Search research articles
Contact Us
Filters
Showing results (71-80 of 109) with videos related to
Page
of 11
Sort By:
The Canadian Journal of Cardiology
|
January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect
Steven C Greenway, Ross McLeod, Stacey Hume, et al.
The Journal of Biological Chemistry
|
April 20, 2011
Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach
Jose Renato Pinto, Shi Wei Yang, Marc-Phillip Hitz, et al.
International Journal of Cancer
|
September 8, 2024
Uncovering possible silent acquired long QT syndrome using exercise stress testing in long-term pediatric acute lymphoblastic leukemia survivors
Audrey Harvey, Maxime Caru, Cecilia Gonzalez Corcia, 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 Quebec
Marie-Pierre Dubé, Jean-Luc Bigras, Maryse Thibeault, et al.
The Canadian Journal of Cardiology
|
January 30, 2022
Regional Vascular Changes and Aortic Dilatation in Pediatric Patients With Bicuspid Aortic Valve
Rawan K Rumman, Cameron Slorach, Wei Hui, et al.
Nature Communications
|
May 22, 2026
Mapping neuro-vascular unit communications reveals distinct angiogenic programs across developing mouse brain regions
Mathilde Bizou, Elise Drapé, Gael Cagnone, et al.
Developmental Cell
|
July 17, 2021
Specialized endothelial tip cells guide neuroretina vascularization and blood-retina-barrier formation
Georgia Zarkada, Joel P Howard, Xue Xiao, 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 Epigenomics
Jessica Piché, Natacha Gosset, Lisa-Marie Legault, et al.
Molecular Psychiatry
|
May 2, 2023
Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories
Marisol Lavertu-Jolin, Bidisha Chattopadhyaya, Pegah Chehrazi, et al.
Circulation
|
May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype
Li Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 109) with videos related to
Sort By:
Page
of 11
The Canadian Journal of Cardiology
|
January 28, 2014
Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect
Steven C Greenway, Ross McLeod, Stacey Hume, et al.
The Journal of Biological Chemistry
|
April 20, 2011
Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach
Jose Renato Pinto, Shi Wei Yang, Marc-Phillip Hitz, et al.
International Journal of Cancer
|
September 8, 2024
Uncovering possible silent acquired long QT syndrome using exercise stress testing in long-term pediatric acute lymphoblastic leukemia survivors
Audrey Harvey, Maxime Caru, Cecilia Gonzalez Corcia, 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 Quebec
Marie-Pierre Dubé, Jean-Luc Bigras, Maryse Thibeault, et al.
The Canadian Journal of Cardiology
|
January 30, 2022
Regional Vascular Changes and Aortic Dilatation in Pediatric Patients With Bicuspid Aortic Valve
Rawan K Rumman, Cameron Slorach, Wei Hui, et al.
Nature Communications
|
May 22, 2026
Mapping neuro-vascular unit communications reveals distinct angiogenic programs across developing mouse brain regions
Mathilde Bizou, Elise Drapé, Gael Cagnone, et al.
Developmental Cell
|
July 17, 2021
Specialized endothelial tip cells guide neuroretina vascularization and blood-retina-barrier formation
Georgia Zarkada, Joel P Howard, Xue Xiao, 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 Epigenomics
Jessica Piché, Natacha Gosset, Lisa-Marie Legault, et al.
Molecular Psychiatry
|
May 2, 2023
Acan downregulation in parvalbumin GABAergic cells reduces spontaneous recovery of fear memories
Marisol Lavertu-Jolin, Bidisha Chattopadhyaya, Pegah Chehrazi, et al.
Circulation
|
May 25, 2005
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype
Li Zhang, D Woodrow Benson, Martin Tristani-Firouzi, et al.
Page
of 11