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Biorxiv : the Preprint Server for Biology
|
May 3, 2023
<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer network
Mason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
An engineered human cardiac tissue model reveals contributions of systemic lupus erythematosus autoantibodies to myocardial injury
Sharon Fleischer, Trevor R Nash, Manuel A Tamargo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation
|
June 5, 2003
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy
Michael Arad, Ivan P Moskowitz, Vickas V Patel, et al.
Nature Communications
|
October 19, 2019
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes
W Scott Watkins, E Javier Hernandez, Sergiusz Wesolowski, et al.
American Journal of Human Genetics
|
June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation. Cardiovascular Genetics
|
May 11, 2013
Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy
Mauro W Costa, Guanglan Guo, Orit Wolstein, et al.
Circulation
|
October 10, 2018
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
Carolyn Y Ho, Sharlene M Day, Euan A Ashley, et al.
Stroke
|
November 30, 2016
THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage
Teresa Santiago-Sim, Xiaoqian Fang, Morgan L Hennessy, et al.
The Journal of Clinical Investigation
|
February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy
Danos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.
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of 54
Search research articles
Search
Showing results (441-450 of 533) with videos related to
Sort By:
Page
of 54
Biorxiv : the Preprint Server for Biology
|
May 3, 2023
<i>Tbx5</i> maintains atrial identity by regulating an atrial enhancer network
Mason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
An engineered human cardiac tissue model reveals contributions of systemic lupus erythematosus autoantibodies to myocardial injury
Sharon Fleischer, Trevor R Nash, Manuel A Tamargo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 28, 2024
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation
|
June 5, 2003
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy
Michael Arad, Ivan P Moskowitz, Vickas V Patel, et al.
Nature Communications
|
October 19, 2019
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes
W Scott Watkins, E Javier Hernandez, Sergiusz Wesolowski, et al.
American Journal of Human Genetics
|
June 21, 2025
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
Circulation. Cardiovascular Genetics
|
May 11, 2013
Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy
Mauro W Costa, Guanglan Guo, Orit Wolstein, et al.
Circulation
|
October 10, 2018
Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe)
Carolyn Y Ho, Sharlene M Day, Euan A Ashley, et al.
Stroke
|
November 30, 2016
THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage
Teresa Santiago-Sim, Xiaoqian Fang, Morgan L Hennessy, et al.
The Journal of Clinical Investigation
|
February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy
Danos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.
Page
of 54