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Showing results (201-210 of 216) with videos related to

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Acta Neuropathologica|July 16, 2014
Germ-line and somatic DICER1 mutations in pineoblastomaLeanne de Kock, Nelly Sabbaghian, Harriet Druker, et al.
Journal of Medical Genetics|October 18, 2015
High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndromeLeanne de Kock, Yu Chang Wang, Timothée Revil, et al.
Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Nathan Youlton, et al.
Plos Genetics|April 9, 2016
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart DefectsJames R Priest, Kazutoyo Osoegawa, Nebil Mohammed, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 2020
Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascadeYing Wang, Vivek Nanda, Daniel Direnzo, et al.
Research Square|December 4, 2023
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Nathan Youlton, et al.
Nature Cardiovascular Research|June 5, 2025
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Michelle Youlton, et al.
Journal of Medical Genetics|January 27, 2011
DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndromeIngrid Slade, Chiara Bacchelli, Helen Davies, et al.
The Journal of Clinical Investigation|November 17, 2020
Congenital heart disease risk loci identified by genome-wide association study in European patientsHarald Lahm, Meiwen Jia, Martina Dreßen, et al.
Circulation. Genomic and Precision Medicine|April 7, 2023
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease PhenotypesMengyao Yu, Matthew Aguirre, Meiwen Jia, et al.
Pageof 22

Showing results (201-210 of 216) with videos related to

Sort By:
Pageof 22
Acta Neuropathologica|July 16, 2014
Germ-line and somatic DICER1 mutations in pineoblastomaLeanne de Kock, Nelly Sabbaghian, Harriet Druker, et al.
Journal of Medical Genetics|October 18, 2015
High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndromeLeanne de Kock, Yu Chang Wang, Timothée Revil, et al.
Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Nathan Youlton, et al.
Plos Genetics|April 9, 2016
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart DefectsJames R Priest, Kazutoyo Osoegawa, Nebil Mohammed, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 17, 2020
Clonally expanding smooth muscle cells promote atherosclerosis by escaping efferocytosis and activating the complement cascadeYing Wang, Vivek Nanda, Daniel Direnzo, et al.
Research Square|December 4, 2023
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Nathan Youlton, et al.
Nature Cardiovascular Research|June 5, 2025
Epistasis regulates genetic control of cardiac hypertrophyQianru Wang, Tiffany M Tang, Michelle Youlton, et al.
Journal of Medical Genetics|January 27, 2011
DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndromeIngrid Slade, Chiara Bacchelli, Helen Davies, et al.
The Journal of Clinical Investigation|November 17, 2020
Congenital heart disease risk loci identified by genome-wide association study in European patientsHarald Lahm, Meiwen Jia, Martina Dreßen, et al.
Circulation. Genomic and Precision Medicine|April 7, 2023
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease PhenotypesMengyao Yu, Matthew Aguirre, Meiwen Jia, et al.
Pageof 22