High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations.
about
Childhood acute myeloid leukaemiaUse of single nucleotide polymorphism array technology to improve the identification of chromosomal lesions in leukemiaSpecific genomic regions are differentially affected by copy number alterations across distinct cancer types, in aggregated cytogenetic data.Integrative analysis of copy number and gene expression data suggests novel pathogenetic mechanisms in primary myelofibrosis.Reexpression of LSAMP inhibits tumor growth in a preclinical osteosarcoma model.Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia.MYC Deregulation in Primary Human Cancers.The genomic landscape of core-binding factor acute myeloid leukemiasCopy number variation analysis on a non-Hodgkin lymphoma case-control study identifies an 11q25 duplication associated with diffuse large B-cell lymphoma8q24 amplified segments involve novel fusion genes between NSMCE2 and long noncoding RNAs in acute myelogenous leukemiaRole of SWI/SNF in acute leukemia maintenance and enhancer-mediated Myc regulation.Epidemiology of childhood acute myeloid leukemia.Identification of recurrent focal copy number variations and their putative targeted driver genes in ovarian cancerLoss of Mll3 Catalytic Function Promotes Aberrant MyelopoiesisSomatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemiaA novel genomic alteration of LSAMP associates with aggressive prostate cancer in African American men.Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia-7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity.Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors.Single-nucleotide polymorphism-array improves detection rate of genomic alterations in core-binding factor leukemia.Different characteristics identified by single nucleotide polymorphism array analysis in leukemia suggest the need for different application strategies depending on disease category.A genome-wide single-nucleotide polymorphism-array can improve the prognostic stratification of the core binding factor acute myeloid leukemia.Molecular and genetic alterations associated with therapy resistance and relapse of acute myeloid leukemia.Genomic architecture and treatment outcome in pediatric acute myeloid leukemia: a Children's Oncology Group report.Clinical Relevance of RUNX1 and CBFB Alterations in Acute Myeloid Leukemia and Other Hematological Disorders.The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes.Prognostic significance of acquired copy-neutral loss of heterozygosity in acute myeloid leukemia.Genome-wide genotyping of acute myeloid leukemia with translocation t(9;11)(p22;q23) reveals novel recurrent genomic alterations.A Myc enhancer cluster regulates normal and leukaemic haematopoietic stem cell hierarchies.SNP-array lesions in core binding factor acute myeloid leukemia.Enhancer dysfunction in leukemia.
P2860
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P2860
High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations.
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
High-resolution genomic profil ...... recurrent genomic alterations.
@ast
High-resolution genomic profil ...... recurrent genomic alterations.
@en
type
label
High-resolution genomic profil ...... recurrent genomic alterations.
@ast
High-resolution genomic profil ...... recurrent genomic alterations.
@en
prefLabel
High-resolution genomic profil ...... recurrent genomic alterations.
@ast
High-resolution genomic profil ...... recurrent genomic alterations.
@en
P2093
P2860
P1433
P1476
High-resolution genomic profil ...... recurrent genomic alterations.
@en
P2093
Arnold Ganser
Asmaa Quessar
Ina Radtke
James R Downing
Jan Krönke
Jeffrey E Rubnitz
Jennifer Edelmann
Jinjun Cheng
Juliane Gohlke
P2860
P304
P356
10.1182/BLOOD-2011-09-380444
P407
P577
2012-01-10T00:00:00Z