847 results on '"Stoll, Monika"'
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2. Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
3. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.
4. In situ lipid-loading activates peripheral dendritic cell subsets characterized by cellular ROS accumulation but compromises their capacity to prime naïve T cells
5. Transcriptomic research in atherosclerosis: Unravelling plaque phenotype and overcoming methodological challenges
6. MicroRNA-216a is essential for cardiac angiogenesis
7. Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death
8. Genomic instability in the naturally and prematurely aged myocardium
9. Assessment of angiogenesis-related parameters in juvenile idiopathic arthritis-associated uveitis
10. Atrial fibrillation in the presence and absence of heart failure enhances expression of genes involved in cardiomyocyte structure, conduction properties, fibrosis, inflammation, and endothelial dysfunction
11. Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
12. Monocyte subpopulation profiling indicates CDK6-derived cell differentiation and identifies subpopulation-specific miRNA expression sets in acute and stable coronary artery disease
13. Polymorphisms in the mTOR-PI3K-Akt pathway, energy balance-related exposures and colorectal cancer risk in the Netherlands Cohort Study
14. Studies in Zebra Fish and Rat Models Support Dual Blockade of EP2 and EP4 (Prostaglandin E2 Receptors Type 2 and 4) for Renoprotection in Glomerular Hyperfiltration and Albuminuria
15. Validation of a predictive model for identifying an increased risk for recurrence in adolescents and young adults with a first provoked thromboembolism
16. Correction to: Role of prothrombin 19,911 A > G polymorphism, blood group and male gender in patients with venous thromboembolism: results of a german cohort study
17. Cpxm2 as a novel candidate for cardiac hypertrophy and failure in hypertension
18. Human atherosclerotic plaque transcriptomics reveals endothelial beta-2 spectrin as a potential regulator a leaky plaque microvasculature phenotype
19. Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study
20. Genotype–Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study
21. LncRNA Bigheart trans-activates gene expression in a feed forward mechanism that facilitates calcineurin-NFAT signaling in myocardial hypertrophy
22. In situ lipid-loading activates peripheral dendritic cell subsets characterized by cellular ROS accumulation but compromises their capacity to prime naïve T cells
23. Nur77 serves as a molecular brake of the metabolic switch during T cell activation to restrict autoimmunity
24. Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
25. Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism
26. Dichotomy between the transcriptomic landscape of naturally versus accelerated aged murine hearts
27. A Genomic-Systems Biology Map for Cardiovascular Function
28. Genotype–Phenotype Relationship among 785 Unrelated White Women with Inherited Congenital Factor VII Deficiency: A Three-Center Database Study.
29. Cell-intrinsic genomic reassortment of pandemic H1N1 2009 and Eurasian avian-like swine influenza viruses results in potentially zoonotic variants.
30. Ablation of biglycan attenuates cardiac hypertrophy and fibrosis after left ventricular pressure overload
31. Autoinhibitory regulation of S100A8/S100A9 alarmin activity locally restricts sterile inflammation
32. Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study
33. PO-02-144 ETIOLOGICAL AND MOLECULAR DETERMINANTS OF ATRIAL ENDOMYSIAL FIBROSIS: RESULTS FROM THE CATCH ME CONSORTIUM
34. MP-453085-5 ATRIAL FIBRILLATION, FEMALE SEX AND HEART HAILURE ARE THE MAIN DRIVERS OF ATRIAL CARDIOMYOPATHY IN CARDIAC SURGERY PATIENTS: RESULTS FROM THE CATCH ME CONSORTIUM
35. DNA methylation links between depression and immunity
36. Supplementary Materials from Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma
37. Supplementary Figures 4 - 6 from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
38. Supplementary Figure 3 from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
39. Supplementary Figure Legend from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
40. Supplementary Figures S1-6 from Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma
41. Supplementary Figure 1 from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
42. Supplementary Tables S1-6 from Deep Sequencing in Conjunction with Expression and Functional Analyses Reveals Activation of FGFR1 in Ewing Sarcoma
43. Supplementary Figure 2 from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
44. Supplementary Tables 1 - 3 from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
45. Supplementary Methods from DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target Genes
46. Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum
47. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
48. DNA repair in cardiomyocytes is critical for maintaining cardiac function in mice
49. Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease
50. Interaktionen in Kindertageseinrichtungen: Theorie und Praxis im interdisziplinären Dialog
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