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Barbara A Sampson

Showing results (11-20 of 25) with videos related to

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Forensic Science International|November 5, 2018
Functional characterization of TRPM4 variants identified in sudden unexpected natural deathEkaterina Subbotina, Nori Williams, Barbara A Sampson, et al.
Pacing and Clinical Electrophysiology : PACE|December 23, 2018
Functional reclassification of variants of uncertain significance in the HCN4 gene identified in sudden unexpected deathJingyun Dong, Ekaterina Subbotina, Nori Williams, et al.
Forensic Science International|June 14, 2019
Functional characterization of SCN10A variants in several cases of sudden unexplained deathIvan Gando, Nori Williams, Glenn I Fishman, et al.
Forensic Science International|March 18, 2019
Functional characterization of ABCC9 variants identified in sudden unexpected natural deathEkaterina Subbotina, Hua-Qian Yang, Ivan Gando, et al.
American Heart Journal|April 9, 2011
Women have less severe and extensive coronary atherosclerosis in fatal cases of ischemic heart disease: an autopsy studyNathaniel R Smilowitz, Barbara A Sampson, Christopher R Abrecht, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 28, 2023
Molecular genetic characterization of sudden deaths due to thoracic aortic dissection or ruptureSarah Saxton, Gregory Dickinson, Dawei Wang, et al.
Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.
Forensic Science International|March 11, 2020
Using postmortem formalin fixed paraffin-embedded tissues for molecular testing of sudden cardiac death: A cautionary tale of utility and limitationsYing Lin, Tatyana Gryazeva, Dawei Wang, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 4, 2018
Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case seriesNori Williams, Robert Marion, Thomas V McDonald, et al.
Circulation. Cardiovascular Genetics|December 17, 2017
Applying High-Resolution Variant Classification to Cardiac Arrhythmogenic Gene Testing in a Demographically Diverse Cohort of Sudden Unexplained DeathsYing Lin, Nori Williams, Dawei Wang, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Forensic Science International|November 5, 2018
Functional characterization of TRPM4 variants identified in sudden unexpected natural deathEkaterina Subbotina, Nori Williams, Barbara A Sampson, et al.
Pacing and Clinical Electrophysiology : PACE|December 23, 2018
Functional reclassification of variants of uncertain significance in the HCN4 gene identified in sudden unexpected deathJingyun Dong, Ekaterina Subbotina, Nori Williams, et al.
Forensic Science International|June 14, 2019
Functional characterization of SCN10A variants in several cases of sudden unexplained deathIvan Gando, Nori Williams, Glenn I Fishman, et al.
Forensic Science International|March 18, 2019
Functional characterization of ABCC9 variants identified in sudden unexpected natural deathEkaterina Subbotina, Hua-Qian Yang, Ivan Gando, et al.
American Heart Journal|April 9, 2011
Women have less severe and extensive coronary atherosclerosis in fatal cases of ischemic heart disease: an autopsy studyNathaniel R Smilowitz, Barbara A Sampson, Christopher R Abrecht, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 28, 2023
Molecular genetic characterization of sudden deaths due to thoracic aortic dissection or ruptureSarah Saxton, Gregory Dickinson, Dawei Wang, et al.
Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.
Forensic Science International|March 11, 2020
Using postmortem formalin fixed paraffin-embedded tissues for molecular testing of sudden cardiac death: A cautionary tale of utility and limitationsYing Lin, Tatyana Gryazeva, Dawei Wang, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|October 4, 2018
Phenotypic variations in carriers of predicted protein-truncating genetic variants in MYBPC3: an autopsy-based case seriesNori Williams, Robert Marion, Thomas V McDonald, et al.
Circulation. Cardiovascular Genetics|December 17, 2017
Applying High-Resolution Variant Classification to Cardiac Arrhythmogenic Gene Testing in a Demographically Diverse Cohort of Sudden Unexplained DeathsYing Lin, Nori Williams, Dawei Wang, et al.
Pageof 3