-
1
-
-
0029550651
-
Inhibition of PDGF-induced phosphoinositide-turnover by glucopiericidin A
-
Ahn, S. C., Kim, B. Y., Park, C. S., Lee, H. S., Suh, P. G., Ryu, S. H., Rho, H. M., Rhee, J. S., Mheen, T. I. and Ahn, J. S. (1995) Inhibition of PDGF-induced phosphoinositide-turnover by glucopiericidin A. Biochem. Mol. Biol. Int. 57: 125-132.
-
(1995)
Biochem. Mol. Biol. Int.
, vol.57
, pp. 125-132
-
-
Ahn, S.C.1
Kim, B.Y.2
Park, C.S.3
Lee, H.S.4
Suh, P.G.5
Ryu, S.H.6
Rho, H.M.7
Rhee, J.S.8
Mheen, T.I.9
Ahn, J.S.10
-
2
-
-
0028898383
-
Sequence requirements for binding of src family tyrosine kinases to activated growth factor receptors
-
Alonso, G., Koegl, M., Mazurenko, N. and Courtneidge, S. A. (1995) Sequence requirements for binding of src family tyrosine kinases to activated growth factor receptors. J. Biol. Chem. 270: 9840-9848.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 9840-9848
-
-
Alonso, G.1
Koegl, M.2
Mazurenko, N.3
Courtneidge, S.A.4
-
3
-
-
0029094297
-
Effects of trapidil and suramin on growth factor-induced calcium response and tyrosine phosphorylation in human glioma cells
-
Bando, K., Kannuki, S., Rokutan, K., Shouno, M. and Matsumoto, K. (1995) Effects of trapidil and suramin on growth factor induced calcium response and tyrosine phosphorylation in human glioma cells. Neurol. Med. Chir. (Tokyo) 35: 631-638.
-
(1995)
Neurol. Med. Chir. (Tokyo)
, vol.35
, pp. 631-638
-
-
Bando, K.1
Kannuki, S.2
Rokutan, K.3
Shouno, M.4
Matsumoto, K.5
-
4
-
-
0030431044
-
Inhibitors of the platelet-derived growth factor receptor tyrosine kinase
-
Bilder, G. E. and Rojas, C. (1996) Inhibitors of the platelet-derived growth factor receptor tyrosine kinase. J. Cardiovasc. Drug Rev. 14: 380-399.
-
(1996)
J. Cardiovasc. Drug Rev.
, vol.14
, pp. 380-399
-
-
Bilder, G.E.1
Rojas, C.2
-
5
-
-
85069025661
-
-
World Patent Application WO 9634867, November 7
-
Blankley, C. J., Boschelli, D. H., Doherty, A. M., Hamby, J. M., Klutchko, S. and Panek, R. L. (1996a) Pyrido[2,3-d]pyrimidines as protein tyrosine kinase-mediated cell proliferation inhibitors. World Patent Application WO 9634867, November 7.
-
(1996)
Pyrido[2,3-d]pyrimidines as Protein Tyrosine Kinase-Mediated Cell Proliferation Inhibitors
-
-
Blankley, C.J.1
Boschelli, D.H.2
Doherty, A.M.3
Hamby, J.M.4
Klutchko, S.5
Panek, R.L.6
-
6
-
-
14444287643
-
-
World Patent Application WO 9615128, May 23
-
Blankley, C. J., Doherty, A. M., Hamby, J. M., Panek, R. L., Schroeder, M. C., Showalter, H. D. H. and Connolly, C. (1996b) 6-Aryl pyrido[2,3-d]pyrimidines and naphthyridines for inhibiting protein tyrosine kinase-mediated cellular proliferation. World Patent Application WO 9615128, May 23.
-
(1996)
6-Aryl Pyrido[2,3-d]pyrimidines and Naphthyridines for Inhibiting Protein Tyrosine Kinase-mediated Cellular Proliferation
-
-
Blankley, C.J.1
Doherty, A.M.2
Hamby, J.M.3
Panek, R.L.4
Schroeder, M.C.5
Showalter, H.D.H.6
Connolly, C.7
-
7
-
-
0010545020
-
Signal transduction by the src family of tyrosine protein kinases
-
Bertino, J. (ed.) Academic Press, San Diego
-
Bolen, J. B., Penhallow, R. C. and Burkhardt, A. L. (1997) Signal transduction by the src family of tyrosine protein kinases. In: Encyclopedia of Cancer, pp. 1657-1668, Bertino, J. (ed.) Academic Press, San Diego.
-
(1997)
Encyclopedia of Cancer
, pp. 1657-1668
-
-
Bolen, J.B.1
Penhallow, R.C.2
Burkhardt, A.L.3
-
8
-
-
0030201070
-
Intracellular signaling in arterial smooth muscle migration versus proliferation
-
Bornfeldt, K. E. (1996) Intracellular signaling in arterial smooth muscle migration versus proliferation. Trends Cardiovasc. Med. 6: 143-151.
-
(1996)
Trends Cardiovasc. Med.
, vol.6
, pp. 143-151
-
-
Bornfeldt, K.E.1
-
9
-
-
0028968622
-
Selective inhibition of the platelet-derived growth factor signal transduction pathway by a protein-tyrosine kinase inhibitor of the 2-phenylaminopyrimidine class
-
Buchdunger, E., Zimmermann, J., Mett, H. Meyer, T., Mueller, M., Regenass, U. and Lydon, N. B. (1995) Selective inhibition of the platelet-derived growth factor signal transduction pathway by a protein-tyrosine kinase inhibitor of the 2-phenylaminopyrimidine class. Proc. Natl. Acad. Sci. USA 92: 2553-2562.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 2553-2562
-
-
Buchdunger, E.1
Zimmermann, J.2
Mett, H.3
Meyer, T.4
Mueller, M.5
Regenass, U.6
Lydon, N.B.7
-
10
-
-
0030031766
-
Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative
-
Buchdunger, E., Zimmermann, J., Mett, H., Meyer, T., Mueller, M., Druker, B. J. and Lydon, N. B. (1996) Inhibition of the Abl protein-tyrosine kinase in vitro and in vivo by a 2-phenylaminopyrimidine derivative.Cancer Res. 56: 100-104.
-
(1996)
Cancer Res.
, vol.56
, pp. 100-104
-
-
Buchdunger, E.1
Zimmermann, J.2
Mett, H.3
Meyer, T.4
Mueller, M.5
Druker, B.J.6
Lydon, N.B.7
-
11
-
-
0028923306
-
Radicicol, a protein tyrosine kinase inhibitor, suppresses the expression of mitogen-inducible cyclooxygenase in macrophages stimulated with lipo-polysaccharide and in experimental glomerulonephritis
-
Chanmugam, P., Feng, L., Liou, S., Jang, B. C., Boudrean, M., Yi, G., Lee, J. H., Kwon, H. J., Beppu, T., Yoshida, M., Xia, Y., Wilson, C. B. and Hwang, D. (1995) Radicicol, a protein tyrosine kinase inhibitor, suppresses the expression of mitogen-inducible cyclooxygenase in macrophages stimulated with lipo-polysaccharide and in experimental glomerulonephritis. J. Biol. Chem. 270: 5413-5426.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 5413-5426
-
-
Chanmugam, P.1
Feng, L.2
Liou, S.3
Jang, B.C.4
Boudrean, M.5
Yi, G.6
Lee, J.H.7
Kwon, H.J.8
Beppu, T.9
Yoshida, M.10
Xia, Y.11
Wilson, C.B.12
Hwang, D.13
-
12
-
-
0029818354
-
Recombinant mitotoxin basic fibroblast growth factor-saporin reduces venons anastomotic intimal hyperplasia in the arterinvenous graft
-
Chen, C. Mattar, S. G., Hughes, J. D., Pierce, G. F., Cock, J. E., Ku, D. N., Hanson, S. R. and Lumsden, A. B. (1996) Recombinant mitotoxin basic fibroblast growth factor-saporin reduces venons anastomotic intimal hyperplasia in the arterinvenous graft. Circulation 94: 1989-1995.
-
(1996)
Circulation
, vol.94
, pp. 1989-1995
-
-
Chen, C.1
Mattar, S.G.2
Hughes, J.D.3
Pierce, G.F.4
Cock, J.E.5
Ku, D.N.6
Hanson, S.R.7
Lumsden, A.B.8
-
13
-
-
0028589148
-
Platelet-derived growth factor receptor signals
-
Claesson-Welsh, L. (1994) Platelet-derived growth factor receptor signals. J. Biol. Chem. 269: 32023-32026.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 32023-32026
-
-
Claesson-Welsh, L.1
-
14
-
-
0030921482
-
Inhibition of growth factor-mediated tyrosine phosphorylation in vascular smooth muscle by PD 089828, a new synthetic protein tyrosine kinase inhibitor
-
Dahring, T. K., Lu, G. H., Hamby, J. M., Batley, B. L., Krakerr, A. J. and Panek, R. L. (1997) Inhibition of growth factor-mediated tyrosine phosphorylation in vascular smooth muscle by PD 089828, a new synthetic protein tyrosine kinase inhibitor. J. Pharmacol. Exp. Ther. 281: 1446-1456.
-
(1997)
J. Pharmacol. Exp. Ther.
, vol.281
, pp. 1446-1456
-
-
Dahring, T.K.1
Lu, G.H.2
Hamby, J.M.3
Batley, B.L.4
Krakerr, A.J.5
Panek, R.L.6
-
16
-
-
0029043860
-
Selective inhibition of the tyrosine kinase pp60src by analogs of 5,10-dihydropyrimido[4,5-b]quinolin-4(1 H)-one
-
Dow, R. L., Bechle, B. M., Chou, T. T., Goddard, C. and Larson, E. R. (1995) Selective inhibition of the tyrosine kinase pp60src by analogs of 5,10-dihydropyrimido[4,5-b]quinolin-4(1 H)-one. Bioorg. Med. Chem. Lett. 5: 1007-1010.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 1007-1010
-
-
Dow, R.L.1
Bechle, B.M.2
Chou, T.T.3
Goddard, C.4
Larson, E.R.5
-
17
-
-
85069020998
-
-
US Patent 5593997, January 14
-
Dow, R. L., Koch, K. and Schulte, G. R. (1997) 4-Aminopyrazolo[3,4-d]pyrimidines and 4-ammopyrazolo[3,4-d]pyridines as tyrosine kinase inhibitors, US Patent 5593997, January 14.
-
(1997)
4-Aminopyrazolo[3,4-d]pyrimidines and 4-ammopyrazolo[3,4-d]pyridines as Tyrosine Kinase Inhibitors
-
-
Dow, R.L.1
Koch, K.2
Schulte, G.R.3
-
18
-
-
0028884325
-
Exploration of the sequence specificity of pp60c-src tyrosine kinase. Minimal peptide sequence required for maximal activity
-
Edison, A. M., Barker, S. C., Kassel, D. B., Luther, M. A. and Knight, W. B. (1995) Exploration of the sequence specificity of pp60c-src tyrosine kinase. Minimal peptide sequence required for maximal activity. J. Biol. Chem. 270: 27112-27115.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27112-27115
-
-
Edison, A.M.1
Barker, S.C.2
Kassel, D.B.3
Luther, M.A.4
Knight, W.B.5
-
19
-
-
0029166660
-
Damnacanthal is a highly potent, selective inhibitor of p56lck tyrosine kinase activity
-
Faltynek, C. R., Schroeder, J., Mauvais, P., Miller, D., Wing, S., Murphy, D, Lehr, R., Kelley, M., Maycock, A., Michne, W., Miski, M. and Thunberg, A. L. (1995a) Damnacanthal is a highly potent, selective inhibitor of p56lck tyrosine kinase activity. Biochemistry 34: 12404-12410.
-
(1995)
Biochemistry
, vol.34
, pp. 12404-12410
-
-
Faltynek, C.R.1
Schroeder, J.2
Mauvais, P.3
Miller, D.4
Wing, S.5
Murphy, D.6
Lehr, R.7
Kelley, M.8
Maycock, A.9
Michne, W.10
Miski, M.11
Thunberg, A.L.12
-
20
-
-
0029007854
-
Inhibition of T lymphocyte activation by a novel p56lck tyrosine kinase inhihitor
-
Faltynek, C. R., Wang, S., Miller, D., Mauvais, P., Gauvin, B., Reid, J., Xie, W., Hoekstra, S., Juniewicz, P., Sarup, J., Lehr, R., Sawutz, D. G. and Murphy, D. (1995b) Inhibition of T lymphocyte activation by a novel p56lck tyrosine kinase inhihitor. J. Enzyme Inhib. 9: 111-122.
-
(1995)
J. Enzyme Inhib.
, vol.9
, pp. 111-122
-
-
Faltynek, C.R.1
Wang, S.2
Miller, D.3
Mauvais, P.4
Gauvin, B.5
Reid, J.6
Xie, W.7
Hoekstra, S.8
Juniewicz, P.9
Sarup, J.10
Lehr, R.11
Sawutz, D.G.12
Murphy, D.13
-
21
-
-
0028821818
-
Protein tyrosine kinase and protein kinase C inhibition by fungal anthraquinones related to emodin
-
Fredenhagen, A., Mett, H., Meyer, T., Buchdunger, E., Regenass, U., Roggo, R. E. and Petersen, F. (1995) Protein tyrosine kinase and protein kinase C inhibition by fungal anthraquinones related to emodin. J. Antibiot. 48: 1355-1358.
-
(1995)
J. Antibiot.
, vol.48
, pp. 1355-1358
-
-
Fredenhagen, A.1
Mett, H.2
Meyer, T.3
Buchdunger, E.4
Regenass, U.5
Roggo, R.E.6
Petersen, F.7
-
22
-
-
0029008798
-
Novel quinone antiproliferame inhibitors of phosphatidylinositol-3-kinase
-
Frew, T., Powis, G., Berggren, M., Gallegos, A., Abraham, R. T., Ashendel, C. L., Zalkow, L. H., Hudson, C., Gruszecka-Kowalik, E., Burgess, E. M., Benedetti-Doctorovich, V., Kerrigan, J. E., Lambropoulos, J., Merriman, R. and Bonjouklian, R. (1995) Novel quinone antiproliferame inhibitors of phosphatidylinositol-3-kinase. Anticancer Drug Des. 10: 347-359.
-
(1995)
Anticancer Drug Des.
, vol.10
, pp. 347-359
-
-
Frew, T.1
Powis, G.2
Berggren, M.3
Gallegos, A.4
Abraham, R.T.5
Ashendel, C.L.6
Zalkow, L.H.7
Hudson, C.8
Gruszecka-Kowalik, E.9
Burgess, E.M.10
Benedetti-Doctorovich, V.11
Kerrigan, J.E.12
Lambropoulos, J.13
Merriman, R.14
Bonjouklian, R.15
-
23
-
-
0028352507
-
Protein tyrosine kinases as therapeutic targets in cancer chemotherapy and recent advances in the development of new inhibitors
-
Fry, D. W. (1994) Protein tyrosine kinases as therapeutic targets in cancer chemotherapy and recent advances in the development of new inhibitors. Expert Opin. Invest. Drugs 3: 577-595.
-
(1994)
Expert Opin. Invest. Drugs
, vol.3
, pp. 577-595
-
-
Fry, D.W.1
-
24
-
-
0028879656
-
Inhibitors of protein tyrosine kinases
-
Fry, D. W. and Bridges, A. J. (1995) Inhibitors of protein tyrosine kinases. Curr. Opin. Biotechnol. 6: 662-667.
-
(1995)
Curr. Opin. Biotechnol.
, vol.6
, pp. 662-667
-
-
Fry, D.W.1
Bridges, A.J.2
-
25
-
-
0029587403
-
Inhibition of basic fibroblast growth factor-mediated tyrosine phosphorylation and protein synthesis by PD 145709, a member of the 2-thioindole class of tyrosine kinase inhibitors
-
Fry, D. W. and Nelson, J. M. (1995) Inhibition of basic fibroblast growth factor-mediated tyrosine phosphorylation and protein synthesis by PD 145709, a member of the 2-thioindole class of tyrosine kinase inhibitors. Anticancer Drug Des. 10: 607-622.
-
(1995)
Anticancer Drug Des.
, vol.10
, pp. 607-622
-
-
Fry, D.W.1
Nelson, J.M.2
-
26
-
-
0030888879
-
Angiogenesis as a target for tumor treatment
-
Gastl, G., Hermann, T., Steurer, M., Zmija, J., Gunsilius, E., Unger, C. and Kraft, A. (1997) Angiogenesis as a target for tumor treatment. Oncology 54: 177-184.
-
(1997)
Oncology
, vol.54
, pp. 177-184
-
-
Gastl, G.1
Hermann, T.2
Steurer, M.3
Zmija, J.4
Gunsilius, E.5
Unger, C.6
Kraft, A.7
-
27
-
-
0029899585
-
Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: Structure-activity relationships in quinoxaliues, quinolines, and indole tyrphostins
-
Gazit, A., App, H., McMahon, G., Chen, J., Levitzki, A. and Bohmer, F. D. (1996) Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxaliues, quinolines, and indole tyrphostins. J. Med. Chem. 39: 2170-2177.
-
(1996)
J. Med. Chem.
, vol.39
, pp. 2170-2177
-
-
Gazit, A.1
App, H.2
McMahon, G.3
Chen, J.4
Levitzki, A.5
Bohmer, F.D.6
-
29
-
-
0010615455
-
-
World Patent Application WO 9614843, May 23
-
Giese, N. A., Lokker, N., Laibelman, A. M. and Scarborough, R. M. (1996) Pharmaceutical pyrzole compositions useful as inhibitors of protein kinase. World Patent Application WO 9614843, May 23.
-
(1996)
Pharmaceutical Pyrzole Compositions Useful as Inhibitors of Protein Kinase
-
-
Giese, N.A.1
Lokker, N.2
Laibelman, A.M.3
Scarborough, R.M.4
-
30
-
-
0031568943
-
Tyrphostins, inhibitors of protein tyrosine kinase, in restenosis
-
Golomb, G. and Fishbein, I. (1997) Tyrphostins, inhibitors of protein tyrosine kinase, in restenosis. Adv. Drug Delivery Rev. 24: 51-62.
-
(1997)
Adv. Drug Delivery Rev.
, vol.24
, pp. 51-62
-
-
Golomb, G.1
Fishbein, I.2
-
31
-
-
14444281388
-
Structure-activity relationships for a novel seties of pyrido[2,3-d]pyrimidine tyrosine kinase inhibitors
-
Hamby, J. M., Connolly, C. J. C., Schroeder, M. C., Winters, R. T., Showalter, H. D. H., Panek, R. L., Major, T. C., Olsewski, B., Ryan, M. J., Dahring, T., Lu, G. H., Keiser, J., Amar, A., Shen, C., Kraker, A. J., Slintak, V., Nelson, J. M., Fry, D. W., Bradlord, L., Hallak, H. and Doherty, A. M. (1997) Structure-activity relationships for a novel seties of pyrido[2,3-d]pyrimidine tyrosine kinase inhibitors. J. Med. Chem. 40: 2296-2303.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2296-2303
-
-
Hamby, J.M.1
Connolly, C.J.C.2
Schroeder, M.C.3
Winters, R.T.4
Showalter, H.D.H.5
Panek, R.L.6
Major, T.C.7
Olsewski, B.8
Ryan, M.J.9
Dahring, T.10
Lu, G.H.11
Keiser, J.12
Amar, A.13
Shen, C.14
Kraker, A.J.15
Slintak, V.16
Nelson, J.M.17
Fry, D.W.18
Bradlord, L.19
Hallak, H.20
Doherty, A.M.21
more..
-
32
-
-
0030029143
-
Discovery of a novel, potent, and src family-selective tyrosine kinase inhibitor. Study of lck- and fynT-dependent T-cell activation
-
Hanke, J. H., Gardner, J. P., Dow, R. L., Changelian, P. S., Brissette, W. H., Weringer, E. J., Pollok, B. A. and Connelly, P. A. (1996) Discovery of a novel, potent, and src family-selective tyrosine kinase inhibitor. Study of lck- and fynT-dependent T-cell activation. J. Biol. Chem. 271: 695-701.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 695-701
-
-
Hanke, J.H.1
Gardner, J.P.2
Dow, R.L.3
Changelian, P.S.4
Brissette, W.H.5
Weringer, E.J.6
Pollok, B.A.7
Connelly, P.A.8
-
33
-
-
0025933703
-
Platelet-derived growth factor and autocrine mechanisms of oncogenic processes
-
Heldin, C.-H. and Westermark, B. (1991) Platelet-derived growth factor and autocrine mechanisms of oncogenic processes. Crit. Rev. Oncol. 2: 109-124.
-
(1991)
Crit. Rev. Oncol.
, vol.2
, pp. 109-124
-
-
Heldin, C.-H.1
Westermark, B.2
-
34
-
-
0010614228
-
-
World Patent Application WO 9519169, July 20
-
Hirth, K. P., Schwartz, D. P., Mann, E., Shawver, L. K., Keri, G., Szckely, I., Bajor, T., Haimichael, J., Orfi, L., Levitzki, A., Gazit, A., Ullrich, A., Lammers, R., Kabbinavar, F. F., Slamon, D. J. and Tang, C. P. (1995) Treatment of platelet-derived growth factor-related disorders such as cancers using inhibitors of platelet-derived growth receptor. World Patent Application WO 9519169, July 20.
-
(1995)
Treatment of Platelet-Derived Growth Factor-Related Disorders Such as Cancers Using Inhibitors of Platelet-Derived Growth Receptor
-
-
Hirth, K.P.1
Schwartz, D.P.2
Mann, E.3
Shawver, L.K.4
Keri, G.5
Szckely, I.6
Bajor, T.7
Haimichael, J.8
Orfi, L.9
Levitzki, A.10
Gazit, A.11
Ullrich, A.12
Lammers, R.13
Kabbinavar, F.F.14
Slamon, D.J.15
Tang, C.P.16
-
35
-
-
0030009278
-
Structure of angelmicin B, a novel src signal transduction inhibitor
-
Hori, H., Higashi, K., Ishiyama, T., Uramoto, M., Uehara, Y. and Oki, T. (1996) Structure of angelmicin B, a novel src signal transduction inhibitor. Tetrahedron Lett. 37: 2785-2788.
-
(1996)
Tetrahedron Lett.
, vol.37
, pp. 2785-2788
-
-
Hori, H.1
Higashi, K.2
Ishiyama, T.3
Uramoto, M.4
Uehara, Y.5
Oki, T.6
-
37
-
-
0028829579
-
Polyhydroxylated 3-(N-phenyl) carbamoyl-2-iminochromene derivatives as potent: Inhibitors of tyrosine kinase p60c-src
-
Huang, C.-K., Wu, F.-Y. and Ai, Y.-X. (1995) Polyhydroxylated 3-(N-phenyl) carbamoyl-2-iminochromene derivatives as potent: inhibitors of tyrosine kinase p60c-src. Bioorg. Med. Chem. Lett. 5: 2423-2428.
-
(1995)
Bioorg. Med. Chem. Lett.
, vol.5
, pp. 2423-2428
-
-
Huang, C.-K.1
Wu, F.-Y.2
Ai, Y.-X.3
-
38
-
-
0026495734
-
Pharmacology of smooth muscle cell replication
-
Jackson, C. L. and Schwartz, S. M. (1992) Pharmacology of smooth muscle cell replication. Hypertension (Dallas) 20: 713-736.
-
(1992)
Hypertension (Dallas)
, vol.20
, pp. 713-736
-
-
Jackson, C.L.1
Schwartz, S.M.2
-
39
-
-
0029833451
-
Epidermal growth factor receptor tyrosine kinase inhibitors as potential cancer chemopreventives
-
Kelloff, G. J., Fay, J. R., Steele, V. E., Lubet, R. A., Boone, C. W., Crowell, J. A. and Sigman, C. C. (1996) Epidermal growth factor receptor tyrosine kinase inhibitors as potential cancer chemopreventives. Cancer Epidemiol. Biomarkers Prev. 5: 657-666.
-
(1996)
Cancer Epidemiol. Biomarkers Prev.
, vol.5
, pp. 657-666
-
-
Kelloff, G.J.1
Fay, J.R.2
Steele, V.E.3
Lubet, R.A.4
Boone, C.W.5
Crowell, J.A.6
Sigman, C.C.7
-
40
-
-
0000166625
-
Antitumor activities of hypericin as a protein tyrosine kinase blocker
-
Kil, K.-S., Yum, Y.-N., Seo, S.-H. and Lee K.-T. (1996) Antitumor activities of hypericin as a protein tyrosine kinase blocker. Arch. Pharmacal Res. 19: 490-496.
-
(1996)
Arch. Pharmacal Res.
, vol.19
, pp. 490-496
-
-
Kil, K.-S.1
Yum, Y.-N.2
Seo, S.-H.3
Lee, K.-T.4
-
41
-
-
0342546626
-
Phosphorylation site-specific inhibition of platelet-derived growth factor β-receptor autophosphorylation by the receptor blocking tyrphostin AG1296
-
Kovalenko, M., Roennstrand, L., Heldin, C.-H., Loubtchenkov, M., Gazit, A., Levitzki, A. and Boehmer, F. D. (1997) Phosphorylation site-specific inhibition of platelet-derived growth factor β-receptor autophosphorylation by the receptor blocking tyrphostin AG1296. Biochemistry 36: 6260-6269.
-
(1997)
Biochemistry
, vol.36
, pp. 6260-6269
-
-
Kovalenko, M.1
Roennstrand, L.2
Heldin, C.-H.3
Loubtchenkov, M.4
Gazit, A.5
Levitzki, A.6
Boehmer, F.D.7
-
42
-
-
0027081145
-
Potent and specific inhibition of p60v-src protein kinase both in vivo and in vitro by radicicol
-
Kown, H. J., Yoshida, M., Fukui, Y., Horinouchi, S. and Beppu, T. (1992) Potent and specific inhibition of p60v-src protein kinase both in vivo and in vitro by radicicol. Cancer Res. 52: 6926-6930.
-
(1992)
Cancer Res.
, vol.52
, pp. 6926-6930
-
-
Kown, H.J.1
Yoshida, M.2
Fukui, Y.3
Horinouchi, S.4
Beppu, T.5
-
43
-
-
0029994470
-
Src as a target for anticancer drugs
-
Levitzki, A. (1996) Src as a target for anticancer drugs. Anticancer Drug Des. 11: 175-182.
-
(1996)
Anticancer Drug Des.
, vol.11
, pp. 175-182
-
-
Levitzki, A.1
-
44
-
-
0027239809
-
Expression of basic fibroblast growth factor and its receptor by smooth muscle cells and endothelium in injured rat arteries. An en face study
-
Lindner, V. and Reidy, M. A. (1993) Expression of basic fibroblast growth factor and its receptor by smooth muscle cells and endothelium in injured rat arteries. An en face study. Circ. Res. 73: 589-595.
-
(1993)
Circ. Res.
, vol.73
, pp. 589-595
-
-
Lindner, V.1
Reidy, M.A.2
-
45
-
-
0029050865
-
A subpopulation of smooth muscle cells in injured rat arteries expresses platelet-derived growth factor-B chain mRNA
-
Lindner, V., Giachelli, C. M., Schwartz, S. M. and Reidy, M. A. (1995) A subpopulation of smooth muscle cells in injured rat arteries expresses platelet-derived growth factor-B chain mRNA. Circ. Res. 76: 951-957.
-
(1995)
Circ. Res.
, vol.76
, pp. 951-957
-
-
Lindner, V.1
Giachelli, C.M.2
Schwartz, S.M.3
Reidy, M.A.4
-
46
-
-
0028872499
-
Antisense oligonucleotides for PDGF-B and its receptor inhibit mechanical strain-induced fetal lung cell growth
-
Liu, M., Liu, J., Buch, S., Tanswell, A. K. and Post, M. (1995) Antisense oligonucleotides for PDGF-B and its receptor inhibit mechanical strain-induced fetal lung cell growth. Can. Am. J. Physiol. 269: L178-L184.
-
(1995)
Can. Am. J. Physiol.
, vol.269
-
-
Liu, M.1
Liu, J.2
Buch, S.3
Tanswell, A.K.4
Post, M.5
-
47
-
-
0029896432
-
Identification of GIYWHHY as a novel peptide substrate for human p60c-src protein tyrosine kinase
-
Lou, Q., Leftwich, M. E. and Lam, K. S. (1996) Identification of GIYWHHY as a novel peptide substrate for human p60c-src protein tyrosine kinase. Bioorg. Med. Chem. 4: 677-682.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 677-682
-
-
Lou, Q.1
Leftwich, M.E.2
Lam, K.S.3
-
48
-
-
0030963144
-
Potent pseudosubstrate-based peptide inhibitors for p60c-src protein tyrosine kinase
-
Lou, Q., Leftwich, M. E., McKay, R. T., Salmon, S. E., Rychetsky, L. and Lam, K. S. (1997) Potent pseudosubstrate-based peptide inhibitors for p60c-src protein tyrosine kinase. Cancer Res. 57: 1877-1881.
-
(1997)
Cancer Res.
, vol.57
, pp. 1877-1881
-
-
Lou, Q.1
Leftwich, M.E.2
McKay, R.T.3
Salmon, S.E.4
Rychetsky, L.5
Lam, K.S.6
-
49
-
-
0030024792
-
Local infusion of FGF-saporin reduces intimal hyperplasia
-
Mattar, S. G., Hanson, S. R., Pierce, G. F., Chen, C., Hughes, J. D., Cook, J. E., Shen, C., Noe, B. A., Suwyn, C. R., Scott, J. R. and Lumsden, A. B. (1996) Local infusion of FGF-saporin reduces intimal hyperplasia. J. Surg. Res. 60: 339-344.
-
(1996)
J. Surg. Res.
, vol.60
, pp. 339-344
-
-
Mattar, S.G.1
Hanson, S.R.2
Pierce, G.F.3
Chen, C.4
Hughes, J.D.5
Cook, J.E.6
Shen, C.7
Noe, B.A.8
Suwyn, C.R.9
Scott, J.R.10
Lumsden, A.B.11
-
50
-
-
0027501428
-
Inhibition of the epidermal growth factor receptor tyrosine kinase activity by leflunomide
-
Mattar, T., Kochhar, K., Bartlett, R., Bremer, E. G. and Finnegan, A. (1993) Inhibition of the epidermal growth factor receptor tyrosine kinase activity by leflunomide. FEBS Lett. 334: 161-164.
-
(1993)
FEBS Lett.
, vol.334
, pp. 161-164
-
-
Mattar, T.1
Kochhar, K.2
Bartlett, R.3
Bremer, E.G.4
Finnegan, A.5
-
51
-
-
0029850505
-
In vivo pharmacology and antitumor evaluation of the tyrpbostin tyrosine kinase inhibitor RG13022
-
McLeod, H. L., Brunton, V. G., Eckardt, N., Lear, M. J., Robins, D. J., Workman, P. and Graham, M. A. (1996) In vivo pharmacology and antitumor evaluation of the tyrpbostin tyrosine kinase inhibitor RG13022. Br. J. Cancer 74: 1714-1718.
-
(1996)
Br. J. Cancer
, vol.74
, pp. 1714-1718
-
-
McLeod, H.L.1
Brunton, V.G.2
Eckardt, N.3
Lear, M.J.4
Robins, D.J.5
Workman, P.6
Graham, M.A.7
-
52
-
-
0028947501
-
Approach to the discovery of novel, selective inhibitors of p56lck tyrosine kinase: Identification of non-hydroxylated chrornones as p56lck inhibitors
-
Miller. D., Wang, S., Reid, J., Xie, W., Gauvin, B., Kelley, M., Sarup, J., Sawutz, D. G., Miski, M., Dolle, R. E. and Faltynek, C. R. (1995) Approach to the discovery of novel, selective inhibitors of p56lck tyrosine kinase: identification of non-hydroxylated chrornones as p56lck inhibitors. Drug Dev. Res. 34: 344-352.
-
(1995)
Drug Dev. Res.
, vol.34
, pp. 344-352
-
-
Miller, D.1
Wang, S.2
Reid, J.3
Xie, W.4
Gauvin, B.5
Kelley, M.6
Sarup, J.7
Sawutz, D.G.8
Miski, M.9
Dolle, R.E.10
Faltynek, C.R.11
-
55
-
-
0029166858
-
Inhibition by 5′-methylthiondenosine of cell growth and tyrosine kinase activity stimulated by fibroblast growth factor receptor in human gliomas
-
Miyaji, K., Tani, E., Nakano, A., Ikemoto, H. and Kaba, K. (1995) Inhibition by 5′-methylthiondenosine of cell growth and tyrosine kinase activity stimulated by fibroblast growth factor receptor in human gliomas. J. Neurosurg. 83: 690-697.
-
(1995)
J. Neurosurg.
, vol.83
, pp. 690-697
-
-
Miyaji, K.1
Tani, E.2
Nakano, A.3
Ikemoto, H.4
Kaba, K.5
-
56
-
-
0030945871
-
Structure of the tyrosine kinase domain of fibroblast factor receptor in complex with inhibitors
-
Mohammadi, M., McMahon, G., Sun, L., Tang, C., Hirth, P., Yeh, B. K., Hubbard, S. R. and Schlessinger, J. (1997) Structure of the tyrosine kinase domain of fibroblast factor receptor in complex with inhibitors. Science 276: 955-960.
-
(1997)
Science
, vol.276
, pp. 955-960
-
-
Mohammadi, M.1
McMahon, G.2
Sun, L.3
Tang, C.4
Hirth, P.5
Yeh, B.K.6
Hubbard, S.R.7
Schlessinger, J.8
-
57
-
-
85069022116
-
-
US Patent 5476851, December 19
-
Myers, M. R., Persons, P. E., Ly, C. Q. and Spada, A. P. (1995) Pyrazolo[3,4-g]quinoxaline compounds which inhibit PDGF receptor protein tyrosine kinase. US Patent 5476851, December 19.
-
(1995)
Pyrazolo[3,4-g]quinoxaline Compounds Which Inhibit PDGF Receptor Protein Tyrosine Kinase
-
-
Myers, M.R.1
Persons, P.E.2
Ly, C.Q.3
Spada, A.P.4
-
58
-
-
0031576843
-
The preparation and SAR of 4-(anilino), 4-(phenoxy), and 4-(thiophenoxy)-quinazolines: Inhibitors of p56lck and EGF-R tyrosine kinase activity
-
Myers, M. R, Setzer, N. N., Spada, A. P., Zulli, A. L., Hsu, C.-Y. J., Zilberstein, A., Johnson, S. E., Hook, L. H. and Jacoski, M. V. (1997) The preparation and SAR of 4-(anilino), 4-(phenoxy), and 4-(thiophenoxy)-quinazolines: inhibitors of p56lck and EGF-R tyrosine kinase activity. Bioorg. Med. Chem. Lett. 7: 417-420.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 417-420
-
-
Myers, M.R.1
Setzer, N.N.2
Spada, A.P.3
Zulli, A.L.4
Hsu, C.-Y.J.5
Zilberstein, A.6
Johnson, S.E.7
Hook, L.H.8
Jacoski, M.V.9
-
60
-
-
0010581856
-
The molecular basis of primary immunodeficiency disorders
-
Interlaken, Switzerland, June 1996, Kazatchkine, M. D. and Morell, A. (eds.) Parthenon Publishiny, New York
-
Ochs, H. D. (1996) The molecular basis of primary immunodeficiency disorders. In: Intravenous Immumonoglobulin Research and Therapy, Proceedings of the Fourth International Symposium on Intravenous Immunoglobulin Therapy, Interlaken, Switzerland, June 1996, pp. 175-191, Kazatchkine, M. D. and Morell, A. (eds.) Parthenon Publishiny, New York.
-
(1996)
Intravenous Immumonoglobulin Research and Therapy, Proceedings of the Fourth International Symposium on Intravenous Immunoglobulin Therapy
, pp. 175-191
-
-
Ochs, H.D.1
-
61
-
-
0029035467
-
Tyrosine kinase inhibitors. 4. Structure-activity relationships among N- and 3-substituted 2,2′-dithiobis(1H-indoles) for in vitro inhibition of receptor and nonreceptor protein tyrosine kinases
-
Palmer, B. D., Rewcastle, G. W., Thompson, A. M., Boyd, M., Showalter, H. D. H., Sercel, A. D., Fry, D. W., Kraker, A. J. and Denny, W. A. (1995) Tyrosine kinase inhibitors. 4. Structure-activity relationships among N- and 3-substituted 2,2′-dithiobis(1H-indoles) for in vitro inhibition of receptor and nonreceptor protein tyrosine kinases. J. Med. Chem. 38: 58-67.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 58-67
-
-
Palmer, B.D.1
Rewcastle, G.W.2
Thompson, A.M.3
Boyd, M.4
Showalter, H.D.H.5
Sercel, A.D.6
Fry, D.W.7
Kraker, A.J.8
Denny, W.A.9
-
62
-
-
0031471249
-
In vitro pharmacological characterization of PD 166285, a new broadly active protein tyrosine kinase inhibitor
-
in press
-
Panek, R. L., Lu, G. H., Klutchko, S. R., Batley, B. L., Dahring, T. K., Hamby, J. M., Hallak, H., Doherty, A. M. and Keiser, J. A. (1997) In vitro pharmacological characterization of PD 166285, a new broadly active protein tyrosine kinase inhibitor. J. Pharmacol. Exp. Ther., in press.
-
(1997)
J. Pharmacol. Exp. Ther.
-
-
Panek, R.L.1
Lu, G.H.2
Klutchko, S.R.3
Batley, B.L.4
Dahring, T.K.5
Hamby, J.M.6
Hallak, H.7
Doherty, A.M.8
Keiser, J.A.9
-
63
-
-
0001128759
-
Protein kinase inhibitors for the treatment of cancer
-
Patrick, D. R. and Heimbrook, D. C. (1996) Protein kinase inhibitors for the treatment of cancer. Drug Discov. Today 1: 325-330.
-
(1996)
Drug Discov. Today
, vol.1
, pp. 325-330
-
-
Patrick, D.R.1
Heimbrook, D.C.2
-
64
-
-
0029910050
-
Radicicol inhibits tyrosine phosphorylation of the antotic src substrate Sam68 and retards subsequent exit from antosis of src-transformed cells
-
Pillay, L, Nakano, H. and Sharma, S. V. (1996) Radicicol inhibits tyrosine phosphorylation of the antotic src substrate Sam68 and retards subsequent exit from antosis of src-transformed cells. Cell Growth Differ. 7: 1487-1499.
-
(1996)
Cell Growth Differ.
, vol.7
, pp. 1487-1499
-
-
Pillay, L.1
Nakano, H.2
Sharma, S.V.3
-
65
-
-
0343214911
-
The development of arterial lesions: A process controlled by multiple factors
-
Reidy, M. A. and Bendeck, M. P. (1997) The development of arterial lesions: a process controlled by multiple factors. Fundam. Clin. Cardiol. 28: 55-67.
-
(1997)
Fundam. Clin. Cardiol.
, vol.28
, pp. 55-67
-
-
Reidy, M.A.1
Bendeck, M.P.2
-
66
-
-
0022457822
-
The biology of platelet-derived growth factor
-
Ross, R., Raines, E. W. and Bowen-Pope, D. F. (1986) The biology of platelet-derived growth factor. Cell 46: 155-169.
-
(1986)
Cell
, vol.46
, pp. 155-169
-
-
Ross, R.1
Raines, E.W.2
Bowen-Pope, D.F.3
-
67
-
-
0003172281
-
Signal transduction pathways as drug targets
-
Saltiel, A. R. (1995) Signal transduction pathways as drug targets. Sci. Am. Sci. Med. 2: 58-67.
-
(1995)
Sci. Am. Sci. Med.
, vol.2
, pp. 58-67
-
-
Saltiel, A.R.1
-
68
-
-
0030007675
-
In vitro characterization of a novel series of platelet-derived growth factor receptor tyrosine kinase inhibitors
-
Sawutz, D. G., Bode, D. C., Briggs, M., Reid, J. R., Canniff, P., Caldwell, L., Faltynek, C. R., Miller, D., Dunn, J. A., de Garavilla, L., Guiles, J. W., Weigelt, C., Michne, W., Treasurywala, A. M. and Silver, P. J. (1996) In vitro characterization of a novel series of platelet-derived growth factor receptor tyrosine kinase inhibitors. Biochem. Pharmacol. 51: 1631-1638.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 1631-1638
-
-
Sawutz, D.G.1
Bode, D.C.2
Briggs, M.3
Reid, J.R.4
Canniff, P.5
Caldwell, L.6
Faltynek, C.R.7
Miller, D.8
Dunn, J.A.9
De Garavilla, L.10
Guiles, J.W.11
Weigelt, C.12
Michne, W.13
Treasurywala, A.M.14
Silver, P.J.15
-
69
-
-
0029112036
-
Tyrosine kinase inhibitors inhibit multiple steps of the cell cycle of vascular smooth muscle cells
-
Shimokado, K., Umezawa, K. and Ogata, J. (1995) Tyrosine kinase inhibitors inhibit multiple steps of the cell cycle of vascular smooth muscle cells. Exp. Cell Re. 220: 266-273.
-
(1995)
Exp. Cell Re.
, vol.220
, pp. 266-273
-
-
Shimokado, K.1
Umezawa, K.2
Ogata, J.3
-
70
-
-
4644279756
-
Tyrosine kinase inhibitors. 6. Structure-activity relationships among N- and 3-substituted 2,2′-diselenobis(1H-indoles) for inhibition of protein tyrosine kinases and comparative in vitro and in vivo studies against selected sulfur congeners
-
Showalter, H. D. H., Sercel, A. D., Leja, B. M., Wolfangel, C. D., Ambroso, L. A., Elliott, W. L., Fry, D. W., Kraker, A. J., Howard, C. T., Lu, G. H., Moore, C. W., Nelson, J. M., Roberts, B. I., Vincent, P. W., Denny, W. A. and Thompson, A. M. (1997) Tyrosine kinase inhibitors. 6. Structure-activity relationships among N- and 3-substituted 2,2′-diselenobis(1H-indoles) for inhibition of protein tyrosine kinases and comparative in vitro and in vivo studies against selected sulfur congeners. J. Med. Chem. 40: 413-426.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 413-426
-
-
Showalter, H.D.H.1
Sercel, A.D.2
Leja, B.M.3
Wolfangel, C.D.4
Ambroso, L.A.5
Elliott, W.L.6
Fry, D.W.7
Kraker, A.J.8
Howard, C.T.9
Lu, G.H.10
Moore, C.W.11
Nelson, J.M.12
Roberts, B.I.13
Vincent, P.W.14
Denny, W.A.15
Thompson, A.M.16
-
71
-
-
0029432632
-
Protein kinase inhibitors - Potential chemotherapeuttc agents
-
Shugar, D. (1995) Protein kinase inhibitors - potential chemotherapeuttc agents. Acta Biochim. Pol. 42: 405-418
-
(1995)
Acta Biochim. Pol.
, vol.42
, pp. 405-418
-
-
Shugar, D.1
-
72
-
-
0031034930
-
Crystal structure of the src family tyrosine kinase hck
-
Sicheri, F., Moarefi, I. and Kuriyan, J. (1997) Crystal structure of the src family tyrosine kinase hck. Nature 385: 602-609.
-
(1997)
Nature
, vol.385
, pp. 602-609
-
-
Sicheri, F.1
Moarefi, I.2
Kuriyan, J.3
-
73
-
-
0026023289
-
Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice
-
Soriano, P., Montgomery, C., Geske, R. and Bradley, A. (1991) Targeted disruption of the c-src proto-oncogene leads to osteopetrosis in mice. Cell 64: 693-702.
-
(1991)
Cell
, vol.64
, pp. 693-702
-
-
Soriano, P.1
Montgomery, C.2
Geske, R.3
Bradley, A.4
-
74
-
-
0029159775
-
Small molecule inhibitors of tyrosine kinase activity
-
Spada, A. P. and Myers, M. R. (1995) Small molecule inhibitors of tyrosine kinase activity. Expert Opin. Ther. Pat. 5: 805-817.
-
(1995)
Expert Opin. Ther. Pat.
, vol.5
, pp. 805-817
-
-
Spada, A.P.1
Myers, M.R.2
-
76
-
-
0027172209
-
The src family tyrosine kinases are required for platelet-derived growth factor-mediated signal transduction in NIH 3T3 cells
-
Twamley-Stein, G. M., Pepperkok, R., Ansorge, W. and Courtneidge, S. A. (1993) The src family tyrosine kinases are required for platelet-derived growth factor-mediated signal transduction in NIH 3T3 cells. Proc. Natl. Acad. Sci. USA 90: 7696-7700.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 7696-7700
-
-
Twamley-Stein, G.M.1
Pepperkok, R.2
Ansorge, W.3
Courtneidge, S.A.4
-
78
-
-
0027272856
-
Angelmicins, new inhibitors of oncogenic src signal transduction
-
Uehara, Y., Li, P.-M., Fukazawa, H., Mizuno, S., Nihei, Y., Nishio, M., Hanada, M., Yamamoto, C., Furumai, T. and Oki, T. (1993) Angelmicins, new inhibitors of oncogenic src signal transduction. J. Antibiot. 46: 1306-1308.
-
(1993)
J. Antibiot.
, vol.46
, pp. 1306-1308
-
-
Uehara, Y.1
Li, P.-M.2
Fukazawa, H.3
Mizuno, S.4
Nihei, Y.5
Nishio, M.6
Hanada, M.7
Yamamoto, C.8
Furumai, T.9
Oki, T.10
-
79
-
-
9344269909
-
Sequence-independent inhibition of in vitro vascular smooth muscle cell proliferation, migration, and in vivo neointimal formation by phosphorothioate oligodeoxynucleotides
-
Wang, W., Chen, H. J., Schwartz, A., Cannon, P. J., Stein, C. A. and Rabbani, L. E. (1996) Sequence-independent inhibition of in vitro vascular smooth muscle cell proliferation, migration, and in vivo neointimal formation by phosphorothioate oligodeoxynucleotides. J. Clin. Invest. 98: 443-450.
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 443-450
-
-
Wang, W.1
Chen, H.J.2
Schwartz, A.3
Cannon, P.J.4
Stein, C.A.5
Rabbani, L.E.6
-
80
-
-
9044228411
-
Inhibitors of protein tyrosine phosphorylation reduce the proliferation of two human glioma cell lines
-
Weemink, P. A. O. Verheul, E., Kerkhof, E., van Veelen, C. W. M. and Rijksen, G. (1996) Inhibitors of protein tyrosine phosphorylation reduce the proliferation of two human glioma cell lines. Neurosurgery 38: 108-114.
-
(1996)
Neurosurgery
, vol.38
, pp. 108-114
-
-
Weemink, P.A.O.1
Verheul, E.2
Kerkhof, E.3
Van Veelen, C.W.M.4
Rijksen, G.5
-
81
-
-
0031025991
-
Three-dimensional structure of the tyrosine kinase c-src
-
Xu, W., Harrison, S. C. and Eck, M. J. (1997) Three-dimensional structure of the tyrosine kinase c-src. Nature 385: 595-602.
-
(1997)
Nature
, vol.385
, pp. 595-602
-
-
Xu, W.1
Harrison, S.C.2
Eck, M.J.3
-
82
-
-
0029052321
-
Inhibition of protein tyrosine phosphorylation in T cells by a novel immunosuppressive agent, leflunomide
-
Xu, X., Williams, J. W., Bremer, E. G., Finnegan, A. and Chong, A. S.-F. (1995) Inhibition of protein tyrosine phosphorylation in T cells by a novel immunosuppressive agent, leflunomide. J. Biol.Chem. 270: 12398-12403.
-
(1995)
J. Biol.chem.
, vol.270
, pp. 12398-12403
-
-
Xu, X.1
Williams, J.W.2
Bremer, E.G.3
Finnegan, A.4
Chong, A.S.-F.5
-
83
-
-
0030014489
-
Two activities of the immunosuppressive metabolite of leflunomide, A77 1726. Inhibition of pyrimidine nucleotide synthesis and protein tyrosine phosphorylation
-
Xu, X., Williams, J. W., Gong, H., Finnegan, A. and Chong, A. S.-F. (1996) Two activities of the immunosuppressive metabolite of leflunomide, A77 1726. Inhibition of pyrimidine nucleotide synthesis and protein tyrosine phosphorylation. Biochem. Pharmacol. 52: 527-534.
-
(1996)
Biochem. Pharmacol.
, vol.52
, pp. 527-534
-
-
Xu, X.1
Williams, J.W.2
Gong, H.3
Finnegan, A.4
Chong, A.S.-F.5
-
84
-
-
0028834626
-
Inhibition of the association with nuclear matrix of pRB, p70 and p40 proteins along with the specific suppression of c-myc expression by geldanamycin, an inhibitor of src tyrosine kinase
-
Yamaki, H., Nakajima, M., Seimiya, H., Saya, H., Sugita, M. and Tsuruo, T. (1995) Inhibition of the association with nuclear matrix of pRB, p70 and p40 proteins along with the specific suppression of c-myc expression by geldanamycin, an inhibitor of src tyrosine kinase. J. Antibiot. 48: 1021-1026.
-
(1995)
J. Antibiot.
, vol.48
, pp. 1021-1026
-
-
Yamaki, H.1
Nakajima, M.2
Seimiya, H.3
Saya, H.4
Sugita, M.5
Tsuruo, T.6
-
85
-
-
0030176410
-
Angelmicin B, a new inhibitor of oncogenic signal transduction, inhibits growth and induces myelomonocytic difterentiation of human myeloid leukemia HL-60 cells
-
Yokoyama, A., Okabe-Kado, J., Uehara, Y., Oki, T., Tomoyasu, S., Tsuruoka, N. and Honma, Y. (1996) Angelmicin B, a new inhibitor of oncogenic signal transduction, inhibits growth and induces myelomonocytic difterentiation of human myeloid leukemia HL-60 cells. Leuk. Res. 20: 491-497.
-
(1996)
Leuk. Res.
, vol.20
, pp. 491-497
-
-
Yokoyama, A.1
Okabe-Kado, J.2
Uehara, Y.3
Oki, T.4
Tomoyasu, S.5
Tsuruoka, N.6
Honma, Y.7
-
86
-
-
0031038098
-
Platelet-derived growth factor stimulates sodium-dependent Pi transport in osteoblastic cells via phospholipase Cγ and phosphatidylinositol 3′-kinase
-
Zhen, X., Bonjour, J.-P. and Caverzasio, J. (1997) Platelet-derived growth factor stimulates sodium-dependent Pi transport in osteoblastic cells via phospholipase Cγ and phosphatidylinositol 3′-kinase. J. Bone Miner. Rev 12: 36-44.
-
(1997)
J. Bone Miner. Rev
, vol.12
, pp. 36-44
-
-
Zhen, X.1
Bonjour, J.-P.2
Caverzasio, J.3
-
87
-
-
0029951570
-
(Phenylamino)pyrimidine (PAP) derivatives: A new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors
-
Zimmermann, J., Buchdunger, E., Mett, H., Meyer, T., Lydon, N. B. and Traxler, P. (1996) (Phenylamino)pyrimidine (PAP) derivatives: a new class of potent and highly selective PDGF-receptor autophosphorylation inhibitors. Bioorg. Med. Chem. Lett. 6: 1221-1226.
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 1221-1226
-
-
Zimmermann, J.1
Buchdunger, E.2
Mett, H.3
Meyer, T.4
Lydon, N.B.5
Traxler, P.6
-
88
-
-
0031026055
-
Potent and selective inhibitors of the abl-kinase: Phenylaminopyrimidine (PAP) derivatives
-
Zimmermann, J., Buchdunger, E., Mett, H., Meyer, T. and Lydon, N. B. (1997) Potent and selective inhibitors of the abl-kinase: phenylaminopyrimidine (PAP) derivatives. Bioorg. Med. Chem. Lett. 7: 187-192.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 187-192
-
-
Zimmermann, J.1
Buchdunger, E.2
Mett, H.3
Meyer, T.4
Lydon, N.B.5
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