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E Seidman

Showing results (471-480 of 533) with videos related to

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JAMA Cardiology|October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgerySimon C Body, Charles D Collard, Stanton K Shernan, et al.
JACC. Basic to Translational Science|June 13, 2026
Targeting Inflammation by Pioglitazone and its R-Enantiomer Mitigates Pathological Myocardial Remodeling in Murine Hypertrophic CardiomyopathyAnna-Theresa Pfaller, Claudia Veneziano, Sarala Raj Murthi, et al.
Nature Cardiovascular Research|February 12, 2024
Tbx5 maintains atrial identity in post-natal cardiomyocytes by regulating an atrial-specific enhancer networkMason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
JACC. Basic to Translational Science|May 6, 2020
Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart DefectsJonathan J Edwards, Andrew D Rouillard, Nicolas F Fernandez, et al.
Nature|June 6, 2020
Complement genes contribute sex-biased vulnerability in diverse disordersNolan Kamitaki, Aswin Sekar, Robert E Handsaker, et al.
Science Translational Medicine|July 9, 2025
Regulatory T cells attenuate chronic inflammation and cardiac fibrosis in hypertrophic cardiomyopathyYing-Jie Wang, Kamayani Singh, Adam B Lokman, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Research Square|March 11, 2024
The BMAL1/HIF2A heterodimer modulates circadian variations of myocardial injuryWei Ruan, Tao Li, Jaewoong Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomiaDaniel Quiat, Andrew T Timberlake, Justin J Curran, et al.
Pageof 54

Showing results (471-480 of 533) with videos related to

Sort By:
Pageof 54
JAMA Cardiology|October 21, 2020
Association of Damaging Variants in Genes With Increased Cancer Risk Among Patients With Congenital Heart DiseaseSarah U Morton, Akiko Shimamura, Peter E Newburger, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgerySimon C Body, Charles D Collard, Stanton K Shernan, et al.
JACC. Basic to Translational Science|June 13, 2026
Targeting Inflammation by Pioglitazone and its R-Enantiomer Mitigates Pathological Myocardial Remodeling in Murine Hypertrophic CardiomyopathyAnna-Theresa Pfaller, Claudia Veneziano, Sarala Raj Murthi, et al.
Nature Cardiovascular Research|February 12, 2024
Tbx5 maintains atrial identity in post-natal cardiomyocytes by regulating an atrial-specific enhancer networkMason E Sweat, Yangpo Cao, Xiaoran Zhang, et al.
JACC. Basic to Translational Science|May 6, 2020
Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart DefectsJonathan J Edwards, Andrew D Rouillard, Nicolas F Fernandez, et al.
Nature|June 6, 2020
Complement genes contribute sex-biased vulnerability in diverse disordersNolan Kamitaki, Aswin Sekar, Robert E Handsaker, et al.
Science Translational Medicine|July 9, 2025
Regulatory T cells attenuate chronic inflammation and cardiac fibrosis in hypertrophic cardiomyopathyYing-Jie Wang, Kamayani Singh, Adam B Lokman, et al.
Nature Communications|July 10, 2025
Genome sequencing is critical for forecasting outcomes following congenital cardiac surgeryW Scott Watkins, Edgar J Hernandez, Thomas A Miller, et al.
Research Square|March 11, 2024
The BMAL1/HIF2A heterodimer modulates circadian variations of myocardial injuryWei Ruan, Tao Li, Jaewoong Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomiaDaniel Quiat, Andrew T Timberlake, Justin J Curran, et al.
Pageof 54