(Q38337753)

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Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance

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scholarly article

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Europe PubMed Central

2 September 2017

Comprehensive array CGH of normal karyotype myelodysplastic syndromes reveals hidden recurrent and individual genomic copy number alterations with prognostic relevance (English)

1 reference

Europe PubMed Central

2 September 2017

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author name string

A Thiel

1

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Europe PubMed Central

2 September 2017

M Beier

2

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Europe PubMed Central

2 September 2017

D Ingenhag

3

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Europe PubMed Central

2 September 2017

K Servan

4

1 reference

Europe PubMed Central

2 September 2017

M Hein

5

1 reference

Europe PubMed Central

2 September 2017

V Moeller

6

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Europe PubMed Central

2 September 2017

B Betz

7

1 reference

Europe PubMed Central

2 September 2017

B Hildebrandt

8

1 reference

Europe PubMed Central

2 September 2017

C Evers

9

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2 September 2017

U Germing

10

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2 September 2017

B Royer-Pokora

11

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2 September 2017

publication date

28 January 2011

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Europe PubMed Central

2 September 2017

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Europe PubMed Central

2 September 2017

25

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2 September 2017

387-399

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2 September 2017

3

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2 September 2017

https://scigraph.springernature.com/pub.10.1038/leu.2010.293

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Proposals for the classification of the myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

High-resolution genomic arrays facilitate detection of novel cryptic chromosomal lesions in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival.

1 reference

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21 January 2018

Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array CGH.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Detection of cryptic chromosomal lesions including acquired segmental uniparental disomy in advanced and low-risk myelodysplastic syndromes

1 reference

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21 January 2018

Accurate detection of uniparental disomy and microdeletions by SNP array analysis in myelodysplastic syndromes with normal cytogenetics

1 reference

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Genomic profiling and identification of high-risk uveal melanoma by array CGH analysis of primary tumors and liver metastases

1 reference

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21 January 2018

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

1 reference

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Genetic characterization of TET1, TET2, and TET3 alterations in myeloid malignancies

1 reference

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EGO, a novel, noncoding RNA gene, regulates eosinophil granule protein transcript expression

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21 January 2018

WWOX: its genomics, partners, and functions

1 reference

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High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

1 reference

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21 January 2018

LRRK2 modulates vulnerability to mitochondrial dysfunction in Caenorhabditis elegans

1 reference

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21 January 2018

Loss of heterozygosity 4q24 and TET2 mutations associated with myelodysplastic/myeloproliferative neoplasms

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Acquired mutations in TET2 are common in myelodysplastic syndromes

1 reference

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21 January 2018

Mutation in TET2 in myeloid cancers

1 reference

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21 January 2018

Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs).

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Haploinsufficiency of EGR1, a candidate gene in the del(5q), leads to the development of myeloid disorders

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Human mortalin (HSPA9): a candidate for the myeloid leukemia tumor suppressor gene on 5q31

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Integrated genomic analysis implicates haploinsufficiency of multiple chromosome 5q31.2 genes in de novo myelodysplastic syndromes pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

A critical role for phosphatase haplodeficiency in the selective suppression of deletion 5q MDS by lenalidomide

1 reference

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21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

21 January 2018

Mutation analysis of transferrin-receptor 2 in patients with atypical hemochromatosis.

1 reference

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21 January 2018

Receptor tyrosine kinase, EphB4 (HTK), accelerates differentiation of select human hematopoietic cells

1 reference

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The ephrinB2/EphB4 axis is dysregulated in osteoprogenitors from myeloma patients and its activation affects myeloma bone disease and tumor growth

1 reference

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Core-binding factors in haematopoiesis and leukaemia

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SNP array analysis in hematologic malignancies: avoiding false discoveries

1 reference

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Time-dependent prognostic scoring system for predicting survival and leukemic evolution in myelodysplastic syndromes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

7 January 2021

based on heuristic

inferred from DOI database lookup

Mortalin is a novel mediator of erythropoietin signaling

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

7 January 2021

based on heuristic

inferred from DOI database lookup

Delineation of multiple deleted regions in 7q in myeloid disorders

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2010.293

7 January 2021

based on heuristic

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Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH

1 reference

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based on heuristic

inferred from DOI database lookup

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10.1038/LEU.2010.293

1 reference

Europe PubMed Central

2 September 2017

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1 reference

Europe PubMed Central

2 September 2017

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