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Showing results (1221-1230 of 1,263) with videos related to

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Cancer Research|September 17, 2020
Cancers from Novel <i>Pole</i>-Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint BlockadeMelissa A Galati, Karl P Hodel, Miki S Gams, et al.
Nature|August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycleMatthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
JACC. Clinical Electrophysiology|September 7, 2024
Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia GenesMajd A El-Harasis, Zachary T Yoneda, Katherine C Anderson, et al.
Contemporary Clinical Trials|September 16, 2018
Putting patients at the center of kidney care transitions: PREPARE NOW, a cluster randomized controlled trialJ A Green, P L Ephraim, F F Hill-Briggs, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Critical Ultrasound Journal|November 22, 2015
The evolution of an integrated ultrasound curriculum (iUSC) for medical students: 9-year experienceRichard A Hoppmann, Victor V Rao, Floyd Bell, et al.
Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
JACC. Cardiovascular Interventions|November 29, 2023
Persistent and Recurrent Device-Related Thrombus After Left Atrial Appendage Closure: Incidence, Predictors, and OutcomesJules Mesnier, Trevor Simard, Richard G Jung, et al.
Journal of the American College of Cardiology|July 23, 2021
Predictors of Device-Related Thrombus Following Percutaneous Left Atrial Appendage OcclusionTrevor Simard, Richard G Jung, Kyle Lehenbauer, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Pageof 127

Showing results (1221-1230 of 1,263) with videos related to

Sort By:
Pageof 127
Cancer Research|September 17, 2020
Cancers from Novel <i>Pole</i>-Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint BlockadeMelissa A Galati, Karl P Hodel, Miki S Gams, et al.
Nature|August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycleMatthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
JACC. Clinical Electrophysiology|September 7, 2024
Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia GenesMajd A El-Harasis, Zachary T Yoneda, Katherine C Anderson, et al.
Contemporary Clinical Trials|September 16, 2018
Putting patients at the center of kidney care transitions: PREPARE NOW, a cluster randomized controlled trialJ A Green, P L Ephraim, F F Hill-Briggs, et al.
Nucleic Acids Research|November 13, 2013
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype dataSebastian Köhler, Sandra C Doelken, Christopher J Mungall, et al.
Critical Ultrasound Journal|November 22, 2015
The evolution of an integrated ultrasound curriculum (iUSC) for medical students: 9-year experienceRichard A Hoppmann, Victor V Rao, Floyd Bell, et al.
Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
JACC. Cardiovascular Interventions|November 29, 2023
Persistent and Recurrent Device-Related Thrombus After Left Atrial Appendage Closure: Incidence, Predictors, and OutcomesJules Mesnier, Trevor Simard, Richard G Jung, et al.
Journal of the American College of Cardiology|July 23, 2021
Predictors of Device-Related Thrombus Following Percutaneous Left Atrial Appendage OcclusionTrevor Simard, Richard G Jung, Kyle Lehenbauer, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Pageof 127