Protein kinase inhibitors as a therapeutic modality.
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[1] A. Levitzki. Tyrphostins: tyrosine kinase blockers as novel antiproliferative agents and dissectors of signal transduction , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[2] S. Bursell,et al. Amelioration of Vascular Dysfunctions in Diabetic Rats by an Oral PKC β Inhibitor , 1996, Science.
[3] A. Levitzki,et al. Tyrphostins--potential antiproliferative agents and novel molecular tools. , 1990, Biochemical pharmacology.
[4] V Hombach,et al. A dual inhibitor of platelet-derived growth factor beta-receptor and Src kinase activity potently interferes with motogenic and mitogenic responses to PDGF in vascular smooth muscle cells. A novel candidate for prevention of vascular remodeling. , 1999, Circulation research.
[5] A. Levitzki,et al. Tyrphostin-induced inhibition of p210bcr-abl tyrosine kinase activity induces K562 to differentiate. , 1993, Blood.
[6] R. Nilakantan,et al. Syntheses and EGFR and HER-2 kinase inhibitory activities of 4-anilinoquinoline-3-carbonitriles: analogues of three important 4-anilinoquinazolines currently undergoing clinical evaluation as therapeutic antitumor agents. , 2002, Bioorganic & medicinal chemistry letters.
[7] A. Levitzki,et al. Tyrosine kinase inhibition ameliorates the hyperdynamic state and decreases nitric oxide production in cirrhotic rats with portal hypertension and ascites. , 1997, The Journal of clinical investigation.
[8] Roy Kk,et al. Early Development of Cyclin Dependent Kinase Modulators , 2001 .
[9] G. Bollag,et al. Discovery of a novel Raf kinase inhibitor. , 2001, Endocrine-related cancer.
[10] A. Levitzki,et al. Selective inhibition of the epidermal growth factor and HER2/neu receptors by tyrphostins. , 1993, The Journal of biological chemistry.
[11] R. Krais,et al. Potential 18F-labeled biomarkers for epidermal growth factor receptor tyrosine kinase , 2001 .
[12] W. Cavenee,et al. Human glioblastoma xenografts overexpressing a tumor-specific mutant epidermal growth factor receptor sensitized to cisplatin by the AG1478 tyrosine kinase inhibitor. , 2001, Journal of neurosurgery.
[13] Kuo‐Ting Chang,et al. Enhancement of chemosensitivity by tyrphostin AG825 in high-p185(neu) expressing non-small cell lung cancer cells. , 1996, Cancer research.
[14] A. Levitzki,et al. Kinetics of phosphorylation of the SH2‐containing domain of phospholipase Cγ1 by the epidermal growth factor receptor , 1994, FEBS letters.
[15] G. Schwartz,et al. Cyclin-dependent kinase and protein kinase C inhibitors: a novel class of antineoplastic agents in clinical development. , 2000, Cancer journal.
[16] A. Levitzki,et al. Tyrphostins. 2. Heterocyclic and alpha-substituted benzylidenemalononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2/neu tyrosine kinases. , 1991, Journal of medicinal chemistry.
[17] A. Levitzki,et al. Tyrphostins that suppress the growth of human papilloma virus 16-immortalized human keratinocytes. , 1999, The Journal of pharmacology and experimental therapeutics.
[18] E. Sausville,et al. Tyrphostin induced growth inhibition: correlation with effect on p210bcr-abl autokinase activity in K562 chronic myelogenous leukemia. , 1994, Anti-cancer drugs.
[19] A. Levitzki,et al. Prevention of lipopolysaccharide-induced lethal toxicity by tyrosine kinase inhibitors. , 1994, Science.
[20] P. Worland,et al. Structure-activity relationship studies of flavopiridol analogues. , 2000, Bioorganic & medicinal chemistry letters.
[21] S. Mani,et al. Cyclin-dependent kinase inhibitors: novel anticancer agents , 2000, Expert opinion on investigational drugs.
[22] A. Levitzki,et al. ROS, stress‐activated kinases and stress signaling in cancer , 2002, EMBO reports.
[23] A. Senderowicz,et al. Flavopiridol: the First Cyclin-Dependent Kinase Inhibitor in Human Clinical Trials , 2004, Investigational New Drugs.
[24] A. Levitzki,et al. Selective interactions of transforming and normal abl proteins with ATP, tyrosine-copolymer substrates, and tyrphostins. , 1992, The Journal of biological chemistry.
[25] A. Levitzki,et al. Tyrphostins as molecular tools and potential antiproliferative drugs. , 1991, Trends in pharmacological sciences.
[26] A. Levitzki,et al. Labeled EGFr‐TK irreversible inhibitor (ML03): In vitro and in vivo properties, potential as PET biomarker for cancer and feasibility as anticancer drug , 2002, International journal of cancer.
[27] A. Levitzki,et al. The inhibition of EGF-dependent proliferation of keratinocytes by tyrphostin tyrosine kinase blockers , 1991, The Journal of cell biology.
[28] B. Druker,et al. Inhibition of c-kit receptor tyrosine kinase activity by STI 571, a selective tyrosine kinase inhibitor. , 2000, Blood.
[29] E. Sausville. Complexities in the development of cyclin-dependent kinase inhibitor drugs. , 2002, Trends in molecular medicine.
[30] G. Koehl,et al. Rapamycin inhibits primary and metastatic tumor growth by antiangiogenesis: involvement of vascular endothelial growth factor , 2002, Nature Medicine.
[31] A. Levitzki,et al. pp60(cSrc) is a caspase-3 substrate and Is essential for the transformed phenotype of A431 cells. , 2000, Molecular cell biology research communications : MCBRC.
[32] A. Levitzki,et al. Tyrphostins I: synthesis and biological activity of protein tyrosine kinase inhibitors. , 1989, Journal of medicinal chemistry.
[33] A. Levitzki,et al. Signal-transduction therapy. A novel approach to disease management. , 1994, European journal of biochemistry.
[34] B. Druker,et al. Perspectives on the development of a molecularly targeted agent. , 2002, Cancer cell.
[35] Beverly A. Teicher,et al. Antiangiogenic effects of a protein kinase Cβ-selective small molecule , 2001, Cancer Chemotherapy and Pharmacology.
[36] S. Keyse,et al. Tyrosine kinase inhibition: an approach to drug development. , 1995, Human & experimental toxicology.
[37] A. Levitzki,et al. Substrate competitive inhibitors of IGF-1 receptor kinase. , 2000, Biochemistry.
[38] A. Levitzki,et al. Blocking of EGF-dependent cell proliferation by EGF receptor kinase inhibitors , 1988, Science.
[39] K. Gibson,et al. ZD1839 (Iressa): an orally active inhibitor of epidermal growth factor signaling with potential for cancer therapy. , 2002, Cancer research.
[40] P. Seeburg,et al. Structural mechanism for STI-571 inhibition of abelson tyrosine kinase. , 2000, Science.
[41] D. Davies,et al. Epidermal growth factor receptor tyrosine kinase. Investigation of catalytic mechanism, structure-based searching and discovery of a potent inhibitor. , 1994, Biochemical pharmacology.
[42] M. Bryckaert,et al. Inhibition of platelet-derived growth factor-induced mitogenesis and tyrosine kinase activity in cultured bone marrow fibroblasts by tyrphostins. , 1992, Experimental cell research.
[43] W. Cavenee,et al. Drug resistance of human glioblastoma cells conferred by a tumor-specific mutant epidermal growth factor receptor through modulation of Bcl-XL and caspase-3-like proteases. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[44] E. Sausville,et al. Early development of cyclin dependent kinase modulators. , 2001, Current pharmaceutical design.
[45] A. Levitzki,et al. Inhibition of acute lymphoblastic leukaemia by a Jak-2 inhibitor , 1996, Nature.
[46] E. Sausville,et al. Inhibition of CDKs as a Therapeutic Modality , 2000, Annals of the New York Academy of Sciences.
[47] A. Levitzki,et al. Tyrosine kinase inhibition: an approach to drug development. , 1995, Science.
[48] A. Levitzki,et al. Kinetics of inhibition by tyrphostins of the tyrosine kinase activity of the epidermal growth factor receptor and analysis by a new computer program. , 1994, Molecular pharmacology.
[49] A. Nicholson,et al. Mutations of the BRAF gene in human cancer , 2002, Nature.
[50] A. Levitzki,et al. Enhanced ROS Production in Oncogenically Transformed Cells Potentiates c-Jun N-Terminal Kinase and p38 Mitogen-Activated Protein Kinase Activation and Sensitization to Genotoxic Stress , 2001, Molecular and Cellular Biology.
[51] Alan R. Saltiel,et al. Blockade of the MAP kinase pathway suppresses growth of colon tumors in vivo , 1999, Nature Medicine.
[52] D. Coppola,et al. Combination therapy with AG-490 and interleukin 12 achieves greater antitumor effects than either agent alone. , 2002, Molecular cancer therapeutics.
[53] C. Heldin,et al. Selective platelet-derived growth factor receptor kinase blockers reverse sis-transformation. , 1994, Cancer research.
[54] R. Krais,et al. Potential (18)F-labeled biomarkers for epidermal growth factor receptor tyrosine kinase. , 2001, Nuclear medicine and biology.
[55] J. Turkson,et al. Constitutive activation of Stat3 signaling confers resistance to apoptosis in human U266 myeloma cells. , 1999, Immunity.
[56] T. Hunter,et al. The Protein Kinase Complement of the Human Genome , 2002, Science.
[57] I. Fishbein,et al. PDGF-receptor tyrosine kinase blocker AG1295 selectively attenuates smooth muscle cell growth in vitro and reduces neointimal formation after balloon angioplasty in swine. , 1998, Circulation.
[58] Jürg Zimmermann,et al. Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr–Abl positive cells , 1996, Nature Medicine.
[59] Alexander Levitzki,et al. Protein tyrosine kinase inhibitors as novel therapeutic agents. , 1999, Pharmacology & therapeutics.
[60] N. Shenoy,et al. Growth inhibition of psoriatic keratinocytes by quinazoline tyrosine kinase inhibitors , 1999, The British journal of dermatology.
[61] A. Levitzki,et al. Printed in U.S.A. Copyright © 1997 by The Endocrine Society Specific Inhibition of Insulin-Like Growth Factor-1 and Insulin Receptor Tyrosine Kinase Activity and Biological Function by Tyrphostins , 2022 .
[62] S. Colla,et al. Effects of the tyrosine kinase inhibitor AG957 and an Anti-Fas receptor antibody on CD34(+) chronic myelogenous leukemia progenitor cells. , 1999, Blood.
[63] A. Levitzki,et al. Late administration of a lipophilic tyrosine kinase inhibitor prevents lipopolysaccharide and Escherichia coli-induced lethal toxicity. , 1996, The Journal of infectious diseases.
[64] A. Levitzki. Signal Transduction Interception as a Novel Approach to Disease Management , 1995, Annals of the New York Academy of Sciences.
[65] A. Levitzki. EGF receptor as a therapeutic target. , 2003, Lung cancer.
[66] A. Levitzki,et al. Epidermal-growth-factor-dependent activation of the src-family kinases. , 1994, European journal of biochemistry.
[67] R. Jove,et al. Inhibition of pp60c-Src reduces Bcl-XL expression and reverses the transformed phenotype of cells overexpressing EGF and HER-2 receptors , 1999, Oncogene.
[68] J. Hanke,et al. Discovery of a Novel, Potent, and Src Family-selective Tyrosine Kinase Inhibitor , 1996, The Journal of Biological Chemistry.
[69] G. Schwartsmann,et al. Targeting protein kinase C: new therapeutic opportunities against high-grade malignant gliomas? , 2002, The oncologist.
[70] Tamar Geiger,et al. Toward a PKB inhibitor: modification of a selective PKA inhibitor by rational design. , 2002, Biochemistry.
[71] S. Bursell,et al. Amelioration of vascular dysfunctions in diabetic rats by an oral PKC beta inhibitor. , 1996, Science.
[72] G. Mcmahon,et al. Tyrphostins. 5. Potent inhibitors of platelet-derived growth factor receptor tyrosine kinase: structure-activity relationships in quinoxalines, quinolines, and indole tyrphostins. , 1996, Journal of medicinal chemistry.
[73] M. Jirousek,et al. Protein kinase C inhibitors as novel anticancer drugs , 2001, Expert opinion on investigational drugs.
[74] A. Levitzki,et al. Tyrphostins suppress the growth of psoriatic keratinocytes , 1995, Experimental dermatology.
[75] A. Zilberstein,et al. Tyrphostins inhibit PDGF-induced DNA synthesis and associated early events in smooth muscle cells. , 1991, The American journal of physiology.
[76] B. Druker,et al. Lessons learned from the development of an abl tyrosine kinase inhibitor for chronic myelogenous leukemia. , 2000, The Journal of clinical investigation.
[77] A. Ullrich,et al. Flk-1 as a target for tumor growth inhibition. , 1996, Cancer research.
[78] G. Golomb,et al. Tricyclic quinoxalines as potent kinase inhibitors of PDGFR kinase, Flt3 and Kit. , 2003, Bioorganic & medicinal chemistry.
[79] C. Heldin,et al. Phosphorylation site-specific inhibition of platelet-derived growth factor beta-receptor autophosphorylation by the receptor blocking tyrphostin AG1296. , 1997, Biochemistry.
[80] L. Kèlland,et al. Flavopiridol, the first cyclin-dependent kinase inhibitor to enter the clinic: current status , 2000, Expert opinion on investigational drugs.
[81] J. Kuriyan,et al. Crystal structure of Hck in complex with a Src family-selective tyrosine kinase inhibitor. , 1999, Molecular cell.
[82] C. Natanson,et al. Tyrphostin AG 556 improves survival and reduces multiorgan failure in canine Escherichia coli peritonitis. , 1997, The Journal of clinical investigation.
[83] M. Carroll,et al. CGP 57148, a tyrosine kinase inhibitor, inhibits the growth of cells expressing BCR-ABL, TEL-ABL, and TEL-PDGFR fusion proteins. , 1997, Blood.
[84] A. Levitzki,et al. Inhibitors of epidermal growth factor receptor kinase and of cyclin-dependent kinase 2 activation induce growth arrest, differentiation, and apoptosis of human papilloma virus 16-immortalized human keratinocytes. , 1997, Cancer research.