Absolute quantitation of Met using mass spectrometry for clinical application: assay precision, stability, and correlation with MET gene amplification in FFPE tumor tissue.
about
Next-generation clinical trials: Novel strategies to address the challenge of tumor molecular heterogeneityMolecular pathology of cancer: how to communicate with diseaseQuantitative measurement of cancer tissue biomarkers in the lab and in the clinic.Mass-spectrometry-based quantitation of Her2 in gastroesophageal tumor tissue: comparison to IHC and FISH.Quantification of HER2 by Targeted Mass Spectrometry in Formalin-Fixed Paraffin-Embedded (FFPE) Breast Cancer Tissues.High HER2 protein levels correlate with increased survival in breast cancer patients treated with anti-HER2 therapy.Optimized Protocol for Quantitative Multiple Reaction Monitoring-Based Proteomic Analysis of Formalin-Fixed, Paraffin-Embedded Tissues.A Timely Shift from Shotgun to Targeted Proteomics and How It Can Be Groundbreaking for Cancer Research.MET tyrosine kinase receptor expression and amplification as prognostic biomarkers of survival in gastroesophageal adenocarcinoma.Prognostic and predictive value of MET deregulation in non-small cell lung cancerCancer proteomics: developments in technology, clinical use and commercialization.Quantification of Anaplastic Lymphoma Kinase Protein Expression in Non-Small Cell Lung Cancer Tissues from Patients Treated with CrizotinibUpdate on Gastroesophageal Adenocarcinoma Targeted Therapies.Novel Targeted Therapies for Esophagogastric Cancer.Tumours with class 3 BRAF mutants are sensitive to the inhibition of activated RAS.Rilotumumab plus epirubicin, cisplatin, and capecitabine as first-line therapy in advanced MET-positive gastric or gastro-oesophageal junction cancer (RILOMET-1): a randomised, double-blind, placebo-controlled, phase 3 trial.Detection of MET mRNA in gastric cancer in situ. Comparison with immunohistochemistry and sandwich immunoassays.An approach to suppress the evolution of resistance in BRAFV600E-mutant cancer.Targeted therapies for targeted populations: Anti-EGFR treatment for EGFR amplified gastroesophageal adenocarcinoma.
P2860
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P2860
Absolute quantitation of Met using mass spectrometry for clinical application: assay precision, stability, and correlation with MET gene amplification in FFPE tumor tissue.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年学术文章
@wuu
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
name
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@ast
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@en
type
label
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@ast
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@en
prefLabel
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@ast
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@en
P2093
P2860
P1433
P1476
Absolute quantitation of Met u ...... fication in FFPE tumor tissue.
@en
P2093
Brittany Rambo
Daniel V T Catenacci
David B Krizman
Jamar Uzzell
Jon Burrows
Kathleen Bengali
Les Henderson
Marlene Darfler
P2860
P304
P356
10.1371/JOURNAL.PONE.0100586
P407
P577
2014-07-01T00:00:00Z