ライフサイエンスコーパス: ATP receptor

1 receptors and at least one G(s)-coupled ADP/ATP receptor.

2 n LN-residing T cells via engagement of P2X7 ATP receptors.

3 TP, and suramin was used to block apical P2Y ATP receptors.

4 cleotide specificity among the family of P2Y ATP receptors.

5 ls in concentrations sufficient to stimulate ATP receptors.

6 Inhibitors of mammalian P2-type ATP receptors abolished ATP-induced O2- production, sugg

7 ygenase/cyclooxygenase, BK(Ca) channels, and ATP receptor activation within astrocytes.

8 ongly affected in mice deficient in the P2X1-ATP receptor and in wild-type (WT) mice treated with CGS

9 These effects involve adenosine A(1) and ATP receptors and depend on decreased extracellular pH.

10 l excitability via adenosine A(1) receptors, ATP receptors, and ecto-ATPase.

11 usly and require connexin hemichannels, P2Y1 ATP receptors, and intracellular IP3-mediated calcium re

12 r, they regulate mucus clearance through P2 (ATP) receptors, and following surface metabolism through

13 Application of the ATP receptor antagonists pyridoxal-5'-phosphate-6-azophe

14 aling pathways downstream of this ionotropic ATP receptor are poorly understood.

15 The results demonstrate that functional P2X ATP receptors are expressed in hippocampal granule cells

16 P2Y ATP receptors are widely expressed in mammalian tissues

17 Blockade of ATP receptors at these sites diminishes the chemosensory

18 In summary, the function of P2X3 ATP receptor can be inhibited by P2Y2-mediated depletion

19 These results suggest that ATP receptors can modulate voltage- as well as ligand-ga

20 mechanisms, and the nociceptor-specific P2X3 ATP receptor channel is considered a target in pain ther

21 Treatments aiming at inhibition of specific ATP receptors could be of a potential therapeutic benefi

22 lts suggest that nicotinic receptors and P2X ATP receptors do not act independently in these sympathe

23 Similar ATP receptors do not exist in plants, although extracell

24 xpression of ionotropic GABA, glutamate, and ATP receptors in oligodendrocytes derived from the optic

25 Blockade of ATP receptors in the VLM (microinjection of P2 receptor

26 rinergic receptors, while the functioning of ATP receptors in thymocytes is reflected by ATP(ext)-ind

27 The [Ca2+]i elevating activity of the ATP receptor is modulated during T cell differentiation.

28 skate Raja erinacea express a primitive P2Y ATP receptor lacking pharmacologic selectivity, so we cl

29 pharmacological studies have indicated that ATP receptors may be involved in the regulation of physi

30 amined the mechanisms by which activation of ATP receptors modulates excitatory neurotransmission to

31 Extracellular ATP receptors monitor tissue damage and activate a Ca(2+

32 how that human beta cells express ionotropic ATP receptors of the P2X(3) type and that activation of

33 We have searched for ATP receptors on a cholinergic presynaptic nerve termina

34 vel of mRNAs encoding GFRalpha2 and Ret, the ATP receptor P2X(3) (found in IB(4)-positive, GFRalpha2-

35 For example, expression of the ATP receptor P2X(3) is strongly implicated in nociceptio

36 n the regenerating liver is modulated by the ATP receptor, P2X1.

37 The ATP receptor P2X3 is selectively expressed by nociceptor

38 The ATP receptor P2X3 is selectively expressed on small diam

39 to neural cell adhesion molecule (NCAM) and ATP receptor P2X3.

40 The ATP receptor P2X7 (P2X7R or P2RX7) has a key role in inf

41 sphocholine inhibits ion-channel function of ATP receptor P2X7 in monocytic cells via nAChR containin

42 unds nor signaling through the extracellular ATP receptor P2X7 Monocyte IL-1beta production was speci

43 Conversely, blocking the ATP receptor P2X7 reduced Th17 responses in LoD cultures

44 ATP is a typical second signal sensed by the ATP receptor P2X7 that triggers activation of the NLRP3-

45 converts ATP to ADP/AMP, and an increase in ATP receptor P2X7.

46 activation, ATP accumulation, expression of ATP receptor P2X7R, and production of thymic stromal lym

47 ese findings support the hypothesis that the ATP receptor P2Y1 is a principal receptor mediating both

48 dicate for the first time a role for the UTP/ATP receptor, P2Y2, in development of intimal hyperplasi

49 Distribution of the two types of ATP receptor responses on individual cells was stochasti

50 ion of the P2x receptor on the platelets (an ATP receptor) resulted in no increase in platelet NO pro

51 The ATP receptor subunit P2X2 was expressed in Xenopus oocyt

52 The ionotropic ATP receptor subunits P2X(1-6) receptors play important

53 s express ionotropic adenosine triphosphate (ATP) receptors, suggesting that ATP signaling participat

54 Despite the prominent expression of P2X-type ATP receptors throughout the hypothalamus, the role of A

55 s were found in the functional expression of ATP receptors, TRPA1 channels, voltage-gated calcium-, p

56 old thermosensors of neonatal mice and rats, ATP receptors were functionally expressed, but the expre

57 The single channel properties of P2X ATP receptors were investigated in outside-out patches f

58 d may be capable of autocrine stimulation of ATP receptors, while conversion to adenosine by ecto-enz

59 er P2Y receptor functions as a primitive P2Y ATP receptor with broad pharmacologic selectivity and is

60 s with 18alpha-glycyrrhetinic acid, blocking ATP receptors with pyridoxal-phosphate-6-azophenyl-2',4'