harry C. Dietz, Elena Gallo-McFarlane, D Woodrow Benson, Claudia Moreau, Damian Labuda, Shing H. Zhan, Yaoqing Shen, Michèle Jomphe, Steven J.M. Jones, Jeroen Bakkers, Grégor Andelfinger
Published 2014Artigo -
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Loss of ADAMTS19 causes progressive non-syndromic heart valve disease by Florian Wünnemann, Asaf Ta‐Shma, Christoph Preuß, Séverine Leclerc, Patrick van Vliet, Andrea Oneglia, Maryse Thibeault, Emily Nordquist, Joy Lincoln, Franka Scharfenberg, Christoph Becker‐Pauly, P. Hofmann, Kirstin Hoff, Enrique Audain, Hans-Heiner Kramer, Wojciech Makałowski, Amiram Nir, Sebastian S. Gerety, Matthew E. Hurles, Johanna Comes, Anne Fournier, Hanna Osińska, Jeffrey Robins, Michel Pucéat, Harry C. Dietz, Andrew S. McCallion, Grégor Andelfinger, Bart Loeys, Lut Van Laer, Per Eriksson, Salah A. Mohamed, Luc Mertens, Anders Franco-Cereceda, Seema Mital, Orly Elpeleg, Marc‐Phillip Hitz, Grégor Andelfinger
Published 2019Artigo
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Biology
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Genetics
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Phenotype
Allele
Amygdala
Anatomy
Cancer research
Chromosome
Cognition
Cohesin
Embryo
Embryonic stem cell
Enhancer
Exome sequencing
Extinction (optical mineralogy)
GABAergic
Heart development
Heart disease
Histone
Histone deacetylase
Histone deacetylase 2
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JAG1
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