48 results on '"London, Barry"'
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2. Abstract 4147419: EKG Abnormalities and Homozygous Embryonic Lethality in Gene-Targeted Mice Mimicking K1479 Acetylation of the Cardiac Na+ Channel Nav1.5
3. Abstract 4142680: Functional Heterogeneity of NaV1.5 in Mouse Heart
4. Abstract 4134792: SIRTUIN5 Modulates Na+/Ca2+ Handling Via Oxidative Stress Dependent Manner In Mouse Heart
5. Abstract 14676: Susceptibility to Cardiac-Targeted Irradiation in Wild-Type and Nos1 Haploinsufficient Mice
6. Abstract 14488: Male Predominant Cardiac Phenotype in Cardiac-Specific Gpd1-l Knockout Mice
7. Abstract 13147: Monitoring Central Arterial Pressure on the Chest Surface: Initial Results From Two Pilot Studies in Human Subjects
8. Abstract 13201: Sex Difference Following Cardiac-Targeted Irradiation in Mice
9. Abstract 16997: Reaffirmation of GPD1L-A280V as a Brugada Syndrome Disease-Causing Variant
10. Letter by London Regarding Article, “Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome”
11. Medical Misinformation: Vet the Message!
12. Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
13. Abstract 19265: Differential Dose-Dependent Effects of Nicotinamide on the Cardiac Sodium Channel: Insights on a Novel Therapeutic Approach for Sudden Cardiac Death
14. Abstract 15138: GWAS Identifies GPC6 as a Novel Predictor of Arrhythmia in Heart Failure
15. Abstract 13735: External Defibrillation During MRI: Feasibility and Safety
16. Abstract 13546: Putative Titin Mutations Associated With Both Long QT Syndrome and Left Ventricular Noncompaction
17. Abstract 11720: Loss of Vascular Smooth-Muscle Activity During Moderate Physical Activity as a Hallmark of Aging in Human Subjects
18. Abstract 14372: The Acquired Long QT-Causing Drugs Haloperidol and Terfenadine Cause Defects in HERG Trafficking
19. Abstract 14053: Sumoylation of the Cardiac Sodium Channel Na V 1.5 Does Not Increase Late Sodium Current
20. Medical Misinformation
21. Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery.
22. Abstract 16940: Serum Amine-based Metabolites and Their Association With Outcomes in Primary Prevention Implantable Cardioverter Defibrillator Patients
23. Abstract 17984: No Longer Silent: A Synonymous Coding SNP Modifying a Novel MicroRNA-24:SCN5A Interaction Associates With Non-Arrhythmic Death in Heart Failure
24. Abstract 19030: High Mortality in Cardiomyopathy Patients Heterozygous for the CFTR ΔF508 Cystic Fibrosis Mutation
25. Abstract 18890: An MYH7 Mutation Causes Inherited Left Ventricular Noncompaction and Sudden Death in a Large Multigenerational Family
26. Abstract 18586: GPD1-L Inhibits the Cardiac Sodium Channel Nav1.5 by decreasing SIRTUIN1 Activity
27. Abstract 19390: Sirtuin 1 Modulates Cardiac Sodium Channels in vivo
28. In Memoriam Tribute to James A. Shaver, MD
29. Abstract 16912: The Incidence of the First Appropriate ICD Shock Remains Stable in Heart Failure Patients Over 6 Years
30. Understanding Cardiac Calcium Channelopathies
31. Abstract 5346: Regulation of Cardiac Na + Current by Pyridine Nucleotides: A Possible Explanation of Glycerol-3-Phosphate Dehydrogenase-Linked Brugada Syndrome
32. Systems Approach to Understanding Electromechanical Activity in the Human Heart
33. Mutation in Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Decreases Cardiac Na + Current and Causes Inherited Arrhythmias
34. Molecular and Functional Characterization of Novel Glycerol-3-Phosphate Dehydrogenase 1–Like Gene ( GPD1-L ) Mutations in Sudden Infant Death Syndrome
35. Abstract 2968: Postmortem Genetic Testing of the GPD1-L-Encoded Glycerol-3-Phosphate Dehydrogenase 1-Like Protein in Sudden Infant Death Syndrome
36. Abstract 2378: The MinK G38S Polymorphism Associates with Atrial Arrhythmias after Subarachnoid Hemorrhage
37. Omega-3 Fatty Acids and Cardiac Arrhythmias: Prior Studies and Recommendations for Future Research
38. Response to Letter Regarding Article, “Upsurge in T-Wave Alternans and Nonalternating Repolarization Instability Precedes Spontaneous Initiation of Ventricular Tachyarrhythmias in Humans”
39. Upsurge in T-Wave Alternans and Nonalternating Repolarization Instability Precedes Spontaneous Initiation of Ventricular Tachyarrhythmias in Humans
40. Transcription Enhancer Factor-1-Related Factor-Transgenic Mice Develop Cardiac Conduction Defects Associated With Altered Connexin Phosphorylation
41. Effect of the Asp 298 Variant of Endothelial Nitric Oxide Synthase on Survival for Patients With Congestive Heart Failure
42. Clinical and Molecular Heterogeneity in the Brugada Syndrome
43. Pharmacogenetic Interactions Between β-Blocker Therapy and the Angiotensin-Converting Enzyme Deletion Polymorphism in Patients With Congestive Heart Failure
44. A Knockout May Not Always Be a Knockout
45. Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias.
46. Abstract 16296: The Acetylatable Lysine Residue of the Cardiac Sodium Channel Regulates Membrane Localization Through Interactions With the Cytoskeletal Anchoring Protein α-Actinin 2.
47. Abstract 15342: Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery.
48. Effect of the Asp298 variant of endothelial nitric oxide synthase on survival for patients with congestive heart failure.
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