(Q44336225)

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Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis

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scholarly article

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2 December 2017

Identification of acquired copy number alterations and uniparental disomies in cytogenetically normal acute myeloid leukemia using high-resolution single-nucleotide polymorphism analysis (English)

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Europe PubMed Central

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2 December 2017

single-nucleotide polymorphism

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based on heuristic

inferred from title

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acute myeloid leukemia

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author name string

L Bullinger

1

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2 December 2017

J Krönke

2

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2 December 2017

C Schön

3

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2 December 2017

I Radtke

4

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2 December 2017

K Urlbauer

5

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2 December 2017

U Botzenhardt

6

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2 December 2017

V Gaidzik

7

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2 December 2017

A Carió

8

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2 December 2017

C Senger

9

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2 December 2017

R F Schlenk

10

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2 December 2017

J R Downing

11

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2 December 2017

K Holzmann

12

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2 December 2017

K Döhner

13

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2 December 2017

H Döhner

14

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2 December 2017

publication date

17 December 2009

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24

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2

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438-449

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2 December 2017

https://scigraph.springernature.com/pub.10.1038/leu.2009.263

0 references

Acute myeloid leukaemia

1 reference

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The clinical significance of cytogenetic abnormalities in acute myeloid leukaemia

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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?

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Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia

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Methods and strategies for analyzing copy number variation using DNA microarrays

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Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

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Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

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Chromosomal abnormalities in cancer

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Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML

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Prognostic impact of WT1 mutations in cytogenetically normal acute myeloid leukemia: a study of the German-Austrian AML Study Group

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Reference alignment of SNP microarray signals for copy number analysis of tumors

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

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Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays

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Whole genome scanning as a cytogenetic tool in hematologic malignancies

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Acquired copy number alterations in adult acute myeloid leukemia genomes

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21 January 2018

Detection of large-scale variation in the human genome

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21 January 2018

Global variation in copy number in the human genome

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21 January 2018

Large-scale copy number polymorphism in the human genome

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Adenoviral-mediated Rybp expression promotes tumor cell-specific apoptosis

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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)

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Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype

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RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer

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Concurrent transcriptional deregulation of AML1/RUNX1 and GATA factors by the AML1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia

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The protein kinase C-eta isoform induces proliferation in glioblastoma cell lines through an ERK/Elk-1 pathway

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Mutation in TET2 in myeloid cancers

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Acquired mutations in TET2 are common in myelodysplastic syndromes

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Del (9q) AML: clinical and cytological characteristics and prognostic implications

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Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia

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hnRNP K: an HDM2 target and transcriptional coactivator of p53 in response to DNA damage

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Suppression of anoikis and induction of metastasis by the neurotrophic receptor TrkB

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Chromosomal translocations involving the MLL gene: molecular mechanisms

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Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia

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Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): biologic and clinical features

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Disclosure of Candidate Genes in Acute Myeloid Leukemia With Complex Karyotypes Using Microarray-Based Molecular Characterization

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BCR–ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros

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Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia

1 reference

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Molecular characterization of acute myeloid leukemia

1 reference

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Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.263

7 January 2021

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Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes

1 reference

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DNA profiling analysis of 100 consecutive de novo acute myeloid leukemia cases reveals patterns of genomic instability that affect all cytogenetic risk groups

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T(3;14)(p14.1;q32) involving IGH and FOXP1 is a novel recurrent chromosomal aberration in MALT lymphoma

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Oligonucleotide array-CGH reveals cryptic gene copy number alterations in karyotypically normal acute myeloid leukemia

1 reference

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Somatic heterozygous mutations in ETV6 (TEL) and frequent absence of ETV6 protein in acute myeloid leukemia

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hCAP-D3 Expression Marks a Prostate Cancer Subtype With Favorable Clinical Behavior and Androgen Signaling Signature

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Acute myeloid leukemia with deletion 9q within a noncomplex karyotype is associated with CEBPA loss-of-function mutations

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Identifiers

10.1038/LEU.2009.263

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 December 2017

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