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6. Biobank-driven genomic discovery yields new insight into atrial fibrillation biology

8. Contributors

10. Mitochondrial oxidative stress contributes to diastolic dysfunction through impaired mitochondrial dynamics

12. Cardiac Kir2.1 and NaV1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

16. SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients

17. Author response: SNTA1 gene rescues ion channel function and is antiarrhythmic in cardiomyocytes derived from induced pluripotent stem cells from muscular dystrophy patients

19. SNTA1 GeneRescues Ion Channel Function in Cardiomyocytes Derived from Induced Pluripotent Stem Cells Reprogrammed from Muscular Dystrophy Patients with Arrhythmias

21. In vitro model of ischemic heart failure using human induced pluripotent stem cell–derived cardiomyocytes

22. Loss of H3K4 methylation destabilizes gene expression patterns and physiological functions in adult murine cardiomyocytes

24. Power output is linearly related to MyHC content in rat skinned myocytes and isolated working hearts

25. Abnormal myocardial expression of SAP97 is associated with arrhythmogenic risk

31. Contributors

32. Brugada syndrome trafficking-defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels

33. HDAC inhibitor valproic acid protects heart function through Foxm1 pathway after acute myocardial infarction

35. Bipolar Patient Specific In vitroDiagnostic Test Reveals Underlying Cardiac Arrhythmia Phenotype Caused by Calcium Channel Genetic Risk Factor

36. Detection of Drug-Induced Torsades de Pointes Arrhythmia Mechanisms Using hiPSC-CM Syncytial Monolayers in a High-Throughput Screening Voltage Sensitive Dye Assay.

37. Brugada syndrome trafficking–defective Nav1.5 channels can trap cardiac Kir2.1/2.2 channels

38. Cardiac Kir2.1 and Na V 1.5 Channels Traffic Together to the Sarcolemma to Control Excitability

39. Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation

40. Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

41. HDAC Inhibitor Valproic Acid Protects Heart Function Through Foxm1 Pathway after Acute Myocardial Infarction

43. Complement Destabilizes Cardiomyocyte Function in Vivo after Polymicrobial Sepsis and In Vitro 2

44. Designing heart performance by gene transfer

47. Functional cardiac fibroblasts derived from human pluripotent stem cells via second heart field progenitors.

48. Loaded shortening and power output in cardiac myocytes are dependent on myosin heavy chain isoform expression

50. Complement Destabilizes Cardiomyocyte Function In Vivo after Polymicrobial Sepsis and In Vitro

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