Genome and transcriptome sequencing in prospective metastatic triple-negative breast cancer uncovers therapeutic vulnerabilities.
about
Characterization of X chromosome inactivation using integrated analysis of whole-exome and mRNA sequencingA pilot study using next-generation sequencing in advanced cancers: feasibility and challengesCurrent Management Strategies in Breast Cancer by Targeting Key Altered Molecular PlayersThe Role of Forkhead Box Protein M1 in Breast Cancer Progression and Resistance to TherapySomatic mutations in breast and serous ovarian cancer young patients: a systematic review and meta-analysisCirculating Tumor Cells: A Window Into Tumor Development and Therapeutic EffectivenessMolecular Technologies in the Clinical Diagnostic LaboratoryStatus of PI3K/Akt/mTOR pathway inhibitors in lymphomaIntegrated genomic characterization reveals novel, therapeutically relevant drug targets in FGFR and EGFR pathways in sporadic intrahepatic cholangiocarcinomaWhole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.Personalized treatment of Sézary syndrome by targeting a novel CTLA4:CD28 fusion.Novel therapeutic strategies for patients with triple-negative breast cancerProspective molecular profiling of canine cancers provides a clinically relevant comparative model for evaluating personalized medicine (PMed) trialsDevelopment of a RSK Inhibitor as a Novel Therapy for Triple-Negative Breast Cancer.A thirteen-gene expression signature predicts survival of patients with pancreatic cancer and identifies new genes of interest.Wnt signaling in triple negative breast cancer is associated with metastasisBayesian methods for expression-based integration of various types of genomics data.Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.Regulators associated with clinical outcomes revealed by DNA methylation data in breast cancer.Data Interoperability of Whole Exome Sequencing (WES) Based Mutational Burden Estimates from Different LaboratoriesTargeting oncogenic vulnerabilities in triple negative breast cancer: biological bases and ongoing clinical studies.Circulating Tumor DNA Mutation Profiling by Targeted Next Generation Sequencing Provides Guidance for Personalized Treatments in Multiple Cancer TypesIntegrated analysis of recurrent properties of cancer genes to identify novel driversPathway-based analysis of breast cancer.Triple-negative breast cancer: challenges and opportunities of a heterogeneous disease.Increased risk of brain metastases in women with breast cancer and p16 expression in metastatic lymph-nodesα-catenin. A tumor suppressor beyond adherens junctions.Novel role of Engrailed 1 as a prosurvival transcription factor in basal-like breast cancer and engineering of interference peptides block its oncogenic function.Translating RNA sequencing into clinical diagnostics: opportunities and challenges.Mutational profiles in triple-negative breast cancer defined by ultradeep multigene sequencing show high rates of PI3K pathway alterations and clinically relevant entity subgroup specific differences.Pharmacological profiling of kinase dependency in cell lines across triple-negative breast cancer subtypes.Triple negative breast tumors in African-American and Hispanic/Latina women are high in CD44+, low in CD24+, and have loss of PTEN.Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer.Revealing the Molecular Portrait of Triple Negative Breast Tumors in an Understudied Population through Omics Analysis of Formalin-Fixed and Paraffin-Embedded Tissues.Molecular heterogeneity in adjacent cells in triple-negative breast cancer.Evaluation and integration of cancer gene classifiers: identification and ranking of plausible drivers.Discovery and functional characterization of a neomorphic PTEN mutation.Capture-based next-generation sequencing reveals multiple actionable mutations in cancer patients failed in traditional testing.Development and clinical application of an integrative genomic approach to personalized cancer therapyNovel insights into breast cancer genetic variance through RNA sequencing.
P2860
Q21131890-D249F003-189C-4928-A654-E99E5C7CFE54Q21132483-75C0D275-77EA-4643-8FC3-63D4ABD54E35Q26765877-AC5D3DE7-8888-4BCD-BC83-CED0E83325CDQ26768290-2B833BA7-02F3-40F5-8062-3B10809B21BCQ26776018-AF6CB661-8059-4973-8047-10BE44B49269Q26827815-D3D06811-6A82-4424-A5E6-14275FB3A8DBQ26996463-E2AA2FAF-59C8-4436-B7E3-E0B00D6C60E0Q27026544-A476AC64-7B47-4CE7-86DC-3798656C6DB5Q27852856-D8781D70-4702-4313-91C3-062C7D61F15AQ27853005-74CE34AE-ABB9-48FE-B57B-5D24529C2C24Q27853146-6CDA2349-66AB-4F9F-AC75-0661ED5C87F9Q28067436-97348491-99C3-4CE2-ACDE-C6DF9F42CB87Q28540955-F14A8CED-5417-40D0-A06D-384B07E075A3Q30275521-FDEA1B86-10A9-4887-A33A-01E48C504E10Q30410836-102E2692-C0C0-4B29-B88E-980E5D9FE484Q30597238-2F14E1E4-C177-4D27-BED9-31310726C093Q30668548-E3C7FD00-B9F0-48B4-A8E7-E1CD924A0D63Q30857788-18DFD77B-046C-4966-BD63-584CCA7D6319Q30956005-62355A7B-4B5C-4612-AB89-AACCCDEEFC2CQ31089220-22AB567A-F904-4C2C-B4CC-8E67623F51E2Q33591876-72257140-020D-4D6A-8601-566D7FBF2A4CQ33673752-92473CFD-8726-459E-AB2D-AB4BC45A4F68Q33742981-415EB2CF-AB3D-42BB-AFAB-320EBED62311Q33758011-774F5D4E-4465-44EF-B800-51C3CA729E93Q33769821-3B77427D-3C45-48F1-97F2-E64C67153083Q33913936-F34662A1-16A4-48DC-8253-2DF1D4A8E4A6Q34028517-E4262791-FF04-4836-9B89-19860192BBEFQ34285190-6588FC9D-74F8-4B7E-B541-1AD611D6CEA4Q34519034-9A6921A0-23C9-4448-93D9-BB454AECDE7AQ34654793-5C5AF34F-3E06-4F32-B66F-0E1E2E9E3CE8Q34978420-043FC467-6128-4DAE-BED4-089CA9D7CB73Q35027892-8730BCBD-32A2-428E-A05F-CE5E086F76C7Q35190834-8D976DDA-F3F9-46C3-BD11-71A7BF09FBC6Q35593154-A14BC2ED-0F8C-48E6-B6EC-615827CD766AQ35965925-1A0D4A56-D4BF-4978-8D12-15F8631B32A7Q36294122-F5026789-206F-46B8-8778-434D3531E832Q36300265-3989A99E-0089-4B4C-A139-B34D8432B876Q36902969-79183442-0389-412F-B466-8F9A11FEB9EAQ36954557-DD74D39B-5D1C-4F38-B6CB-C177B2ABA0ADQ37043550-2EC0D596-1402-488D-92B3-162FA6F7DAF4
P2860
Genome and transcriptome sequencing in prospective metastatic triple-negative breast cancer uncovers therapeutic vulnerabilities.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@en
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@nl
type
label
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@en
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@nl
prefLabel
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@en
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@nl
P2093
P1476
Genome and transcriptome seque ...... s therapeutic vulnerabilities.
@en
P2093
Ahmet Kurdoglu
Alexis Christoforides
Angela Baker
Anthony W Tolcher
Asim Siddiqui
Bodour Salhia
Catalin Barbacioru
Cristi L Aitelli
Cynthia R Osborne
Daniel Von Hoff
P304
P356
10.1158/1535-7163.MCT-12-0781
P577
2012-11-19T00:00:00Z