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Acquired copy number alterations in adult acute myeloid leukemia genomes.

Acquired copy number alterations in adult acute myeloid leukemia genomes.

http://www.wikidata.org/entity/Q37276767

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Advances in understanding benzene health effects and susceptibility C8orf4 negatively regulates self-renewal of liver cancer stem cells via suppression of NOTCH2 signalling Micro-RNAs and copy number changes: new levels of gene regulation in acute myeloid leukemia Recurring mutations found by sequencing an acute myeloid leukemia genome Synthetic lethality and cancer: cohesin and PARP at the replication fork Genomics of acute myeloid leukemia The Polo-Like Kinase 1 (PLK1) inhibitor NMS-P937 is effective in a new model of disseminated primary CD56+ acute monoblastic leukaemia Use of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemia Abnormal dosage of ultraconserved elements is highly disfavored in healthy cells but not cancer cells TC1(C8orf4) regulates hematopoietic stem/progenitor cells and hematopoiesis The origin and evolution of mutations in acute myeloid leukemia Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.The complexity of interpreting genomic data in patients with acute myeloid leukemia.Chromosomal minimal critical regions in therapy-related leukemia appear different from those of de novo leukemia by high-resolution aCGH.Array CGH in human leukemia: from somatics to genetics.Next-generation sequencing.Clinical impact of gene mutations and lesions detected by SNP-array karyotyping in acute myeloid leukemia patients in the context of gemtuzumab ozogamicin treatment: results of the ALFA-0701 trial.Public data archives for genomic structural variation.The DNA double-strand break response is abnormal in myeloblasts from patients with therapy-related acute myeloid leukemia.Homozygous deletion mapping in myeloma samples identifies genes and an expression signature relevant to pathogenesis and outcome Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia.SNP array analysis in hematologic malignancies: avoiding false discoveries Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype.Identification of clinically important chromosomal aberrations in acute myeloid leukemia by array-based comparative genomic hybridization.NF1 inactivation in adult acute myelogenous leukemia Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion.The association between the copy-number variations of ZMAT4 and hematological malignancy.Analysis of the coding genome of diffuse large B-cell lymphoma SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3.A novel insertion ins(18;5)(q21.1;q31.2q35.1) in acute myeloid leukemia associated with microdeletions at 5q31.2, 5q35.1q35.2 and 18q12.3q21.1 detected by oligobased array comparative genomic hybridization Gain of MYC underlies recurrent trisomy of the MYC chromosome in acute promyelocytic leukemia Acquired genomic copy number aberrations and survival in adult acute myelogenous leukemia Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression Biology, risk stratification, and therapy of pediatric acute leukemias: an update.In vitro histone lysine methylation by NSD1, NSD2/MMSET/WHSC1 and NSD3/WHSC1L.Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia Autophagy in the pathogenesis of myelodysplastic syndrome and acute myeloid leukemia.Identification of novel genomic aberrations in AML-M5 in a level of array CGH Acquired genomic copy number aberrations and survival in chronic lymphocytic leukemia.Older patients with normal karyotype acute myeloid leukemia have a higher rate of genomic changes compared to young patients as determined by SNP array analysis

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P2860

Acquired copy number alterations in adult acute myeloid leukemia genomes.

http://www.wikidata.org/entity/Q37276767

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 27 July 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@en

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@nl

type

label

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@en

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@nl

prefLabel

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@en

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@nl

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PNAS.0903091106

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Acquired copy number alterations in adult acute myeloid leukemia genomes.

@en

P2093

Brian P O'Gara

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Daniel C Link

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

Elaine R Mardis

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Hrishikesh Deshmukh

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Jack Baty

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Jacob Kitzman

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Jacqueline E Payton

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Joel Geoghegan

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

John F DiPersio

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

Mark A Watson

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P2860

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia.

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)

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

Fusion of a novel gene, BTL, to ETV6 in acute myeloid leukemias with a t(4;12)(q11-q12;p13).

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification?

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.

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12950-12955

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10.1073/PNAS.0903091106

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31

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106

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Clara D. Bloomfield

Krzysztof Mrózek

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2009-07-27T00:00:00Z

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26713892

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19651600

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