All Stories

  1. 3D Carbon-Nanotube-Based Composites for Cardiac Tissue Engineering
  2. Carbon Nanotube Facilitation of Myocardial Ablation with Radiofrequency Energy
  3. Decreased Levels of BAG3 in a Family With a Rare Variant and in Idiopathic Dilated Cardiomyopathy
  4. Exploring the elasticity and adhesion behavior of cardiac fibroblasts by atomic force microscopy indentation
  5. Family Members of Patients With ARVC
  6. Pharmacogenetics of heart failure
  7. Inhibition of Proto-Oncogene c-Src Tyrosine Kinase
  8. Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update
  9. Whole Exome Sequencing Identifies a Troponin T Mutation Hot Spot in Familial Dilated Cardiomyopathy
  10. Poor Prognosis of Rare Sarcomeric Gene Variants in Patients with Dilated Cardiomyopathy
  11. Cardiac Hypertrophy, Accessory Pathway, and Conduction System Disease in an Adolescent
  12. Atomic force microscopy of 3T3 and SW-13 cell lines: An investigation of cell elasticity changes due to fixation
  13. Carbon Nanotubes Instruct Physiological Growth and Functionally Mature Syncytia: Nongenetic Engineering of Cardiac Myocytes
  14. Improving cardiac myocytes performance by carbon nanotubes platforms†
  15. Utility of Cardiac Magnetic Resonance Imaging to Differentiate Cardiac Sarcoidosis from Arrhythmogenic Right Ventricular Cardiomyopathy
  16. Carbon Nanotubes Promote Growth and Spontaneous Electrical Activity in Cultured Cardiac Myocytes
  17. Truncations of Titin Causing Dilated Cardiomyopathy
  18. Sudden Death Associated With Danon Disease in Women
  19. High-throughput Genotyping Robot-assisted Method for Mutation Detection in Patients With Hypertrophic Cardiomyopathy
  20. Genetic Variation in Titin in Arrhythmogenic Right Ventricular Cardiomyopathy–Overlap Syndromes
  21. Hearing the Noise
  22. SCN5A Mutations Associate With Arrhythmic Dilated Cardiomyopathy and Commonly Localize to the Voltage-Sensing Mechanism
  23. Prognostic predictors in arrhythmogenic right ventricular cardiomyopathy: results from a 10-year registry
  24. Heart failure and personalized medicine
  25. Prognostic impact of familial screening in dilated cardiomyopathy
  26. Phenotypic Heterogeneity of Sarcomeric Gene Mutations
  27. Genetic Evaluation of Cardiomyopathy—A Heart Failure Society of America Practice Guideline
  28. Pharmacogenetic effect of an endothelin-1 haplotype on response to bucindolol therapy in chronic heart failure
  29. Lamin A/C Gene and the Heart
  30. Cardiomyopathy and carnitine deficiency
  31. The challenge of cardiomyopathies in 2007
  32. Are Nonsustained Ventricular Tachycardias Predictive of Major Arrhythmias in Patients with Dilated Cardiomyopathy on Optimal Medical Treatment?
  33. Danon disease presenting with dilated cardiomyopathy and a complex phenotype
  34. Prevalence of Desmin Mutations in Dilated Cardiomyopathy
  35. Ophthalmic Manifestations of Danon Disease
  36. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy
  37. α-Myosin Heavy Chain
  38. Drug Therapy in the Heart Transplant Recipient
  39. Drug Therapy in the Heart Transplant Recipient
  40. SCN5A Mutation Associated With Dilated Cardiomyopathy, Conduction Disorder, and Arrhythmia
  41. Analysis of Genetic Variations of Lamin A/C Gene (LMNA) by Denaturing High-Performance Liquid Chromatography
  42. Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing
  43. Familial Dilated Cardiomyopathy
  44. Genomic medicine and atrial fibrillation**Editorials published in the Journal of the American College of Cardiologyreflect the views of the authors and do not necessarily represent the views of JACCor the American College of Cardiology.
  45. Natural history of dilated cardiomyopathy due to lamin A/C gene mutations
  46. Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement
  47. Familial dilated cardiomyopathy
  48. Long-term effects of carvedilol in idiopathic dilated cardiomyopathy with persistent left ventricular dysfunction despite chronic metoprolol
  49. Guidelines for the study of familial dilated cardiomyopathies
  50. ADVANCES IN MOLECULAR GENETICS OF DILATED CARDIOMYOPATHY
  51. Dilated cardiomyopathy: a genetic approach.
  52. A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy
  53. A New Locus for Arrhythmogenic Right Ventricular Dysplasia on the Long Arm of Chromosome 14
  54. A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart.
  55. Familial dilated cardiomyopathy
  56. Absence of linkage between idiopathic dilated cardiomyopathy and candidate genes involved in the immune function in a large Italian pedigree.
  57. Low frequency of detection by nested polymerase chain reaction of enterovirus ribonucleic acid in endomyocardial tissue of patients with idiopathic dilated cardiomyopathy
  58. Evidence from family studies for autoimmunity in dilated cardiomyopathy
  59. Parental origin of the X chromosome in a patient with a Robertsonian translocation and Turner's syndrome.
  60. Clinical and pathologic study of familial dilated cardiomyopathy
  61. Correlation between histomorphometric findings on endomyocardial biopsy and clinical findings in idiopathic dilated cardiomyopathy
  62. Ventricular arrhythmias in dilated cardiomyopathy: Efficacy of amiodarone
  63. Arrhythmias in dilated cardiomyopathy.