NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis
Authors
Keywords
-
Journal
LEUKEMIA
Volume 31, Issue 3, Pages 565-572
Publisher
Springer Nature
Online
2016-10-03
DOI
10.1038/leu.2016.267
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Recurrent abnormalities can be used for risk group stratification in pediatric AMKL: a retrospective intergroup study
- (2016) Jasmijn D. E. de Rooij et al. BLOOD
- Identification of MYC mutations in acute myeloid leukemias with NUP98–NSD1 translocations
- (2016) V-P Lavallée et al. LEUKEMIA
- Collaborative Efforts Driving Progress in Pediatric Acute Myeloid Leukemia
- (2015) C. Michel Zwaan et al. JOURNAL OF CLINICAL ONCOLOGY
- Identification of the NUP98-PHF23 fusion gene in pediatric cytogenetically normal acute myeloid leukemia by whole-transcriptome sequencing
- (2015) Marco Togni et al. Journal of Hematology & Oncology
- NUP98/NSD1 and FLT3/ITD coexpression is more prevalent in younger AML patients and leads to induction failure: a COG and SWOG report
- (2014) F. Ostronoff et al. BLOOD
- Potent co-operation between the NUP98-NSD1 fusion and the FLT3-ITD mutation in acute myeloid leukemia induction
- (2014) A. Thanasopoulou et al. HAEMATOLOGICA
- NUP98-NSD1fusion in association withFLT3-ITD mutation identifies a prognostically relevant subgroup of pediatric acute myeloid leukemia patients suitable for monitoring by real time quantitative PCR
- (2013) Susanna Akiki et al. GENES CHROMOSOMES & CANCER
- Improved Outcome in Pediatric Relapsed Acute Myeloid Leukemia: Results of a Randomized Trial on Liposomal Daunorubicin by the International BFM Study Group
- (2013) Gertjan J.L. Kaspers et al. JOURNAL OF CLINICAL ONCOLOGY
- POU1F1 is a novel fusion partner of NUP98 in acute myeloid leukemia with t(3;11)(p11;p15)
- (2013) Susana Lisboa et al. Molecular Cancer
- Identification of GSX2 and AF10 as NUP98 partner genes in myeloid malignancies
- (2013) G Soler et al. Blood Cancer Journal
- TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions
- (2013) Daehwan Kim et al. GENOME BIOLOGY
- Diagnosis and management of acute myeloid leukemia in children and adolescents: recommendations from an international expert panel
- (2012) U. Creutzig et al. BLOOD
- A rare but specific subset of adult AML patients can be defined by the cytogenetically cryptic NUP98–NSD1 fusion gene
- (2012) A Fasan et al. LEUKEMIA
- Analysis of NUP98/NSD1 translocations in adult AML and MDS patients
- (2012) F Thol et al. LEUKEMIA
- Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks
- (2012) Cole Trapnell et al. Nature Protocols
- NUP98 gene fusions and hematopoietic malignancies: common themes and new biologic insights
- (2011) S. M. Gough et al. BLOOD
- NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern
- (2011) I. H. I. M. Hollink et al. BLOOD
- The Structure of NSD1 Reveals an Autoregulatory Mechanism Underlying Histone H3K36 Methylation
- (2011) Qi Qiao et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- High frequencies of simultaneous FLT3-ITD, WT1 and KIT mutations in hematological malignancies with NUP98-fusion genes
- (2010) T Taketani et al. LEUKEMIA
- 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
- (2009) W-C Chou et al. LEUKEMIA
- Haematopoietic malignancies caused by dysregulation of a chromatin-binding PHD finger
- (2009) Gang G. Wang et al. NATURE
- Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia
- (2009) I. Radtke et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Monosomal Karyotype in Acute Myeloid Leukemia: A Better Indicator of Poor Prognosis Than a Complex Karyotype
- (2008) Dimitri A. Breems et al. JOURNAL OF CLINICAL ONCOLOGY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started