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2. Single-Nuclear RNA Sequencing of Endomyocardial Biopsies Identifies Persistence of Donor-Recipient Chimerism With Distinct Signatures in Severe Cardiac Allograft Vasculopathy

3. A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos)

5. SnRNA sequencing defines signaling by RBC-derived extracellular vesicles in the murine heart

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

8. Transcriptome variation in human tissues revealed by long-read sequencing

9. Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy

11. Deep learning enables genetic analysis of the human thoracic aorta

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

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

15. Loss of the Atrial Fibrillation-Related Gene, Zfhx3 , Results in Atrial Dilation and Arrhythmias

16. Transcriptional and Cellular Diversity of the Human Heart

18. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation

19. Multi-ethnic genome-wide association study for atrial fibrillation

21. Deep learning enables genetic analysis of the human thoracic aorta

23. Sex-specific responses to slow progressive pressure overload in a large animal model of HFpEF

24. COVID-19 and Cardiovascular Disease

25. Single-nuclear RNA sequencing of endomyocardial biopsies identifies persistence of donor-recipient chimerism with distinct signatures in severe cardiac allograft vasculopathy

27. Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential

29. Clinico-histopathologic and single-nuclei RNA-sequencing insights into cardiac injury and microthrombi in critical COVID-19

31. Deep learning enables genetic analysis of the human thoracic aorta

32. Abstract 14422: Molecular Pathogenesis of Cardiac Microthrombi in Fatal Covid-19: Insights from Clinico-histopathologic and Single Nuclei RNA Sequencing Analyses

33. Abstract 8955: Cardiopulmonary Phenotyping of Sex-Based Differences in a Feline Model of HFpEF

34. Molecular Pathophysiology of Cardiac Injury and Cardiac Microthrombi in Fatal COVID-19: Insights from Clinico-histopathologic and Single Nuclei RNA Sequencing Analyses

35. Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear (Ursus arctos).

36. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

37. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation

38. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

39. Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation

40. Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

41. Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 Mediated Myocarditis

42. Deep learning enables genetic analysis of the human thoracic aorta

43. Transcriptional and Cellular Diversity of the Human Heart

44. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

45. Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

46. Genome-Wide Association Study–Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse

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

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

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

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