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Showing results (471-480 of 599) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|February 19, 2026
Prdm16 Amplifies Notch Signaling and Suppresses Venous Lineage Specification to Prevent Arteriovenous Malformations During Vascular DevelopmentJore Van Wauwe, Pavithra Janarthanan, Sander Craps, et al.
Heart Rhythm|October 19, 2011
Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathyMarwan M Refaat, Steven A Lubitz, Seiko Makino, et al.
Nature Reviews. Cardiology|September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicineAndrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|September 15, 2025
The Effect of Butyrylated Starch on Bowel Polyps in Familial Adenomatous Polyposis: Results of a Randomized, Double-blind, Placebo-Controlled Crossover TrialJulie M Clarke, Trevor J Lockett, Karen L Harrap, et al.
Nature Communications|August 27, 2015
Chamber identity programs drive early functional partitioning of the heartChristian Mosimann, Daniela Panáková, Andreas A Werdich, et al.
Familial Cancer|June 15, 2023
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case reportRomy Walker, Mark Clendenning, Jihoon E Joo, et al.
Circulation|January 20, 2018
Complement Receptor C5aR1 Plays an Evolutionarily Conserved Role in Successful Cardiac RegenerationNiranjana Natarajan, Yamen Abbas, Donald M Bryant, et al.
Circulation. Genomic and Precision Medicine|May 31, 2018
Interdisciplinary Models for Research and Clinical Endeavors in Genomic Medicine: A Scientific Statement From the American Heart AssociationKiran Musunuru, Pankaj Arora, John P Cooke, et al.
Familial Cancer|July 9, 2026
Lynch syndrome caused by a pathogenic SINE-VNTR-Alu (SVA) insertion in MSH2 gene identified by long-read DNA sequencingJihoon E Joo, Khalid Mahmood, Mark Clendenning, et al.
Molecular Genetics & Genomic Medicine|September 5, 2019
The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communicationStephanie Harris, Allison L Cirino, Christina W Carr, et al.
Pageof 60

Showing results (471-480 of 599) with videos related to

Sort By:
Pageof 60
Arteriosclerosis, Thrombosis, and Vascular Biology|February 19, 2026
Prdm16 Amplifies Notch Signaling and Suppresses Venous Lineage Specification to Prevent Arteriovenous Malformations During Vascular DevelopmentJore Van Wauwe, Pavithra Janarthanan, Sander Craps, et al.
Heart Rhythm|October 19, 2011
Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathyMarwan M Refaat, Steven A Lubitz, Seiko Makino, et al.
Nature Reviews. Cardiology|September 1, 2025
Creating an atlas of variant effects to resolve variants of uncertain significance and guide cardiovascular medicineAndrew M Glazer, Daniel R Tabet, Victoria N Parikh, et al.
Cancer Prevention Research (Philadelphia, Pa.)|September 15, 2025
The Effect of Butyrylated Starch on Bowel Polyps in Familial Adenomatous Polyposis: Results of a Randomized, Double-blind, Placebo-Controlled Crossover TrialJulie M Clarke, Trevor J Lockett, Karen L Harrap, et al.
Nature Communications|August 27, 2015
Chamber identity programs drive early functional partitioning of the heartChristian Mosimann, Daniela Panáková, Andreas A Werdich, et al.
Familial Cancer|June 15, 2023
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case reportRomy Walker, Mark Clendenning, Jihoon E Joo, et al.
Circulation|January 20, 2018
Complement Receptor C5aR1 Plays an Evolutionarily Conserved Role in Successful Cardiac RegenerationNiranjana Natarajan, Yamen Abbas, Donald M Bryant, et al.
Circulation. Genomic and Precision Medicine|May 31, 2018
Interdisciplinary Models for Research and Clinical Endeavors in Genomic Medicine: A Scientific Statement From the American Heart AssociationKiran Musunuru, Pankaj Arora, John P Cooke, et al.
Familial Cancer|July 9, 2026
Lynch syndrome caused by a pathogenic SINE-VNTR-Alu (SVA) insertion in MSH2 gene identified by long-read DNA sequencingJihoon E Joo, Khalid Mahmood, Mark Clendenning, et al.
Molecular Genetics & Genomic Medicine|September 5, 2019
The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communicationStephanie Harris, Allison L Cirino, Christina W Carr, et al.
Pageof 60