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Heterogeneity of resistance mutations detectable by next-generation sequencing in TKI-treated lung adenocarcinoma
scientific article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
27304188
retrieved
13 November 2016
title
Heterogeneity of resistance mutations detectable by next-generation sequencing in TKI-treated lung adenocarcinoma
(English)
1 reference
stated in
PubMed
PubMed ID
27304188
retrieved
13 November 2016
main subject
adenocarcinoma
1 reference
based on heuristic
inferred from title
heterogeneity
1 reference
based on heuristic
inferred from title
author name string
Deborah A Belchis
series ordinal
1
0 references
Li-Hui Tseng
series ordinal
2
0 references
Thomas Gniadek
series ordinal
3
0 references
Lisa Haley
series ordinal
4
0 references
Parvez Lokhandwala
series ordinal
5
0 references
Peter Illei
series ordinal
6
0 references
Christopher D Gocke
series ordinal
7
0 references
Patrick Forde
series ordinal
8
0 references
Julie Brahmer
series ordinal
9
0 references
Frederic B Askin
series ordinal
10
0 references
James R Eshleman
series ordinal
11
0 references
Ming-Tseh Lin
series ordinal
12
0 references
language of work or name
English
0 references
publication date
9 June 2016
0 references
published in
Oncotarget
0 references
describes a project that uses
massive parallel sequencing
1 reference
based on heuristic
inferred from title
cites work
Acquired Resistance of EGFR-Mutant Lung Cancer to a T790M-Specific EGFR Inhibitor: Emergence of a Third Mutation (C797S) in the EGFR Tyrosine Kinase Domain
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MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling
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Novel D761Y and common secondary T790M mutations in epidermal growth factor receptor-mutant lung adenocarcinomas with acquired resistance to kinase inhibitors
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PubMed Central
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20 March 2017
Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer
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PubMed Central
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Acquired resistance of lung adenocarcinomas to gefitinib or erlotinib is associated with a second mutation in the EGFR kinase domain
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EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy
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Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib
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PubMed Central
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BIM mediates EGFR tyrosine kinase inhibitor-induced apoptosis in lung cancers with oncogenic EGFR mutations
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PubMed Central
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Epidermal growth factor receptor mutations in lung cancer
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PubMed Central
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The mechanism of acquired resistance to irreversible EGFR tyrosine kinase inhibitor-afatinib in lung adenocarcinoma patients
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29 September 2017
Contribution of KRAS mutations and c.2369C > T (p.T790M) EGFR to acquired resistance to EGFR-TKIs in EGFR mutant NSCLC: a study on circulating tumor DNA.
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PubMed Central
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L858R-positive lung adenocarcinoma with KRAS G12V, EGFR T790M and EGFR L858R mutations: A case report
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PubMed Central
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29 September 2017
Mechanisms of resistance to EGFR tyrosine kinase inhibitors
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PubMed Central
reference URL
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Clinical detection and categorization of uncommon and concomitant mutations involving BRAF.
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29 September 2017
Detection of T790M, the Acquired Resistance EGFR Mutation, by Tumor Biopsy versus Noninvasive Blood-Based Analyses
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PubMed Central
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Treatment approaches for EGFR-inhibitor-resistant patients with non-small-cell lung cancer
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PubMed Central
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Digital PCR analysis of plasma cell-free DNA for non-invasive detection of drug resistance mechanisms in EGFR mutant NSCLC: Correlation with paired tumor samples
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Impact of Concurrent PIK3CA Mutations on Response to EGFR Tyrosine Kinase Inhibition in EGFR-Mutant Lung Cancers and on Prognosis in Oncogene-Driven Lung Adenocarcinomas
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PIK3CA Mutations are Common in Many Tumor Types and are Often Associated With Other Driver Mutations
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The Allelic Context of the C797S Mutation Acquired upon Treatment with Third-Generation EGFR Inhibitors Impacts Sensitivity to Subsequent Treatment Strategies
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29 September 2017
Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
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29 September 2017
Multi-institutional Oncogenic Driver Mutation Analysis in Lung Adenocarcinoma: The Lung Cancer Mutation Consortium Experience
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PubMed Central
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29 September 2017
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29 September 2017
Tumor cellularity as a quality assurance measure for accurate clinical detection of BRAF mutations in melanoma.
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29 September 2017
Mechanisms of acquired resistance to EGFR-tyrosine kinase inhibitor in Korean patients with lung cancer.
1 reference
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PubMed Central
reference URL
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29 September 2017
Comparison study of the performance of the QIAGEN EGFR RGQ and EGFR pyro assays for mutation analysis in non-small cell lung cancer
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PubMed Central
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29 September 2017
Overcoming acquired resistance to anticancer therapy: focus on the PI3K/AKT/mTOR pathway
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216719
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29 September 2017
Preclinical rationale for PI3K/Akt/mTOR pathway inhibitors as therapy for epidermal growth factor receptor inhibitor-resistant non-small-cell lung cancer
1 reference
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29 September 2017
HER2 amplification: a potential mechanism of acquired resistance to EGFR inhibition in EGFR-mutant lung cancers that lack the second-site EGFRT790M mutation
1 reference
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PubMed Central
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29 September 2017
Lung cancers with acquired resistance to EGFR inhibitors occasionally harbor BRAF gene mutations but lack mutations in KRAS, NRAS, or MEK1.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216719
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29 September 2017
Phosphoinositide-3-kinase catalytic alpha and KRAS mutations are important predictors of resistance to therapy with epidermal growth factor receptor tyrosine kinase inhibitors in patients with advanced non-small cell lung cancer
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216719
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29 September 2017
Somatic EGFR mutations and efficacy of tyrosine kinase inhibitors in NSCLC.
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PubMed Central
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29 September 2017
Acquired resistance to epidermal growth factor receptor kinase inhibitors associated with a novel T854A mutation in a patient with EGFR-mutant lung adenocarcinoma
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PubMed Central
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29 September 2017
Irreversible inhibitors of the EGF receptor may circumvent acquired resistance to gefitinib
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PubMed Central
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29 September 2017
Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor Treatment Response in Advanced Lung Adenocarcinomas with G719X/L861Q/S768I Mutations.
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PubMed Central
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2 June 2018
Non-p.V600E BRAF Mutations Are Common Using a More Sensitive and Broad Detection Tool.
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27 November 2018
Analytical performance of the cobas EGFR mutation assay for Japanese non-small-cell lung cancer.
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27 November 2018
Efficiency of the Therascreen® RGQ PCR kit for the detection of EGFR mutations in non-small cell lung carcinomas.
1 reference
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216719
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27 November 2018
Epidermal growth factor receptor gene mutations and increased copy numbers predict gefitinib sensitivity in patients with recurrent non-small-cell lung cancer
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5216719
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27 November 2018
Non-responsiveness to gefitinib in a patient with lung adenocarcinoma having rare EGFR mutations S768I and V769L
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27304188
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Challenges posed to pathologists in the detection of KRAS mutations in colorectal cancers
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/27304188
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.18632/ONCOTARGET.9931
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4784744
OpenCitations bibliographic resource ID
4784744
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4784744
PMCID
5216719
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4784744
PubMed ID
27304188
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4784744
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