(Q80594737)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15382262%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

title

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

1 reference

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1 January 2020

1 reference

5

1 reference

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1 January 2020

Massimo Negrini

8

1 reference

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1 January 2020

author name string

Roberta La Starza

1

1 reference

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1 January 2020

Paolo Gorello

2

1 reference

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1 January 2020

Roberto Rosati

3

1 reference

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1 January 2020

Antonio Riezzo

4

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1 January 2020

Eros Ferrazzi

6

1 reference

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1 January 2020

Massimo F Martelli

7

1 reference

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1 January 2020

Cristina Mecucci

9

1 reference

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1 January 2020

publication date

1 December 2004

1 reference

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Genes, Chromosomes and Cancer

1 January 2020

published in

1 reference

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1 January 2020

volume

41

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1 January 2020

issue

4

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1 January 2020

page(s)

395-399

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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 January 2020

cites work

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7 January 2021

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

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7 January 2021

Successful use of the same slide for consecutive fluorescence in situ hybridization experiments

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7 January 2021

NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes

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7 January 2021

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

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7 January 2021

Molecular characterization of NSD1, a human homologue of the mouse Nsd1 gene

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7 January 2021

Haploinsufficiency of NSD1 causes Sotos syndrome

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7 January 2021

NUP98 gene fusions in hematologic malignancies.

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7 January 2021

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

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7 January 2021

NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15).

1 reference

7 January 2021

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20103

1 reference

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1 January 2020

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