Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
about
The Human Kinome Targeted by FDA Approved Multi-Target Drugs and Combination Products: A Comparative Study from the Drug-Target Interaction Network PerspectiveTargeting the Raf-MEK-ERK mitogen-activated protein kinase cascade for the treatment of cancerEpigenetic assays for chemical biology and drug discovery.ErbB expression, activation, and inhibition with lapatinib and tyrphostin (AG825) in human vestibular schwannomas.FOXO3a represses VEGF expression through FOXM1-dependent and -independent mechanisms in breast cancer.FoxM1 mediated resistance to gefitinib in non-small-cell lung cancer cellsMolecular mechanisms of acquired resistance to tyrosine kinase targeted therapyThe escalating role of epidermal growth factor receptor inhibitors in cancer management: clinical considerations for the health system pharmacist.Lapatinib for the treatment of breast cancer in the People's Republic of China.Clinical Experience with Lapatinib in Patients with ErbB2-Overexpressing Metastatic Breast CancerLapatinib - Member of a New Generation of ErbB-Targeting Drugs.Development of prediction tools for diarrhea and rash in breast cancer patients receiving lapatinib in combination with capecitabine.FoxM1 is a downstream target and marker of HER2 overexpression in breast cancerErbB receptor-driven prolactinomas respond to targeted lapatinib treatment in female transgenic miceTyrosine kinase inhibitors: Multi-targeted or single-targeted?Deciphering the role of forkhead transcription factors in cancer therapyAn HPLC method for the determination of a novel anti-hypertension agent 6,7-dimethoxy-3-(4-(4-fluorobenzyloxy)-3-methoxyphenylmethyl)quinazolin-4(3H)-one in rat plasma: application to pharmacokinetic study.N⁴-(3-Bromophenyl)-7-(substituted benzyl) pyrrolo[2,3-d]pyrimidines as potent multiple receptor tyrosine kinase inhibitors: design, synthesis, and in vivo evaluation.The Akt signaling pathway: an emerging therapeutic target in malignant melanoma.Activation of multiple ERBB family receptors mediates glioblastoma cancer stem-like cell resistance to EGFR-targeted inhibition.Plant lectin can target receptors containing sialic acid, exemplified by podoplanin, to inhibit transformed cell growth and migration.Understanding drugs in breast cancer through drug sensitivity screeningDevelopment of a test that measures real-time HER2 signaling function in live breast cancer cell lines and primary cells.Induction of caspase-dependent extrinsic apoptosis by apigenin through inhibition of signal transducer and activator of transcription 3 (STAT3) signalling in HER2-overexpressing BT-474 breast cancer cells.Mechanisms of drug inhibition of signalling molecules.N2-Trimethylacetyl substituted and unsubstituted-N4-phenylsubstituted-6-(2-pyridin-2-ylethyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamines: design, cellular receptor tyrosine kinase inhibitory activities and in vivo evaluation as antiangiogenic, antimetA review of lapatinib ditosylate in the treatment of refractory or advanced breast cancer.Design, synthesis and biological evaluation of substituted pyrrolo[2,3-d]pyrimidines as multiple receptor tyrosine kinase inhibitors and antiangiogenic agentsMelanoma adapts to RAF/MEK inhibitors through FOXD3-mediated upregulation of ERBB3Jumping higher: is it still possible? The ALTTO trial challenge.Role of ErbB family receptor tyrosine kinases in intrahepatic cholangiocarcinomaGenomic and proteomic biomarkers for cancer: a multitude of opportunities.The Paradox of Oestradiol-Induced Breast Cancer Cell Growth and Apoptosis.Safety of triazole antifungal drugs in patients with cancer.Growth factors as active participants in carcinogenesis: a perspective.Radiosensitizing effect of lapatinib in human epidermal growth factor receptor 2-positive breast cancer cells.Clinical pharmacokinetics of tyrosine kinase inhibitors: focus on 4-anilinoquinazolines.Boron-Based Drug Design.Mechanisms of tumor cell resistance to the current targeted-therapy agents.Antibody and lectin target podoplanin to inhibit oral squamous carcinoma cell migration and viability by distinct mechanisms.
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P2860
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
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2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
name
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@ast
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@en
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@nl
type
label
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@ast
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@en
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@nl
prefLabel
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@ast
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@en
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@nl
P2860
P3181
P356
P1476
Lapatinib: a novel dual tyrosine kinase inhibitor with activity in solid tumors
@en
P2093
Christian R Dolder
Michael H Nelson
P2860
P3181
P356
10.1345/APH.1G387
P407
P577
2006-02-01T00:00:00Z