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Showing results (211-220 of 216) with videos related to

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HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Stem Cells (Dayton, Ohio)|February 21, 2019
Coordinating Tissue Regeneration Through Transforming Growth Factor-β Activated Kinase 1 Inactivation and ReactivationHsiao Hsin Sung Hsieh, Shailesh Agarwal, David J Cholok, et al.
Communications Medicine|March 19, 2024
AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathyIris Wu, Aliya Zeng, Amara Greer-Short, et al.
Acta Neuropathologica|May 21, 2014
Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutationsLeanne de Kock, Nelly Sabbaghian, François Plourde, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartX Rosa Ma, Stephanie D Conley, Michael Kosicki, et al.
Human Mutation|July 16, 2015
Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan SyndromeViviana Cordeddu, Jiani C Yin, Cecilia Gunnarsson, et al.
Pageof 22

Showing results (211-220 of 216) with videos related to

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Pageof 22
You have reached the last page of results.This site can display upto 216 results.
HGG Advances|September 4, 2023
Rare variants in <i>CAPN2</i> increase risk for isolated hypoplastic left heart syndromeElizabeth E Blue, Janson J White, Michael K Dush, et al.
Stem Cells (Dayton, Ohio)|February 21, 2019
Coordinating Tissue Regeneration Through Transforming Growth Factor-β Activated Kinase 1 Inactivation and ReactivationHsiao Hsin Sung Hsieh, Shailesh Agarwal, David J Cholok, et al.
Communications Medicine|March 19, 2024
AAV9:PKP2 improves heart function and survival in a Pkp2-deficient mouse model of arrhythmogenic right ventricular cardiomyopathyIris Wu, Aliya Zeng, Amara Greer-Short, et al.
Acta Neuropathologica|May 21, 2014
Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutationsLeanne de Kock, Nelly Sabbaghian, François Plourde, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Molecular convergence of risk variants for congenital heart defects leveraging a regulatory map of the human fetal heartX Rosa Ma, Stephanie D Conley, Michael Kosicki, et al.
Human Mutation|July 16, 2015
Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan SyndromeViviana Cordeddu, Jiani C Yin, Cecilia Gunnarsson, et al.
Pageof 22