The use of high pressure liquid chromatography (HPLC) for the separation of radiolabeled arachidonic acid and its metabolites produced by thrombin-treated human platelets. II. Establishment of optimal assay conditions.
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[1] A. Schafer,et al. Platelet resistance to prostaglandin D2 in patients with myeloproliferative disorders , 1978 .
[2] D. Deykin,et al. Mobilization of arachidonic acid in human platelets. Kinetics and Ca2+ dependency. , 1977, Biochimica et biophysica acta.
[3] E. Lapetina,et al. Cyclic adenosine 3',5'-monophosphate and prostacyclin inhibit membrane phospholipase activity in platelets. , 1977, Biochemical and biophysical research communications.
[4] E. Goetzl,et al. Stimulation of human eosinophil and neutrophil polymorphonuclear leukocyte chemotaxis and random migration by 12-L-hydroxy-5,8,10,14-eicosatetraenoic acid. , 1977, The Journal of clinical investigation.
[5] D. Deykin,et al. Transfer of arachidonic acid to human platelet plasmalogen in response to thrombin. , 1976, Biochemical and biophysical research communications.
[6] D. Deykin,et al. Isolation of membranes from normal and thrombin-treated gel-filtered platelets using a lectin marker. , 1976, Biochimica et biophysica acta.
[7] J. Tainer,et al. Biogenesis of chemotactic molecules by the arachidonate lipoxygenase system of platelets , 1975, Nature.
[8] R. Koch. Calcium ion activation of lipoxidase. , 1968, Archives of biochemistry and biophysics.
[9] R. F. Chen,et al. Removal of fatty acids from serum albumin by charcoal treatment. , 1967, The Journal of biological chemistry.