scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1476-5381.1996.TB15341.X |
P8608 | Fatcat ID | release_avmodsr3trbbjca2ebybgs6ska |
P932 | PMC publication ID | 1909568 |
P698 | PubMed publication ID | 8732278 |
P5875 | ResearchGate publication ID | 14470781 |
P2093 | author name string | Dalpiaz A | |
Borea PA | |||
Varani K | |||
Gessi S | |||
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Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction | Q27860958 | ||
Adenosine receptor-induced cyclic AMP generation and inhibition of 5-hydroxytryptamine release in human platelets | Q28644646 | ||
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Soluble and membrane-associated human low-affinity adenosine binding protein (adenotin): properties and homology with mammalian and avian stress proteins | Q34352397 | ||
Adenosine regulates via two different types of receptors, the accumulation of cyclic AMP in cultured brain cells | Q34660775 | ||
8-(3-Chlorostyryl)caffeine (CSC) is a selective A2-adenosine antagonist in vitro and in vivo | Q36308893 | ||
The thermodynamics of the self-association of the reduced and carboxymethylated form of apoA-II from the human high density lipoprotein complex | Q39075296 | ||
Pharmacokinetic modelling of the haemodynamic effects of the A2a adenosine receptor agonist CGS 21680C in conscious normotensive rats | Q40996025 | ||
[3H]CGS 21680, a selective A2 adenosine receptor agonist directly labels A2 receptors in rat brain | Q41954440 | ||
Characterization of the A2 adenosine receptor labeled by [3H]NECA in rat striatal membranes | Q42205750 | ||
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A rapid filtration assay for soluble receptors using polyethylenimine-treated filters | Q48789289 | ||
3H5?-N-ethylcarboxamide adenosine binds to both Ra and Ri adenosine receptors in rat striatum | Q53838720 | ||
Separation of solubilized A2 adenosine receptors of human platelets from non-receptor [3H]NECA binding sites by gel filtration | Q57903620 | ||
Thermodynamic analysis of agonist and antagonist binding to membrane-bound and solubilized A1 adenosine receptors | Q60050359 | ||
Ra Adenosine receptors in human platelets | Q61012553 | ||
Adenosine binding sites of rat pheochromocytoma PC 12 cell membranes: partial characterization and solubilization | Q68058221 | ||
A modification of a protein-binding method for rapid quantification of cAMP in cell-culture supernatants and body fluid | Q68494696 | ||
Comparison of three paf-acether receptor antagonist ginkgolides | Q69846304 | ||
Agonist binding at alpha 2-adrenoceptors of human platelets using 3H-UK-14,304: regulation by Gpp(NH)p and cations | Q69905458 | ||
Binding thermodynamics of adenosine A2a receptor ligands | Q71676594 | ||
Purification and characterization of an adenotin-like adenosine binding protein from human platelets | Q72124037 | ||
2-Alkynyl derivatives of adenosine-5'-N-ethyluronamide: selective A2 adenosine receptor agonists with potent inhibitory activity on platelet aggregation | Q72505516 | ||
Binding characteristics of the adenosine A2 receptor ligand [3H]CGS 21680 to human platelet membranes | Q72857155 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1693-1701 | |
P577 | publication date | 1996-04-01 | |
P1433 | published in | British Journal of Pharmacology | Q919631 |
P1476 | title | Pharmacological and biochemical characterization of purified A2a adenosine receptors in human platelet membranes by [3H]-CGS 21680 binding | |
P478 | volume | 117 |
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