303 results on '"Barajas-Martinez, Hector"'
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2. Gene and stem cell therapy for inherited cardiac arrhythmias
3. Underlying mechanism of atrial fibrillation–associated Nppa-I137T mutation and cardiac effect of potential drug therapy
4. Abstract 17335: Novel Functional Genomic Studies in Scn1bb Variant Associated With Brugada Syndrome and the Ameliorative Effect of Acacetin
5. Abstract 17334: Association of BIN1 Deletion With Electrical and Structural Remodeling in a Transgenic BIN1 KO Mouse Model of Heart Failure-Novel Option for Effective Therapy Using VK-II-86
6. Abstract 11956: Arumenamide-787 Suppresses Arrhythmogenesis Associated With the J Wave Syndrome as Well as Hypothermia
7. Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome
8. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
9. Role of multimodality imaging in a patient with posterior left ventricular aneurysm and non-compaction: Review of the literature.
10. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
11. J Wave Syndromes: Brugada and Early Repolarization Syndromes
12. Intracellular uptake of agents that block the hERG channel can confound the assessment of QT interval prolongation and arrhythmic risk
13. Frequency of Irritable Bowel Syndrome in Patients with Brugada Syndrome and Drug-Induced Type 1 Brugada Pattern
14. Rings and ovoid heart: OCIR. A new cardiomyopathy? Family genetic findings and multimodality imaging analysis. A rare cardiac phenotype and review of the literature
15. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
16. Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease
17. Editorial: Arrhythmias in women
18. A novel three base-pair deletion in domain two of the cardiac sodium channel causes Brugada syndrome
19. Relation of the Brugada Phenocopy to Hyperkalemia (from the International Registry on Brugada Phenocopy)
20. Prevalence of spontaneous Brugada ECG pattern recorded at standard intercostal leads: A meta-analysis
21. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility
22. The Phenotypic Spectrum of a Mutation Hotspot Responsible for the Short QT Syndrome
23. The Small Conductance Calcium-Activated Potassium Channel Inhibitors NS8593 and UCL1684 Prevent the Development of Atrial Fibrillation Through Atrial-Selective Inhibition of Sodium Channel Activity
24. Mechanisms underlying the antiarrhythmic effect of ARumenamide-787 in experimental models of the J wave syndromes and hypothermia
25. Functional identification of hot-spot mutations in cardiac calcium channel genes associated with the J wave syndromes
26. Advances in basic and translational research in atrial fibrillation
27. Cellular and ionic mechanisms underlying the effects of cilostazol, milrinone, and isoproterenol to suppress arrhythmogenesis in an experimental model of early repolarization syndrome
28. Mechanisms underlying atrial-selective block of sodium channels by Wenxin Keli: Experimental and theoretical analysis
29. Biophysical and molecular comparison of sodium current in cells isolated from canine atria and pulmonary vein
30. Acacetin, a Potent Transient Outward Current Blocker, May Be a Novel Therapeutic for KCND3 -Encoded Kv4.3 Gain-of-Function-Associated J-Wave Syndromes
31. Mechanisms underlying the development of the electrocardiographic and arrhythmic manifestations of early repolarization syndrome
32. ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene
33. Effect of Wenxin Keli and quinidine to suppress arrhythmogenesis in an experimental model of Brugada syndrome
34. Clinical Characteristics and Electrophysiologic Properties of SCN5A Variants in Fever-Induced Brugada Syndrome
35. Abstract 21344: Mutations in CACNA1C and KCNE2 Genes are Associated With Brugada Syndrome and Epilepsy
36. About half of the late sodium current in cardiac myocytes from dog ventricle is due to non-cardiac-type Na+ channels
37. Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant
38. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Nav1.5 and Kv4.3 channel currents
39. Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8
40. Atrial-selective inhibition of sodium-channel current by Wenxin Keli is effective in suppressing atrial fibrillation
41. PO-615-05 ACACETIN, A POTENT TRANSIENT OUTWARD CURRENT BLOCKER, MAY BE A NOVEL THERAPEUTIC FOR KCND3-ENCODED KV4.3 GAIN-OF-FUNCTION-ASSOCIATED J-WAVE SYNDROMES
42. Modulation of canine cardiac sodium current by Apelin
43. Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
44. Abstract 12296: Clinical and Functional Genetic Characterization of the Role of Cardiac Calcium Channel Variants in the Early Repolarization Syndrome
45. Abrogation of CC Chemokine Receptor 9 Ameliorates Ventricular Electrical Remodeling in Mice After Myocardial Infarction
46. SCN5A Mutation associated with acute myocardial infarction
47. Common variants in SCN10A gene associated with Brugada syndrome
48. Overlap Arrhythmia Syndromes Resulting from Multiple Genetic Variations Studied in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
49. Novel polygenetic variants evidenced in a patient with Jervell and Lange-Nielsen syndrome
50. BS10 A carvedilol analogue, VKII-86, prevents hypokalaemia-induced ventricular arrhythmia through novel multi-channel effects
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