Identification of a novel fusion gene involvingRUNX1and the antisense strand ofSV2Bin aBCR-ABL1-positive acute leukemia-Reference-Cited by-同舟云学术

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Identification of a novel fusion gene involvingRUNX1and the antisense strand ofSV2Bin aBCR-ABL1-positive acute leukemia

Published:2013-10-03 Issue:12 Volume:52 Page:1114-1122
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Giguère Amélie¹²,Hébert Josée¹²

Affiliation:

1. Quebec Leukemia Cell Bank and Hematology-Oncology Division; Maisonneuve-Rosemont Hospital; 5415 L'Assomption Blvd., Montréal H1T 2M4 Canada

2. Department of Medicine; Université de Montréal; C.P. 6128, succursale Centre-ville, Montréal H3C 3J7 Canada

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gcc.22105/fullpdf

Reference32 articles.

1. Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome;Agerstam;Genes Chromosomes Cancer,2007

2. Simultaneous occurrence of ETV6-RUNX1 and BCR-ABL1 (e1a2) transcripts in a child with B-cell acute lymphoblastic leukemia;Balatzenko;Cancer Genet,2013

3. Elucidation of a novel pathogenomic mechanism using genome-wide long mate-pair sequencing of a congenital t(16;21) in a series of three RUNX1-mutated FPD/AML pedigrees;Buijs;Leukemia,2012

4. Runx1 isoforms show differential expression patterns during hematopoietic development but have similar functional effects in adult hematopoietic stem cells;Challen;Exp Hematol,2010

5. Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter;Chen;Nature,2009

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neoplasia-associated Chromosome Translocations Resulting in Gene Truncation;Cancer Genomics - Proteomics;2022

2. Bioinformatics analysis of potential core genes for glioblastoma;Bioscience Reports;2020-07

3. Truncated RUNX1 Generated by the Fusion of RUNX1 to Antisense GRIK2 via a Cryptic Chromosome Translocation Enhances Sensitivity to Granulocyte Colony-Stimulating Factor;Cytogenetic and Genome Research;2020

4. Identification of a novel fusion gene, RUNX1-PRPF38A , in acute myeloid leukemia;International Journal of Laboratory Hematology;2017-03-06

5. FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia;Oncology Letters;2017-02-08

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