scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00395-015-0485-6 |
P698 | PubMed publication ID | 25851234 |
P50 | author | Manolis Mavroidis | Q63974769 |
Constantinos H Davos | Q64515124 | ||
P2093 | author name string | J Peter van Tintelen | |
Aimilia Varela | |||
Yassemi Capetanaki | |||
Axel Vater | |||
Christian Maasch | |||
Ioanna Kostavasili | |||
Stelios Psarras | |||
Michalis Katsimpoulas | |||
Nikolaos C Athanasiadis | |||
P2860 | cites work | Effects of complement activation in the isolated heart. Role of the terminal complement components | Q43804974 |
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Changes and regulation of the C5a receptor on neutrophils during septic shock in humans | Q44402512 | ||
Recombinant human complement C5a receptor antagonist reduces infarct size after surgical revascularization | Q47233244 | ||
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The C5a chemoattractant receptor mediates mucosal defence to infection | Q24318486 | ||
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The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death | Q28114840 | ||
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Myocyte necrosis underlies progressive myocardial dystrophy in mouse dsg2-related arrhythmogenic right ventricular cardiomyopathy | Q37292752 | ||
A novel C5a-neutralizing mirror-image (l-)aptamer prevents organ failure and improves survival in experimental sepsis | Q37393792 | ||
Complement-mediated ischemia-reperfusion injury: lessons learned from animal and clinical studies | Q37498110 | ||
Animal models of arrhythmogenic cardiomyopathy | Q37628322 | ||
Desmin-related myopathy | Q37780788 | ||
Oxidation-specific epitopes are danger-associated molecular patterns recognized by pattern recognition receptors of innate immunity | Q37830940 | ||
Arrhythmogenic cardiomyopathy: transgenic animal models provide novel insights into disease pathobiology | Q37889542 | ||
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A missense mutation in desmin tail domain linked to human dilated cardiomyopathy promotes cleavage of the head domain and abolishes its Z-disc localization. | Q43184436 | ||
P433 | issue | 3 | |
P304 | page(s) | 27 | |
P577 | publication date | 2015-04-08 | |
P1433 | published in | Basic Research in Cardiology | Q2453360 |
P1476 | title | Complement system modulation as a target for treatment of arrhythmogenic cardiomyopathy | |
P478 | volume | 110 |
Q42377369 | Desmin and αB-crystallin interplay in the maintenance of mitochondrial homeostasis and cardiomyocyte survival. |
Q39948025 | Desmin enters the nucleus of cardiac stem cells and modulates Nkx2.5 expression by participating in transcription factor complexes that interact with the nkx2.5 gene |
Q28115277 | Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect |
Q60046136 | Identification of Crucial Genes and Pathways in Human Arrhythmogenic Right Ventricular Cardiomyopathy by Coexpression Analysis |
Q38599642 | Impaired calcium homeostasis is associated with sudden cardiac death and arrhythmias in a genetic equivalent mouse model of the human HRC-Ser96Ala variant |
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Q33757711 | Metformin protects against infection-induced myocardial dysfunction |
Q36100438 | Netrin-1 Reduces Monocyte and Macrophage Chemotaxis towards the Complement Component C5a. |
Q64084317 | Three in a Box: Understanding Cardiomyocyte, Fibroblast, and Innate Immune Cell Interactions to Orchestrate Cardiac Repair Processes |
Q36322072 | Transgenic mice overexpressing desmocollin-2 (DSC2) develop cardiomyopathy associated with myocardial inflammation and fibrotic remodeling |
Q33641786 | Tumor necrosis factor-α confers cardioprotection through ectopic expression of keratins K8 and K18. |
Q47340446 | Type III Intermediate Filaments Desmin, Glial Fibrillary Acidic Protein (GFAP), Vimentin, and Peripherin |
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