Robert L. Wykle spends much of his time researching Biochemistry, Platelet-activating factor, Choline, Arachidonic acid and Phosphatidylinositol. The study incorporates disciplines such as Stimulation and Acyl group in addition to Biochemistry. His Stimulation research incorporates elements of Phosphatidic acid and Biosynthesis.
The concepts of his Platelet-activating factor study are interwoven with issues in Ionophore, Degranulation, Cytochalasin B and Platelet. His Choline research focuses on Phosphatidylcholine and how it relates to Canine kidney, Palmitic acid and Diglyceride. His study in Phosphatidylinositol is interdisciplinary in nature, drawing from both Ether and Sphingomyelin.
Robert L. Wykle mainly investigates Biochemistry, Platelet-activating factor, Arachidonic acid, Phospholipid and Stereochemistry. His research on Biochemistry often connects related areas such as Stimulation. His Platelet-activating factor study combines topics from a wide range of disciplines, such as Platelet, Receptor, Ionophore, Phosphocholine and Pharmacology.
As a part of the same scientific family, Robert L. Wykle mostly works in the field of Arachidonic acid, focusing on Phospholipase A2 and, on occasion, Cell biology, Leukotriene B4, Phosphorylation and Cytosol. His Phospholipid research integrates issues from Fatty acid, Nuclear magnetic resonance spectroscopy and Membrane lipids. His Stereochemistry research is multidisciplinary, relying on both Structure–activity relationship and Alkyl.
Robert L. Wykle mostly deals with Biochemistry, Platelet-activating factor, Arachidonic acid, Phospholipase A2 and Cell biology. His research on Biochemistry frequently connects to adjacent areas such as Ether. His Platelet-activating factor study combines topics in areas such as High-performance liquid chromatography, Chromatography, Mass spectrometry, Lipid metabolism and Pharmacology.
His studies in Arachidonic acid integrate themes in fields like Diglyceride, Chemotaxis, Cytosol and Protein kinase C, Phosphorylation. His work carried out in the field of Chemotaxis brings together such families of science as In vitro, G protein, Pertussis toxin, Degranulation and Eicosanoid. His Cell biology research focuses on subjects like Leukotriene B4, which are linked to Zileuton, Exocytosis, Lipoxygenase, Arachidonate 5-lipoxygenase and Stimulation.
His scientific interests lie mostly in Biochemistry, Leukotriene B4, Chemotaxis, Tyrosine phosphorylation and Kinase. His work in Cyclin-dependent kinase 2, Cyclin-dependent kinase 9, ASK1, Phosphatidylethanolamine and Cholesterol is related to Biochemistry. His research in Leukotriene B4 intersects with topics in Phospholipase A2, Arachidonic acid and Cell biology.
His Arachidonic acid research is multidisciplinary, incorporating elements of Exocytosis, Lipoxygenase and Stimulation. The various areas that Robert L. Wykle examines in his Chemotaxis study include Protein kinase A, Pertussis toxin, Degranulation, MAPK/ERK pathway and Eicosanoid. His biological study spans a wide range of topics, including Acetyltransferase and Molecular biology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
1-O-alkyl-2-arachidonoyl-sn-glycero-3-phosphocholine. A common source of platelet-activating factor and arachidonate in human polymorphonuclear leukocytes.
F H Chilton;J M Ellis;S C Olson;R L Wykle.
Journal of Biological Chemistry (1984)
1-O-Alkyl-sn-glyceryl-3-phosphorylcholines: a novel class of neutrophil stimulants.
J. T. O'Flaherty;R. L. Wykle;C. H. Miller;J. C. Lewis.
American Journal of Pathology (1981)
A novel mechanism of diglyceride formation. 12-O-tetradecanoylphorbol-13-acetate stimulates the cyclic breakdown and resynthesis of phosphatidylcholine.
L W Daniel;M Waite;R L Wykle.
Journal of Biological Chemistry (1986)
Choline-linked Phosphoglycerides A SOURCE OF PHOSPHATIDIC ACID AND DIGLYCERIDES IN STIMULATED NEUTROPHILS*
D E Agwu;L C McPhail;M C Chabot;L W Daniel.
Journal of Biological Chemistry (1989)
Platelet activating factor. Stimulation of the lipoxygenase pathway in polymorphonuclear leukocytes by 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine.
F H Chilton;J T O'Flaherty;C E Walsh;M J Thomas.
Journal of Biological Chemistry (1982)
1-O-alkyl-linked glycerophospholipids of human neutrophils: distribution of arachidonate and other acyl residues in the ether-linked and diacyl species.
H W Mueller;J T O'Flaherty;D G Greene;M P Samuel.
Journal of Lipid Research (1984)
Biosynthesis of platelet activating factor in rabbit polymorphonuclear neutrophils.
H W Mueller;J T O'Flaherty;R L Wykle.
Journal of Biological Chemistry (1983)
Binding and metabolism of platelet-activating factor by human neutrophils.
J. T. O'Flaherty;Jefferson R. Surles;Jimmy Redman;David Jacobson.
Journal of Clinical Investigation (1986)
The molecular species distribution of platelet-activating factor synthesized by rabbit and human neutrophils.
H W Mueller;J T O'Flaherty;R L Wykle.
Journal of Biological Chemistry (1984)
Selective acylation of lyso platelet activating factor by arachidonate in human neutrophils.
F H Chilton;J T O'Flaherty;J M Ellis;C L Swendsen.
Journal of Biological Chemistry (1983)
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