[PDF][PDF] A t (16; 21)(p11; q22) in acute myeloid leukemia (AML) resulting in fusion of the FUS/TLS and ERG genes: a review of the literature
J Buchanan, CA Tirado - J Assoc Genet Technol, 2016 - researchgate.net
Abstract The t (16; 21)(p11; q22) is a rare chromosomal abnormality that appears in
approximately 1% of acute myeloid leukemia (AML) cases. Previously, between 50 and 60 …
approximately 1% of acute myeloid leukemia (AML) cases. Previously, between 50 and 60 …
Molecular analysis of more than 140 gene fusion variants and aberrant activation of EVI1 and TLX1 in hematological malignancies
Gene fusions are observed in abnormal chromosomal rearrangements such as
translocations in hematopoietic malignancies, especially leukemia subtypes. Hence, it is …
translocations in hematopoietic malignancies, especially leukemia subtypes. Hence, it is …
Establishment and characterization of a rare atypical chronic myeloid leukemia cell line NT-1
J Qian, QR Wang, J Liu, SH Jiang, XQ Ni, ZH Lin… - Leukemia Research, 2014 - Elsevier
Human leukemia cell lines are of great value in leukemia research. In this study, we
established and described the biological characteristics of a rare atypical chronic myeloid …
established and described the biological characteristics of a rare atypical chronic myeloid …