Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity - Wikidata - wikimedia - TriplyDB

Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

http://www.wikidata.org/entity/Q36918993

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Circulating Tumor Cells in the Adenocarcinoma of the Esophagus Emerging therapeutic targets in esophageal adenocarcinoma Genomic characterization of esophageal squamous cell carcinoma: Insights from next-generation sequencing Reactivation of telomerase in cancer Genetic Biomarkers of Barrett's Esophagus Susceptibility and Progression to Dysplasia and Cancer: A Systematic Review and Meta-Analysis Advances in targeted therapies and new promising targets in esophageal cancer Mutational signatures: the patterns of somatic mutations hidden in cancer genomes Surgery in the era of the 'omics revolution SWI/SNF chromatin remodeling complexes and cancer Signaling pathways in the molecular pathogenesis of adenocarcinomas of the esophagus and gastroesophageal junction Loss-of-Function PTPRD Mutations Lead to Increased STAT3 Activation and Sensitivity to STAT3 Inhibition in Head and Neck Cancer Structural integrity of centromeric chromatin and faithful chromosome segregation requires Pat1 Molecular predictive markers in tumors of the gastrointestinal tract Etiology and Prevention of Esophageal Cancer Evidence of cancer-promoting roles for AMPK and related kinases Systematic review and meta-analysis of immunohistochemical prognostic biomarkers in resected oesophageal adenocarcinoma Neoadjuvant treatment for advanced esophageal cancer: response assessment before surgery and how to predict response to chemoradiation before starting treatment High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families Comprehensive molecular characterization of gastric adenocarcinoma Hypermutation in human cancer genomes: footprints and mechanisms Genome-Wide Transcriptional Regulation Mediated by Biochemically Distinct SWI/SNF Complexes Inactivating CUX1 mutations promote tumorigenesis Signatures of mutational processes in human cancer Translating genomic profiling to gastrointestinal cancer treatment.Base changes in tumour DNA have the power to reveal the causes and evolution of cancer.Clearance of Dying Cells by Phagocytes: Mechanisms and Implications for Disease Pathogenesis.Novel insight into mutational landscape of head and neck squamous cell carcinoma Disease mutant analysis identifies a new function of DAXX in telomerase regulation and telomere maintenance.Collection, integration and analysis of cancer genomic profiles: from data to insight.A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE)Data on affected cancer-related genes in pediatric t(12;21)-positive acute lymphoblastic leukemia patients harboring unbalanced der(6)t(X;6) translocations.Recent advances in preoperative management of esophageal adenocarcinoma Mutations of Chromatin Structure Regulating Genes in Human Malignancies.Genomics, Endoscopy, and Control of Gastroesophageal Cancers: A Perspective.Association of BRM promoter polymorphisms and esophageal adenocarcinoma outcome A comparative analysis of whole genome sequencing of esophageal adenocarcinoma pre- and post-chemotherapy Impact of mutations in Toll-like receptor pathway genes on esophageal carcinogenesis.Ribosomal DNA copy number loss and sequence variation in cancer Metformin sensitizes chemotherapy by targeting cancer stem cells and the mTOR pathway in esophageal cancer Chromatin-regulating proteins as targets for cancer therapy.

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Exome and whole-genome sequencing of esophageal adenocarcinoma identifies recurrent driver events and mutational complexity

http://www.wikidata.org/entity/Q36918993

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2013 nî lūn-bûn

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2013年论文

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2013年论文

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2013年论文

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Exome and whole-genome sequenc ...... ents and mutational complexity

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Exome and whole-genome sequenc ...... ents and mutational complexity

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Nature Genetics

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Exome and whole-genome sequenc ...... ents and mutational complexity

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Aaron McKenna

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Adam J Bass

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Alex H Ramos

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Andrey Sivachenko

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Arjun Pennathur

http://www.w3.org/2001/XMLSchema#string

Austin M Dulak

http://www.w3.org/2001/XMLSchema#string

Cameron Fox

http://www.w3.org/2001/XMLSchema#string

Chip Stewart

http://www.w3.org/2001/XMLSchema#string

David G Beer

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Douglas Voet

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P2860

Profiling critical cancer gene mutations in clinical tumor samples

Non-adherent cell-specific expression of DOCK2, a member of the human CDM-family proteins

MOZ and MORF histone acetyltransferases interact with the Runt-domain transcription factor Runx2

The structural basis of lipopolysaccharide recognition by the TLR4-MD-2 complex

Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma

A landscape of driver mutations in melanoma

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

dbSNP: the NCBI database of genetic variation

Melanoma genome sequencing reveals frequent PREX2 mutations

miRBase: integrating microRNA annotation and deep-sequencing data

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478-486

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10.1038/NG.2591

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5

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45

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Candace Guiducci

Kristian Cibulskis

Andrew C. Chang

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2013-03-24T00:00:00Z

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236076959

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23525077

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3678719

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