ライフサイエンスコーパス: TXA2 receptor

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1 sphorylation of the carboxyl terminus of the TXA2 receptor.

2 ng to the third intracytoplasmic loop of the TXA2 receptor.

3 ssion (Bmax = 95 +/- 6 pmol/mg) of the C-His-TxA2 receptors.

4 y different from those of the wild type (wt)-TxA2 receptors.

5 ficantly different between C-His-TxA2 and wt-TxA2 receptors.

6 ased structure-function and other studies of TxA2 receptors.

7 y another G-protein associated with platelet TXA2 receptors.

8 ligand and immunoaffinity chromatography, 2) TXA2 receptor activation stimulates GTPgammaS binding to

9 separate experiments, it was found that the TXA2 receptor agonist U46619 stimulated [35S]guanosine 5

10 ed as potent dual-acting agents to block the TXA2 receptor and to inhibit the thromboxane synthase (T

11 ation of a high level of expression of C-His-TxA2 receptors and a rapid purification procedure follow

12 haq and Galpha13 are functionally coupled to TXA2 receptors and dissociate upon agonist activation.

13 (C-His) was ligated to the alpha-isoform of TxA2 receptors and expressed in COS-7 and Chinese hamste

14 upled agonist receptors, the thromboxane A2 (TXA2) receptor, and protease-activated receptors (PARs).

15 pecifically blocked by pretreatment with the TXA2 receptor antagonist, BM13.505.

16 al angiogenesis are similarly inhibited by a TXA2 receptor antagonist, SQ29548.

17 These data identify TXA2 receptors as cGMP-dependent protein kinase substrat

18 lets deficient in PLC gamma 2, G alpha q, or TxA2 receptors, as well as platelets treated with a prot

19 Thromboxane A2 (TxA2) receptors belong to the class of G-protein-coupled

20 The C-His-TxA2 receptors bound the radioligands 125I-7-[(1R,2S,3S,

21 affinity methods, in vivo phosphorylation of TXA2 receptors by cyclic GMP was demonstrated from 32P-l

22 that in addition to Galphaq, purification of TXA2 receptors by ligand (SQ31,491)-affinity chromatogra

23 o Galpha13, and 3) Galpha13 affinity for the TXA2 receptor can be modulated by agonist-receptor activ

24 irect evidence that endogenous Galpha13 is a TXA2 receptor-coupled G-protein, as: 1) its alpha-subuni

25 de mapping studies of in vivo phosphorylated TXA2 receptors demonstrated cGMP mediates phosphorylatio

26 The requirement for Btk and TxA2 receptor function in GPIb-dependent arterial thromb

27 to purify the human platelet thromboxane A2 (TXA2) receptor-Galphaq complex.

28 let inhibition by NO, activation of platelet TXA2 receptors in the presence of cGMP was studied.

29 vitro, but not Galphaq copurifying with the TXA2 receptors in these experiments.

30 to catalyze the phosphorylation of platelet TXA2 receptors in vitro, but not Galphaq copurifying wit

31 he relationship of structure to function for TxA2 receptors is limited because of their low levels of

32 aphy using an antibody raised against native TXA2 receptor protein.

33 ism of purinergic receptors (suramin+RB2) or TXA2 receptor (SQ29548), or by intratracheal apyrase.

34 r thromboxane A2 (TxA2), we created a mutant TxA2 receptor (TP receptor) in which serines at position

35 Human EC express both TXA2 receptor (TP) isoforms; however, the effects of ind

36 pressed in mice genetically deficient in the TxA2 receptor (TP) or treated with a TP antagonist.

37 Deletion of the TxA2 receptor (TP) reduces the hyperplastic response to

38 Endothelial cells express TXA2 receptors (TP) but the effects of TP stimulation on

39 S18886 is an orally active thromboxane A2 (TXA2) receptor (TP) antagonist in clinical development f

40 The TXA2 receptor (TXA2R) is a member of the G protein-coupl

41 Two subtypes of the thromboxane A2 (TxA2) receptor (TxA2R-E and TxA2R-P), which differ in th

42 r evidence for functional coupling of G13 to TXA2 receptors was provided in studies where solubilized

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