-
1
-
-
0026035523
-
Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation
-
Vu TK, Hung DT, Wheaton VI, Coughlin SR, (1991) Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activation. Cell 64: 1057-1068.
-
(1991)
Cell
, vol.64
, pp. 1057-1068
-
-
Vu, T.K.1
Hung, D.T.2
Wheaton, V.I.3
Coughlin, S.R.4
-
2
-
-
0032514474
-
A dual thrombin receptor system for platelet activation
-
Kahn M, Zheng Y, Huang W, Bigornia V, Zeng D, et al. (1998) A dual thrombin receptor system for platelet activation. Nature 394: 690-694.
-
(1998)
Nature
, vol.394
, pp. 690-694
-
-
Kahn, M.1
Zheng, Y.2
Huang, W.3
Bigornia, V.4
Zeng, D.5
-
3
-
-
0033559805
-
Protease-activated receptors 1 and 4 mediate activation of human platelets by thrombin
-
Kahn ML, Nakanishi-Matsui M, Shapiro MJ, Ishihara H, Coughlin SR, (1999) Protease-activated receptors 1 and 4 mediate activation of human platelets by thrombin. The Journal of clinical investigation 103: 879-887.
-
(1999)
The Journal of Clinical Investigation
, vol.103
, pp. 879-887
-
-
Kahn, M.L.1
Nakanishi-Matsui, M.2
Shapiro, M.J.3
Ishihara, H.4
Coughlin, S.R.5
-
4
-
-
0032499696
-
Cloning and characterization of human protease-activated receptor 4
-
Xu WF, Andersen H, Whitmore TE, Presnell SR, Yee DP, et al. (1998) Cloning and characterization of human protease-activated receptor 4. Proceedings of the National Academy of Sciences of the United States of America 95: 6642-6646.
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, pp. 6642-6646
-
-
Xu, W.F.1
Andersen, H.2
Whitmore, T.E.3
Presnell, S.R.4
Yee, D.P.5
-
5
-
-
0035817822
-
Role of thrombin signalling in platelets in haemostasis and thrombosis
-
Sambrano GR, Weiss EJ, Zheng YW, Huang W, Coughlin SR, (2001) Role of thrombin signalling in platelets in haemostasis and thrombosis. Nature 413: 74-78.
-
(2001)
Nature
, vol.413
, pp. 74-78
-
-
Sambrano, G.R.1
Weiss, E.J.2
Zheng, Y.W.3
Huang, W.4
Coughlin, S.R.5
-
6
-
-
13244273430
-
Impaired hemostasis and protection against thrombosis in protease-activated receptor 4-deficient mice is due to lack of thrombin signaling in platelets
-
Hamilton JR, Cornelissen I, Coughlin SR, (2004) Impaired hemostasis and protection against thrombosis in protease-activated receptor 4-deficient mice is due to lack of thrombin signaling in platelets. J Thromb Haemost 2: 1429-1435.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 1429-1435
-
-
Hamilton, J.R.1
Cornelissen, I.2
Coughlin, S.R.3
-
7
-
-
0029758276
-
Development of potent thrombin receptor antagonist peptides
-
Bernatowicz MS, Klimas CE, Hartl KS, Peluso M, Allegretto NJ, et al. (1996) Development of potent thrombin receptor antagonist peptides. J Med Chem 39: 4879-4887.
-
(1996)
J Med Chem
, vol.39
, pp. 4879-4887
-
-
Bernatowicz, M.S.1
Klimas, C.E.2
Hartl, K.S.3
Peluso, M.4
Allegretto, N.J.5
-
8
-
-
13044257730
-
Design, synthesis, and biological characterization of a peptide-mimetic antagonist for a tethered-ligand receptor
-
Andrade-Gordon P, Maryanoff BE, Derian CK, Zhang HC, Addo MF, et al. (1999) Design, synthesis, and biological characterization of a peptide-mimetic antagonist for a tethered-ligand receptor. Proceedings of the National Academy of Sciences of the United States of America 96: 12257-12262.
-
(1999)
Proceedings of the National Academy of Sciences of the United States of America
, vol.96
, pp. 12257-12262
-
-
Andrade-Gordon, P.1
Maryanoff, B.E.2
Derian, C.K.3
Zhang, H.C.4
Addo, M.F.5
-
9
-
-
0034670162
-
Inhibition of cellular action of thrombin by N3-cyclopropyl-7-[[4-(1-methylethyl)phenyl]methyl]-7H-pyrrolo[3, 2-f]quinazoline-1,3-diamine (SCH 79797), a nonpeptide thrombin receptor antagonist
-
Ahn HS, Foster C, Boykow G, Stamford A, Manna M, et al. (2000) Inhibition of cellular action of thrombin by N3-cyclopropyl-7-[[4-(1-methylethyl)phenyl]methyl]-7H-pyrrolo[3, 2-f]quinazoline-1,3-diamine (SCH 79797), a nonpeptide thrombin receptor antagonist. Biochem Pharmacol 60: 1425-1434.
-
(2000)
Biochem Pharmacol
, vol.60
, pp. 1425-1434
-
-
Ahn, H.S.1
Foster, C.2
Boykow, G.3
Stamford, A.4
Manna, M.5
-
10
-
-
32044441604
-
Discovery and synthesis of a novel series of quinoline-based thrombin receptor (PAR-1) antagonists
-
Clasby MC, Chackalamannil S, Czarniecki M, Doller D, Eagen K, et al. (2006) Discovery and synthesis of a novel series of quinoline-based thrombin receptor (PAR-1) antagonists. Bioorg Med Chem Lett 16: 1544-1548.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 1544-1548
-
-
Clasby, M.C.1
Chackalamannil, S.2
Czarniecki, M.3
Doller, D.4
Eagen, K.5
-
11
-
-
84859555815
-
Vorapaxar in the secondary prevention of atherothrombotic events
-
Morrow DA, Braunwald E, Bonaca MP, Ameriso SF, Dalby AJ, et al. (2012) Vorapaxar in the secondary prevention of atherothrombotic events. New England Journal of Medicine 366: 1404-2817.
-
(2012)
New England Journal of Medicine
, vol.366
, pp. 1404-2817
-
-
Morrow, D.A.1
Braunwald, E.2
Bonaca, M.P.3
Ameriso, S.F.4
Dalby, A.J.5
-
12
-
-
83655177669
-
Thrombin-receptor antagonist vorapaxar in acute coronary syndromes
-
Tricoci P, Huang Z, Held C, Moliterno D, Armstrong P, et al. (2012) Thrombin-receptor antagonist vorapaxar in acute coronary syndromes. The New England journal of medicine 366: 20-53.
-
(2012)
The New England Journal of Medicine
, vol.366
, pp. 20-53
-
-
Tricoci, P.1
Huang, Z.2
Held, C.3
Moliterno, D.4
Armstrong, P.5
-
13
-
-
84867336413
-
Vorapaxar for secondary prevention of thrombotic events for patients with previous myocardial infarction: a prespecified subgroup analysis of the TRA 2 degrees P-TIMI 50 trial
-
Scirica BM, Bonaca MP, Braunwald E, De Ferrari GM, Isaza D, et al. (2012) Vorapaxar for secondary prevention of thrombotic events for patients with previous myocardial infarction: a prespecified subgroup analysis of the TRA 2 degrees P-TIMI 50 trial. Lancet 380: 1317-1324.
-
(2012)
Lancet
, vol.380
, pp. 1317-1324
-
-
Scirica, B.M.1
Bonaca, M.P.2
Braunwald, E.3
De Ferrari, G.M.4
Isaza, D.5
-
14
-
-
84875410453
-
Protease-activated Receptor (PAR) 1 and PAR4 Differentially Regulate Factor V Expression from Human Platelets
-
Duvernay MT, Young S, Gailani D, Schoenecker J, Hamm HE (2013) Protease-activated Receptor (PAR) 1 and PAR4 Differentially Regulate Factor V Expression from Human Platelets. Mol Pharmacol.
-
(2013)
Mol Pharmacol
-
-
Duvernay, M.T.1
Young, S.2
Gailani, D.3
Schoenecker, J.4
Hamm, H.E.5
-
15
-
-
33645509877
-
Differential regulation of endothelial exocytosis of P-selectin and von Willebrand factor by protease-activated receptors and cAMP
-
Cleator J, Zhu W, Vaughan D, Hamm H, (2006) Differential regulation of endothelial exocytosis of P-selectin and von Willebrand factor by protease-activated receptors and cAMP. Blood 107: 2736-2780.
-
(2006)
Blood
, vol.107
, pp. 2736-2780
-
-
Cleator, J.1
Zhu, W.2
Vaughan, D.3
Hamm, H.4
-
16
-
-
79551480210
-
Protease-activated receptor signaling in platelets activates cytosolic phospholipase A2α differently for cyclooxygenase-1 and 12-lipoxygenase catalysis
-
Holinstat M, Boutaud O, Apopa P, Vesci J, Bala M, et al. (2011) Protease-activated receptor signaling in platelets activates cytosolic phospholipase A2α differently for cyclooxygenase-1 and 12-lipoxygenase catalysis. Arteriosclerosis, thrombosis, and vascular biology 31: 435-477.
-
(2011)
Arteriosclerosis, Thrombosis, and Vascular Biology
, vol.31
, pp. 435-477
-
-
Holinstat, M.1
Boutaud, O.2
Apopa, P.3
Vesci, J.4
Bala, M.5
-
17
-
-
33748745670
-
PAR4, but not PAR1, signals human platelet aggregation via Ca2+ mobilization and synergistic P2Y12 receptor activation
-
Holinstat M, Voss B, Bilodeau M, McLaughlin J, Cleator J, et al. (2006) PAR4, but not PAR1, signals human platelet aggregation via Ca2+ mobilization and synergistic P2Y12 receptor activation. The Journal of biological chemistry 281: 26665-26739.
-
(2006)
The Journal of Biological Chemistry
, vol.281
, pp. 26665-26739
-
-
Holinstat, M.1
Voss, B.2
Bilodeau, M.3
McLaughlin, J.4
Cleator, J.5
-
18
-
-
0034682810
-
Protease-activated receptors 1 and 4 are shut off with distinct kinetics after activation by thrombin
-
Shapiro MJ, Weiss EJ, Faruqi TR, Coughlin SR, (2000) Protease-activated receptors 1 and 4 are shut off with distinct kinetics after activation by thrombin. The Journal of biological chemistry 275: 25216-25221.
-
(2000)
The Journal of Biological Chemistry
, vol.275
, pp. 25216-25221
-
-
Shapiro, M.J.1
Weiss, E.J.2
Faruqi, T.R.3
Coughlin, S.R.4
-
19
-
-
34247545661
-
PAR1, but not PAR4, activates human platelets through a Gi/o/phosphoinositide-3 kinase signaling axis
-
Voss B, McLaughlin J, Holinstat M, Zent R, Hamm H, (2007) PAR1, but not PAR4, activates human platelets through a Gi/o/phosphoinositide-3 kinase signaling axis. Molecular pharmacology 71: 1399-1805.
-
(2007)
Molecular Pharmacology
, vol.71
, pp. 1399-1805
-
-
Voss, B.1
McLaughlin, J.2
Holinstat, M.3
Zent, R.4
Hamm, H.5
-
20
-
-
38849168285
-
Synthesis and antiplatelet activity of ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) derivatives
-
Chen H-S, Kuo S-C, Teng C-M, Lee F-Y, Wang J-P, et al. (2008) Synthesis and antiplatelet activity of ethyl 4-(1-benzyl-1H-indazol-3-yl)benzoate (YD-3) derivatives. Bioorganic & medicinal chemistry 16: 1262-1340.
-
(2008)
Bioorganic & Medicinal Chemistry
, vol.16
, pp. 1262-1340
-
-
Chen, H.-S.1
Kuo, S.-C.2
Teng, C.-M.3
Lee, F.-Y.4
Wang, J.-P.5
-
21
-
-
78649631367
-
The indazole derivative YD-3 specifically inhibits thrombin-induced angiogenesis in vitro and in vivo
-
Peng C-Y, Pan S-L, Pai H-C, Tsai A-C, Guh J-H, et al. (2010) The indazole derivative YD-3 specifically inhibits thrombin-induced angiogenesis in vitro and in vivo. Shock (Augusta, Ga) 34: 580-585.
-
(2010)
Shock (Augusta, Ga)
, vol.34
, pp. 580-585
-
-
Peng, C.-Y.1
Pan, S.-L.2
Pai, H.-C.3
Tsai, A.-C.4
Guh, J.-H.5
-
22
-
-
0033943590
-
YD-3, a novel inhibitor of protease-induced platelet activation
-
Wu C, Huang S, Hwang T, Kuo S, Lee F, et al. (2000) YD-3, a novel inhibitor of protease-induced platelet activation. British journal of pharmacology 130: 1289-1385.
-
(2000)
British Journal of Pharmacology
, vol.130
, pp. 1289-1385
-
-
Wu, C.1
Huang, S.2
Hwang, T.3
Kuo, S.4
Lee, F.5
-
23
-
-
0036285450
-
Selective inhibition of protease-activated receptor 4-dependent platelet activation by YD-3
-
Wu C-C, Hwang T-L, Liao C-H, Kuo S-C, Lee F-Y, et al. (2002) Selective inhibition of protease-activated receptor 4-dependent platelet activation by YD-3. Thrombosis and haemostasis 87: 1026-1059.
-
(2002)
Thrombosis and Haemostasis
, vol.87
, pp. 1026-1059
-
-
Wu, C.-C.1
Hwang, T.-L.2
Liao, C.-H.3
Kuo, S.-C.4
Lee, F.-Y.5
-
24
-
-
0035950053
-
Synthesis of 1-benzyl-3-(5'-hydroxymethyl-2'-furyl)indazole analogues as novel antiplatelet agents
-
Lee F, Lien J, Huang L, Huang T, Tsai S, et al. (2001) Synthesis of 1-benzyl-3-(5'-hydroxymethyl-2'-furyl)indazole analogues as novel antiplatelet agents. Journal of medicinal chemistry 44: 3746-3755.
-
(2001)
Journal of Medicinal Chemistry
, vol.44
, pp. 3746-3755
-
-
Lee, F.1
Lien, J.2
Huang, L.3
Huang, T.4
Tsai, S.5
-
25
-
-
78649631367
-
The indazole derivative YD-3 specifically inhibits thrombin-induced angiogenesis in vitro and in vivo
-
Peng CY, Pan SL, Pai HC, Tsai AC, Guh JH, et al. (2010) The indazole derivative YD-3 specifically inhibits thrombin-induced angiogenesis in vitro and in vivo. Shock 34: 580-585.
-
(2010)
Shock
, vol.34
, pp. 580-585
-
-
Peng, C.Y.1
Pan, S.L.2
Pai, H.C.3
Tsai, A.C.4
Guh, J.H.5
-
26
-
-
45149106841
-
Application of combinatorial chemistry science on modern drug discovery
-
Kennedy JP, Williams L, Bridges TM, Daniels RN, Weaver D, et al. (2008) Application of combinatorial chemistry science on modern drug discovery. J Comb Chem 10: 345-354.
-
(2008)
J Comb Chem
, vol.10
, pp. 345-354
-
-
Kennedy, J.P.1
Williams, L.2
Bridges, T.M.3
Daniels, R.N.4
Weaver, D.5
-
27
-
-
19944431003
-
Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors
-
Lindsley CW, Zhao Z, Leister WH, Robinson RG, Barnett SF, et al. (2005) Allosteric Akt (PKB) inhibitors: discovery and SAR of isozyme selective inhibitors. Bioorg Med Chem Lett 15: 761-764.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 761-764
-
-
Lindsley, C.W.1
Zhao, Z.2
Leister, W.H.3
Robinson, R.G.4
Barnett, S.F.5
-
28
-
-
0000344058
-
A superior synthethic method for the bromination of indoles and benzimidazoles
-
Mistry AG, Smith K, Bye MR, (1986) A superior synthethic method for the bromination of indoles and benzimidazoles. Tetrahedron letters 27: 1051-2105.
-
(1986)
Tetrahedron Letters
, vol.27
, pp. 1051-2105
-
-
Mistry, A.G.1
Smith, K.2
Bye, M.R.3
-
30
-
-
0028984532
-
Two classes of agonist-sensitive Ca2+ stores in platelets, as identified by their differential sensitivity to 2,5-di-(tert-butyl)-1,4-benzohydroquinone and thapsigargin
-
Cavallini L, Coassin M, Alexandre A, (1995) Two classes of agonist-sensitive Ca2+ stores in platelets, as identified by their differential sensitivity to 2,5-di-(tert-butyl)-1,4-benzohydroquinone and thapsigargin. Biochem J 310 (Pt 2): 449-452.
-
(1995)
Biochem J
, vol.310
, Issue.PART 2
, pp. 449-452
-
-
Cavallini, L.1
Coassin, M.2
Alexandre, A.3
-
31
-
-
33846279424
-
Differential involvement of thrombin receptors in Ca2+ release from two different intracellular stores in human platelets
-
Jardin I, Ben Amor N, Bartegi A, Pariente JA, Salido GM, et al. (2007) Differential involvement of thrombin receptors in Ca2+ release from two different intracellular stores in human platelets. Biochem J 401: 167-174.
-
(2007)
Biochem J
, vol.401
, pp. 167-174
-
-
Jardin, I.1
Ben Amor, N.2
Bartegi, A.3
Pariente, J.A.4
Salido, G.M.5
-
32
-
-
0033003760
-
A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays
-
Zhang JH, Chung TD, Oldenburg KR, (1999) A Simple Statistical Parameter for Use in Evaluation and Validation of High Throughput Screening Assays. J Biomol Screen 4: 67-73.
-
(1999)
J Biomol Screen
, vol.4
, pp. 67-73
-
-
Zhang, J.H.1
Chung, T.D.2
Oldenburg, K.R.3
-
33
-
-
0036285450
-
Selective inhibition of protease-activated receptor 4-dependent platelet activation by YD-3
-
Wu CC, Hwang TL, Liao CH, Kuo SC, Lee FY, et al. (2002) Selective inhibition of protease-activated receptor 4-dependent platelet activation by YD-3. Thromb Haemost 87: 1026-1033.
-
(2002)
Thromb Haemost
, vol.87
, pp. 1026-1033
-
-
Wu, C.C.1
Hwang, T.L.2
Liao, C.H.3
Kuo, S.C.4
Lee, F.Y.5
-
34
-
-
0034089122
-
Incomplete inhibition of platelet aggregation and glycoprotein IIb-IIIa receptor blockade by abciximab: importance of internal pool of glycoprotein IIb-IIIa receptors
-
Gawaz M, Ruf A, Pogatsa-Murray G, Dickfeld T, Rudiger S, et al. (2000) Incomplete inhibition of platelet aggregation and glycoprotein IIb-IIIa receptor blockade by abciximab: importance of internal pool of glycoprotein IIb-IIIa receptors. Thromb Haemost 83: 915-922.
-
(2000)
Thromb Haemost
, vol.83
, pp. 915-922
-
-
Gawaz, M.1
Ruf, A.2
Pogatsa-Murray, G.3
Dickfeld, T.4
Rudiger, S.5
-
35
-
-
0028807209
-
Differential inhibition of platelet aggregation induced by adenosine diphosphate or a thrombin receptor-activating peptide in patients treated with bolus chimeric 7E3 Fab: implications for inhibition of the internal pool of GPIIb/IIIa receptors
-
Kleiman NS, Raizner AE, Jordan R, Wang AL, Norton D, et al. (1995) Differential inhibition of platelet aggregation induced by adenosine diphosphate or a thrombin receptor-activating peptide in patients treated with bolus chimeric 7E3 Fab: implications for inhibition of the internal pool of GPIIb/IIIa receptors. J Am Coll Cardiol 26: 1665-1671.
-
(1995)
J Am Coll Cardiol
, vol.26
, pp. 1665-1671
-
-
Kleiman, N.S.1
Raizner, A.E.2
Jordan, R.3
Wang, A.L.4
Norton, D.5
-
36
-
-
0034307532
-
The GPIb thrombin-binding site is essential for thrombin-induced platelet procoagulant activity
-
Dormann D, Clemetson KJ, Kehrel BE, (2000) The GPIb thrombin-binding site is essential for thrombin-induced platelet procoagulant activity. Blood 96: 2469-2478.
-
(2000)
Blood
, vol.96
, pp. 2469-2478
-
-
Dormann, D.1
Clemetson, K.J.2
Kehrel, B.E.3
|