-
1
-
-
0028884033
-
PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo
-
Alessi DR, Cuenda A, Cohen P, Dudley DT, and Saltiel AR (1995) PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo. J Biol Chem 270:27489-27494.
-
(1995)
J Biol Chem
, vol.270
, pp. 27489-27494
-
-
Alessi, D.R.1
Cuenda, A.2
Cohen, P.3
Dudley, D.T.4
Saltiel, A.R.5
-
2
-
-
36549040859
-
The selectivity of protein kinase inhibitors: A further update
-
Bain J, Plater L, Elliott M, Shpiro N, Hastie CJ, McLauchlan H, Klevernic I, Arthur JS, Alessi DR, and Cohen P (2007) The selectivity of protein kinase inhibitors: a further update. Biochem J 408:297-315.
-
(2007)
Biochem J
, vol.408
, pp. 297-315
-
-
Bain, J.1
Plater, L.2
Elliott, M.3
Shpiro, N.4
Hastie, C.J.5
McLauchlan, H.6
Klevernic, I.7
Arthur, J.S.8
Alessi, D.R.9
Cohen, P.10
-
3
-
-
34447625738
-
Multiple GPCR conformations and signalling pathways: Implications for antagonist affinity estimates
-
Baker JG and Hill SJ (2007) Multiple GPCR conformations and signalling pathways: implications for antagonist affinity estimates. Trends Pharmacol Sci 28:374-381.
-
(2007)
Trends Pharmacol Sci
, vol.28
, pp. 374-381
-
-
Baker, J.G.1
Hill, S.J.2
-
4
-
-
31044443609
-
Relaxin-3: Improved synthesis strategy and demonstration of its high-affinity interaction with the relaxin receptor LGR7 both in vitro and in vivo
-
DOI 10.1021/bi052233e
-
Bathgate RA, Lin F, Hanson NF, Otvos L, Jr., Guidolin A, Giannakis C, Bastiras S, Layfield SL, Ferraro T, Ma S, Zhao C, Gundlach AL, Samuel CS, Tregear GW, and Wade JD (2006) Relaxin-3: improved synthesis strategy and demonstration of its high-affinity interaction with the relaxin receptor LGR7 both in vitro and in vivo. Biochemistry 45:1043-1053. (Pubitemid 43122269)
-
(2006)
Biochemistry
, vol.45
, Issue.3
, pp. 1043-1053
-
-
Bathgate, R.A.D.1
Lin, F.2
Hanson, N.F.3
Otvos Jr., L.4
Guidolin, A.5
Giannakis, C.6
Bastiras, S.7
Layfield, S.L.8
Ferraro, T.9
Ma, S.10
Zhao, C.11
Gundlach, A.L.12
Samuel, C.S.13
Tregear, G.W.14
Wade, J.D.15
-
5
-
-
0037059750
-
Human relaxin gene 3 (H3) and the equivalent mouse relaxin (M3) gene: Novel members of the relaxin peptide family
-
DOI 10.1074/jbc.M107882200
-
Bathgate RA, Samuel CS, Burazin TC, Layfield S, Claasz AA, Reytomas IG, Dawson NF, Zhao C, Bond C, Summers RJ, et al. (2002) Human relaxin gene 3 (H3) and the equivalent mouse relaxin (M3) gene. Novel members of the relaxin peptide family. J Biol Chem 277:1148-1157. (Pubitemid 34968862)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.2
, pp. 1148-1157
-
-
Bathgate, R.A.D.1
Samuel, C.S.2
Burazin, T.C.D.3
Layfield, S.4
Claasz, A.A.5
Reytomas, I.G.T.6
Dawson, N.F.7
Zhao, C.8
Bond, C.9
Summers, R.J.10
Parry, L.J.11
Wade, J.D.12
Tregear, G.W.13
-
6
-
-
19444382560
-
Delta opioid peptide (D-Ala 2, D-Leu 5) enkephalin: Linking hibernation and neuroprotection
-
Borlongan CV, Wang Y, and Su TP (2004) Delta opioid peptide (D-Ala 2, D-Leu 5) enkephalin: linking hibernation and neuroprotection. Front Biosci 9:3392-3398.
-
(2004)
Front Biosci
, vol.9
, pp. 3392-3398
-
-
Borlongan, C.V.1
Wang, Y.2
Su, T.P.3
-
7
-
-
0035369623
-
Transcription-dependent and -independent control of neuronal survival by the PI3K-Akt signaling pathway
-
DOI 10.1016/S0959-4388(00)00211-7
-
Brunet A, Datta SR, and Greenberg ME (2001) Transcription-dependent and -independent control of neuronal survival by the PI3K-Akt signaling pathway. Curr Opin Neurobiol 11:297-305. (Pubitemid 32524094)
-
(2001)
Current Opinion in Neurobiology
, vol.11
, Issue.3
, pp. 297-305
-
-
Brunet, A.1
Datta, S.R.2
Greenberg, M.E.3
-
8
-
-
2342451911
-
G-protein coupled receptors in lipid rafts and caveolae: How, when and why do they go there?
-
DOI 10.1677/jme.0.0320325
-
Chini B and Parenti M (2004) G-protein coupled receptors in lipid rafts and caveolae: how, when and why do they go there? J Mol Endocrinol 32:325-338. (Pubitemid 38584639)
-
(2004)
Journal of Molecular Endocrinology
, vol.32
, Issue.2
, pp. 325-338
-
-
Chini, B.1
Parenti, M.2
-
9
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies SP, Reddy H, Caivano M, and Cohen P (2000) Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 351:95-105.
-
(2000)
Biochem J
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
Cohen, P.4
-
10
-
-
0034644522
-
Signal transduction by the JNK group of MAP kinases
-
Davis RJ (2000) Signal transduction by the JNK group of MAP kinases. Cell 103: 239-252.
-
(2000)
Cell
, vol.103
, pp. 239-252
-
-
Davis, R.J.1
-
11
-
-
33751162165
-
Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy
-
Galandrin S and Bouvier M (2006) Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy. Mol Pharmacol 70:1575-1584.
-
(2006)
Mol Pharmacol
, vol.70
, pp. 1575-1584
-
-
Galandrin, S.1
Bouvier, M.2
-
12
-
-
33845939640
-
Comparison of signaling pathways activated by the relaxin family peptide receptors, RXFP1 and RXFP2, using reporter genes
-
Halls ML, Bathgate RA, and Summers RJ (2007) Comparison of signaling pathways activated by the relaxin family peptide receptors, RXFP1 and RXFP2, using reporter genes. J Pharmacol Exp Ther 320:281-290.
-
(2007)
J Pharmacol Exp Ther
, vol.320
, pp. 281-290
-
-
Halls, M.L.1
Bathgate, R.A.2
Summers, R.J.3
-
13
-
-
18044378198
-
Multiple binding sites revealed by interaction of relaxin family peptides with native and chimeric relaxin family peptide receptors 1 and 2 (LGR7 and LGR8)
-
DOI 10.1124/jpet.104.080655
-
Halls ML, Bond CP, Sudo S, Kumagai J, Ferraro T, Layfield S, Bathgate RA, and Summers RJ (2005) Multiple binding sites revealed by interaction of relaxin family peptides with native and chimeric relaxin family peptide receptors 1 and 2 (LGR7 and LGR8). J Pharmacol Exp Ther 313:677-687. (Pubitemid 40604168)
-
(2005)
Journal of Pharmacology and Experimental Therapeutics
, vol.313
, Issue.2
, pp. 677-687
-
-
Halls, M.L.1
Bond, C.P.2
Sudo, S.3
Kumagai, J.4
Ferraro, T.5
Layfield, S.6
Bathgate, R.A.D.7
Summers, R.J.8
-
14
-
-
0033543549
-
Activation of the protein kinase ERK5/BMK1 by receptor tyrosine kinases: Identification and characterization of a signaling pathway to the nucleus
-
Kamakura S, Moriguchi T, and Nishida E (1999) Activation of the protein kinase ERK5/BMK1 by receptor tyrosine kinases. Identification and characterization of a signaling pathway to the nucleus. J Biol Chem 274:26563-26571. (Pubitemid 129520095)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.37
, pp. 26563-26571
-
-
Kamakura, S.1
Moriguchi, T.2
Nishida, E.3
-
15
-
-
0043235844
-
Ligand-selective receptor conformations revisited: The promise and the problem
-
Kenakin T (2003) Ligand-selective receptor conformations revisited: the promise and the problem. Trends Pharmacol Sci 24:346-354.
-
(2003)
Trends Pharmacol Sci
, vol.24
, pp. 346-354
-
-
Kenakin, T.1
-
16
-
-
34548471964
-
R3(BDelta23-27)R/I5 chimeric peptide, a selective antagonist for GPCR135 and GPCR142 over relaxin receptor LGR7: In vitro and in vivo characterization
-
DOI 10.1074/jbc.M701416200
-
Kuei C, Sutton S, Bonaventure P, Pudiak C, Shelton J, Zhu J, Nepomuceno D, Wu J, Chen J, Kamme F, et al. (2007) R3(BDelta23 27)R/I5 chimeric peptide, a selective antagonist for GPCR135 and GPCR142 over relaxin receptor LGR7: in vitro and in vivo characterization. J Biol Chem 282:25425-25435. (Pubitemid 47372825)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.35
, pp. 25425-25435
-
-
Kuei, C.1
Sutton, S.2
Bonaventure, P.3
Pudiak, C.4
Shelton, J.5
Zhu, J.6
Nepomuceno, D.7
Wu, J.8
Chen, J.9
Kamme, F.10
Seierstad, M.11
Hack, M.D.12
Bathgate, R.A.D.13
Hossain, M.A.14
Wade, J.D.15
Atack, J.16
Lovenberg, T.W.17
Liu, C.18
-
17
-
-
0030026314
-
Purification and characterization of porcine prorelaxin
-
Layden SS and Tregear GW (1996) Purification and characterization of porcine prorelaxin. J Biochem Biophys Methods 31:69-80.
-
(1996)
J Biochem Biophys Methods
, vol.31
, pp. 69-80
-
-
Layden, S.S.1
Tregear, G.W.2
-
18
-
-
11244347812
-
Relaxin-3/insulin-like peptide 5 chimeric peptide, a selective ligand for G protein-coupled receptor (GPCR)135 and GPCR142 over leucine-rich repeat-containing G protein-coupled receptor 7
-
DOI 10.1124/mol.104.006700
-
Liu C, Chen J, Kuei C, Sutton S, Nepomuceno D, Bonaventure P, and Lovenberg TW (2005) Relaxin-3/insulin-like peptide 5 chimeric peptide, a selective ligand for G protein-coupled receptor (GPCR)135 and GPCR142 over leucine-rich repeat-containing G protein-coupled receptor 7. Mol Pharmacol 67:231-240. (Pubitemid 40069983)
-
(2005)
Molecular Pharmacology
, vol.67
, Issue.1
, pp. 231-240
-
-
Liu, C.1
Chen, J.2
Kuei, C.3
Sutton, S.4
Nepomuceno, D.5
Bonaventure, P.6
Lovenberg, T.W.7
-
19
-
-
10744224962
-
Identification of Relaxin-3/INSL7 as an Endogenous Ligand for the Orphan G-protein-coupled Receptor GPCR135
-
DOI 10.1074/jbc.M308995200
-
Liu C, Eriste E, Sutton S, Chen J, Roland B, Kuei C, Farmer N, Jörnvall H, Sillard R, and Lovenberg TW (2003) Identification of relaxin-3/INSL7 as an endogenous ligand for the orphan G-protein-coupled receptor GPCR135. J Biol Chem 278: 50754-50764. (Pubitemid 37548924)
-
(2003)
Journal of Biological Chemistry
, vol.278
, Issue.50
, pp. 50754-50764
-
-
Liu, C.1
Eriste, E.2
Sutton, S.3
Chen, J.4
Roland, B.5
Kuei, C.6
Farmer, N.7
Jornvall, H.8
Sillard, R.9
Lovenberg, T.W.10
-
20
-
-
0032977187
-
2-terminal kinase, p38s, and extracellular signal-regulated kinase 5
-
Marinissen MJ, Chiariello M, Pallante M, and Gutkind JS (1999) A network of mitogen-activated protein kinases links G protein-coupled receptors to the c-jun promoter: a role for c-Jun NH2-terminal kinase, p38s, and extracellular signal-regulated kinase 5. Mol Cell Biol 19:4289-4301. (Pubitemid 29242004)
-
(1999)
Molecular and Cellular Biology
, vol.19
, Issue.6
, pp. 4289-4301
-
-
Marinissen, M.J.1
Chiariello, M.2
Pallante, M.3
Gutkind, J.S.4
-
21
-
-
33947169889
-
Hypothalamic mapping of orexigenic action and Fos-like immunoreactivity following relaxin-3 administration in male Wistar rats
-
DOI 10.1152/ajpendo.00346.2006
-
McGowan BM, Stanley SA, White NE, Spangeus A, Patterson M, Thompson EL, Smith KL, Donovan J, Gardiner JV, Ghatei MA, et al. (2007) Hypothalamic mapping of orexigenic action and Fos-like immunoreactivity following relaxin-3 administration in male Wistar rats. Am J Physiol Endocrinol Metab 292:E913-919. (Pubitemid 46411072)
-
(2007)
American Journal of Physiology - Endocrinology and Metabolism
, vol.292
, Issue.3
-
-
McGowan, B.M.1
Stanley, S.A.2
White, N.E.3
Spangeus, A.4
Patterson, M.5
Thompson, E.L.6
Smith, K.L.7
Donovan, J.8
Gardiner, J.V.9
Ghatei, M.A.10
Bloom, S.R.11
-
22
-
-
26944466076
-
GPCR screening via ERK 1/2: A novel platform for screening G protein-coupled receptors
-
DOI 10.1177/1087057105277968
-
Osmond RI, Sheehan A, Borowicz R, Barnett E, Harvey G, Turner C, Brown A, Crouch MF, and Dyer AR (2005) GPCR screening via ERK 1/2: a novel platform for screening G protein-coupled receptors. J Biomol Screen 10:730-737. (Pubitemid 41476808)
-
(2005)
Journal of Biomolecular Screening
, vol.10
, Issue.7
, pp. 730-737
-
-
Osmond, R.I.W.1
Sheehan, A.2
Borowicz, R.3
Barnett, E.4
Harvey, G.5
Turner, C.6
Brown, A.7
Crouch, M.F.8
Dyer, A.R.9
-
23
-
-
0035896513
-
ERK5 and ERK2 Cooperate to Regulate NF-kappaB and Cell Transformation
-
DOI 10.1074/jbc.M009764200
-
Pearson G, English JM, White MA, and Cobb MH (2001) ERK5 and ERK2 cooperate to regulate NF-kappaB and cell transformation. J Biol Chem 276:7927-7931. (Pubitemid 37385589)
-
(2001)
Journal of Biological Chemistry
, vol.276
, Issue.11
, pp. 7927-7931
-
-
Pearson, G.1
English, J.M.2
White, M.A.3
Cobb, M.H.4
-
24
-
-
0029827366
-
The p38 and ERK MAP kinase pathways cooperate to activate ternary complex factors and c-fos transcription in response to UV light
-
Price MA, Cruzalegui FH, and Treisman R (1996) The p38 and ERK MAP kinase pathways cooperate to activate ternary complex factors and c-fos transcription in response to UV light. EMBO J 15:6552-6563.
-
(1996)
EMBO J
, vol.15
, pp. 6552-6563
-
-
Price, M.A.1
Cruzalegui, F.H.2
Treisman, R.3
-
25
-
-
2942530310
-
ERK and p38 MAPK-activated protein kinases: A family of protein kinases with diverse biological functions
-
Roux PP and Blenis J (2004) ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions. Microbiol Mol Biol Rev 68: 320-344.
-
(2004)
Microbiol Mol Biol Rev
, vol.68
, pp. 320-344
-
-
Roux, P.P.1
Blenis, J.2
-
26
-
-
0022979263
-
Localization of binding sites for calcitonin gene-related peptide in rat brain by in vitro autoradiography
-
DOI 10.1016/0306-4522(86)90137-5
-
Sexton PM, McKenzie JS, Mason RT, Moseley JM, Martin TJ, and Mendelsohn FA (1986) Localization of binding sites for calcitonin gene-related peptide in rat brain by in vitro autoradiography. Neuroscience 19:1235-1245. (Pubitemid 17217018)
-
(1986)
Neuroscience
, vol.19
, Issue.4
, pp. 1235-1245
-
-
Sexton, P.M.1
McKenzie, J.S.2
Mason, R.T.3
-
27
-
-
0033524913
-
Lysophosphatidic acid activates NF-kappaB in fibroblasts. a requirement for multiple inputs
-
DOI 10.1074/jbc.274.6.3828
-
Shahrestanifar M, Fan X, and Manning DR (1999) Lysophosphatidic acid activates NF-kappaB in fibroblasts. A requirement for multiple inputs. J Biol Chem 274: 3828-3833. (Pubitemid 29077232)
-
(1999)
Journal of Biological Chemistry
, vol.274
, Issue.6
, pp. 3828-3833
-
-
Shahrestanifar, M.1
Fan, X.2
Manning, D.R.3
-
28
-
-
12944268757
-
Activation of Erk and JNK MAPK pathways by acute swim stress in rat brain regions
-
DOI 10.1186/1471-2202-5-36
-
Shen CP, Tsimberg Y, Salvadore C, and Meller E (2004) Activation of Erk and JNK MAPK pathways by acute swim stress in rat brain regions. BMC Neurosci 5:36. (Pubitemid 40177045)
-
(2004)
BMC Neuroscience
, vol.5
, pp. 36
-
-
Shen, C.-P.1
Tsimberg, Y.2
Salvadore, C.3
Meller, E.4
-
29
-
-
15544378102
-
Distribution of G-protein-coupled receptor (GPCR)135 binding sites and receptor mRNA in the rat brain suggests a role for relaxin-3 in neuroendocrine and sensory processing
-
DOI 10.1159/000083656
-
Sutton SW, Bonaventure P, Kuei C, Roland B, Chen J, Nepomuceno D, Lovenberg TW, and Liu C (2004) Distribution of G-protein-coupled receptor (GPCR)135 binding sites and receptor mRNA in the rat brain suggests a role for relaxin-3 in neuroendocrine and sensory processing. Neuroendocrinology 80:298-307. (Pubitemid 40470238)
-
(2004)
Neuroendocrinology
, vol.80
, Issue.5
, pp. 298-307
-
-
Sutton, S.W.1
Bonaventure, P.2
Kuei, C.3
Roland, B.4
Chen, J.5
Nepomuceno, D.6
Lovenberg, T.W.7
Liu, C.8
-
30
-
-
18444395865
-
Neurons expressing relaxin 3/INSL 7 in the nucleus incertus respond to stress
-
DOI 10.1111/j.1460-9568.2005.03980.x
-
Tanaka M, Iijima N, Miyamoto Y, Fukusumi S, Itoh Y, Ozawa H, and Ibata Y (2005) Neurons expressing relaxin 3/INSL 7 in the nucleus incertus respond to stress. Eur J Neurosci 21:1659-1670. (Pubitemid 40646611)
-
(2005)
European Journal of Neuroscience
, vol.21
, Issue.6
, pp. 1659-1670
-
-
Tanaka, M.1
Iijima, N.2
Miyamoto, Y.3
Fukusumi, S.4
Itoh, Y.5
Ozawa, H.6
Ibata, Y.7
-
31
-
-
64549159372
-
Addition of a carboxy-terminal green fluorescent protein does not alter the binding and signaling properties of relaxin family peptide receptor 3
-
van der Westhuizen ET, Wade JD, Sexton PM, and Summers RJ (2009) Addition of a carboxy-terminal green fluorescent protein does not alter the binding and signaling properties of relaxin family peptide receptor 3. Ann NY Acad Sci 1160:105-107.
-
(2009)
Ann NY Acad Sci
, vol.1160
, pp. 105-107
-
-
Van Der Westhuizen, E.T.1
Wade, J.D.2
Sexton, P.M.3
Summers, R.J.4
-
32
-
-
34347338779
-
The relaxin family peptide receptor 3 activates extracellular signal-regulated kinase 1/2 through a protein kinase C-dependent mechanism
-
van der Westhuizen ET, Werry TD, Sexton PM, and Summers RJ (2007) The relaxin family peptide receptor 3 activates extracellular signal-regulated kinase 1/2 through a protein kinase C-dependent mechanism. Mol Pharmacol 71:1618-1629.
-
(2007)
Mol Pharmacol
, vol.71
, pp. 1618-1629
-
-
Van Der Westhuizen, E.T.1
Werry, T.D.2
Sexton, P.M.3
Summers, R.J.4
-
33
-
-
0032745423
-
RWJ 67657, a potent, orally active inhibitor of p38 mitogen-activated protein kinase
-
Wadsworth SA, Cavender DE, Beers SA, Lalan P, Schafer PH, Malloy EA, Wu W, Fahmy B, Olini GC, Davis JE, et al. (1999) RWJ 67657, a potent, orally active inhibitor of p38 mitogen-activated protein kinase. J Pharmacol Exp Ther 291:680-687. (Pubitemid 29503541)
-
(1999)
Journal of Pharmacology and Experimental Therapeutics
, vol.291
, Issue.2
, pp. 680-687
-
-
Wadsworth, S.A.1
Cavender, D.E.2
Beers, S.A.3
Lalan, P.4
Schafer, P.H.5
Malloy, E.A.6
Wu, W.7
Fahmy, B.8
Olini, G.C.9
Davis, J.E.10
Pellegrino-Gensey, J.L.11
Wachter, M.P.12
Siekierka, J.J.13
-
34
-
-
0029808748
-
Transcription factor AP-1 regulation by mitogen-activated protein kinase signal transduction pathways
-
Whitmarsh AJ and Davis RJ (1996) Transcription factor AP-1 regulation by mitogen-activated protein kinase signal transduction pathways. J Mol Med 74:589-607.
-
(1996)
J Mol Med
, vol.74
, pp. 589-607
-
-
Whitmarsh, A.J.1
Davis, R.J.2
-
35
-
-
0034641936
-
Apoptosis in the nervous system
-
Yuan J and Yankner BA (2000) Apoptosis in the nervous system. Nature 407:802-809.
-
(2000)
Nature
, vol.407
, pp. 802-809
-
-
Yuan, J.1
Yankner, B.A.2
|