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1  receptors and at least one G(s)-coupled ADP/ATP receptor.
2 range diffusible signals and involves the P2 ATP receptor.
3 TP, and suramin was used to block apical P2Y ATP receptors.
4 n LN-residing T cells via engagement of P2X7 ATP receptors.
5 cleotide specificity among the family of P2Y ATP receptors.
6 ls in concentrations sufficient to stimulate ATP receptors.
7 lective ligand gated adenosine-triphosphate (ATP) receptor 7 (P2X7).
8              Inhibitors of mammalian P2-type ATP receptors abolished ATP-induced O2- production, sugg
9 ygenase/cyclooxygenase, BK(Ca) channels, and ATP receptor activation within astrocytes.
10 ongly affected in mice deficient in the P2X1-ATP receptor and in wild-type (WT) mice treated with CGS
11     These effects involve adenosine A(1) and ATP receptors and depend on decreased extracellular pH.
12 l excitability via adenosine A(1) receptors, ATP receptors, and ecto-ATPase.
13 usly and require connexin hemichannels, P2Y1 ATP receptors, and intracellular IP3-mediated calcium re
14 r, they regulate mucus clearance through P2 (ATP) receptors, and following surface metabolism through
15                           Application of the ATP receptor antagonists pyridoxal-5'-phosphate-6-azophe
16 aling pathways downstream of this ionotropic ATP receptor are poorly understood.
17  The results demonstrate that functional P2X ATP receptors are expressed in hippocampal granule cells
18                                          P2Y ATP receptors are widely expressed in mammalian tissues
19                                  Blockade of ATP receptors at these sites diminishes the chemosensory
20             In summary, the function of P2X3 ATP receptor can be inhibited by P2Y2-mediated depletion
21                   These results suggest that ATP receptors can modulate voltage- as well as ligand-ga
22 mechanisms, and the nociceptor-specific P2X3 ATP receptor channel is considered a target in pain ther
23  Treatments aiming at inhibition of specific ATP receptors could be of a potential therapeutic benefi
24 ceptor P2K1 (DORN1, LecRK-I.9; extracellular ATP receptor) directly interacts with and phosphorylates
25 lts suggest that nicotinic receptors and P2X ATP receptors do not act independently in these sympathe
26                                      Similar ATP receptors do not exist in plants, although extracell
27 xpression of ionotropic GABA, glutamate, and ATP receptors in oligodendrocytes derived from the optic
28                                  Blockade of ATP receptors in the VLM (microinjection of P2 receptor
29 rinergic receptors, while the functioning of ATP receptors in thymocytes is reflected by ATP(ext)-ind
30        The [Ca2+]i elevating activity of the ATP receptor is modulated during T cell differentiation.
31  skate Raja erinacea express a primitive P2Y ATP receptor lacking pharmacologic selectivity, so we cl
32  pharmacological studies have indicated that ATP receptors may be involved in the regulation of physi
33 BAA or GABAB receptors, NMDA receptors, P2Y1 ATP receptors, metabotropic glutamate receptor 5, and TR
34 amined the mechanisms by which activation of ATP receptors modulates excitatory neurotransmission to
35                                Extracellular ATP receptors monitor tissue damage and activate a Ca(2+
36 how that human beta cells express ionotropic ATP receptors of the P2X(3) type and that activation of
37                         We have searched for ATP receptors on a cholinergic presynaptic nerve termina
38 M)) express high levels of the extracellular ATP receptor P2RX7 in mice.
39 vel of mRNAs encoding GFRalpha2 and Ret, the ATP receptor P2X(3) (found in IB(4)-positive, GFRalpha2-
40               For example, expression of the ATP receptor P2X(3) is strongly implicated in nociceptio
41  we then demonstrated that activation of the ATP receptors P2X or P2Y(1) increases the neuronal firin
42 n the regenerating liver is modulated by the ATP receptor, P2X1.
43                                          The ATP receptor P2X3 is selectively expressed by nociceptor
44                                          The ATP receptor P2X3 is selectively expressed on small diam
45  to neural cell adhesion molecule (NCAM) and ATP receptor P2X3.
46 nosine receptor ADORA2B and the pH-sensitive ATP receptor P2X4.
47                                          The ATP receptor P2X7 (P2X7R or P2RX7) has a key role in inf
48 sphocholine inhibits ion-channel function of ATP receptor P2X7 in monocytic cells via nAChR containin
49 unds nor signaling through the extracellular ATP receptor P2X7 Monocyte IL-1beta production was speci
50                     Conversely, blocking the ATP receptor P2X7 reduced Th17 responses in LoD cultures
51 ATP is a typical second signal sensed by the ATP receptor P2X7 that triggers activation of the NLRP3-
52  converts ATP to ADP/AMP, and an increase in ATP receptor P2X7.
53  activation, ATP accumulation, expression of ATP receptor P2X7R, and production of thymic stromal lym
54 ese findings support the hypothesis that the ATP receptor P2Y1 is a principal receptor mediating both
55 dicate for the first time a role for the UTP/ATP receptor, P2Y2, in development of intimal hyperplasi
56             Distribution of the two types of ATP receptor responses on individual cells was stochasti
57 ion of the P2x receptor on the platelets (an ATP receptor) resulted in no increase in platelet NO pro
58 s point to the existence of additional plant ATP receptor(s) and provide crucial downstream targets f
59 nisin-B1 toxicity, suggesting that different ATP receptor(s) are operational in this process.
60                                          The ATP receptor subunit P2X2 was expressed in Xenopus oocyt
61                               The ionotropic ATP receptor subunits P2X(1-6) receptors play important
62 s express ionotropic adenosine triphosphate (ATP) receptors, suggesting that ATP signaling participat
63 Despite the prominent expression of P2X-type ATP receptors throughout the hypothalamus, the role of A
64 O NUCLEOTIDES 1 (DORN1), was the first plant ATP receptor to be identified but key downstream protein
65 s were found in the functional expression of ATP receptors, TRPA1 channels, voltage-gated calcium-, p
66                               In particular, ATP receptors up-regulated on day 1 postinjury, whereas
67 old thermosensors of neonatal mice and rats, ATP receptors were functionally expressed, but the expre
68         The single channel properties of P2X ATP receptors were investigated in outside-out patches f
69 d may be capable of autocrine stimulation of ATP receptors, while conversion to adenosine by ecto-enz
70 er P2Y receptor functions as a primitive P2Y ATP receptor with broad pharmacologic selectivity and is
71 s with 18alpha-glycyrrhetinic acid, blocking ATP receptors with pyridoxal-phosphate-6-azophenyl-2',4'