Search Results - "LONDON, Barry"
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1
JAHA : The End of the Beginning
Published in Journal of the American Heart Association (20-12-2022)Get full text
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2
Reviewing Peer Review
Published in Journal of the American Heart Association (03-08-2021)Get full text
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3
Diversity, Equity, and Inclusiveness in Medicine and Cardiology
Published in Journal of the American Heart Association (01-09-2020)Get full text
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4
Mouse models of long QT syndrome
Published in The Journal of physiology (01-01-2007)“…Congenital long QT syndrome is a rare inherited condition characterized by prolongation of action potential duration (APD) in cardiac myocytes, prolongation of…”
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5
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
Published in Circulation (New York, N.Y.) (22-01-2019)“…BACKGROUND:Heart failure (HF) is a morbid and heritable disorder for which the biological mechanisms are incompletely understood. We therefore examined genetic…”
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6
Study familial hypertrophic cardiomyopathy using patient-specific induced pluripotent stem cells
Published in Cardiovascular research (01-11-2014)“…Familial hypertrophic cardiomyopathy (HCM) is one the most common heart disorders, with gene mutations in the cardiac sarcomere. Studying HCM with…”
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7
Cardiac Implantable Electronic Device Infections: Who is at Greatest Risk?
Published in Heart rhythm (01-06-2017)“…Abstract Background Cardiac Implantable Electronic Device (CIED) infections are associated with hospitalization, mortality, increased costs and adverse…”
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8
Genetics of Atrial Fibrillation
Published in Journal of the American Heart Association (16-10-2018)“…Background Atrial fibrillation ( AF ) is a common arrhythmia seen in clinical practice. Occasionally, no common risk factors are present in patients with this…”
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9
Mechanism of automaticity in cardiomyocytes derived from human induced pluripotent stem cells
Published in Journal of molecular and cellular cardiology (01-04-2015)“…Abstract Background and objectives. The creation of cardiomyocytes derived from human induced pluripotent stem cells (hiPS-CMs) has spawned broad excitement…”
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10
Deficiency of endothelial sirtuin1 in mice stimulates skeletal muscle insulin sensitivity by modifying the secretome
Published in Nature communications (11-09-2023)“…Downregulation of endothelial Sirtuin1 (Sirt1) in insulin resistant states contributes to vascular dysfunction. Furthermore, Sirt1 deficiency in skeletal…”
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11
Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias
Published in Circulation (New York, N.Y.) (13-11-2007)“…Brugada syndrome is a rare, autosomal-dominant, male-predominant form of idiopathic ventricular fibrillation characterized by a right bundle-branch block and…”
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12
Current Perspectives on Coronavirus Disease 2019 and Cardiovascular Disease: A White Paper by the JAHA Editors
Published in Journal of the American Heart Association (16-06-2020)“…Coronavirus Disease 2019 (COVID-19) has infected more than 3.0 million people worldwide and killed more than 200,000 as of April 27, 2020. In this White Paper,…”
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13
The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome
Published in Frontiers in medicine (19-06-2024)“…Brugada Syndrome (BrS) is an inherited arrhythmia syndrome in which mutations in the cardiac sodium channel (Na 1.5) account for approximately 20% of cases…”
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14
Knockout of Sorbin And SH3 Domain Containing 2 (Sorbs2) in Cardiomyocytes Leads to Dilated Cardiomyopathy in Mice
Published in Journal of the American Heart Association (05-07-2022)“…Background Sorbin and SH3 domain containing 2 (Sorbs2) protein is a cytoskeletal adaptor with an emerging role in cardiac biology and disease; yet, its…”
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15
Cardiac Arrhythmias: From (Transgenic) Mice to Men
Published in Journal of cardiovascular electrophysiology (01-09-2001)“…Cardiac Arrhythmias. Transgenic and gene‐targeted mice now are frequently used to study cardiac arrhythmias due to the ease with which the mouse genome can be…”
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16
Molecular and functional characterization of novel glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) mutations in sudden infant death syndrome
Published in Circulation (New York, N.Y.) (13-11-2007)“…Autopsy-negative sudden unexplained death, including sudden infant death syndrome, can be caused by cardiac channelopathies such as Brugada syndrome (BrS)…”
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17
Left Ventricular Diameter and Risk Stratification for Sudden Cardiac Death
Published in Journal of the American Heart Association (16-09-2014)“…Background Left ventricular (LV) diameter is routinely measured on the echocardiogram but has not been jointly evaluated with the ejection fraction (EF) for…”
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18
Cardiac Adverse Events Associated With Chemo-Radiation Versus Chemotherapy for Resectable Stage III Non-Small-Cell Lung Cancer: A Surveillance, Epidemiology and End Results-Medicare Study
Published in Journal of the American Heart Association (06-12-2022)“…Background We compared cardiac outcomes for surgery-eligible patients with stage III non-small-cell lung cancer treated adjuvantly or neoadjuvantly with…”
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19
Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy
Published in Heart rhythm (01-03-2012)“…Background Dilated cardiomyopathy (DCM) is a leading cause of heart failure and death. The etiology of DCM is genetically heterogeneous. Objectives We sought…”
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Estimated Cardiac Risk Associated With Macrolides and Fluoroquinolones Decreases Substantially When Adjusting for Patient Characteristics and Comorbidities
Published in Journal of the American Heart Association (01-05-2018)“…Background Some studies have found that antimicrobials, especially macrolides, increase the risk of cardiovascular death. We investigated potential…”
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