(Q82480890)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

editorial

0 references

title

Myelodysplastic syndromes: lost between two states? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

C Acquaviva

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

V Gelsi-Boyer

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

publication date

1 January 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

page(s)

1-5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20068572%20AND%20SRC:MED&resulttype=core&format=json

The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: rationale and important changes

16 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Gene silencing by DNA methylation in haematological malignancies

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

DNA methylation profiling of myelodysplastic syndrome hematopoietic progenitor cells during in vitro lineage-specific differentiation.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Aberrant promotor methylation in MDS hematopoietic cells during in vitro lineage specific differentiation is differently associated with DNMT isoforms

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Apoptotic pathways to death in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

SNP array karyotyping allows for the detection of uniparental disomy and cryptic chromosomal abnormalities in MDS/MPD-U and MPD.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

250K single nucleotide polymorphism array karyotyping identifies acquired uniparental disomy and homozygous mutations, including novel missense substitutions of c-Cbl, in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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.2009.157

7 January 2021

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

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Genome-wide DNA-mapping of CD34+ cells from patients with myelodysplastic syndrome using 500K SNP arrays identifies significant regions of deletion and uniparental disomy

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Mutation in TET2 in myeloid cancers

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Detection of mutant TET2 in myeloid malignancies other than myeloproliferative neoplasms: CMML, MDS, MDS/MPN and AML.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Acquired mutations in TET2 are common in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Characterization of Asxl1, a murine homolog of Additional sex combs, and analysis of the Asx-like gene family

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Functional conservation of Asxl2, a murine homolog for the Drosophila enhancer of trithorax and polycomb group gene Asx

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Additional sex comb-like 1 (ASXL1), in cooperation with SRC-1, acts as a ligand-dependent coactivator for retinoic acid receptor

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Deletion 5q in myelodysplastic syndrome: a paradigm for the study of hemizygous deletions in cancer

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Genome profiling of acute myelomonocytic leukemia: alteration of the MYB locus in MYST3-linked cases

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Functional involvement of RINF, retinoid-inducible nuclear factor (CXXC5), in normal and tumoral human myelopoiesis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

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.2009.157

7 January 2021

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.2009.157

7 January 2021

Fluorescence in situ hybridization characterization of ider(20q) in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

L3MBTL1, a histone-methylation-dependent chromatin lock

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Epigenetic silencing of the tumor suppressor microRNA Hsa-miR-124a regulates CDK6 expression and confers a poor prognosis in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

MicroRNA-29b induces global DNA hypomethylation and tumor suppressor gene reexpression in acute myeloid leukemia by targeting directly DNMT3A and 3B and indirectly DNMT1.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Tumor suppressor gene inactivation in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Polycomb complexes repress developmental regulators in murine embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Control of developmental regulators by Polycomb in human embryonic stem cells

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Stem cell regulation by polycomb repressors: postponing commitment

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Biochemical mechanisms of gene regulation by polycomb group protein complexes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Genetic and epigenetic alterations in myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Transformation from committed progenitor to leukaemia stem cell initiated by MLL-AF9.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

MLL translocations, histone modifications and leukaemia stem-cell development

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Chromatin maps, histone modifications and leukemia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

The PHD finger, a nuclear protein-interaction domain

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

PHD fingers in human diseases: disorders arising from misinterpreting epigenetic marks

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

The emerging functions of histone demethylases

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

A histone H3 lysine 27 demethylase regulates animal posterior development

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Control of differentiation in a self-renewing mammalian tissue by the histone demethylase JMJD3

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

SMRT-mediated repression of an H3K27 demethylase in progression from neural stem cell to neuron

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Polycomb complexes and epigenetic states

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

H3K79 methylation profiles define murine and human MLL-AF4 leukemias

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Aberrant chromatin at genes encoding stem cell regulators in human mixed-lineage leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Haematopoietic malignancies caused by dysregulation of a chromatin-binding PHD finger

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

NUP98-HOX translocations lead to myelodysplastic syndrome in mice and men

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

The AML1-ETO fusion gene and the FLT3 length mutation collaborate in inducing acute leukemia in mice

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Role of nucleophosmin in embryonic development and tumorigenesis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Histone demethylase JMJD3 contributes to epigenetic control of INK4a/ARF by oncogenic RAS

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

The H3K27me3 demethylase JMJD3 contributes to the activation of the INK4A-ARF locus in response to oncogene- and stress-induced senescence

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Altered nucleophosmin transport in acute myeloid leukaemia with mutated NPM1: molecular basis and clinical implications.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

TET2 mutations and their clinical correlates in polycythemia vera, essential thrombocythemia and myelofibrosis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Frequent TET2 mutations in systemic mastocytosis: clinical, KITD816V and FIP1L1-PDGFRA correlates

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Mutations of ASXL1 gene in myeloproliferative neoplasms.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021

Frequent CBL mutations associated with 11q acquired uniparental disomy in myeloproliferative neoplasms

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.157

7 January 2021