(Q45405305)

English

From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype

scientific article published on 17 January 2012

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scholarly article

1 reference

Europe PubMed Central

14 December 2017

From cryptic chromosomal lesions to pathologically relevant genes: integration of SNP-array with gene expression profiling in myelodysplastic syndrome with normal karyotype (English)

1 reference

Europe PubMed Central

14 December 2017

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myelodysplastic syndrome

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based on heuristic

inferred from title

7

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Europe PubMed Central

14 December 2017

Kyra Michalová

9

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Europe PubMed Central

14 December 2017

Michaela Dostalova Merkerova

object named as

Michaela Dostalova Merkerova

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Zuzana Zemanová

object named as

Zuzana Zemanova

5

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author name string

Dagmar Bystricka

2

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Europe PubMed Central

14 December 2017

Monika Belickova

3

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Europe PubMed Central

14 December 2017

Zdenek Krejcik

4

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Europe PubMed Central

14 December 2017

Jaroslav Polak

6

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Europe PubMed Central

14 December 2017

Jana Brezinova

8

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Europe PubMed Central

14 December 2017

Jaroslav Cermak

10

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14 December 2017

publication date

17 January 2012

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Europe PubMed Central

14 December 2017

Genes, Chromosomes and Cancer

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Europe PubMed Central

14 December 2017

51

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14 December 2017

5

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14 December 2017

419-428

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Europe PubMed Central

14 December 2017

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

The human SWI/SNF complex associates with RUNX1 to control transcription of hematopoietic target genes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Clinical effect of point mutations in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Real-time quantitative polymerase chain reaction detection of minimal residual disease by standardized WT1 assay to enhance risk stratification in acute myeloid leukemia: a European LeukemiaNet study.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

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/10.1002%2FGCC.21927

21 January 2018

Cytogenetic features in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Pathogenesis and consequences of uniparental disomy in cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Novel TET2 mutations associated with UPD4q24 in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Pathobiology, classification, and diagnosis of myelodysplastic syndrome

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https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Prognostic impact of SNP array karyotyping in myelodysplastic syndromes and related myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

A distinct expression of various gene subsets in CD34+ cells from patients with early and advanced myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

Tribbles in disease: Signaling pathways important for cellular function and neoplastic transformation

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

The presence of clonal cell subpopulations in peripheral blood and bone marrow of patients with refractory cytopenia with multilineage dysplasia but not in patients with refractory anemia may reflect a multistep pathogenesis of myelodysplasia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

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/10.1002%2FGCC.21927

7 January 2021

based on heuristic

inferred from DOI database lookup

Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia (AML) with a normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

7 January 2021

based on heuristic

inferred from DOI database lookup

Copy number alterations at polymorphic loci may be acquired somatically in patients with myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

7 January 2021

based on heuristic

inferred from DOI database lookup

del11(p11-13) with overexpression of Wilms' tumor gene during leukemic transformation of myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.21927

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.21927

1 reference

Europe PubMed Central

14 December 2017

1 reference

Europe PubMed Central

14 December 2017

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