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1. The G4 resolvase Dhx36 modulates cardiomyocyte differentiation and ventricular conduction system development

4. Author Correction: Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferation

5. Endogenous IL-1 receptor antagonist restricts healthy and malignant myeloproliferation

6. Heteroplasmy of Wild-Type Mitochondrial DNA Variants in Mice Causes Metabolic Heart Disease With Pulmonary Hypertension and Frailty

7. Incongruence between transcriptional and vascular pathophysiological cell states

10. Extreme downregulation of Y chromosome in blood confers increased risk of atherosclerotic disease

11. SpatialDDLS: an R package to deconvolute spatial transcriptomics data using neural networks.

12. Incongruence between transcriptional and vascular pathophysiological cell states

13. A Human Hereditary Cardiomyopathy Shares a Genetic Substrate with Bicuspid Aortic Valve:[Inkl. Correction]

14. Definition of a cell surface signature for human cardiac progenitor cells after comprehensive comparative transcriptomic and proteomic characterization

15. A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve

17. Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing

19. Pluripotency factors regulate the onset of Hox cluster activation in the early embryo

20. Wt1 transcription factor impairs cardiomyocyte specification and drives a phenotypic switch from myocardium to epicardium

21. Pluripotency factors regulate the onset of Hox cluster activation in the early embryo

22. Corrigendum: Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing

23. Correction: Wt1 transcription factor impairs cardiomyocyte specification and drives a phenotypic switch from myocardium to epicardium

24. Abstract 418: 18 FDG-PET Monitors Atherosclerosis Disease Activity In Minipigs.

25. Wt1 transcription factor impairs cardiomyocyte specification and drives a phenotypic switch from myocardium to epicardium

28. Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve.

29. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

30. Downregulation of WT1 transcription factor gene expression is required to promote myocardial fate

31. The zebrafish reference genome sequence and its relationship to the human genome

33. Definition of a cell surface signature for human cardiac progenitor cells after comprehensive comparative transcriptomic and proteomic characterization

34. Nanog regulates Pou3f1 expression at the exit from pluripotency during gastrulation

35. Nanog regulates Pou3f1 expression at the exit from pluripotency during gastrulation

37. Nanog regulates Pou3f1 expression and represses anterior fate at the exit from pluripotency

38. Pluripotency factors regulate the onset of Hox cluster activation in the early embryo

39. Ablation of the stress protease OMA1 protects against heart failure in mice

41. CTCF counter-regulates cardiomyocyte development and maturation programs in the embryonic heart

42. CXCL6 is an important paracrine factor in the pro-angiogenic human cardiac progenitor-like cell secretome

43. CTCF counter-regulates cardiomyocyte development and maturation programs in the embryonic heart

44. Erratum: Corrigendum: Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing

46. Sequential Notch activation regulates ventricular chamber development

47. Meis1 coordinates a network of genes implicated in eye development and microphthalmia

48. Hedgehog lipid modifications are required for Hedgehog stabilization in the extracellular matrix

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