review article | Q7318358 |
scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1001305932 |
P356 | DOI | 10.2165/00003495-200060001-00003 |
P698 | PubMed publication ID | 11129169 |
P2093 | author name string | F Ciardiello | |
P2860 | cites work | Epidermal growth factor-related peptides and their receptors in human malignancies | Q28293442 |
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Protein tyrosine kinase inhibitors as novel therapeutic agents | Q33716122 | ||
The epidermal growth factor receptor and its inhibition in cancer therapy | Q33716127 | ||
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Tyrosine kinase inhibitors in preclinical development | Q33832624 | ||
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ZD1839 ('Iressa') as an anticancer agent | Q34112985 | ||
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Phase I studies of anti-epidermal growth factor receptor chimeric antibody C225 alone and in combination with cisplatin. | Q34507119 | ||
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Specific inhibition of epidermal growth factor receptor tyrosine kinase by 4-anilinoquinazolines | Q36821859 | ||
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Antitumor activity of sequential treatment with topotecan and anti-epidermal growth factor receptor monoclonal antibody C225. | Q40959114 | ||
Anti-epidermal growth factor receptor antibody C225 inhibits angiogenesis in human transitional cell carcinoma growing orthotopically in nude mice | Q40971116 | ||
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Inhibitors of tyrosine kinase | Q41643303 | ||
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Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD-1839 (Iressa), an epidermal growth factor receptor-selective tyrosine kinase inhibitor | Q57424632 | ||
Antitumor Activity of Combined Blockade of Epidermal Growth Factor Receptor and Protein Kinase A | Q57424743 | ||
Cytotoxicity against human tumor cells mediated by the conjugate of anti-epidermal growth factor receptor monoclonal antibody to recombinant ricin A chain | Q69739616 | ||
Antitumor effect of anti-epidermal growth factor receptor monoclonal antibodies plus cis-diamminedichloroplatinum on well established A431 cell xenografts | Q70487549 | ||
Tyrosine kinase inhibitors. 10. Isomeric 4-[(3-bromophenyl)amino]pyrido[d]-pyrimidines are potent ATP binding site inhibitors of the tyrosine kinase function of the epidermal growth factor receptor | Q71072552 | ||
Tyrphostins. 6. Dimeric benzylidenemalononitrile tyrophostins: potent inhibitors of EGF receptor tyrosine kinase in vitro | Q71875718 | ||
Epidermal growth factor receptors in human breast carcinoma cells: a potential selective target for transforming growth factor alpha-Pseudomonas exotoxin 40 fusion protein | Q72132785 | ||
Antitumor effects of doxorubicin in combination with anti-epidermal growth factor receptor monoclonal antibodies | Q72856071 | ||
Epidermal growth factor receptor family and chemosensitization | Q73133036 | ||
Epidermal growth factor receptor blockade with C225 plus gemcitabine results in regression of human pancreatic carcinoma growing orthotopically in nude mice by antiangiogenic mechanisms | Q73803447 | ||
Induction of apoptosis and cell cycle arrest by CP-358,774, an inhibitor of epidermal growth factor receptor tyrosine kinase | Q73838278 | ||
Blockade of the epidermal growth factor receptor signaling by a novel tyrosine kinase inhibitor leads to apoptosis of endothelial cells and therapy of human pancreatic carcinoma | Q73886918 | ||
Genistein exerts multiple suppressive effects on human breast carcinoma cells | Q77536071 | ||
PD153035, a tyrosine kinase inhibitor, prevents epidermal growth factor receptor activation and inhibits growth of cancer cells in a receptor number-dependent manner | Q77553678 | ||
Biological efficacy of a chimeric antibody to the epidermal growth factor receptor in a human tumor xenograft model | Q77555291 | ||
Phase I clinical trial of the flavonoid quercetin: pharmacokinetics and evidence for in vivo tyrosine kinase inhibition | Q77556839 | ||
P304 | page(s) | 25-32; discussion 41-2 | |
P577 | publication date | 2000-01-01 | |
P1433 | published in | Drugs | Q3040094 |
P1476 | title | Epidermal growth factor receptor tyrosine kinase inhibitors as anticancer agents | |
P478 | volume | 60 Suppl 1 |
Q44224981 | 25th European Society for Medical Oncology Congress. Hamburg, Germany. October 13-17, 2000. |
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