Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials
about
Melanoma: oncogenic drivers and the immune systemBeyond BRAF: where next for melanoma therapy?Clinical advances in molecular biomarkers for cancer diagnosis and therapyBRAF(L597) mutations in melanoma are associated with sensitivity to MEK inhibitorsBRAF fusions define a distinct molecular subset of melanomas with potential sensitivity to MEK inhibitionSurveying Recent Themes in Translational Bioinformatics: Big Data in EHRs, Omics for Drugs, and Personal GenomicsA graph theoretic approach to utilizing protein structure to identify non-random somatic mutations.VarWalker: personalized mutation network analysis of putative cancer genes from next-generation sequencing dataGuiding Oncology Patients Through the Maze of Precision Medicine.In-depth genomic data analyses revealed complex transcriptional and epigenetic dysregulations of BRAFV600E in melanoma.Beyond histology: translating tumor genotypes into clinically effective targeted therapies.Enabling a genetically informed approach to cancer medicine: a retrospective evaluation of the impact of comprehensive tumor profiling using a targeted next-generation sequencing panelCharacterization of breast cancers with PI3K mutations in an academic practice setting using SNaPshot profilingEfficacy and safety of nilotinib in patients with KIT-mutated metastatic or inoperable melanoma: final results from the global, single-arm, phase II TEAM trialEfficacy and safety of BRAF inhibition alone versus combined BRAF and MEK inhibition in melanoma: a meta-analysis of randomized controlled trials.A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance.Feasibility of real time next generation sequencing of cancer genes linked to drug response: results from a clinical trial.BRAFV600E-mutant melanoma presenting with cardiac involvement.The clinical response to vemurafenib in a patient with a rare BRAFV600DK601del mutation-positive melanoma.Combined BRAF (Dabrafenib) and MEK inhibition (Trametinib) in patients with BRAFV600-mutant melanoma experiencing progression with single-agent BRAF inhibitorSnowball: resampling combined with distance-based regression to discover transcriptional consequences of a driver mutationUpdate on Molecular Pathology of Cutaneous Melanocytic Lesions: What is New in Diagnosis and Molecular Testing for Treatment?Impact of NRAS mutations for patients with advanced melanoma treated with immune therapies.Clinically relevant genes and regulatory pathways associated with NRASQ61 mutations in melanoma through an integrative genomics approach.MicroRNA expression profiling predicts clinical outcome of carboplatin/paclitaxel-based therapy in metastatic melanoma treated on the ECOG-ACRIN trial E2603.[(18)F]-FLT PET to predict early response to neoadjuvant therapy in KRAS wild-type rectal cancer: a pilot study.The Clinicopathological Features of BRAF Mutated Papillary Thyroid Cancers in Chinese PatientsDetection of BRAF Mutations Using a Fully Automated Platform and Comparison with High Resolution Melting, Real-Time Allele Specific Amplification, Immunohistochemistry and Next Generation Sequencing Assays, for Patients with Metastatic Melanoma.Feasibility of Large-Scale Genomic Testing to Facilitate Enrollment Onto Genomically Matched Clinical TrialsClinical Activity of Ipilimumab in Acral Melanoma: A Retrospective Review.MGDB: a comprehensive database of genes involved in melanoma.ERBB activation modulates sensitivity to MEK1/2 inhibition in a subset of driver-negative melanomaCirculating tumor DNA to monitor treatment response and detect acquired resistance in patients with metastatic melanomaGenetics of melanomaThymic neoplasm: a rare disease with a complex clinical presentationRare BRAF mutations in melanoma patients: implications for molecular testing in clinical practice.Correlation between KRAS mutation status and response to chemotherapy in patients with advanced non-small cell lung cancer☆.Building a personalized medicine infrastructure at a major cancer center.Dabrafenib in an elderly patient with metastatic melanoma and BRAF V600R mutation: a case reportCUSTOM-SEQ: a prototype for oncology rapid learning in a comprehensive EHR environment.
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P2860
Routine multiplex mutational profiling of melanomas enables enrollment in genotype-driven therapeutic trials
description
2012 թուականին հրատարակուած գիտական յօդուած
@hyw
2012 թվականին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2012
@ast
im Januar 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific article (publication date: 2012)
@en
vedecký článok (publikovaný 2012)
@sk
vědecký článek publikovaný v roce 2012
@cs
wetenschappelijk artikel (gepubliceerd in 2012)
@nl
наукова стаття, опублікована у 2012
@uk
مقالة علمية (نشرت عام 2012)
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name
Routine multiplex mutational p ...... type-driven therapeutic trials
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Routine multiplex mutational p ...... type-driven therapeutic trials
@en
Routine multiplex mutational p ...... type-driven therapeutic trials
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type
label
Routine multiplex mutational p ...... type-driven therapeutic trials
@ast
Routine multiplex mutational p ...... type-driven therapeutic trials
@en
Routine multiplex mutational p ...... type-driven therapeutic trials
@nl
prefLabel
Routine multiplex mutational p ...... type-driven therapeutic trials
@ast
Routine multiplex mutational p ...... type-driven therapeutic trials
@en
Routine multiplex mutational p ...... type-driven therapeutic trials
@nl
P2093
P2860
P3181
P1433
P1476
Routine multiplex mutational p ...... type-driven therapeutic trials
@en
P2093
A John Iafrate
Ann Richmond
Charles Terry
Cindy L Vnencak-Jones
Donald Hucks
Donna J Hicks
Dora Dias-Santagata
Elizabeth Berry
Jeffrey Sosman
Kimberly Brown Dahlman
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0035309
P407
P577
2012-01-01T00:00:00Z