-
1
-
-
33745742679
-
International union of pharmacology lviii: Update on the p2y g protein-coupled nucleotide receptors: From molecular mechanisms and pathophysiology to therapy
-
Abbracchio MP, Burnstock G, Boeynaems JM, Barnard EA, Boyer JL, Kennedy C, Knight GE, Fumagalli M, Gachet C, and Jacobson KA et al. (2006) International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy. Pharmacol Rev 58:281-341.
-
(2006)
Pharmacol Rev
, vol.58
, pp. 281-341
-
-
Abbracchio, M.P.1
Burnstock, G.2
Boeynaems, J.M.3
Barnard, E.A.4
Boyer, J.L.5
Kennedy, C.6
Knight, G.E.7
Fumagalli, M.8
Gachet, C.9
Jacobson, K.A.10
-
2
-
-
67449161529
-
The udp-glucose receptor p2ry14 triggers innate mucosal immunity in the female reproductive tract by inducing il-8
-
Arase T, Uchida H, Kajitani T, Ono M, Tamaki K, Oda H, Nishikawa S, Kagami M, Nagashima T, and Masuda H, et al. (2009) The UDP-glucose receptor P2RY14 triggers innate mucosal immunity in the female reproductive tract by inducing IL-8. J Immunol 182:7074-7084.
-
(2009)
J Immunol
, vol.182
, pp. 7074-7084
-
-
Arase, T.1
Uchida, H.2
Kajitani, T.3
Ono, M.4
Tamaki, K.5
Oda, H.6
Nishikawa, S.7
Kagami, M.8
Nagashima, T.9
Masuda, H.10
-
3
-
-
84879078240
-
-
WO 2009/070873A1. 2010 Nov 25
-
Belly M, Deschenes D, Fortin R, Fournier JF, Gagne S, Gareau Y, Gautheir JY, Li L, Robichaud J, Therien M, Tranmer GK, and Wang Z (2009) inventors, Merck Frosst Canada LTD, assignee. Substituted 2-naphthoic acids as antagonists of GPR105 activity. WO 2009/070873A1. 2010 Nov 25.
-
(2009)
Inventors, Merck Frosst Canada LTD, assignee. Substituted 2-naphthoic acids as antagonists of GPR105 activity
-
-
Belly, M.1
Deschenes, D.2
Fortin, R.3
Fournier, J.F.4
Gagne, S.5
Gareau, Y.6
Gautheir, J.Y.7
Li, L.8
Robichaud, J.9
Therien, M.10
Tranmer, G.K.11
Wang, Z.12
-
4
-
-
0030036747
-
Synthesis, chemical properties, and preliminary evaluation of substituted cbi analogs of cc-1065 and the duocarmycins incorporating the 7-cyano-1,299a-tetrahydrocyclopropa [c]benz[e]indol-4-one alkylation subunit hammett quantitation of the magnitude of electronic effects on functional reactivity
-
Boger DL, Han N, Tarby CM, Boyce CW, Cai H, Jin Q, and Kitos PA (1996) Synthesis, chemical properties, and preliminary evaluation of substituted CBI analogs of CC-1065 and the duocarmycins incorporating the 7-cyano-1,2,9,9a- tetrahydrocyclopropa [c]benz[e]indol-4-one alkylation subunit: Hammett quantitation of the magnitude of electronic effects on functional reactivity. J Org Chem 61:4894-4912.
-
(1996)
J Org Chem
, vol.61
, pp. 4894-4912
-
-
Boger, D.L.1
Han, N.2
Tarby, C.M.3
Boyce, C.W.4
Cai, H.5
Jin, Q.6
Kitos, P.A.7
-
5
-
-
0025721122
-
Evidence that utp and atp regulate phospholipase c through a common extracellular 59-nucleotide receptor in human airway epithelial cells
-
Brown HA, Lazarowski ER, Boucher RC, and Harden TK (1991) Evidence that UTP and ATP regulate phospholipase C through a common extracellular 59-nucleotide receptor in human airway epithelial cells. Mol Pharmacol 40:648-655.
-
(1991)
Mol Pharmacol
, vol.40
, pp. 648-655
-
-
Brown, H.A.1
Lazarowski, E.R.2
Boucher, R.C.3
Harden, T.K.4
-
6
-
-
34248576759
-
Physiology and pathophysiology of purinergic neurotransmission
-
Burnstock G (2007) Physiology and pathophysiology of purinergic neurotransmission. Physiol Rev 87:659-797.
-
(2007)
Physiol Rev
, vol.87
, pp. 659-797
-
-
Burnstock, G.1
-
7
-
-
73149122802
-
Quantification of gi-mediated inhibition of adenylyl cyclase activity reveals that udp is a potent agonist of the human p2y14 receptor
-
Carter RL, Fricks IP, Barrett MO, Burianek LE, Zhou Y, Ko H, Das A, Jacobson KA, Lazarowski ER, and Harden TK (2009) Quantification of Gi-mediated inhibition of adenylyl cyclase activity reveals that UDP is a potent agonist of the human P2Y14 receptor. Mol Pharmacol 76:1341-1348
-
(2009)
Mol Pharmacol
, vol.76
, pp. 1341-1348
-
-
Carter, R.L.1
Fricks, I.P.2
Barrett, M.O.3
Burianek, L.E.4
Zhou, Y.5
Ko, H.6
Das, A.7
Jacobson, K.A.8
Lazarowski, E.R.9
Harden, T.K.10
-
8
-
-
0034646649
-
A g protein-coupled receptor for udp-glucose
-
Chambers JK, Macdonald LE, Sarau HM, Ames RS, Freeman K, Foley JJ, Zhu Y, McLaughlin MM, Murdock P, and McMillan L et al. (2000) A G protein-coupled receptor for UDP-glucose. J Biol Chem 275:10767-10771.
-
(2000)
J Biol Chem
, vol.275
, pp. 10767-10771
-
-
Chambers, J.K.1
Macdonald, L.E.2
Sarau, H.M.3
Ames, R.S.4
Freeman, K.5
Foley, J.J.6
Zhu, Y.7
McLaughlin, M.M.8
Murdock, P.9
McMillan, L.10
-
9
-
-
0033151694
-
Chimeric g proteins allow a high-throughput signaling assay of gi-coupled receptors
-
Coward P, Chan SD, Wada HG, Humphries GM, and Conklin BR (1999) Chimeric G proteins allow a high-throughput signaling assay of Gi-coupled receptors. Anal Biochem 270:242-248
-
(1999)
Anal Biochem
, vol.270
, pp. 242-248
-
-
Coward, P.1
Chan, S.D.2
Wada, H.G.3
Humphries, G.M.4
Conklin, B.R.5
-
10
-
-
74849131078
-
Human p2y14 receptor agonists: Truncation of the hexose moiety of uridine-59-diphosphoglucose and its replacement with alkyl and aryl groups
-
Das A, Ko H, Burianek LE, Barrett MO, Harden TK, and Jacobson KA (2010) Human P2Y14 receptor agonists: truncation of the hexose moiety of uridine-59-diphosphoglucose and its replacement with alkyl and aryl groups. J Med Chem 53: 471-480.
-
(2010)
J Med Chem
, vol.53
, pp. 471-480
-
-
Das, A.1
Ko, H.2
Burianek, L.E.3
Barrett, M.O.4
Harden, T.K.5
Jacobson, K.A.6
-
11
-
-
0035885861
-
Cloning, pharmacology, and tissue distribution of g-protein-coupled receptor gpr105 (kiaa0001) rodent orthologs
-
Freeman K, Tsui P, Moore D, Emson PC, Vawter L, Naheed S, Lane P, Bawagan H, Herrity N, and Murphy K et al. (2001) Cloning, pharmacology, and tissue distribution of G-protein-coupled receptor GPR105 (KIAA0001) rodent orthologs. Genomics 78:124-128
-
(2001)
Genomics
, vol.78
, pp. 124-128
-
-
Freeman, K.1
Tsui, P.2
Moore, D.3
Emson, P.C.4
Vawter, L.5
Naheed, S.6
Lane, P.7
Bawagan, H.8
Herrity, N.9
Murphy, K.10
-
12
-
-
42449109538
-
Udp is a competitive antagonist at the human p2y14 receptor
-
Fricks IP, Maddileti S, Carter RL, Lazarowski ER, Nicholas RA, Jacobson KA, and Harden TK (2008) UDP is a competitive antagonist at the human P2Y14 receptor. J Pharmacol Exp Ther 325:588-594.
-
(2008)
J Pharmacol Exp Ther
, vol.325
, pp. 588-594
-
-
Fricks, I.P.1
Maddileti, S.2
Carter, R.L.3
Lazarowski, E.R.4
Nicholas, R.A.5
Jacobson, K.A.6
Harden, T.K.7
-
13
-
-
67649884495
-
Gi-dependent cell signaling responses of the human p2y14 receptor in model cell systems
-
Fricks IP, Carter RL, Lazarowski ER, and Harden TK (2009) Gi-dependent cell signaling responses of the human P2Y14 receptor in model cell systems. J Pharmacol Exp Ther 330:162-168
-
(2009)
J Pharmacol Exp Ther
, vol.330
, pp. 162-168
-
-
Fricks, I.P.1
Carter, R.L.2
Lazarowski, E.R.3
Harden, T.K.4
-
14
-
-
84873745806
-
The role of p2y14 and other p2y receptors in degranulation of human lad2 mast cells
-
Gao ZG, Wei Q, Jayasekara MP, and Jacobson KA (2013) The role of P2Y14 and other P2Y receptors in degranulation of human LAD2 mast cells. Purinergic Signal 9: 31-40.
-
(2013)
Purinergic Signal
, vol.9
, pp. 31-40
-
-
Gao, Z.G.1
Wei, Q.2
Jayasekara, M.P.3
Jacobson, K.A.4
-
15
-
-
79955552171
-
The identification of 4,7-disubstituted naphthoic acid derivatives as udp-competitive antagonists of p2y14
-
Gauthier JY, Belley M, Deschênes D, Fournier JF, Gagné S, Gareau Y, Hamel M, Hénault M, Hyjazie H, and Kargman S et al. (2011) The identification of 4,7-disubstituted naphthoic acid derivatives as UDP-competitive antagonists of P2Y14. Bioorg Med Chem Lett 21:2836-2839.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 2836-2839
-
-
Gauthier, J.Y.1
Belley, M.2
Deschênes, D.3
Fournier, J.F.4
Gagné, S.5
Gareau, Y.6
Hamel, M.7
Hénault, M.8
Hyjazie, H.9
Kargman, S.10
-
16
-
-
79955555317
-
Synthesis and sar of pyrimidine-based, non-nucleotide p2y14 receptor antagonists
-
Guay D, Beaulieu C, Belley M, Crane SN, DeLuca JC, Gareau Y, Hamel M, Henault M, Hyjazie H, and Kargman S et al. (2011) Synthesis and SAR of pyrimidine-based, non-nucleotide P2Y14 receptor antagonists. Bioorg Med Chem Lett 21:2832-2835.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 2832-2835
-
-
Guay, D.1
Beaulieu, C.2
Belley, M.3
Crane, S.N.4
DeLuca, J.C.5
Gareau, Y.6
Hamel, M.7
Henault, M.8
Hyjazie, H.9
Kargman, S.10
-
17
-
-
80053543466
-
Discovery of novel p2y14 agonist and antagonist using conventional and nonconventional methods
-
Hamel M, Henault M, Hyjazie H, Morin N, Bayly C, Skorey K, Therien AG, Mancini J, Brideau C, and Kargman S (2011) Discovery of novel P2Y14 agonist and antagonist using conventional and nonconventional methods. J Biomol Screen 16: 1098-1105.
-
(2011)
J Biomol Screen
, vol.16
, pp. 1098-1105
-
-
Hamel, M.1
Henault, M.2
Hyjazie, H.3
Morin, N.4
Bayly, C.5
Skorey, K.6
Therien, A.G.7
Mancini, J.8
Brideau, C.9
Kargman, S.10
-
18
-
-
0020049863
-
Differential modification of the interaction of cardiac muscarinic cholinergic and beta-Adrenergic receptors with a guanine nucleotide binding component(s)
-
Harden TK, Scheer AG, and Smith MM (1982) Differential modification of the interaction of cardiac muscarinic cholinergic and beta-Adrenergic receptors with a guanine nucleotide binding component(s). Mol Pharmacol 21:570-580.
-
(1982)
Mol Pharmacol
, vol.21
, pp. 570-580
-
-
Harden, T.K.1
Scheer, A.G.2
Smith, M.M.3
-
20
-
-
0031711820
-
Transporters of nucleotide sugars, atp, and nucleotide sulfate in the endoplasmic reticulum and golgi apparatus
-
Hirschberg CB, Robbins PW, and Abeijon C (1998) Transporters of nucleotide sugars, ATP, and nucleotide sulfate in the endoplasmic reticulum and Golgi apparatus. Annu Rev Biochem 67:49-69.
-
(1998)
Annu Rev Biochem
, vol.67
, pp. 49-69
-
-
Hirschberg, C.B.1
Robbins, P.W.2
Abeijon, C.3
-
22
-
-
34848851105
-
Coordinated release of nucleotides and mucin from human airway epithelial calu-3 cells
-
Kreda SM, Okada SF, van Heusden CA, O'Neal W, Gabriel S, Abdullah L, Davis CW, Boucher RC, and Lazarowski ER (2007) Coordinated release of nucleotides and mucin from human airway epithelial Calu-3 cells. J Physiol 584:245-259.
-
(2007)
J Physiol
, vol.584
, pp. 245-259
-
-
Kreda, S.M.1
Okada, S.F.2
Van Heusden, C.A.3
O'Neal, W.4
Gabriel, S.5
Abdullah, L.6
Davis, C.W.7
Boucher, R.C.8
Lazarowski, E.R.9
-
23
-
-
0038745422
-
Release of cellular udp-glucose as a potential extracellular signaling molecule
-
Lazarowski ER, Shea DA, Boucher RC, and Harden TK (2003) Release of cellular UDP-glucose as a potential extracellular signaling molecule. Mol Pharmacol 63: 1190-1197.
-
(2003)
Mol Pharmacol
, vol.63
, pp. 1190-1197
-
-
Lazarowski, E.R.1
Shea, D.A.2
Boucher, R.C.3
Harden, T.K.4
-
25
-
-
70149083748
-
P2x1 ion channels promote neutrophil chemotaxis through rho kinase activation
-
Lecut C, Frederix K, Johnson DM, Deroanne C, Thiry M, Faccinetto C, Marée R, Evans RJ, Volders PG, and Bours V et al. (2009) P2X1 ion channels promote neutrophil chemotaxis through Rho kinase activation. J Immunol 183:2801-2809.
-
(2009)
J Immunol
, vol.183
, pp. 2801-2809
-
-
Lecut, C.1
Frederix, K.2
Johnson, D.M.3
Deroanne, C.4
Thiry, M.5
Faccinetto, C.6
Marée, R.7
Evans, R.J.8
Volders, P.G.9
Bours, V.10
-
26
-
-
0037663449
-
P2y-like receptor, gpr105 (p2y14), identifies and mediates chemotaxis of bone-marrow hematopoietic stem cells
-
Lee BC, Cheng T, Adams GB, Attar EC, Miura N, Lee SB, Saito Y, Olszak I, Dombkowski D, and Olson DP et al. (2003) P2Y-like receptor, GPR105 (P2Y14), identifies and mediates chemotaxis of bone-marrow hematopoietic stem cells. Genes Dev 17:1592-1604.
-
(2003)
Genes Dev
, vol.17
, pp. 1592-1604
-
-
Lee, B.C.1
Cheng, T.2
Adams, G.B.3
Attar, E.C.4
Miura, N.5
Lee, S.B.6
Saito, Y.7
Olszak, I.8
Dombkowski, D.9
Olson, D.P.10
-
27
-
-
1542704056
-
Gpr105, a novel gi/o-coupled udp-glucose receptor expressed on brain glia and peripheral immune cells, is regulated by immunologic challenge: Possible role in neuroimmune function
-
Moore DJ, Murdock PR, Watson JM, Faull RL, Waldvogel HJ, Szekeres PG, Wilson S, Freeman KB, and Emson PC (2003) GPR105, a novel Gi/o-coupled UDP-glucose receptor expressed on brain glia and peripheral immune cells, is regulated by immunologic challenge: possible role in neuroimmune function. Brain Res Mol Brain Res 118:10-23.
-
(2003)
Brain Res Mol Brain Res
, vol.118
, pp. 10-23
-
-
Moore, D.J.1
Murdock, P.R.2
Watson, J.M.3
Faull, R.L.4
Waldvogel, H.J.5
Szekeres, P.G.6
Wilson, S.7
Freeman, K.B.8
Emson, P.C.9
-
28
-
-
0029788548
-
Uridine nucleotide selectivity of three phospholipase c-Activating p2 receptors: Identification of a udp-selective, a utp-selective, and an atp-And utp-specific receptor
-
Nicholas RA, Watt WC, Lazarowski ER, Li Q, and Harden K (1996) Uridine nucleotide selectivity of three phospholipase C-Activating P2 receptors: identification of a UDP-selective, a UTP-selective, and an ATP-And UTP-specific receptor. Mol Pharmacol 50:224-229.
-
(1996)
Mol Pharmacol
, vol.50
, pp. 224-229
-
-
Nicholas, R.A.1
Watt, W.C.2
Lazarowski, E.R.3
Li, Q.4
Harden, K.5
-
29
-
-
80051642490
-
Coupled nucleotide and mucin hypersecretion from gobletcell metaplastic human airway epithelium
-
Okada SF, Zhang L, Kreda SM, Abdullah LH, Davis CW, Pickles RJ, Lazarowski ER, and Boucher RC (2011) Coupled nucleotide and mucin hypersecretion from gobletcell metaplastic human airway epithelium. Am J Respir Cell Mol Biol 45:253-260.
-
(2011)
Am J Respir Cell Mol Biol
, vol.45
, pp. 253-260
-
-
Okada, S.F.1
Zhang, L.2
Kreda, S.M.3
Abdullah, L.H.4
Davis, C.W.5
Pickles, R.J.6
Lazarowski, E.R.7
Boucher, R.C.8
-
30
-
-
0035143199
-
Differential coupling of the human p2y11 receptor to phospholipase c and adenylyl cyclase
-
Qi AD, Kennedy C, Harden TK, and Nicholas RA (2001) Differential coupling of the human P2Y11 receptor to phospholipase C and adenylyl cyclase. Br J Pharmacol 132:318-326.
-
(2001)
Br J Pharmacol
, vol.132
, pp. 318-326
-
-
Qi, A.D.1
Kennedy, C.2
Harden, T.K.3
Nicholas, R.A.4
-
31
-
-
0031754497
-
Receptors for purines and pyrimidines
-
Ralevic V and Burnstock G (1998) Receptors for purines and pyrimidines. Pharmacol Rev 50:413-492.
-
(1998)
Pharmacol Rev
, vol.50
, pp. 413-492
-
-
Ralevic, V.1
Burnstock, G.2
-
32
-
-
79959886815
-
Applying the pro-drug approach to afford highly bioavailable antagonists of p2y14
-
Robichaud J, Fournier JF, Gagné S, Gauthier JY, Hamel M, Han Y, Hénault M, Kargman S, Levesque JF, and Mamane Y et al. (2011) Applying the pro-drug approach to afford highly bioavailable antagonists of P2Y14. Bioorg Med Chem Lett 21:4366-4368
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 4366-4368
-
-
Robichaud, J.1
Fournier, J.F.2
Gagné, S.3
Gauthier, J.Y.4
Hamel, M.5
Han, Y.6
Hénault, M.7
Kargman, S.8
Levesque, J.F.9
Mamane, Y.10
-
33
-
-
0016374975
-
A highly sensitive adenylate cyclase assay
-
Salomon Y, Londos C, and Rodbell M (1974) A highly sensitive adenylate cyclase assay. Anal Biochem 58:541-548
-
(1974)
Anal Biochem
, vol.58
, pp. 541-548
-
-
Salomon, Y.1
Londos, C.2
Rodbell, M.3
-
34
-
-
0029926077
-
Second messenger cascade specificity and pharmacological selectivity of the human p2y1-purinoceptor
-
Schachter JB, Li Q, Boyer JL, Nicholas RA, and Harden TK (1996) Second messenger cascade specificity and pharmacological selectivity of the human P2Y1-purinoceptor. Br J Pharmacol 118:167-173.
-
(1996)
Br J Pharmacol
, vol.118
, pp. 167-173
-
-
Schachter, J.B.1
Li, Q.2
Boyer, J.L.3
Nicholas, R.A.4
Harden, T.K.5
-
35
-
-
33746198758
-
Functional expression of the p2y14 receptor in human neutrophils
-
Scrivens M and Dickenson JM (2006) Functional expression of the P2Y14 receptor in human neutrophils. Eur J Pharmacol 543:166-173.
-
(2006)
Eur J Pharmacol
, vol.543
, pp. 166-173
-
-
Scrivens, M.1
Dickenson, J.M.2
-
36
-
-
66449127496
-
Endoplasmic reticulum/golgi nucleotide sugar transporters contribute to the cellular release of udp-sugar signaling molecules
-
Sesma JI, Esther CR, Jr., Kreda SM, Jones L, O'Neal W, Nishihara S, Nicholas RA, and Lazarowski ER (2009) Endoplasmic reticulum/golgi nucleotide sugar transporters contribute to the cellular release of UDP-sugar signaling molecules. J Biol Chem 284:12572-12583.
-
(2009)
J Biol Chem
, vol.284
, pp. 12572-12583
-
-
Sesma, J.I.1
Esther, C.R.2
Jr. Kreda, S.M.3
Jones, L.4
O'Neal, W.5
Nishihara, S.6
Nicholas, R.A.7
Lazarowski, E.R.8
-
37
-
-
84865721456
-
The UDP-sugar-sensing P2Y14 receptor promotes rhomediated signaling chemotaxis in human neutrophils
-
Sesma JI, Kreda SM, Steinckwich-Besancon N, Dang H, García-Mata R, Harden TK, and Lazarowski ER (2012) The UDP-sugar-sensing P2Y14 receptor promotes Rhomediated signaling and chemotaxis in human neutrophils. Am J Physiol Cell Physiol 303:C490-C498
-
(2012)
Am J Physiol Cell Physiol
, vol.303
-
-
Sesma, J.I.1
Kreda, S.M.2
Steinckwich-Besancon, N.3
Dang, H.4
García-Mata, R.5
Harden, T.K.6
Lazarowski, E.R.7
-
38
-
-
0042134893
-
Human immature monocytederived dendritic cells express the g protein-coupled receptor gpr105 (kiaa0001, p2y14) and increase intracellular calcium in response to its agonist, uridine diphosphoglucose
-
Skelton L, Cooper M, Murphy M, and Platt A (2003) Human immature monocytederived dendritic cells express the G protein-coupled receptor GPR105 (KIAA0001, P2Y14) and increase intracellular calcium in response to its agonist, uridine diphosphoglucose. J Immunol 171:1941-1949.
-
(2003)
J Immunol
, vol.171
, pp. 1941-1949
-
-
Skelton, L.1
Cooper, M.2
Murphy, M.3
Platt, A.4
-
39
-
-
40049087904
-
Inhibition of neutrophil apoptosis by atp is mediated by the p2y11 receptor
-
Vaughan KR, Stokes L, Prince LR, Marriott HM, Meis S, Kassack MU, Bingle CD, Sabroe I, Surprenant A, and Whyte MK (2007) Inhibition of neutrophil apoptosis by ATP is mediated by the P2Y11 receptor. J Immunol 179:8544-8553.
-
(2007)
J Immunol
, vol.179
, pp. 8544-8553
-
-
Vaughan, K.R.1
Stokes, L.2
Prince, L.R.3
Marriott, H.M.4
Meis, S.5
Kassack, M.U.6
Bingle, C.D.7
Sabroe, I.8
Surprenant, A.9
Whyte, M.K.10
-
40
-
-
0029666263
-
P2u agonists induce chemotaxis and actin polymerization in human neutrophils and differentiated hl60 cells
-
Verghese MW, Kneisler TB, and Boucheron JA (1996) P2U agonists induce chemotaxis and actin polymerization in human neutrophils and differentiated HL60 cells. J Biol Chem 271:15597-15601.
-
(1996)
J Biol Chem
, vol.271
, pp. 15597-15601
-
-
Verghese, M.W.1
Kneisler, T.B.2
Boucheron, J.A.3
-
41
-
-
84864804711
-
Gpr105 ablation prevents inflammation and improves insulin sensitivity in mice with diet-induced obesity
-
Xu J, Morinaga H, Oh D, Li P, Chen A, Talukdar S, Mamane Y, Mancini JA, Nawrocki AR, and Lazarowski E et al. (2012) GPR105 ablation prevents inflammation and improves insulin sensitivity in mice with diet-induced obesity. J Immunol 189:1992-1999.
-
(2012)
J Immunol
, vol.189
, pp. 1992-1999
-
-
Xu, J.1
Morinaga, H.2
Oh, D.3
Li, P.4
Chen, A.5
Talukdar, S.6
Mamane, Y.7
Mancini, J.A.8
Nawrocki, A.R.9
Lazarowski, E.10
-
42
-
-
79955961675
-
Molecular pharmacology, physiology, and structure of the p2y receptors
-
von Küglegen V and Harden TK (2012) Molecular pharmacology, physiology, and structure of the P2Y receptors. Adv Pharmacol 61:373-451.
-
(2012)
Adv Pharmacol
, vol.61
, pp. 373-451
-
-
Von Küglegen, V.1
Harden, T.K.2
-
43
-
-
0033766981
-
Extracellular metabolism of atp and other nucleotides
-
Zimmermann H (2000) Extracellular metabolism of ATP and other nucleotides. Naunyn Schmiedebergs Arch Pharmacol 362:299-309.
-
(2000)
Naunyn Schmiedebergs Arch Pharmacol
, vol.362
, pp. 299-309
-
-
Zimmermann, H.1
|