-
1
-
-
0028883178
-
Phospholipid signaling
-
Divecha, N. and Irvine, R. F. (1995) Phospholipid signaling. Cell 80, 269-278.
-
(1995)
Cell
, vol.80
, pp. 269-278
-
-
Divecha, N.1
Irvine, R.F.2
-
2
-
-
0029060391
-
Protein kinase C and lipid signaling for sustained cellular responses
-
Nishizuka, Y. (1995) Protein kinase C and lipid signaling for sustained cellular responses. FASEB. J. 9, 484-496.
-
(1995)
FASEB. J.
, vol.9
, pp. 484-496
-
-
Nishizuka, Y.1
-
4
-
-
0025942516
-
The bisindolylmaleimide GF 109203X is potent and selective inhibitor of protein kinase C
-
Toullec, D., Pianetti, P., Coste, H., Bellevergue, P., Grand-Perret, T., Ajakane, M., Baudet, V., Boissin, P., Boursier, E., Loriolle, F., Duhamel, L., Charon, D. and Kirilovsky, J. (1991) The bisindolylmaleimide GF 109203X is potent and selective inhibitor of protein kinase C. J. Biol. Chem. 266, 15771-15781.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 15771-15781
-
-
Toullec, D.1
Pianetti, P.2
Coste, H.3
Bellevergue, P.4
Grand-Perret, T.5
Ajakane, M.6
Baudet, V.7
Boissin, P.8
Boursier, E.9
Loriolle, F.10
Duhamel, L.11
Charon, D.12
Kirilovsky, J.13
-
5
-
-
64149103614
-
Protein kinase C intervention: the state of play
-
Roffey, J., Rosse, C., Linch, M., Hilbbert, A., McDonald, N. Q. and Parker, P. J. (2009) Protein kinase C intervention: the state of play. Curr. Opin. Cell Biol. 21, 268-279.
-
(2009)
Curr. Opin. Cell Biol.
, vol.21
, pp. 268-279
-
-
Roffey, J.1
Rosse, C.2
Linch, M.3
Hilbbert, A.4
McDonald, N.Q.5
Parker, P.J.6
-
6
-
-
37049100024
-
X-Ray crystal structure of staurosporine: a new alkaloid from a Streptomyces strain
-
Furusaki, A., Hashiba, N., Matsumoto, T., Hirano, A., Iwai, Y. and Omura, S. (1978) X-Ray crystal structure of staurosporine: a new alkaloid from a Streptomyces strain. J. Chem. Soc. Chem. Commun. 18, 800-801.
-
(1978)
J. Chem. Soc. Chem. Commun.
, vol.18
, pp. 800-801
-
-
Furusaki, A.1
Hashiba, N.2
Matsumoto, T.3
Hirano, A.4
Iwai, Y.5
Omura, S.6
-
7
-
-
0028866845
-
Different susceptibility of protein kinases to staurosporine inhibition Kinetic studies and molecular bases for the resistance of protein kinase CK2
-
Meggio, F., Donella Deana, A., Ruzzene, M., Brunati, A. M., Cesaro, L., Guerra, B., Meyer, T., Mett, H., Fabbro, D., Furet, P., Dobrowolska, G. and Pinna, L. A. (1995) Different susceptibility of protein kinases to staurosporine inhibition. Kinetic studies and molecular bases for the resistance of protein kinase CK2. Eur. J. Biochem. 234, 317-322.
-
(1995)
Eur. J. Biochem.
, vol.234
, pp. 317-322
-
-
Meggio, F.1
Donella Deana, A.2
Ruzzene, M.3
Brunati, A.M.4
Cesaro, L.5
Guerra, B.6
Meyer, T.7
Mett, H.8
Fabbro, D.9
Furet, P.10
Dobrowolska, G.11
Pinna, L.A.12
-
8
-
-
8944246315
-
(S)-13-[(dimethylamino) methyl]-10,11,14,15-tetrahydro-4,9:16,21-dimetheno-1H,13H-dibenzo [e,k] pyrrol [3,4-h] [1,4,13] oxadiazacyclohexadecene-1 3 (2H)-dione (LY333531) and related analogues: isozyme selective inhibitors of protein kinase C beta
-
Jirousek, M. R., Giling, J. R., Gonzalez, C. M., Heath, W. F., McDonald, J. H. 3rd, Neel, D. A., Rito, C. J., Singh, U., Stramm, L. E., Melikian-Badalian, A., Baevsky, M., Ballas, L. M., Hall, S. E., Winneroski, L. L. and Faul, M. M. (1996) (S)-13-[(dimethylamino) methyl]-10,11,14,15-tetrahydro-4,9:16,21-dimetheno-1H,13H-dibenzo [e,k] pyrrol [3,4-h] [1,4,13] oxadiazacyclohexadecene-1,3 (2H)-dione (LY333531) and related analogues: isozyme selective inhibitors of protein kinase C beta. J. Med. Chem. 39, 2664-2671.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2664-2671
-
-
Jirousek, M.R.1
Giling, J.R.2
Gonzalez, C.M.3
Heath, W.F.4
McDonald 3rd, J.H.5
Neel, D.A.6
Rito, C.J.7
Singh, U.8
Stramm, L.E.9
Melikian-Badalian, A.10
Baevsky, M.11
Ballas, L.M.12
Hall, S.E.13
Winneroski, L.L.14
Faul, M.M.15
-
9
-
-
33745204140
-
Development and validation of a drug activity biomarker that shows target inhibition in cancer patients receiving enzastaurin, a novel protein kinase C-beta inhibitor
-
Green, L. J., Marder, P., Ray, C., Cook, C. A., Jaken, S., Musib, L. C., Herbst, R. S., Carducci, M., Britten, C. D., Basche, M., Eckhardt, S. G. and Thornton, D. (2006) Development and validation of a drug activity biomarker that shows target inhibition in cancer patients receiving enzastaurin, a novel protein kinase C-beta inhibitor. Clin. Cancer Res. 12, 3408-3415.
-
(2006)
Clin. Cancer Res.
, vol.12
, pp. 3408-3415
-
-
Green, L.J.1
Marder, P.2
Ray, C.3
Cook, C.A.4
Jaken, S.5
Musib, L.C.6
Herbst, R.S.7
Carducci, M.8
Britten, C.D.9
Basche, M.10
Eckhardt, S.G.11
Thornton, D.12
-
10
-
-
0024438833
-
Calphostins (UCN-1028), novel and specific inhibitors of protein kinase C. I. Fermentation, isolation, physic-chemical properties and biological activities
-
Kobayashi, E., Ando, K., Nakano, H., Iida, T., Ohno, H., Morimoto, M. and Tamaoki, T. (1989) Calphostins (UCN-1028), novel and specific inhibitors of protein kinase C. I. Fermentation, isolation, physic-chemical properties and biological activities. J. Antibiot (Tokyo). 42, 1470-1474.
-
(1989)
J. Antibiot (Tokyo).
, vol.42
, pp. 1470-1474
-
-
Kobayashi, E.1
Ando, K.2
Nakano, H.3
Iida, T.4
Ohno, H.5
Morimoto, M.6
Tamaoki, T.7
-
11
-
-
0028914673
-
Characterization of the cysteine-rich region of the Caenorhabditis elegans protein Unc-13 as a high affinity phorbol ester receptor. Analysis of ligandbinding interactions, lipid cofactor requirements, and inhibitor sensitivity
-
Kazanietz, M. G., Lewin, N. E., Bruns, J. D. and Blumberg, P. M. (1995) Characterization of the cysteine-rich region of the Caenorhabditis elegans protein Unc-13 as a high affinity phorbol ester receptor. Analysis of ligandbinding interactions, lipid cofactor requirements, and inhibitor sensitivity. J. Biol. Chem. 270, 10777-10783.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 10777-10783
-
-
Kazanietz, M.G.1
Lewin, N.E.2
Bruns, J.D.3
Blumberg, P.M.4
-
12
-
-
0025784927
-
Inhibition of protein kinase C by calphostin C is light-dependent
-
Bruns, R. F., Miller, F. D., Merriman, R. L., Howbert, J. J., Heath, W. F., Kobayashi, E., Takahashi, I., Tamaoki, T. and Nakano, H. (1991) Inhibition of protein kinase C by calphostin C is light-dependent. Biochem. Biophys. Res. Commun. 176, 288-293.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.176
, pp. 288-293
-
-
Bruns, R.F.1
Miller, F.D.2
Merriman, R.L.3
Howbert, J.J.4
Heath, W.F.5
Kobayashi, E.6
Takahashi, I.7
Tamaoki, T.8
Nakano, H.9
-
13
-
-
58149175775
-
Rationally designed peptide regulators of protein kinase C
-
Churchill, E. N., Qvit, N. and Mochly-Rosen, D. (2009) Rationally designed peptide regulators of protein kinase C. Trends Endocrinol. Metab. 20, 25-33.
-
(2009)
Trends Endocrinol. Metab.
, vol.20
, pp. 25-33
-
-
Churchill, E.N.1
Qvit, N.2
Mochly-Rosen, D.3
-
14
-
-
0025258567
-
chelerythrine is a potent and specific inhibitor of protein kinase C
-
Herbert, J. M., Augereau, J. M., Gleye, J. and Maffrand, J. P. (1990) chelerythrine is a potent and specific inhibitor of protein kinase C. Biochem. Biophys. Res. Commun. 172, 993-999.
-
(1990)
Biochem. Biophys. Res. Commun.
, vol.172
, pp. 993-999
-
-
Herbert, J.M.1
Augereau, J.M.2
Gleye, J.3
Maffrand, J.P.4
-
15
-
-
0031564602
-
Chelerythrine, a protein kinase C inhibitor, interacts with cyclic nucleotide phosphodiesterases
-
Eckly-Michel, A. E., Le Bec, A. and Lugnier, C. (1997) Chelerythrine, a protein kinase C inhibitor, interacts with cyclic nucleotide phosphodiesterases. Eur. J. Pharmacol. 324, 85-88.
-
(1997)
Eur. J. Pharmacol.
, vol.324
, pp. 85-88
-
-
Eckly-Michel, A.E.1
Le Bec, A.2
Lugnier, C.3
-
16
-
-
0027686284
-
BQ123, and ETA receptor antagonist, inhibits endothelin-1-mediated proliferation of human artery smooth muscle cells
-
Zamora, M. A., Dempsey, E. C., Walchak, S. J. and Stelzner, T. J. (1993) BQ123, and ETA receptor antagonist, inhibits endothelin-1-mediated proliferation of human artery smooth muscle cells. Am. J. Respir. Cell Mol. Biol. 9, 429-433.
-
(1993)
Am. J. Respir. Cell Mol. Biol.
, vol.9
, pp. 429-433
-
-
Zamora, M.A.1
Dempsey, E.C.2
Walchak, S.J.3
Stelzner, T.J.4
-
17
-
-
0030987070
-
Regulation of protein kinase C
-
Newton, A. C. (1997) Regulation of protein kinase C. Curr. Opin. Cell Biol. 9, 161-167.
-
(1997)
Curr. Opin. Cell Biol.
, vol.9
, pp. 161-167
-
-
Newton, A.C.1
-
19
-
-
0033621019
-
Requirement for protein kinase C in reactive oxygen species-induced apoptosis of vascular smooth muscle cells
-
Li, P. F., Maasch, C., Haller, H., Dietz, R. and von Harsdorf, R. (1999) Requirement for protein kinase C in reactive oxygen species-induced apoptosis of vascular smooth muscle cells. Circulation 100, 967-973.
-
(1999)
Circulation
, vol.100
, pp. 967-973
-
-
Li, P.F.1
Maasch, C.2
Haller, H.3
Dietz, R.4
von Harsdorf, R.5
-
20
-
-
0025219317
-
Endothelin augments unitary calcium channel currents on the smooth muscle cell membrane of guinea-pig portal vein
-
Inoue, Y., Oike, M., Nakao, K., Kitamura, K. and Kuriyama, H. (1990) Endothelin augments unitary calcium channel currents on the smooth muscle cell membrane of guinea-pig portal vein. J. Physiol. 423, 171-191.
-
(1990)
J. Physiol.
, vol.423
, pp. 171-191
-
-
Inoue, Y.1
Oike, M.2
Nakao, K.3
Kitamura, K.4
Kuriyama, H.5
-
21
-
-
0027422769
-
Endothelin and vasopressin activate low conductance chloride channels in aortic smooth muscle cells
-
Van Renterghem, C. and Lazdunski, M. (1993) Endothelin and vasopressin activate low conductance chloride channels in aortic smooth muscle cells. Pflugers. Arch. 425, 156-163.
-
(1993)
Pflugers. Arch.
, vol.425
, pp. 156-163
-
-
Van Renterghem, C.1
Lazdunski, M.2
-
22
-
-
0029878089
-
2+ influx
-
2+ influx. J. Mol. Cell Cardiol. 28, 707-722.
-
(1996)
J. Mol. Cell Cardiol.
, vol.28
, pp. 707-722
-
-
Nakajima, T.1
Hazama, H.2
Hamada, E.3
Wu, S.N.4
Igarashi, K.5
Yamashita, T.6
Seyama, Y.7
Omata, M.8
Kurachi, Y.9
-
23
-
-
12844250012
-
Endothelin-1 acts via protein kinase C to block KATP channels in rabbit coronary and pulmonary arterial smooth muscle cells
-
Park, W. S., Ko, E. A., Han, J., Kim, N. and Earm, Y. E. (2005) Endothelin-1 acts via protein kinase C to block KATP channels in rabbit coronary and pulmonary arterial smooth muscle cells. J. Cardiovasc. Pharmacol. 45, 99-108.
-
(2005)
J. Cardiovasc. Pharmacol.
, vol.45
, pp. 99-108
-
-
Park, W.S.1
Ko, E.A.2
Han, J.3
Kim, N.4
Earm, Y.E.5
-
24
-
-
27144496593
-
+ channels in rabbit coronary arterial smooth muscle cells through protein kinase C
-
+ channels in rabbit coronary arterial smooth muscle cells through protein kinase C. J. Cardiovasc. Pharmacol. 46, 681-689.
-
(2005)
J. Cardiovasc. Pharmacol.
, vol.46
, pp. 681-689
-
-
Park, W.S.1
Han, J.2
Kim, N.3
Youm, J.B.4
Joo, H.5
Kim, H.K.6
Ko, J.H.7
Earm, Y.E.8
-
25
-
-
14744273136
-
+ current through a PKC-independent mechanism in isolated coronary arterial smooth muscle cells
-
+ current through a PKC-independent mechanism in isolated coronary arterial smooth muscle cells. J. Cardiovasc. Pharmacol. 45, 260-269.
-
(2005)
J. Cardiovasc. Pharmacol.
, vol.45
, pp. 260-269
-
-
Park, W.S.1
Son, Y.K.2
Han, J.3
Kim, N.4
Ko, J.H.5
Bae, Y.M.6
Earm, Y.E.7
-
26
-
-
0019419445
-
Blockage of squid axon potassium conductance by internal tetra-N-alkylammonium ions of various sizes
-
French, R. J. and Shoukimas, J. J. (1981) Blockage of squid axon potassium conductance by internal tetra-N-alkylammonium ions of various sizes. Biophys. J. 34, 271-291.
-
(1981)
Biophys. J.
, vol.34
, pp. 271-291
-
-
French, R.J.1
Shoukimas, J.J.2
-
27
-
-
0025224223
-
Biophysical and molecular mechanisms of Shaker potas sium channel inactivation
-
Hoshi, T., Zagotta, W. N. and Aldrich, R. W. (1990) Biophysical and molecular mechanisms of Shaker potas sium channel inactivation. Science 250, 533-538.
-
(1990)
Science
, vol.250
, pp. 533-538
-
-
Hoshi, T.1
Zagotta, W.N.2
Aldrich, R.W.3
-
28
-
-
0026560616
-
The aromatic binding site for tetraethylammonium ion on potassium channels
-
Heginbotham, L. and MacKinnon, R. (1992) The aromatic binding site for tetraethylammonium ion on potassium channels. Neuron 8, 483-491.
-
(1992)
Neuron
, vol.8
, pp. 483-491
-
-
Heginbotham, L.1
MacKinnon, R.2
-
29
-
-
0029130666
-
Determinants of antiarrhythmic drug action Electrostatic and hydrophobic components of block of the human cardiac hKv1.5 channel
-
Snyders, D. J. and Yeola, S. W. (1995) Determinants of antiarrhythmic drug action. Electrostatic and hydrophobic components of block of the human cardiac hKv1.5 channel. Circ. Res. 77, 575-583.
-
(1995)
Circ. Res.
, vol.77
, pp. 575-583
-
-
Snyders, D.J.1
Yeola, S.W.2
-
31
-
-
0026329937
-
Is staurosporine a specific inhibitor of protein kinase C in intact porcine coronary arteries?
-
Kageyama, M., Mori, T., Yanagisawa, T. and Taira, N. (1991) Is staurosporine a specific inhibitor of protein kinase C in intact porcine coronary arteries? J. Pharmacol. Exp. Ther. 259, 1019-1026.
-
(1991)
J. Pharmacol. Exp. Ther.
, vol.259
, pp. 1019-1026
-
-
Kageyama, M.1
Mori, T.2
Yanagisawa, T.3
Taira, N.4
-
33
-
-
33644897306
-
Slowing of the inactivation of voltage-dependent sodium channels by staurosporine, the protein kinase C inhibitor, in rabbit atrial myocytes
-
Ko, J. H., Park, W. S., Kim, S. J. and Earm, Y. E. (2006) Slowing of the inactivation of voltage-dependent sodium channels by staurosporine, the protein kinase C inhibitor, in rabbit atrial myocytes. Eur. J. Pharmacol. 534, 48-54.
-
(2006)
Eur. J. Pharmacol.
, vol.534
, pp. 48-54
-
-
Ko, J.H.1
Park, W.S.2
Kim, S.J.3
Earm, Y.E.4
-
34
-
-
0029681986
-
Neuronal ion channels as the target sites of insecticides
-
Narahashi, T. (1996) Neuronal ion channels as the target sites of insecticides. Pharmacol. Toxico. 79, 1-14.
-
(1996)
Pharmacol. Toxico.
, vol.79
, pp. 1-14
-
-
Narahashi, T.1
-
35
-
-
0033694833
-
From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels
-
Catterall, W. A. (2000) From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels. Neuron 26, 13-25.
-
(2000)
Neuron
, vol.26
, pp. 13-25
-
-
Catterall, W.A.1
-
36
-
-
0035050571
-
Resurgence of sodium channel research
-
Goldin, A. L. (2001) Resurgence of sodium channel research. Annu. Rev. Physiol. 63, 871-894.
-
(2001)
Annu. Rev. Physiol.
, vol.63
, pp. 871-894
-
-
Goldin, A.L.1
-
38
-
-
0032951891
-
Staurosporine directly blocks Kv1 3 channels expressed in chinese hamster ovary cells
-
Choi, J. S., Hahn, S. J., Rhie, D. J., Jo, Y. H. and Kim, M. S. (1999) Staurosporine directly blocks Kv1.3 channels expressed in chinese hamster ovary cells. Naunyn Schmiedebergs Arch. Pharmacol. 359, 256-261.
-
(1999)
Naunyn Schmiedebergs Arch. Pharmacol.
, vol.359
, pp. 256-261
-
-
Choi, J.S.1
Hahn, S.J.2
Rhie, D.J.3
Jo, Y.H.4
Kim, M.S.5
-
39
-
-
0029790924
-
Class III antiarrhythmic effects of zatebradine. Time-, state-, use-, and voltage-dependent block of hKv1.5 channels
-
Valenzuela, C., Delpon, E., Franqueza, L., Gray, P., Perez, O., Tamargo, J. and Snyders, D. J. (1996) Class III antiarrhythmic effects of zatebradine. Time-, state-, use-, and voltage-dependent block of hKv1.5 channels. Circulation 94, 562-570.
-
(1996)
Circulation
, vol.94
, pp. 562-570
-
-
Valenzuela, C.1
Delpon, E.2
Franqueza, L.3
Gray, P.4
Perez, O.5
Tamargo, J.6
Snyders, D.J.7
-
40
-
-
19344378611
-
+ channels in coronary arterial smooth muscle cells
-
+ channels in coronary arterial smooth muscle cells. Life Sci. 77, 512-527.
-
(2005)
Life Sci
, vol.77
, pp. 512-527
-
-
Park, W.S.1
Son, Y.K.2
Ko, E.A.3
Ko, J.H.4
Lee, H.A.5
Park, K.S.6
Earm, Y.E.7
-
41
-
-
0347948524
-
+ currents of rat mesenteric arterial smooth muscle
-
+ currents of rat mesenteric arterial smooth muscle. Eur. J. Pharmacol. 483, 117-126.
-
(2004)
Eur. J. Pharmacol.
, vol.483
, pp. 117-126
-
-
Kim, A.1
Bae, Y.M.2
Kim, J.3
Kim, B.4
Ho, W.K.5
Earm, Y.E.6
Cho, S.I.7
-
42
-
-
0037432607
-
Chelerythrine and bisindolylmaleimide I prolong cardiac action potentials by protein kinase C-independent mechanism
-
Voutilainen-Mylylä, S., Tavi, P. and Weckström, M. (2003) Chelerythrine and bisindolylmaleimide I prolong cardiac action potentials by protein kinase C-independent mechanism. Eur. J. Pharmacol. 466, 41-51.
-
(2003)
Eur. J. Pharmacol.
, vol.466
, pp. 41-51
-
-
Voutilainen-Mylylä, S.1
Tavi, P.2
Weckström, M.3
-
43
-
-
0035958638
-
+ current by chelerythrine and bisindolylmaleimide I in atrial myocytes from mice
-
+ current by chelerythrine and bisindolylmaleimide I in atrial myocytes from mice. Eur. J. Pharmacol. 424, 173-178.
-
(2001)
Eur. J. Pharmacol.
, vol.424
, pp. 173-178
-
-
Cho, H.1
Youm, J.B.2
Earm, Y.E.3
Ho, W.K.4
-
44
-
-
77954921590
-
+ channels in rabbit ventricular myocytes
-
+ channels in rabbit ventricular myocytes. Korean J. Physiol. Pharmacol. 14, 119-125.
-
(2010)
Korean J. Physiol. Pharmacol.
, vol.14
, pp. 119-125
-
-
Park, W.S.1
Son, Y.K.2
Ko, E.A.3
Choi, S.W.4
Kim, N.R.5
Choi, T.H.6
Youn, H.J.7
Jo, S.H.8
Hong, D.H.9
Han, J.10
-
45
-
-
8644254252
-
Direct block of hERG potassium channels by the protein kinase C inhibitor bisindolylmaleimide I (GF109203X)
-
Thomas, D., Hammerling, B. C., Wimmer, A. B., Wu, K., Ficker, E., Kuryshev, Y. A., Scherer, D., Kiehn, J., Katus, H. A., Schoels, W. and Karle, C. A. (2004) Direct block of hERG potassium channels by the protein kinase C inhibitor bisindolylmaleimide I (GF109203X). Cardiovasc. Res. 64, 467-476.
-
(2004)
Cardiovasc. Res.
, vol.64
, pp. 467-476
-
-
Thomas, D.1
Hammerling, B.C.2
Wimmer, A.B.3
Wu, K.4
Ficker, E.5
Kuryshev, Y.A.6
Scherer, D.7
Kiehn, J.8
Katus, H.A.9
Schoels, W.10
Karle, C.A.11
-
46
-
-
3042528658
-
Mechanisms of arsenic-induced prolongation of cardiac repolarization
-
Ficker, E., Kuryshev, Y. A., Dennis, A. T., Obejero-Paz, C., Wang, L., Hawryluk, P., Wible, B. A. and Brown, A. M. (2004) Mechanisms of arsenic-induced prolongation of cardiac repolarization. Mol. Pharmacol. 66, 33-44.
-
(2004)
Mol. Pharmacol.
, vol.66
, pp. 33-44
-
-
Ficker, E.1
Kuryshev, Y.A.2
Dennis, A.T.3
Obejero-Paz, C.4
Wang, L.5
Hawryluk, P.6
Wible, B.A.7
Brown, A.M.8
-
47
-
-
0343527303
-
Direct block by bisindolylmaleimide of rat Kv1 5 expressed in chinese hamster ovary cells
-
Choi, B. H., Choi, J. S., Jeong, S. W., Hahn, S. J., Yoon, S. H., Jo, Y. H. and Kim, M. S. (2000) Direct block by bisindolylmaleimide of rat Kv1.5 expressed in chinese hamster ovary cells. J. Pharmacol. Exp. Ther. 293, 634-640.
-
(2000)
J. Pharmacol. Exp. Ther.
, vol.293
, pp. 634-640
-
-
Choi, B.H.1
Choi, J.S.2
Jeong, S.W.3
Hahn, S.J.4
Yoon, S.H.5
Jo, Y.H.6
Kim, M.S.7
-
48
-
-
0034640214
-
Inhibition of voltage-dependent sodium channels by Ro 31-8220, a 'specific' protein kinase C inhibitor
-
Lingameneni, R., Vysotskaya, T. N., Duch, D. S. and Hemmings, H. C. Jr. (2000) Inhibition of voltage-dependent sodium channels by Ro 31-8220, a 'specific' protein kinase C inhibitor. FEBS Lett. 473, 265-268.
-
(2000)
FEBS Lett
, vol.473
, pp. 265-268
-
-
Lingameneni, R.1
Vysotskaya, T.N.2
Duch, D.S.3
Hemmings Jr., H.C.4
-
49
-
-
0033179362
-
Inhibitory effect of the kinase inhibitor chelerythrine on acetylcholine-induced current in PC12 cells
-
Shi, L. and Wang, C. (1999) Inhibitory effect of the kinase inhibitor chelerythrine on acetylcholine-induced current in PC12 cells. Arch. Biochem. Biophys. 368, 40-44.
-
(1999)
Arch. Biochem. Biophys.
, vol.368
, pp. 40-44
-
-
Shi, L.1
Wang, C.2
-
50
-
-
0026576854
-
Selective inhibition of protein kinase C Effect on platelet-activating-factor-induced platelet functional responses
-
Murphy, C. T. and Westwick, J. (1992) Selective inhibition of protein kinase C. Effect on platelet-activating-factor-induced platelet functional responses. Biochem. J. 283, 159-164.
-
(1992)
Biochem. J.
, vol.283
, pp. 159-164
-
-
Murphy, C.T.1
Westwick, J.2
-
51
-
-
0030829055
-
Isoform specificity of activators and inhibitors of protein kinase C gamma and delta
-
Keenan, C., Goode, N. and Pears, C. (1997) Isoform specificity of activators and inhibitors of protein kinase C gamma and delta. FEBS Lett. 415, 101-108.
-
(1997)
FEBS Lett.
, vol.415
, pp. 101-108
-
-
Keenan, C.1
Goode, N.2
Pears, C.3
-
52
-
-
24744455900
-
Activation of the BK (SLO1) potassium channel by mallotoxin
-
Zakharov, S. I., Morrow, J. P., Liu, G., Yang, L. and Marx, S. O. (2005) Activation of the BK (SLO1) potassium channel by mallotoxin. J. Biol. Chem. 280, 30882-30887.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 30882-30887
-
-
Zakharov, S.I.1
Morrow, J.P.2
Liu, G.3
Yang, L.4
Marx, S.O.5
-
53
-
-
33846610522
-
+ channels by rottlerin, an inhibitor of protein kinase C-delta, in pituitary tumor (GH3) cells and in cortical neuronal (HCN-1A) cells
-
+ channels by rottlerin, an inhibitor of protein kinase C-delta, in pituitary tumor (GH3) cells and in cortical neuronal (HCN-1A) cells. J. Cell Physiol. 210, 656-666.
-
(2007)
J. Cell Physiol.
, vol.210
, pp. 656-666
-
-
Wu, S.N.1
Wang, Y.J.2
Lin, M.W.3
-
54
-
-
0027161159
-
mSlo, a complex mouse gene encoding "maxi" calcium-activated potassium channels
-
Butler, A., Tsunoda, S., McCobb, D. P., Wei, A. and Salkoff, L. (1993) mSlo, a complex mouse gene encoding "maxi" calcium-activated potassium channels. Science 261, 221-224.
-
(1993)
Science
, vol.261
, pp. 221-224
-
-
Butler, A.1
Tsunoda, S.2
McCobb, D.P.3
Wei, A.4
Salkoff, L.5
-
55
-
-
32644488717
-
Large-conductance, calcium-activated potassium channels: Structural and functional implications
-
Ghatta, S., Nimmagadda, D., Xu, X. P. and O'Rourke, S. T. (2006) Large-conductance, calcium-activated potassium channels: Structural and functional implications. Pharmacol. Ther. 110, 103-116.
-
(2006)
Pharmacol. Ther.
, vol.110
, pp. 103-116
-
-
Ghatta, S.1
Nimmagadda, D.2
Xu, X.P.3
O'Rourke, S.T.4
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