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3. Somatic RIT1 delins in arteriovenous malformations hyperactivate RAS-MAPK signaling amenable to MEK inhibition

5. A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome

6. Identification of a non-canonical chemokine-receptor pathway suppressing regulatory T cells to drive atherosclerosis

9. (Multi-) omics studies of ILC2s in inflammation and metabolic diseases.

10. Targeting platelet-derived CXCL12 impedes arterial thrombosis

13. Gut microbial metabolite imidazole propionate impairs endothelial cell function and promotes the development of atherosclerosis

16. Non‐Hotspot PIK3CA Variants Have Higher Variant Allele Frequency and are More Common in Syndromic Vascular Malformations.

18. MicroRNA-26b protects against MASH development and can be efficiently targeted with lipid nanoparticles

19. Non-activatable mutant of inhibitor of kappa B kinase α (IKKα) exerts vascular site-specific effects on atherosclerosis in Apoe-deficient mice

23. Parkes Weber Syndrome: Contribution of the Genotype to the Diagnosis

24. Simultaneous assessment of mechanical and electrical function in Langendorff-perfused ex-vivo mouse hearts

25. Targeting a cell-specific microRNA repressor of CXCR4 ameliorates atherosclerosis in mice

33. NETs-Induced Thrombosis Impacts on Cardiovascular and Chronic Kidney Disease

35. Chemokines and galectins form heterodimers to modulate inflammation

36. Endotoxinemia Accelerates Atherosclerosis Through Electrostatic Charge–Mediated Monocyte Adhesion

39. Native, Intact Glucagon-Like Peptide-1 Is a Natural Suppressor of Thrombus Growth Under Physiological Flow Conditions

41. GIP receptor agonism improves dyslipidemia and atherosclerosis independently of body weight loss in preclinical mouse model for cardio-metabolic disease

42. WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome

43. Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease

44. Hematopoietic ChemR23 (Chemerin Receptor 23) Fuels Atherosclerosis by Sustaining an M1 Macrophage-Phenotype and Guidance of Plasmacytoid Dendritic Cells to Murine Lesions—Brief Report

47. Targeting mannose receptor expression on macrophages in atherosclerotic plaques of apolipoprotein E-knockout mice using 111In-tilmanocept

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