Recurring mutations found by sequencing an acute myeloid leukemia genome - Test2 - elhamkhani - TriplyDB

Recurring mutations found by sequencing an acute myeloid leukemia genome

Recurring mutations found by sequencing an acute myeloid leukemia genome

http://www.wikidata.org/entity/Q24634204

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Bacteria-human somatic cell lateral gene transfer is enriched in cancer samples Human genetics and genomics a decade after the release of the draft sequence of the human genome Mutational profiling of kinases in glioblastoma.Personal genome sequencing: current approaches and challenges Advances in understanding benzene health effects and susceptibility Identification and functional characterization of isocitrate dehydrogenase 1 (IDH1) mutations in thyroid cancer Cancer-associated IDH1 mutations produce 2-hydroxyglutarate The R882H DNMT3A mutation associated with AML dominantly inhibits wild-type DNMT3A by blocking its ability to form active tetramers IDH1 and IDH2 mutations in gliomas NCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomes A small-cell lung cancer genome with complex signatures of tobacco exposure The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate The Cancer Genome Atlas Pan-Cancer analysis project Integrative analysis of the melanoma transcriptome COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer International network of cancer genome projects.The genomic complexity of primary human prostate cancer Network of Cancer Genes (NCG 3.0): integration and analysis of genetic and network properties of cancer genes Mutational processes molding the genomes of 21 breast cancers Data-independent proteomic screen identifies novel tamoxifen agonist that mediates drug resistance A comprehensive catalogue of somatic mutations from a human cancer genome VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma Massive genomic rearrangement acquired in a single catastrophic event during cancer development Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases Whole-genome cancer analysis as an approach to deeper understanding of tumour biology Fundamentals of cancer metabolism Epimutational profile of hematologic malignancies as attractive target for new epigenetic therapies Metabolic, autophagic, and mitophagic activities in cancer initiation and progression Structural Mechanisms and Drug Discovery Prospects of Rho GTPases Circulating tumor DNA: a promising biomarker in the liquid biopsy of cancer Mitochondrial metabolic remodeling in response to genetic and environmental perturbations Epigenetic regulators and their impact on therapy in acute myeloid leukemia Genetics and Epigenetics of Glioblastoma: Applications and Overall Incidence of IDH1 Mutation Molecular landscape of acute myeloid leukemia in younger adults and its clinical relevance Pathogenesis of Myeloproliferative Neoplasms: Role and Mechanisms of Chronic Inflammation Cancer Metabolism and Drug Resistance Next-Generation Sequencing in Clinical Molecular Diagnostics of Cancer: Advantages and Challenges Applications of Next-generation Sequencing in Systemic Autoimmune Diseases Pediatric AML: From Biology to Clinical Management

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Recurring mutations found by sequencing an acute myeloid leukemia genome

http://www.wikidata.org/entity/Q24634204

description

2009 nî lūn-bûn

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2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2009年の論文

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2009年論文

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2009年論文

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2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

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name

Recurring mutations found by sequencing an acute myeloid leukemia genome

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Recurring mutations found by sequencing an acute myeloid leukemia genome

@en

Recurring mutations found by sequencing an acute myeloid leukemia genome

@nl

type

label

Recurring mutations found by sequencing an acute myeloid leukemia genome

@ast

Recurring mutations found by sequencing an acute myeloid leukemia genome

@en

Recurring mutations found by sequencing an acute myeloid leukemia genome

@nl

prefLabel

Recurring mutations found by sequencing an acute myeloid leukemia genome

@ast

Recurring mutations found by sequencing an acute myeloid leukemia genome

@en

Recurring mutations found by sequencing an acute myeloid leukemia genome

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The New England Journal of Medicine

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Recurring mutations found by sequencing an acute myeloid leukemia genome

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Adam F Dukes

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Anthony M Brummett

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Carrie Haipek

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Christopher C Harris

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Craig S Pohl

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Daniel C Koboldt

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Daniel C Link

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David E Larson

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David J Dooling

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Devin P Locke

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P2860

A turning point in cancer research: sequencing the human genome

Accurate whole human genome sequencing using reversible terminator chemistry

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

Mapping short DNA sequencing reads and calling variants using mapping quality scores

IDH1 and IDH2 mutations in gliomas

Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype.

Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia.

The consensus coding sequences of human breast and colorectal cancers

Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461)

Clinical outcome of de novo acute myeloid leukaemia patients with normal cytogenetics is affected by molecular genetic alterations: a concise review

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1058-66

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scholarly article

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851424

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10.1056/NEJMOA0903840

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P433

11

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361

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Timothy A. Graubert

Michael H Tomasson

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2009-09-10T00:00:00Z

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19657110

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acute myeloid leukemia

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3201812

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