(Q55057111)

16 June 2018

title

NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern. (English)

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16 June 2018

acute megakaryoblastic leukemia

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J D E de Rooij

1

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16 June 2018

I H I M Hollink

2

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16 June 2018

S T C J M Arentsen-Peters

3

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16 June 2018

J F van Galen

4

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16 June 2018

H Berna Beverloo

5

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16 June 2018

A Baruchel

6

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16 June 2018

J Trka

7

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16 June 2018

D Reinhardt

8

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16 June 2018

E Sonneveld

9

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16 June 2018

M Zimmermann

10

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16 June 2018

T A Alonzo

11

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16 June 2018

R Pieters

12

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16 June 2018

S Meshinchi

13

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16 June 2018

M M van den Heuvel-Eibrink

14

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16 June 2018

C Michel Zwaan

15

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16 June 2018

publication date

27 March 2013

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16 June 2018

published in

Leukemia

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16 June 2018

volume

27

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16 June 2018

issue

12

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16 June 2018

page(s)

2280-2288

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16 June 2018

https://scigraph.springernature.com/pub.10.1038/leu.2013.87

exact match

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cites work

Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

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Biology, risk stratification, and therapy of pediatric acute leukemias: an update

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Pediatric acute myeloid leukemia: towards high-quality cure of all patients

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Treatment strategy and long-term results in paediatric patients treated in consecutive UK AML trials

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Genetics of myeloid leukemias

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Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype

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Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

Analysis of NUP98/NSD1 translocations in adult AML and MDS patients

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

Pediatric acute myeloid leukemia with NPM1 mutations is characterized by a gene expression profile with dysregulated HOX gene expression distinct from MLL-rearranged leukemias

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia

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7 January 2021

Characterization of novel genomic alterations and therapeutic approaches using acute megakaryoblastic leukemia xenograft models

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7 January 2021

Childhood and adolescent lymphoid and myeloid leukemia

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7 January 2021

Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel

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7 January 2021

Mononuclear cells contaminating acute lymphoblastic leukaemic samples tested for cellular drug resistance using the methyl-thiazol-tetrazolium assay

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7 January 2021

Prognostically useful gene-expression profiles in acute myeloid leukemia.

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7 January 2021

The heterogeneity of pediatric MLL-rearranged acute myeloid leukemia

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7 January 2021

Evaluation of gene expression signatures predictive of cytogenetic and molecular subtypes of pediatric acute myeloid leukemia

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7 January 2021

A novel NUP98-PHF23 fusion resulting from a cryptic translocation t(11;17)(p15;p13) in acute myeloid leukemia

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

NUP98 gene fusions and hematopoietic malignancies: common themes and new biologic insights

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7 January 2021

Acute megakaryoblastic leukemia in children and adolescents, excluding Down's syndrome: improved outcome with intensified induction treatment

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

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7 January 2021

Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patients.

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

MLL-rearranged leukemia is dependent on aberrant H3K79 methylation by DOT1L.

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

CREB binding protein interacts with nucleoporin-specific FG repeats that activate transcription and mediate NUP98-HOXA9 oncogenicity

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

NUP98-NSD1 links H3K36 methylation to Hox-A gene activation and leukaemogenesis.

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

How chromatin-binding modules interpret histone modifications: lessons from professional pocket pickers

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FLEU.2013.87

7 January 2021

Identifiers

DOI

10.1038/LEU.2013.87

1 reference

16 June 2018

Dimensions Publication ID

1015516040

0 references

1 reference

16 June 2018