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Journal of Cardiovascular Development and Disease
|
November 24, 2023
<i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy
Manal Alaamery, Nour Albesher, Fahad Alhabshan, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
December 19, 2021
Neuregulin-1 enhances cell-cycle activity, delays cardiac fibrosis, and improves cardiac performance in rat pups with right ventricular pressure load
Guido P L Bossers, Marie Günthel, Diederik E van der Feen, et al.
Circulation
|
February 3, 2022
Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction
Antoinette F van Ouwerkerk, Fernanda M Bosada, Karel van Duijvenboden, et al.
Genes & Development
|
May 3, 2007
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria
Willem M H Hoogaars, Angela Engel, Janynke F Brons, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 18, 2020
T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system
Rajiv A Mohan, Fernanda M Bosada, Jan H van Weerd, et al.
Circulation
|
July 2, 2019
Conserved NPPB+ Border Zone Switches From MEF2- to AP-1-Driven Gene Program
Karel van Duijvenboden, Dennis E M de Bakker, Joyce C K Man, et al.
The Journal of Experimental Medicine
|
July 29, 2009
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy
Kalliopi Pilichou, Carol Ann Remme, Cristina Basso, et al.
Nature Communications
|
October 20, 2019
Identification of atrial fibrillation associated genes and functional non-coding variants
Antoinette F van Ouwerkerk, Fernanda M Bosada, Karel van Duijvenboden, et al.
European Heart Journal
|
February 20, 2025
SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias
Jianan Wang, Arie O Verkerk, Ronald Wilders, et al.
The Journal of Clinical Investigation
|
March 20, 2014
A common genetic variant within SCN10A modulates cardiac SCN5A expression
Malou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Journal of Cardiovascular Development and Disease
|
November 24, 2023
<i>TGFBR1</i> Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy
Manal Alaamery, Nour Albesher, Fahad Alhabshan, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
December 19, 2021
Neuregulin-1 enhances cell-cycle activity, delays cardiac fibrosis, and improves cardiac performance in rat pups with right ventricular pressure load
Guido P L Bossers, Marie Günthel, Diederik E van der Feen, et al.
Circulation
|
February 3, 2022
Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction
Antoinette F van Ouwerkerk, Fernanda M Bosada, Karel van Duijvenboden, et al.
Genes & Development
|
May 3, 2007
Tbx3 controls the sinoatrial node gene program and imposes pacemaker function on the atria
Willem M H Hoogaars, Angela Engel, Janynke F Brons, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 18, 2020
T-box transcription factor 3 governs a transcriptional program for the function of the mouse atrioventricular conduction system
Rajiv A Mohan, Fernanda M Bosada, Jan H van Weerd, et al.
Circulation
|
July 2, 2019
Conserved NPPB+ Border Zone Switches From MEF2- to AP-1-Driven Gene Program
Karel van Duijvenboden, Dennis E M de Bakker, Joyce C K Man, et al.
The Journal of Experimental Medicine
|
July 29, 2009
Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy
Kalliopi Pilichou, Carol Ann Remme, Cristina Basso, et al.
Nature Communications
|
October 20, 2019
Identification of atrial fibrillation associated genes and functional non-coding variants
Antoinette F van Ouwerkerk, Fernanda M Bosada, Karel van Duijvenboden, et al.
European Heart Journal
|
February 20, 2025
SCN10A-short gene therapy to restore conduction and protect against malignant cardiac arrhythmias
Jianan Wang, Arie O Verkerk, Ronald Wilders, et al.
The Journal of Clinical Investigation
|
March 20, 2014
A common genetic variant within SCN10A modulates cardiac SCN5A expression
Malou van den Boogaard, Scott Smemo, Ozanna Burnicka-Turek, et al.
Page
of 6