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51. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

52. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

53. Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

54. GWAS-driven Pathway Analyses and Functional Validation Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse

55. Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

57. Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects

58. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

59. Gain-of-function mutations in GATA6 lead to atrial fibrillation

60. Long-range Pitx2c enhancer-promoter interactions prevent predisposition to atrial fibrillation.

61. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

62. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

63. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

66. PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance

67. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

68. Author response: Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

69. Myocyte-Specific Upregulation of in Cardiovascular Disease: Implications for SARS-CoV-2-Mediated Myocarditis.

70. Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.

71. Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects.

74. Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

75. Myocyte-Specific Upregulation of ACE2in Cardiovascular Disease

76. Abstract 18865: Identification of a Functional SNP Regulating PRRX1 at the 1q24 Locus for Atrial Fibrillation

77. Integrating Genetic, Transcriptional, and Functional Analyses to Identify 5 Novel Genes for Atrial Fibrillation

78. A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation

80. Overexpression of KCNN3 results in sudden cardiac death

82. Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures.

83. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

85. Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

86. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

87. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

88. Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation (vol 49, pg 946, 2017)

89. Increased atrial effectiveness of flecainide conferred by altered biophysical properties of sodium channels

91. Abstract 10573: Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

92. Genome-Wide Association Study–Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1as a Susceptibility Gene for Mitral Valve Prolapse

94. Highlights From the Family of Journals.

96. Novel Mutation in FLNC(Filamin C) Causes Familial Restrictive Cardiomyopathy

97. Diminished PRRX1Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential

98. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

99. Cardiomyocyte-derived circulating extracellular vesicles allow a non-invasive liquid biopsy of myocardium in health and disease.

100. Transcriptional profile of the rat cardiovascular system at single cell resolution.

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