816 results on '"London, Barry"'
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52. Abstract P2010: Cardiomyocyte Knockout Of Sorbs2 Rewires Cytoskeleton And Causes Dilated Cardiomyopathy
53. Abstract P3034: Acute Reduction Of Cardiac Sodium Channel Nav1.5 Increases Mitochondrial Calcium And Rewires Cardiac Metabolism
54. Evaluation of potential ionizing irradiation protectors and mitigators using clonogenic survival of human umbilical cord blood hematopoietic progenitor cells
55. Use of Transgenic and Gene-Targeted Mice to Study K+Channel Function in the Cardiovascular System
56. United We Stand; Divided We Fibrillate?
57. Abstract 19265: Differential Dose-Dependent Effects of Nicotinamide on the Cardiac Sodium Channel: Insights on a Novel Therapeutic Approach for Sudden Cardiac Death
58. Abstract 15138: GWAS Identifies GPC6 as a Novel Predictor of Arrhythmia in Heart Failure
59. Abstract 13735: External Defibrillation During MRI: Feasibility and Safety
60. Genetics of Sudden Cardiac Death
61. Angiotensin Receptor Type 1 Single Nucleotide Polymorphism 1166A/C is Associated With Malignant Arrhythmias and Altered Circulating miR-155 Levels in Patients With Chronic Heart Failure
62. Genetic variation in the alternative splicing regulator RBM20 is associated with dilated cardiomyopathy
63. Cardiac levels of NOS1AP RNA from right ventricular tissue recovered during lead extraction
64. Survival Benefit of Implantable Cardioverter-Defibrillators in Left Ventricular Assist Device–Supported Heart Failure Patients
65. Knockout of Sorbin And SH3 Domain Containing 2 (Sorbs2) in Cardiomyocytes Leads to Dilated Cardiomyopathy in Mice
66. Metabolic rescue ameliorates mitochondrial encephalo‐cardiomyopathy in murine and human iPSC models of Leigh syndrome
67. PO-676-01 A VERSATILE CHEMICAL-GENETIC APPROACH TO DETERMINE BASES FOR ARRHYTHMOGENESIS AND SODIUM CHANNELOPATHIES
68. Cardiac Arrhythmias
69. Knockout of Sorbs2 in Cardiomyocytes Leads to Dilated Cardiomyopathy in Mice
70. Defining the Complexity of the Junctional Membrane Complex
71. Impact of Neuroeffector Adrenergic Receptor Polymorphisms on Incident Ventricular Fibrillation During Acute Myocardial Ischemia.
72. Targeting Device Therapy: Genomics of Sudden Death
73. Sex-differences in sodium/calcium exchange expression is a determinant of the arrhythmia phenotype in pre-pubertal rabbit hearts with Long QT type 2
74. Metabolic rescue ameliorates mitochondrial encephalo-cardiomyopathy in murine and human iPSC models of Leigh syndrome
75. The microRNA‐204‐5p inhibits APJ signalling and confers resistance to cardiac hypertrophy and dysfunction
76. Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction
77. Abstract 11720: Loss of Vascular Smooth-Muscle Activity During Moderate Physical Activity as a Hallmark of Aging in Human Subjects
78. Abstract 14372: The Acquired Long QT-Causing Drugs Haloperidol and Terfenadine Cause Defects in HERG Trafficking
79. Abstract 14053: Sumoylation of the Cardiac Sodium Channel Na V 1.5 Does Not Increase Late Sodium Current
80. The role of cardiac magnetic resonance imaging in the evaluation of malignant ventricular arrhythmias in Brugada syndrome
81. Reconciling computer models and stem cell models of human cardiac repolarization: reply
82. The many faces of repolarization instability: which one is prognostic?
83. Complex Trust Taxation: A Proposed Reform
84. Admission to the Pennsylvania Bar: The Need for Sweeping Change
85. Reviewing Peer Review
86. Dissection of the voltage-activated potassium outward currents in adult mouse ventricular myocytes: I to,f, I to,s, I K,slow1, I K,slow2, and I ss
87. Prevention of adverse electrical and mechanical remodeling with biventricular pacing in a rabbit model of myocardial infarction
88. Design of a Phase 1/2 Trial of Intracoronary Administration of AAV1/SERCA2a in Patients With Heart Failure
89. Adrenergic stimulation promotes T-wave alternans and arrhythmia inducibility in a TNF-[alpha] genetic mouse model of congestive heart failure
90. Study familial hypertrophic cardiomyopathy using patient-specific induced pluripotent stem cells
91. Ventricular Arrhythmia Risk After Subarachnoid Hemorrhage
92. Arrhythmia phenotype in mouse models of human long QT
93. A sodium channel pore mutation causing Brugada syndrome
94. Electrical remodeling of cardiac myocytes from mice with heart failure due to the overexpression of tumor necrosis factor-[alpha]
95. Renal insufficiency predicts the time to first appropriate defibrillator shock
96. Recurrent exercise-induced ventricular tachycardia in a patient with Brugada syndrome
97. Contributors
98. Arrhythmias
99. Atrial contractile dysfunction, fibrosis, and arrhythmias in a mouse model of cardiomyopathy secondary to cardiac-specific overexpression of tumor necrosis factor-[alpha]
100. Clinical Importance of β-Adrenoceptor Polymorphisms in Cardiovascular Disease
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