(Q44123939)

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NUP98-NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia

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Europe PubMed Central

PubMed publication ID

30 November 2017

NUP98-NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia (English)

1 reference

Europe PubMed Central

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30 November 2017

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Norio Shiba

1

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Europe PubMed Central

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30 November 2017

Hitoshi Ichikawa

2

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30 November 2017

Tomohiko Taki

3

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30 November 2017

Myoung-Ja Park

4

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30 November 2017

Aoi Jo

5

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30 November 2017

Sachiyo Mitani

6

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30 November 2017

Tohru Kobayashi

7

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30 November 2017

Akira Shimada

8

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30 November 2017

Manabu Sotomatsu

9

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30 November 2017

Hirokazu Arakawa

10

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30 November 2017

Souichi Adachi

11

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30 November 2017

Akio Tawa

12

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30 November 2017

Keizo Horibe

13

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30 November 2017

Masahiro Tsuchida

14

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30 November 2017

Ryoji Hanada

15

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30 November 2017

Ichiro Tsukimoto

16

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30 November 2017

Yasuhide Hayashi

17

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30 November 2017

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30 April 2013

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30 November 2017

Genes, Chromosomes and Cancer

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30 November 2017

52

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30 November 2017

7

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30 November 2017

683-693

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30 November 2017

Prdm16 is a physiologic regulator of hematopoietic stem cells.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

A cryptic t(5;11)(q35;p15.5) in 2 children with acute myeloid leukemia with apparently normal karyotypes, identified by a multiplex fluorescence in situ hybridization telomere assay

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Cluster analysis and display of genome-wide expression patterns

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Genetics of myeloid malignancies: pathogenetic and clinical implications

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

The pathophysiology of HOX genes and their role in cancer.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Prospective study of a pirarubicin, intermediate-dose cytarabine, and etoposide regimen in children with Down syndrome and acute myeloid leukemia: the Japanese Childhood AML Cooperative Study Group

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Molecular genetics of adult acute myeloid leukemia: prognostic and therapeutic implications

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Deletion of IKZF1 and prognosis in acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

NUP98 fusion in human leukemia: dysregulation of the nuclear pore and homeodomain proteins

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Genetic alterations activating kinase and cytokine receptor signaling in high-risk acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Risk-stratified therapy and the intensive use of cytarabine improves the outcome in childhood acute myeloid leukemia: the AML99 trial from the Japanese Childhood AML Cooperative Study Group

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Acquired copy number alterations in adult acute myeloid leukemia genomes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

21 January 2018

Cryptic t(5;11)(q35;p15.5) in adult de novo acute myelocytic leukemia with normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequency of NUP98-NSD1 fusion transcript in childhood acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Common gene expression signatures in t(8;21)- and inv(16)-acute myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Prospective study of a therapeutic regimen with all‐trans retinoic acid and anthracyclines in combination of cytarabine in children with acute promyelocytic leukaemia: the Japanese childhood acute myeloid leukaemia cooperative study

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.22064

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.22064

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 November 2017

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