Zoekresultaten - Maryse Thibeault
- Toon 1 - 4 resultaten van 4
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1
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease door 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
Gepubliceerd in 2016Artigo -
2
Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease door Marc‐Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian R. Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath C. Lionel, Guylaine D’Amours, Emmanuelle Lemyre, Rebecca Cullum, Jean‐Luc Bigras, Maryse Thibeault, Philippe Chétaille, Alexandre Montpetit, Paul Khairy, Bert Overduin, Sabine Klaassen, Pamela A. Hoodless, Philip Awadalla, Julie Hussin, Youssef Idaghdour, Mona Nemer, Alexandre F.R. Stewart, Cornelius F. Boerkoel, Stephen W. Scherer, Andréa Richter, Marie‐Pierre Dubé, Grégor Andelfinger
Gepubliceerd in 2012Artigo -
3
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm door 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
Gepubliceerd in 2014Artigo -
4
Loss of ADAMTS19 causes progressive non-syndromic heart valve disease door 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
Gepubliceerd in 2019Artigo
Zoekinstrumenten:
Gerelateerde Onderwerpen
Biology
Gene
Genetics
Internal medicine
Medicine
Heart disease
Aortic valve
Bicuspid aortic valve
Cell biology
Chromosome
Cohesin
Cohort
Copy-number variation
Disease
Embryonic stem cell
Endocrinology
Enhancer
Exome sequencing
Genome
Heart development
JAG1
Missense mutation
Notch signaling pathway
Pathological
Phenotype
Transcription factor
Zebrafish