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Steven R DePalma

Showing results (21-30 of 47) with videos related to

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Journal of the American Heart Association|March 3, 2025
Modeling <i>SMAD2</i> Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease PathogenesisTarsha Ward, Sarah U Morton, Gabriela Venturini, et al.
Circulation. Genomic and Precision Medicine|August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant CardiomyopathyParth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 4, 2015
CORRIGENDUM: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivityAhmed A Alfares, Melissa A Kelly, Gregory McDermott, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2015
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivityAhmed A Alfares, Melissa A Kelly, Gregory McDermott, et al.
Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Circulation Research|January 1, 2014
Increased burden of cardiovascular disease in carriers of APOL1 genetic variantsKaoru Ito, Alexander G Bick, Jason Flannick, et al.
Plos One|October 8, 2011
Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgeryAmanda A Fox, Mias Pretorius, Kuang-Yu Liu, et al.
Stroke|November 30, 2016
THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid HemorrhageTeresa Santiago-Sim, Xiaoqian Fang, Morgan L Hennessy, et al.
Plos Genetics|November 20, 2020
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profilesAlejandro Martin-Trujillo, Nihir Patel, Felix Richter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Journal of the American Heart Association|March 3, 2025
Modeling <i>SMAD2</i> Mutations in Induced Pluripotent Stem Cells Provides Insights Into Cardiovascular Disease PathogenesisTarsha Ward, Sarah U Morton, Gabriela Venturini, et al.
Circulation. Genomic and Precision Medicine|August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant CardiomyopathyParth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 4, 2015
CORRIGENDUM: Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivityAhmed A Alfares, Melissa A Kelly, Gregory McDermott, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 23, 2015
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivityAhmed A Alfares, Melissa A Kelly, Gregory McDermott, et al.
Nature Communications|September 28, 2016
Loss of RNA expression and allele-specific expression associated with congenital heart diseaseDavid M McKean, Jason Homsy, Hiroko Wakimoto, et al.
Circulation Research|January 1, 2014
Increased burden of cardiovascular disease in carriers of APOL1 genetic variantsKaoru Ito, Alexander G Bick, Jason Flannick, et al.
Plos One|October 8, 2011
Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgeryAmanda A Fox, Mias Pretorius, Kuang-Yu Liu, et al.
Stroke|November 30, 2016
THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid HemorrhageTeresa Santiago-Sim, Xiaoqian Fang, Morgan L Hennessy, et al.
Plos Genetics|November 20, 2020
Rare genetic variation at transcription factor binding sites modulates local DNA methylation profilesAlejandro Martin-Trujillo, Nihir Patel, Felix Richter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
Pageof 5