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Science, ISSN 0036-8075, 1/2010, Volume 327, Issue 5965, pp. 580 - 583
Journal Article
Handbook of Experimental Pharmacology, ISSN 0171-2004, 2012, Volume 210, Issue 210, pp. 3 - 22
Platelets are anucleate, discoid cells, roughly 2-3 μm in diameter that function primarily as regulators of hemostasis, but also play secondary roles in... 
Proplatelet production | Megakaryocyte maturation | Preplatelet interconversion | Ultrastructure | Morphology | Platelet release | Animals | Organelles - ultrastructure | Blood Platelets - cytology | Blood Platelets - ultrastructure | Humans | Megakaryocytes - physiology | Blood Platelets - physiology | Cytoskeleton - ultrastructure
Conference Proceeding
STEM CELLS Translational Medicine, ISSN 2157-6564, 07/2019, Volume 8, Issue 7, pp. 658 - 670
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2012, Volume 7, Issue 1, p. e30193
Background: All three nitric oxide synthase (NOS) isoforms are expressed in atherosclerotic plaques. NOS enzymes in general catalyse NO production. However,... 
NITRIC-OXIDE SYNTHASE | ACCELERATED ATHEROSCLEROSIS | MULTIDISCIPLINARY SCIENCES | IN-VIVO | LESION FORMATION | ENDOTHELIAL CELL-INTERACTIONS | DOUBLE-KNOCKOUT MICE | DEFICIENT MICE | LEUKOCYTE ADHESION | PLATELET-ADHESION | APOLIPOPROTEIN-E | Reactive Oxygen Species - metabolism | Nitric Oxide - pharmacology | Atherosclerosis - genetics | Blood Vessels - metabolism | Blood Vessels - pathology | Mice, Inbred C57BL | Gene Expression Regulation, Enzymologic - physiology | Nitric Oxide Synthase Type III - genetics | Atherosclerosis - metabolism | Mice, Knockout | Atherosclerosis - enzymology | Animals | Apolipoproteins E - genetics | Superoxides - metabolism | Cytoprotection - genetics | Nitric Oxide Synthase Type III - physiology | Mice | Nitric Oxide Synthase Type III - metabolism | Nitric Oxide - metabolism | Oxidative stress | Vascular cell adhesion molecule 1 | Aneurysms | Smooth muscle | Macrophages | Electron spin | Carotid arteries | Arteries | Cell adhesion molecules | Clonal deletion | Blood platelets | Ischemia | Apolipoprotein E | Rodents | Atherosclerosis | Cell adhesion | Deletion | Physiology | Carotid artery | Plaques | Enzymes | Hyperlipidemia | Muscles | Blood vessels | Superoxide | Pharmacology | Bioavailability | Apolipoproteins | Gene expression | Nitric-oxide synthase | Endothelium | White blood cells | Studies | Microscopy | Nitric oxide | Arteriosclerosis | Isoforms | Infiltration | Electron paramagnetic resonance | Spin resonance
Journal Article
BBA - Molecular and Cell Biology of Lipids, ISSN 1388-1981, 2008, Volume 1781, Issue 9, pp. 513 - 518
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 01/2007, Volume 49, Issue 3, pp. 304 - 310
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2016, Volume 11, Issue 4, p. e0153118
Inflammation has an important role in the development of liver fibrosis in general and the activation of hepatic stellate cells (HSCs) in particular. It is... 
FIBROSIS | TGF-BETA | MULTIDISCIPLINARY SCIENCES | DOUBLE-BLIND | NECROSIS-FACTOR-ALPHA | NONALCOHOLIC STEATOHEPATITIS | MICE | ALCOHOLIC HEPATITIS | CARBON-TETRACHLORIDE | FACTOR RECEPTOR | INDUCED LIVER-INJURY | Tumor Necrosis Factor-alpha - metabolism | Cell Line | Matrix Metalloproteinases - genetics | Cytokines - metabolism | Interleukin-1beta - metabolism | Humans | Hepatic Stellate Cells - metabolism | Collagen - biosynthesis | Gene Expression Profiling | Matrix Metalloproteinases - metabolism | Tissue Inhibitor of Metalloproteinases - metabolism | Tissue Inhibitor of Metalloproteinases - genetics | Drugs | Tissue inhibitor of metalloproteinases | Cell culture | Collagen (type I) | Endothelin | Platelet-derived growth factor | Liver | Clinical trials | Gallbladder diseases | Activation | Matrix metalloproteinase | Drug development | Experiments | Interleukin 6 | Proteins | Hepatitis | Infliximab | Rodents | Interleukin 1 | Tumor necrosis factor-TNF | Collagen (type IV) | Metalloproteinase | Growth factors | Interleukin 8 | Interstitial collagenase | Recombinant | Stellate cells | Liver diseases | Cytokines | Interleukin 1 receptor antagonist | Inflammation | Endothelin 1 | Platelet-derived growth factor BB | Gelatinase B | Signaling | Collagen | Fibrosis | Monoclonal antibodies | Sepsis | Chemokines | Monocyte chemoattractant protein 1 | Bile | Life Sciences
Journal Article
Cellular Microbiology, ISSN 1462-5814, 06/2019, Volume 21, Issue 6, pp. e13017 - n/a
α‐Haemolysin (HlyA) from uropathogenic Escherichia coli has been demonstrated to be a significant virulence factor for ascending urinary tract infections. Once... 
α‐haemolysin | infection | E. coli | sepsis | bacteraemia | ACTIVATION | INTERLEUKIN-1 RECEPTOR ANTAGONIST | coli | MICROBIOLOGY | RELEASE | VIRULENCE | ADP | CELL BIOLOGY | ERYTHROCYTES | TUMOR NECROSIS FACTOR | PLATELETS | IL-1-BETA | MOLECULAR-BASIS | alpha-haemolysin | Kidneys | Cytokines | Virulence | Thrombocytes | Inflammation | Exposure | Urinary tract | Gene deletion | Bacteremia | Clonal deletion | E coli | hlyA gene | Deletion | Sepsis | Bacteria | Mice | Platelets | ATP | Adenosine triphosphate
Journal Article