Stewart O. Sage mainly investigates Cell biology, Biochemistry, Platelet, Intracellular and Biophysics. His research in Cell biology intersects with topics in Platelet activation and Transient receptor potential channel. His study explores the link between Platelet and topics such as Fura-2 that cross with problems in EGTA and Thrombin.
Stewart O. Sage combines subjects such as Extracellular and Receptor with his study of Intracellular. Stewart O. Sage has researched Biophysics in several fields, including Patch clamp and Calcium. His Thapsigargin research incorporates themes from Membrane channel, Tyrosine kinase and Tyrosine phosphorylation.
His primary areas of study are Cell biology, Platelet, Biochemistry, Biophysics and Thapsigargin. His Cell biology study combines topics in areas such as Platelet activation and Receptor. His Platelet research is multidisciplinary, relying on both Secretion, Endocrinology and Fura-2.
Biochemistry is closely attributed to Calcium in his study. His Biophysics research is multidisciplinary, incorporating perspectives in Extracellular, Patch clamp and Agonist. His work carried out in the field of Thapsigargin brings together such families of science as Inositol trisphosphate receptor, Immunoprecipitation, Wortmannin, Membrane channel and Kinase.
Platelet, Cell biology, Store-operated calcium entry, Biochemistry and Platelet activation are his primary areas of study. Stewart O. Sage has included themes like Secretion, Biophysics, Autocrine signalling and Pharmacology in his Platelet study. The Biophysics study combines topics in areas such as Endoplasmic reticulum and Intracellular.
His biological study spans a wide range of topics, including Thrombin and TRPC. Within one scientific family, Stewart O. Sage focuses on topics pertaining to Thapsigargin under Store-operated calcium entry, and may sometimes address concerns connected to Colchicine. His research integrates issues of Endocrinology and Phosphorylation in his study of Platelet activation.
Stewart O. Sage focuses on Cell biology, Store-operated calcium entry, Platelet, Thapsigargin and Platelet activation. His research related to STIM1, SOC channels and ORAI1 might be considered part of Cell biology. His studies deal with areas such as Signal transduction, Autocrine signalling and Phosphorylation as well as Platelet.
His Thapsigargin study is related to the wider topic of Biochemistry. As part of his studies on Platelet activation, Stewart O. Sage often connects relevant subjects like Endocrinology. In his research, Extracellular is intimately related to Receptor, which falls under the overarching field of Calcium metabolism.
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The kinetics of changes in intracellular calcium concentration in fura-2-loaded human platelets.
SO Sage;TJ Rink.
Journal of Biological Chemistry (1987)
Receptor-mediated calcium entry in fura-2-loaded human platelets stimulated with ADP and thrombin. Dual-wavelengths studies with Mn2+.
S O Sage;J E Merritt;T J Hallam;T J Rink.
Biochemical Journal (1989)
Activation of receptor-operated cation channels via P2X1 not P2T purinoceptors in human platelets.
Amanda B. MacKenzie;Martyn P. Mahaut-Smith;Stewart O. Sage.
Journal of Biological Chemistry (1996)
A Role for the Actin Cytoskeleton in the Initiation and Maintenance of Store-mediated Calcium Entry in Human Platelets EVIDENCE FOR CONFORMATIONAL COUPLING
Juan A. Rosado;Susanne Jenner;Stewart O. Sage.
Journal of Biological Chemistry (2000)
ADP- and thapsigargin-evoked Ca2+ entry and protein-tyrosine phosphorylation are inhibited by the tyrosine kinase inhibitors genistein and methyl-2,5-dihydroxycinnamate in fura-2-loaded human platelets.
P Sargeant;R W Farndale;S O Sage.
Journal of Biological Chemistry (1993)
Coupling between inositol 1,4,5-trisphosphate receptors and human transient receptor potential channel 1 when intracellular Ca2+ stores are depleted.
Juan A. Rosado;Stewart O. Sage.
Biochemical Journal (2000)
Calcium-activated potassium channels in the endothelium of intact rat aorta
S M Marchenko;S O Sage.
The Journal of Physiology (1996)
ADP evokes biphasic Ca2+ influx in fura-2-loaded human platelets. Evidence for Ca2+ entry regulated by the intracellular Ca2+ store.
S O Sage;R Reast;T J Rink.
Biochemical Journal (1990)
Endogenously Expressed Trp1 Is Involved in Store-mediated Ca2+ Entry by Conformational Coupling in Human Platelets
Juan A. Rosado;Sharon L. Brownlow;Stewart O. Sage.
Journal of Biological Chemistry (2002)
The actin cytoskeleton in store‐mediated calcium entry
Juan A. Rosado;Stewart O. Sage.
The Journal of Physiology (2000)
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