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222 results on '"Ishikawa, Taisuke"'

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1. TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

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

5. Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci

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

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

16. Targeted deep sequencing analyses of long QT syndrome in a Japanese population

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

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.

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

35. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families

37. Cardiac Emerinopathy

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

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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