(Q38740563)

English

Immunophenotypic, cytogenetic, and mutational characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia

scientific article published on 17 October 2016

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scholarly article

1 reference

Europe PubMed Central

6 September 2017

Immunophenotypic, cytogenetic, and mutational characterization of cell lines derived from myelodysplastic syndrome patients after progression to acute myeloid leukemia (English)

1 reference

Europe PubMed Central

6 September 2017

myelodysplastic syndrome

1 reference

based on heuristic

inferred from title

Jeannine Diesch

5

object named as

Jeannine Diesch

1 reference

Europe PubMed Central

6 September 2017

Hans Guenter Drexler

9

object named as

Hans G Drexler

1 reference

Europe PubMed Central

6 September 2017

author name string

Anna Palau

1

1 reference

Europe PubMed Central

6 September 2017

Mar Mallo

2

1 reference

Europe PubMed Central

6 September 2017

Laura Palomo

3

1 reference

Europe PubMed Central

6 September 2017

Ines Rodríguez-Hernández

4

1 reference

Europe PubMed Central

6 September 2017

Diana Campos

6

1 reference

Europe PubMed Central

6 September 2017

Isabel Granada

7

1 reference

Europe PubMed Central

6 September 2017

Jordi Juncà

8

1 reference

Europe PubMed Central

6 September 2017

Francesc Solé

10

1 reference

Europe PubMed Central

6 September 2017

Marcus Buschbeck

11

1 reference

Europe PubMed Central

6 September 2017

publication date

17 October 2016

1 reference

Europe PubMed Central

6 September 2017

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

6 September 2017

56

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Europe PubMed Central

6 September 2017

243-252

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Europe PubMed Central

6 September 2017

3

1 reference

Europe PubMed Central

6 September 2017

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Single nucleotide polymorphism array karyotyping: a diagnostic and prognostic tool in myelodysplastic syndromes with unsuccessful conventional cytogenetic testing.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Detectable FLT3-ITD or RAS mutation at the time of transformation from MDS to AML predicts for very poor outcomes

1 reference

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21 January 2018

The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Unraveling the molecular pathophysiology of myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Clinical effect of point mutations in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

The development of imatinib as a therapeutic agent for chronic myeloid leukemia

1 reference

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21 January 2018

Disruption of SF3B1 results in deregulated expression and splicing of key genes and pathways in myelodysplastic syndrome hematopoietic stem and progenitor cells.

1 reference

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21 January 2018

Many are called MDS cell lines: one is chosen

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

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/10.1002%2FGCC.22430

21 January 2018

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Epidemiology, classification and prognosis of adults and children with myelodysplastic syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Revised international prognostic scoring system for myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Cytogenetic features in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Landscape of genetic lesions in 944 patients with myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Development and applications of CRISPR-Cas9 for genome engineering

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

The immunophenotype of adult acute myeloid leukemia: high frequency of lymphoid antigen expression and comparison of immunophenotype, French-American-British classification, and karyotypic abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Multiple mechanisms deregulate EZH2 and histone H3 lysine 27 epigenetic changes in myeloid malignancies.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Mutations of IDH1 and IDH2 genes in early and accelerated phases of myelodysplastic syndromes and MDS/myeloproliferative neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

The Sequence Alignment/Map format and SAMtools

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Lenalidomide in the myelodysplastic syndrome with chromosome 5q deletion

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Mutations in CBL occur frequently in juvenile myelomonocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Mutations of e3 ubiquitin ligase cbl family members constitute a novel common pathogenic lesion in myeloid malignancies.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Response to lenalidomide in myelodysplastic syndromes with del(5q): influence of cytogenetics and mutations.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Recurring mutations found by sequencing an acute myeloid leukemia genome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Two acute monocytic leukemia (AML-M5a) cell lines (MOLM-13 and MOLM-14) with interclonal phenotypic heterogeneity showing MLL-AF9 fusion resulting from an occult chromosome insertion, ins(11;9)(q23;p22p23).

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Alterations of p53 and Rb genes in a novel human GM-CSF-dependent myeloid cell line (OHN-GM) established from therapy-related leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Copy neutral loss of heterozygosity: a novel chromosomal lesion in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Targeted deep sequencing improves outcome stratification in chronic myelomonocytic leukemia with low risk cytogenetic features

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Clinical and biological implications of driver mutations in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

FLT3 mutations in acute myeloid leukemia cell lines

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

CD56 antigenic expression in acute myeloid leukemia identifies patients with poor clinical prognosis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Role of casein kinase 1A1 in the biology and targeted therapy of del(5q) MDS.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Cytogenetic Nomenclature: Changes in the ISCN 2013 Compared to the 2009 Edition

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

1,25-dihydroxyvitamin D3 enhances the apoptotic activity of MDM2 antagonist nutlin-3a in acute myeloid leukemia cells expressing wild-type p53.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

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.22430

21 January 2018

Definitions and standards in the diagnosis and treatment of the myelodysplastic syndromes: Consensus statements and report from a working conference

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

The role of histone methyltransferase EZH2 in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Frequent pathway mutations of splicing machinery in myelodysplasia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Clonal architecture of chronic myelomonocytic leukemias

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

21 January 2018

Tandem duplications of the FLT3 receptor gene are associated with leukemic transformation of myelodysplasia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrent genetic defects on chromosome 7q in myeloid neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel homo- and hemizygous mutations in EZH2 in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Establishment of a leukaemic cell line from a patient with acquisition of chromosomal abnormalities during disease progression in myelodysplastic syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Biological characteristics and prognosis of adult acute myeloid leukemia with internal tandem duplications in the Flt3 gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical usefulness of fluorescence in situ hybridization for detection of MLL rearrangements in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22430

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.22430

1 reference

Europe PubMed Central

6 September 2017

1 reference

Europe PubMed Central

6 September 2017

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