Acquired copy number alterations in adult acute myeloid leukemia genomes.
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Advances in understanding benzene health effects and susceptibilityC8orf4 negatively regulates self-renewal of liver cancer stem cells via suppression of NOTCH2 signallingMicro-RNAs and copy number changes: new levels of gene regulation in acute myeloid leukemiaRecurring mutations found by sequencing an acute myeloid leukemia genomeSynthetic lethality and cancer: cohesin and PARP at the replication forkGenomics of acute myeloid leukemiaThe Polo-Like Kinase 1 (PLK1) inhibitor NMS-P937 is effective in a new model of disseminated primary CD56+ acute monoblastic leukaemiaUse of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemiaAbnormal dosage of ultraconserved elements is highly disfavored in healthy cells but not cancer cellsTC1(C8orf4) regulates hematopoietic stem/progenitor cells and hematopoiesisThe origin and evolution of mutations in acute myeloid leukemiaGenomic 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 outcomeSingle-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia.SNP array analysis in hematologic malignancies: avoiding false discoveriesGenomic 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 leukemiaCopy 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 lymphomaSNP 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 hybridizationGain of MYC underlies recurrent trisomy of the MYC chromosome in acute promyelocytic leukemiaAcquired genomic copy number aberrations and survival in adult acute myelogenous leukemiaSequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progressionBiology, 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 leukemiaAutophagy in the pathogenesis of myelodysplastic syndrome and acute myeloid leukemia.Identification of novel genomic aberrations in AML-M5 in a level of array CGHAcquired 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.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 27 July 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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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
P2093
P2860
P356
P1476
Acquired copy number alterations in adult acute myeloid leukemia genomes.
@en
P2093
Brian P O'Gara
Daniel C Link
Elaine R Mardis
Hrishikesh Deshmukh
Jacob Kitzman
Jacqueline E Payton
Joel Geoghegan
John F DiPersio
Mark A Watson
P2860
P304
12950-12955
P356
10.1073/PNAS.0903091106
P407
P577
2009-07-27T00:00:00Z