-
1
-
-
0031577677
-
3 adenosine receptor mediates cell spreading, reorganization of actin cytoskeleton, and distribution of Bcl-XL: Studies in human astroglioma cells
-
3 adenosine receptor mediates cell spreading, reorganization of actin cytoskeleton, and distribution of Bcl-XL: studies in human astroglioma cells. Biochem Biophys Res Commun 1997; 241: 297-304.
-
(1997)
Biochem Biophys Res Commun
, vol.241
, pp. 297-304
-
-
Abbracchio, M.P.1
Rainaldi, G.2
Giammarioli, A.M.3
Ceruti, S.4
Brambilla, R.5
Cattabeni, F.6
-
2
-
-
0023895875
-
A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man
-
Bennett GJ, Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man. Pain 1988; 33: 87-107.
-
(1988)
Pain
, vol.33
, pp. 87-107
-
-
Bennett, G.J.1
Xie, Y.K.2
-
3
-
-
84876373418
-
Adenosine kinase: Exploitation for therapeutic gain
-
Boison D. Adenosine kinase: exploitation for therapeutic gain. Pharmacol Rev 2013; 65: 906-43.
-
(2013)
Pharmacol Rev
, vol.65
, pp. 906-943
-
-
Boison, D.1
-
5
-
-
0032520875
-
Electrophysiological characterization of spinal neuronal response properties in anaesthetized rats after ligation of spinal nerves L5-L6
-
Chapman V, Suzuki R, Dickenson AH. Electrophysiological characterization of spinal neuronal response properties in anaesthetized rats after ligation of spinal nerves L5-L6. J Physiol 1998; 507 (Pt 3): 881-94.
-
(1998)
J Physiol
, vol.507
, Issue.3
, pp. 881-894
-
-
Chapman, V.1
Suzuki, R.2
Dickenson, A.H.3
-
7
-
-
0034255439
-
Spared nerve injury: An animal model of persistent peripheral neuropathic pain
-
Decosterd I, Woolf CJ. Spared nerve injury: an animal model of persistent peripheral neuropathic pain. Pain 2000; 87: 149-58.
-
(2000)
Pain
, vol.87
, pp. 149-158
-
-
Decosterd, I.1
Woolf, C.J.2
-
10
-
-
79952033865
-
International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors - An update
-
Fredholm BB, IJzerman AP, Jacobson KA, Linden J, Muller CE. International Union of Basic and Clinical Pharmacology. LXXXI. Nomenclature and classification of adenosine receptors - an update. Pharmacol Rev 2011; 63: 1-34.
-
(2011)
Pharmacol Rev
, vol.63
, pp. 1-34
-
-
Fredholm, B.B.1
IJzerman, A.P.2
Jacobson, K.A.3
Linden, J.4
Muller, C.E.5
-
11
-
-
0021054336
-
Yohimbine: A pharmacological probe for study of the alpha 2-adrenoreceptor
-
Goldberg MR, Robertson D. Yohimbine: a pharmacological probe for study of the alpha 2-adrenoreceptor. Pharmacol Rev 1983; 35: 143-80.
-
(1983)
Pharmacol Rev
, vol.35
, pp. 143-180
-
-
Goldberg, M.R.1
Robertson, D.2
-
12
-
-
0028183017
-
International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin)
-
Hoyer D, Clarke DE, Fozard JR, Hartig PR, Martin GR, Mylecharane EJ, et al. International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin). Pharmacol Rev 1994; 46: 157-203.
-
(1994)
Pharmacol Rev
, vol.46
, pp. 157-203
-
-
Hoyer, D.1
Clarke, D.E.2
Fozard, J.R.3
Hartig, P.R.4
Martin, G.R.5
Mylecharane, E.J.6
-
14
-
-
0033680092
-
ABT-702 (4-amino-5-(3-bromophenyl)-7-(6-morpholinopyridin-3-yl)pyrido[2, 3-d]pyrimidine), a novel orally effective adenosine kinase inhibitor with analgesic and anti-inflammatory properties: I. In vitro characterization and acute antinociceptive effects in the mouse
-
Jarvis MF, Yu H, Kohlhaas K, Alexander K, Lee CH, Jiang M, et al. ABT-702 (4-amino-5-(3-bromophenyl)-7-(6-morpholinopyridin-3-yl)pyrido[2, 3-d]pyrimidine), a novel orally effective adenosine kinase inhibitor with analgesic and anti-inflammatory properties: I. In vitro characterization and acute antinociceptive effects in the mouse. J Pharmacol Exp Ther 2000; 295: 1156-64.
-
(2000)
J Pharmacol Exp Ther
, vol.295
, pp. 1156-1164
-
-
Jarvis, M.F.1
Yu, H.2
Kohlhaas, K.3
Alexander, K.4
Lee, C.H.5
Jiang, M.6
-
15
-
-
0024272147
-
Dose-dependent inhibition by naloxone of nociceptive activity evoked in the rat thalamus
-
Jurna I. Dose-dependent inhibition by naloxone of nociceptive activity evoked in the rat thalamus. Pain 1988; 35: 349-54.
-
(1988)
Pain
, vol.35
, pp. 349-354
-
-
Jurna, I.1
-
16
-
-
0026727999
-
An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat
-
Kim SH, Chung JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain 1992; 50: 355-63.
-
(1992)
Pain
, vol.50
, pp. 355-363
-
-
Kim, S.H.1
Chung, J.M.2
-
17
-
-
74949100800
-
Unmasking the tonic-aversive state in neuropathic pain
-
King T, Vera-Portocarrero L, Gutierrez T, Vanderah TW, Dussor G, Lai J, et al. Unmasking the tonic-aversive state in neuropathic pain. Nat Neurosci 2009; 12: 1364-6.
-
(2009)
Nat Neurosci
, vol.12
, pp. 1364-1366
-
-
King, T.1
Vera-Portocarrero, L.2
Gutierrez, T.3
Vanderah, T.W.4
Dussor, G.5
Lai, J.6
-
18
-
-
0033697042
-
ABT-702 (4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin- 3-yl)pyrido[2,3-d]pyrimidine), a novel orally effective adenosine kinase inhibitor with analgesic and anti-inflammatory properties. II. In vivo characterization in the rat
-
Kowaluk EA, Mikusa J, Wismer CT, Zhu CZ, Schweitzer E, Lynch JJ, et al. ABT-702 (4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin- 3-yl)pyrido[2,3-d]pyrimidine), a novel orally effective adenosine kinase inhibitor with analgesic and anti-inflammatory properties. II. In vivo characterization in the rat. J Pharmacol Exp Ther 2000; 295: 1165-74.
-
(2000)
J Pharmacol Exp Ther
, vol.295
, pp. 1165-1174
-
-
Kowaluk, E.A.1
Mikusa, J.2
Wismer, C.T.3
Zhu, C.Z.4
Schweitzer, E.5
Lynch, J.J.6
-
19
-
-
0032514382
-
Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists
-
Li AH, Moro S, Melman N, Ji XD, Jacobson KA. Structure-activity relationships and molecular modeling of 3, 5-diacyl-2,4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists. J Med Chem 1998; 41: 3186-201.
-
(1998)
J Med Chem
, vol.41
, pp. 3186-3201
-
-
Li, A.H.1
Moro, S.2
Melman, N.3
Ji, X.D.4
Jacobson, K.A.5
-
20
-
-
84864844175
-
Supraspinal peroxynitrite modulates pain signaling by suppressing the endogenous opioid pathway
-
Little JW, Chen Z, Doyle T, Porreca F, Ghaffari M, Bryant L, et al. Supraspinal peroxynitrite modulates pain signaling by suppressing the endogenous opioid pathway. J Neurosci 2012; 32: 10797-808.
-
(2012)
J Neurosci
, vol.32
, pp. 10797-10808
-
-
Little, J.W.1
Chen, Z.2
Doyle, T.3
Porreca, F.4
Ghaffari, M.5
Bryant, L.6
-
22
-
-
84872849804
-
Disease modification of breast cancer-induced bone remodeling by cannabinoid 2 receptor agonists
-
Lozano-Ondoua AN, Hanlon KE, Symons-Liguori AM, Largent-Milnes TM, Havelin JJ, Ferland HL III, et al. Disease modification of breast cancer-induced bone remodeling by cannabinoid 2 receptor agonists. J Bone Miner Res 2013; 28: 92-107.
-
(2013)
J Bone Miner Res
, vol.28
, pp. 92-107
-
-
Lozano-Ondoua, A.N.1
Hanlon, K.E.2
Symons-Liguori, A.M.3
Largent-Milnes, T.M.4
Havelin, J.J.5
Ferland, H.L.6
-
23
-
-
0036277865
-
Descending control of pain
-
Millan MJ. Descending control of pain. Prog Neurobiol 2002; 66: 355-474.
-
(2002)
Prog Neurobiol
, vol.66
, pp. 355-474
-
-
Millan, M.J.1
-
24
-
-
84874444262
-
Pain relief produces negative reinforcement through activation of mesolimbic reward-valuation circuitry
-
Navratilova E, Xie JY, Okun A, Qu C, Eyde N, Ci S, et al. Pain relief produces negative reinforcement through activation of mesolimbic reward-valuation circuitry. Proc Natl Acad Sci USA 2012; 109: 20709-13.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 20709-20713
-
-
Navratilova, E.1
Xie, J.Y.2
Okun, A.3
Qu, C.4
Eyde, N.5
Ci, S.6
-
26
-
-
84856186694
-
Alleviating suffering 101 - Pain relief in the United States
-
Pizzo PA, Clark NM. Alleviating suffering 101 - pain relief in the United States. N Engl J Med 2012; 366: 197-9.
-
(2012)
N Engl J Med
, vol.366
, pp. 197-199
-
-
Pizzo, P.A.1
Clark, N.M.2
-
27
-
-
0029034879
-
Biochemical and pharmacological characterisation of SR141716A, the first potent and selective brain cannabinoid receptor antagonist
-
Rinaldi-Carmona M, Barth F, Heaulme M, Alonso R, Shire D, Congy C, et al. Biochemical and pharmacological characterisation of SR141716A, the first potent and selective brain cannabinoid receptor antagonist. Life Sci 1995; 56: 1941-7.
-
(1995)
Life Sci
, vol.56
, pp. 1941-1947
-
-
Rinaldi-Carmona, M.1
Barth, F.2
Heaulme, M.3
Alonso, R.4
Shire, D.5
Congy, C.6
-
28
-
-
5644254040
-
SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor
-
Rinaldi-Carmona M, Barth F, Millan J, Derocq JM, Casellas P, Congy C, et al. SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor. J Pharmacol Exp Ther 1998; 284: 644-50.
-
(1998)
J Pharmacol Exp Ther
, vol.284
, pp. 644-650
-
-
Rinaldi-Carmona, M.1
Barth, F.2
Millan, J.3
Derocq, J.M.4
Casellas, P.5
Congy, C.6
-
30
-
-
0034635486
-
Disruption of the A(3) adenosine receptor gene in mice and its effect on stimulated inflammatory cells
-
Salvatore CA, Tilley SL, Latour AM, Fletcher DS, Koller BH, Jacobson MA. Disruption of the A(3) adenosine receptor gene in mice and its effect on stimulated inflammatory cells. J Biol Chem 2000; 275: 4429-34.
-
(2000)
J Biol Chem
, vol.275
, pp. 4429-4434
-
-
Salvatore, C.A.1
Tilley, S.L.2
Latour, A.M.3
Fletcher, D.S.4
Koller, B.H.5
Jacobson, M.A.6
-
32
-
-
27444435891
-
Antinociception of intrathecal adenosine receptor subtype agonists in rat formalin test
-
Yoon MH, Bae HB, Choi JI. Antinociception of intrathecal adenosine receptor subtype agonists in rat formalin test. Anesth Analg 2005; 101: 1417-21.
-
(2005)
Anesth Analg
, vol.101
, pp. 1417-1421
-
-
Yoon, M.H.1
Bae, H.B.2
Choi, J.I.3
-
33
-
-
79954578322
-
Pain-relieving prospects for adenosine receptors and ectonucleotidases
-
Zylka MJ. Pain-relieving prospects for adenosine receptors and ectonucleotidases. Trends Mol Med 2011; 17: 188-96.
-
(2011)
Trends Mol Med
, vol.17
, pp. 188-196
-
-
Zylka, M.J.1
|