Search Results - "Moyer, James D"
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Combination Therapy Enhances the Inhibition of Tumor Growth with the Fully Human Anti–Type 1 Insulin-Like Growth Factor Receptor Monoclonal Antibody CP-751,871
Published in Clinical cancer research (01-03-2005)“…Purpose: The insulin-like growth factor (IGF) signaling pathway is implicated in cellular mitogenesis, angiogenesis, tumor cell survival, and tumorigenesis…”
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PF-03814735, an orally bioavailable small molecule aurora kinase inhibitor for cancer therapy
Published in Molecular cancer therapeutics (01-04-2010)“…The Aurora family of highly related serine/threonine kinases plays a key role in the regulation of mitosis. Aurora1 and Aurora2 play important but distinct…”
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The discovery of highly selective erbB2 (Her2) inhibitors for the treatment of cancer
Published in Bioorganic & medicinal chemistry letters (01-06-2007)“…The synthesis and biological evaluation of potent and selective inhibitors of the erbB2 kinase is presented. The vast majority of these compounds are found to…”
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Prevention of Organ Allograft Rejection by a Specific Janus Kinase 3 Inhibitor
Published in Science (American Association for the Advancement of Science) (31-10-2003)“…Because of its requirement for signaling by multiple cytokines, Janus kinase 3 (JAK3) is an excellent target for clinical immunosuppression. We report the…”
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Discovery and pharmacologic characterization of CP-724,714, a selective ErbB2 tyrosine kinase inhibitor
Published in Cancer research (Chicago, Ill.) (15-10-2007)“…Amplification and overexpression of erbB2 (Her-2/neu) proto-oncogene has been linked to human malignancies including tumors of the breast, ovary, and stomach…”
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Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase
Published in Cancer research (Chicago, Ill.) (01-11-1997)“…The epidermal growth factor receptor (EGFR) is overexpressed in a significant percentage of carcinomas and contributes to the malignant phenotype. CP-358,774…”
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Inhibition of epidermal growth factor receptor-associated tyrosine phosphorylation in human carcinomas with CP-358,774: dynamics of receptor inhibition in situ and antitumor effects in athymic mice
Published in The Journal of pharmacology and experimental therapeutics (01-11-1999)“…Phosphorylation of tyrosine residues on the epidermal growth factor (EGF) receptor (EGFr) is an important early event in signal transduction, leading to cell…”
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Bivalence of EGF-like ligands drives the ErbB signaling network
Published in The EMBO journal (15-08-1997)“…Signaling by epidermal growth factor (EGF)‐like ligands is mediated by an interactive network of four ErbB receptor tyrosine kinases, whose mechanism of…”
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9
ErbB Tyrosine Kinases and the Two Neuregulin Families Constitute a Ligand-Receptor Network
Published in Molecular and Cellular Biology (01-10-1998)“…AUTHOR'S CORRECTION ( vol. 19 , p. 8695 ) ERRATUM ( vol. 18 , p. 7602 ) Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content…”
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The biological and biochemical effects of CP-654577, a selective erbB2 kinase inhibitor, on human breast cancer cells
Published in Cancer research (Chicago, Ill.) (01-08-2003)“…Aberrant expression or activity of epidermal growth factor receptor (EGFr) or the closely related p185(erbB2) can promote cell proliferation and survival and…”
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11
Pathogenic poxviruses reveal viral strategies to exploit the ErbB signaling network
Published in The EMBO journal (15-10-1998)“…Virulence of poxviruses, the causative agents of smallpox, depends on virus‐encoded growth factors related to the mammalian epidermal growth factor (EGF). Here…”
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LAS, a novel selective estrogen receptor modulator with chemopreventive and therapeutic activity in the N-nitroso-N-methylurea-induced rat mammary tumor model
Published in Cancer research (Chicago, Ill.) (15-12-2001)“…The N-nitroso-N-methylurea-induced rat mammary tumor model was used to conduct two types of studies: a prevention study designed to test the ability of the…”
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13
Novel Single-Pass Exchange of Circulating Uridine in Rat Liver
Published in Science (American Association for the Advancement of Science) (14-08-1981)“…Evidence is presented that the liver effects an essentially complete degradation of plasma uridine in a single pass and replaces it largely from hepatic pools…”
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Achieving selectivity between highly homologous tyrosine kinases: a novel selective erbB2 inhibitor
Published in Biochemical and biophysical research communications (25-07-2003)“…The discovery of small molecule kinase inhibitors for use as drugs is a promising approach for the treatment of cancer and other diseases, but the discovery of…”
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The Structural Basis for the Specificity of Epidermal Growth Factor and Heregulin Binding
Published in The Journal of biological chemistry (21-04-1995)“…Heregulin is a ligand for the erb B3 and erb B4 receptors, with a region of high homology to epidermal growth factor (EGF). Despite this homology, these…”
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Antitumor activity and biochemical effects of aphidicolin glycinate (NSC 303812) alone and in combination with cisplatin in vivo
Published in Cancer research (Chicago, Ill.) (01-02-1994)“…Aphidicolin, an inhibitor of DNA polymerases alpha and delta, is cytotoxic in vitro against tumor cells. The poor solubility of aphidicolin has led to the…”
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Synthesis, biological testing, and stereochemical assignment of an end group modified retro-inverso bombesin C-terminal nonapeptide
Published in Journal of organic chemistry (01-05-1990)Get full text
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18
Salvage of circulating pyrimidine nucleosides in the rat
Published in Cancer research (Chicago, Ill.) (01-08-1981)“…A new procedure was developed to measure uridine and cytidine in plasma. These nucleosides are present in micromolar concentrations in the plasma of rats,…”
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Cyclopentenyluridine and cyclopentenylcytidine analogs as inhibitors of uridine-cytidine kinase
Published in Journal of medicinal chemistry (01-12-1984)Get full text
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Antitumor activity and biochemical effects of cyclopentenyl cytosine in mice
Published in Cancer research (Chicago, Ill.) (01-07-1986)“…Cyclopentenyl cytosine, a recently synthesized inhibitor of cytidine 5'-triphosphate synthesis, has marked antitumor activity. Treatment with 1 mg/kg i.p. on…”
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