Chronic Myeloid Leukemia With Rare Variant b2a3 (e13a3) BCR-ABL1 Fusion
Author:
Affiliation:
1. Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
2. Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea
Funder
National Research Foundation of Korea
Ministry of Education, Science and Technology
Publisher
Annals of Laboratory Medicine
Subject
Biochemistry, medical,Clinical Biochemistry,General Medicine
Link
http://synapse.koreamed.org/pdf/10.3343/alm.2016.36.3.287
Reference10 articles.
1. Chronic myelogenous leukemia with e13a3 (b2a3) type of BCR-ABL transcript having a DNA breakpoint betweenABL exons a2 and a3
2. CML patient with rare b2a3 (e13a3) variant of BCR–ABL transcript: Complete molecular response to imatinib
3. Complete cytogenetic and molecular response after imatinib treatment for chronic myeloid leukemia in a patient with atypical karyotype and BCR-ABL b2a3 transcript
4. A chronic myeloid leukemia patient with atypical karyotype and BCR–ABL e13a3 transcript caused by complex chromosome rearrangement
5. A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes
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1. Impact of the Breakpoint Region on the Leukemogenic Potential and the TKI Responsiveness of Atypical BCR-ABL1 Transcripts;Frontiers in Pharmacology;2021-06-30
2. Clinical characteristics and prognostic significance of chronic myeloid leukemia with rare BCR-ABL1 transcripts;Leukemia & Lymphoma;2019-07-01
3. Molecular Monitoring in Adult Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia with the Variant e13a3 BCR-ABL1 Fusion;Case Reports in Hematology;2019-06-27
4. Blast crisis of chronic myeloid leukemia with plasmacytoid dendritic cell phenotype associated with a rare fusion transcript, e13a3 BCR–ABL1;Leukemia & Lymphoma;2019-06-11
5. Chronic myeloid leukemia with a rare fusion transcript, b2a3 (e13a3) BCR–ABL1: A report of four cases from India;South Asian Journal of Cancer;2019-04
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