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Philippe Chetaille

Showing results (21-30 of 29) with videos related to

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Plos Genetics|October 21, 2016
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart DiseaseChristoph Preuss, Melanie Capredon, Florian Wünnemann, et al.
Cardiology in the Young|July 7, 2011
Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in QuebecMarie-Pierre Dubé, Jean-Luc Bigras, Maryse Thibeault, et al.
Circulation|January 4, 2008
Implantable cardioverter-defibrillators in tetralogy of FallotPaul Khairy, Louise Harris, Michael J Landzberg, et al.
Stroke|November 24, 2006
Enhanced thrombogenesis but not platelet activation is associated with transcatheter closure of patent foramen ovale in patients with cryptogenic strokeElisabeth Bédard, Josep Rodés-Cabau, Christine Houde, et al.
Open Heart|October 18, 2024
Effect of aortic valve phenotype and sex on aorta dilation in patients with aortic stenosisMarie-Ange Fleury, Lionel Tastet, Jérémy Bernard, et al.
Cellular and Molecular Gastroenterology and Hepatology|February 12, 2019
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and EpigenomicsJessica Piché, Natacha Gosset, Lisa-Marie Legault, et al.
International Journal of Cardiology|December 31, 2010
Structure and process measures of quality of care in adult congenital heart disease patients: a pan-Canadian studyLuc M Beauchesne, Judith Therrien, Nanette Alvarez, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Plos Genetics|October 21, 2016
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart DiseaseChristoph Preuss, Melanie Capredon, Florian Wünnemann, et al.
Cardiology in the Young|July 7, 2011
Design and rationale of a genetic cohort study on congenital cardiac disease: experiences from a multi-institutional platform in QuebecMarie-Pierre Dubé, Jean-Luc Bigras, Maryse Thibeault, et al.
Circulation|January 4, 2008
Implantable cardioverter-defibrillators in tetralogy of FallotPaul Khairy, Louise Harris, Michael J Landzberg, et al.
Stroke|November 24, 2006
Enhanced thrombogenesis but not platelet activation is associated with transcatheter closure of patent foramen ovale in patients with cryptogenic strokeElisabeth Bédard, Josep Rodés-Cabau, Christine Houde, et al.
Open Heart|October 18, 2024
Effect of aortic valve phenotype and sex on aorta dilation in patients with aortic stenosisMarie-Ange Fleury, Lionel Tastet, Jérémy Bernard, et al.
Cellular and Molecular Gastroenterology and Hepatology|February 12, 2019
Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and EpigenomicsJessica Piché, Natacha Gosset, Lisa-Marie Legault, et al.
International Journal of Cardiology|December 31, 2010
Structure and process measures of quality of care in adult congenital heart disease patients: a pan-Canadian studyLuc M Beauchesne, Judith Therrien, Nanette Alvarez, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Nature Genetics|October 6, 2014
Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythmPhilippe Chetaille, Christoph Preuss, Silja Burkhard, et al.
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