WZ4002

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2012-2018
0246820122018

Papers overview

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2015
2015
PURPOSE Mutant selective irreversible pyrimidine-based EGFR kinase inhibitors, including WZ4002, CO-1686, and AZD9291, are… (More)
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2015
2015
Resistance to targeted EGFR inhibitors is likely to develop in EGFR-mutant lung cancers. Early identification of innate or… (More)
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2015
2015
UNLABELLED Irreversible pyrimidine-based EGFR inhibitors, including WZ4002, selectively inhibit both EGFR-activating and EGFR… (More)
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Highly Cited
2013
Highly Cited
2013
The clinical efficacy of EGF receptor (EGFR) kinase inhibitors gefitinib and erlotinib is limited by the development of drug… (More)
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2013
2013
PURPOSE Although EGF receptor tyrosine kinase inhibitors (EGFR-TKI) have shown dramatic effects against EGFR mutant lung cancer… (More)
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2012
2012
Src has a role in the anoikis resistance in lung adenocarcinomas. We focused on two epidermal growth factor receptor (EGFR… (More)
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Highly Cited
2012
Highly Cited
2012
The clinical efficacy of epidermal growth factor receptor (EGFR) kinase inhibitors is limited by the development of drug… (More)
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Is this relevant?
2012
2012
PURPOSE Hepatocyte growth factor (HGF) induces resistance to reversible and irreversible epidermal growth factor receptor… (More)
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2012
2012
Although the EGF receptor tyrosine kinase inhibitors (EGFR-TKI) erlotinib and gefitinib have shown dramatic effects against EGFR… (More)
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2012
2012
UNLABELLED Epidermal growth factor receptor (EGFR) mutational status, activation of downstream signaling, and effective apoptotic… (More)
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