Identification ofNUP98 abnormalities in acute leukemia:JARID1A (12p13) as a new partner gene-Reference-Cited by-同舟云学术

Identification ofNUP98 abnormalities in acute leukemia:JARID1A (12p13) as a new partner gene

Published:2006 Issue:5 Volume:45 Page:437-446
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

van Zutven Laura J. C. M.,Önen Emine,Velthuizen Sandra C. J. M.,van Drunen Ellen,von Bergh Anne R. M.,van den Heuvel-Eibrink Marry M.,Veronese Angelo,Mecucci Cristina,Negrini Massimo,de Greef Georgine E.,Beverloo H. Berna

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference40 articles.

1. The t(11;20)(p15;q11) Chromosomal Translocation Associated With Therapy-Related Myelodysplastic Syndrome Results in anNUP98-TOP1 Fusion

2. The inv(11)(p15q22) Chromosome Translocation of De Novo and Therapy-Related Myeloid Malignancies Results in Fusion of the Nucleoporin Gene, NUP98, With the Putative RNA Helicase Gene, DDX10

3. Overview

4. The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9

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