A novel gene,FGA7, is fused toRUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Reference37 articles.
1. A unique AML1 (CBF2A) rearrangement, t(1;21)(p32;q22), observed in a patient with acute myelomonocytic leukemia
2. The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family
3. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.
4. PU.1 (Spi-1) and C/EBP alpha regulate expression of the granulocyte-macrophage colony-stimulating factor receptor alpha gene
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1. Neoplasia-associated Chromosome Translocations Resulting in Gene Truncation;Cancer Genomics - Proteomics;2022
2. Identification of a novel fusion gene, RUNX1-PRPF38A , in acute myeloid leukemia;International Journal of Laboratory Hematology;2017-03-06
3. FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia;Oncology Letters;2017-02-08
4. Pediatric T-cell acute lymphoblastic leukemia;Genes, Chromosomes and Cancer;2016-10-25
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