(Q37138662)

English

Next-generation sequencing of paired tyrosine kinase inhibitor-sensitive and -resistant EGFR mutant lung cancer cell lines identifies spectrum of DNA changes associated with drug resistance

scientific article published on 03 June 2013

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scholarly article

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Europe PubMed Central

18 August 2017

Next-generation sequencing of paired tyrosine kinase inhibitor-sensitive and -resistant EGFR mutant lung cancer cell lines identifies spectrum of DNA changes associated with drug resistance (English)

1 reference

Europe PubMed Central

18 August 2017

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inferred from title

Katerina Politi

9

Katerina Politi

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Europe PubMed Central

18 August 2017

12

William Pao

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Europe PubMed Central

18 August 2017

Valentina Pirazzoli

7

Valentina Pirazzoli

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Europe PubMed Central

18 August 2017

1

Peilin Jia

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Europe PubMed Central

18 August 2017

11

Zhongming Zhao

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Europe PubMed Central

18 August 2017

author name string

Hailing Jin

2

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Europe PubMed Central

18 August 2017

Catherine B Meador

3

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Europe PubMed Central

18 August 2017

Junfeng Xia

4

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Europe PubMed Central

18 August 2017

Kadoaki Ohashi

5

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Europe PubMed Central

18 August 2017

Lin Liu

6

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Europe PubMed Central

18 August 2017

Kimberly B Dahlman

8

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Europe PubMed Central

18 August 2017

Franziska Michor

10

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Europe PubMed Central

18 August 2017

publication date

3 June 2013

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Europe PubMed Central

18 August 2017

Genome Research

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18 August 2017

23

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18 August 2017

1434-1445

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describes a project that uses

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Genome and transcriptome sequencing of lung cancers reveal diverse mutational and splicing events.

1 reference

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1 reference

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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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Copy number variation detection and genotyping from exome sequence data

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Using transcriptome sequencing to identify mechanisms of drug action and resistance.

1 reference

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VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

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Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV

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Optimization of dosing for EGFR-mutant non-small cell lung cancer with evolutionary cancer modeling

1 reference

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1 reference

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1 reference

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Genotypic and histological evolution of lung cancers acquiring resistance to EGFR inhibitors

1 reference

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Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization

1 reference

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A map of human genome variation from population-scale sequencing

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Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer

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Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR

1 reference

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Novel mutant-selective EGFR kinase inhibitors against EGFR T790M

1 reference

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Gefitinib versus cisplatin plus docetaxel in patients with non-small-cell lung cancer harbouring mutations of the epidermal growth factor receptor (WJTOG3405): an open label, randomised phase 3 trial

1 reference

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Sequencing newly replicated DNA reveals widespread plasticity in human replication timing

1 reference

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1 reference

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Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

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TopHat: discovering splice junctions with RNA-Seq

1 reference

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High-resolution mapping of copy-number alterations with massively parallel sequencing.

1 reference

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Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions

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Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

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MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib

1 reference

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1 reference

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MET amplification leads to gefitinib resistance in lung cancer by activating ERBB3 signaling

1 reference

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1 reference

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1 reference

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Identifiers

10.1101/GR.152322.112

1 reference

Europe PubMed Central

18 August 2017

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Europe PubMed Central

18 August 2017

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Europe PubMed Central

18 August 2017

ResearchGate publication ID

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