222 results on '"Ishikawa, Taisuke"'
Search Results
2. Alkali ion-to-neutral atom converter for the magneto-optical trap of a radioactive isotope
3. Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model
4. Arrhythmogenic right ventricular cardiomyopathy in a Japanese patient with a homozygous founder variant of DSG2 in the East Asian population
5. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
6. Pathological findings of myocardium in a patient with cardiac conduction defect associated with an SCN5A mutation
7. Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
8. Cardiac Emerinopathy: A Non-syndromic Nuclear Envelopathy with Increased Risk of Thromboembolic Stroke due to Progressive Atrial Standstill and Left Ventricular Non-compaction
9. Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction
10. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
11. EN-452414-5 VENTRICULAR CONDUCTION IS A MARKER FOR ARRHYTHMIC RISK IN OVERLAP SODIUM CHANNEL DISEASE
12. Letter regarding “SCN9Avariant in a family of mixed breed dogs with congenital insensitivity to pain”—Navigating the pathogenicity of candidate gene mutations: Spotlight on paralog Nav genes
13. Inherited bradyarrhythmia: A diverse genetic background
14. Genotype-dependent differences in age of manifestation and arrhythmia complications in short QT syndrome
15. Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death
16. Targeted deep sequencing analyses of long QT syndrome in a Japanese population
17. Molecular mechanisms of heart failure progression associated with implantable cardioverter-defibrillator shocks for ventricular tachyarrhythmias
18. HCN4 pacemaker channels attenuate the parasympathetic response and stabilize the spontaneous firing of the sinoatrial node
19. Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers
20. Abstract 21144: Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation Carriers in Japan
21. Abstract 17926: CALM2-D134H Mutation Associated With Long-QT Syndrome Delayed Inactivation of L-type Ca2+ Currents in Human iPS Cells Derived Cardiomyocytes
22. Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder
23. BS-515-01 NON-CODING DELETION INDUCES 3D CHROMATIN REMODELLING AND PITX2 EXPRESSION DYSREGULATION ASSOCIATED WITH A SYNDROMIC CARDIAC DISORDER
24. Genetic defects in a His-Purkinje system transcription factor, IRX3, cause lethal cardiac arrhythmias
25. Correction: Targeted deep sequencing analyses of long QT syndrome in a Japanese population.
26. Heart-specific Small Subunit of Myosin Light Chain Phosphatase Activates Rho-associated Kinase and Regulates Phosphorylation of Myosin Phosphatase Target Subunit 1
27. Novel Mechanisms of Trafficking Defect Caused by KCNQ1 Mutations Found in Long QT Syndrome
28. Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants
29. Novel electrocardiographic criteria for short QT syndrome in children and adolescents
30. Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome
31. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
32. Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations
33. Dilated cardiomyopathy-associated BAG3 mutations impair Z-disc assembly and enhance sensitivity to apoptosis in cardiomyocytes
34. Ligand-free trifluoromethylation of iodoarenes by use of 2-Aryl-2-trifluoromethylbenzimidazoline as new trifluoromethylating reagent
35. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families
36. A Case Report: Two Young Children with Long QT Syndrome Type-2 Diagnosed by Presymptomatic Genetic Testing
37. Cardiac Emerinopathy
38. Catalytic trifluoromethylation of iodoarenes by use of 2-trifluoromethylated benzimidazoline as trifluoromethylating reagent
39. Pathological Features of Lamin Cardiomyopathy
40. TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway
41. Identification of transmembrane protein 168 mutation in familial Brugada syndrome
42. Desmin‐related myopathy characterized by non‐compaction cardiomyopathy, cardiac conduction defect, and coronary artery dissection
43. Comparative effects of amlodipine and benazepril on Left Atrial Pressure in Dogs with experimentally-induced Mitral Valve Regurgitation
44. Clinical Manifestations and Long-Term Mortality in Lamin A/C Mutation Carriers From a Japanese Multicenter Registry
45. Overexpression of heart-specific small subunit of myosin light chain phosphatase results in heart failure and conduction disturbance
46. Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation
47. Allele-specific ablation rescues electrophysiological abnormalities in a human iPS cell model of long-QT syndrome with a CALM2 mutation
48. A novel de novo calmodulin mutation in a 6-year-old boy who experienced an aborted cardiac arrest
49. Letter regarding "SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain"—Navigating the pathogenicity of candidate gene mutations: Spotlight on paralog Nav genes.
50. Clinical characteristics and risk of arrhythmia recurrences in patients with idiopathic ventricular fibrillation associated with early repolarization
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