Frequent rearrangements of retinoic acid receptor alpha gene and myl gene, and rare mutations of RAS and FMS genes in acute promyelocytic leukemia
Author:
Publisher
Wiley
Subject
Hematology
Reference36 articles.
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2. : “Catalog of Chromosome Aberrations in Cancer,” 3rd Ed. New York: Alan R. Liss; 1988.
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4. Molecular Analysis of Acute Promyelocytic Leukemia Breakpoint Cluster Region on Chromosome 17
5. Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus.
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1. NRAS mutations are rare in acute myeloid leukaemias with t(8;21) or inv(16);European Journal of Haematology;2009-04-24
2. Secondary near-tetraploidy with double der(15)t(15;17) in acute promyelocytic leukemia in relapse;Cancer Genetics and Cytogenetics;2004-03
3. Fusion ofMLL andMSF in Adult De Novo Acute Myelomonocytic Leukemia (M4) with T(11;17)(Q23;Q25);International Journal of Hematology;2002-06
4. Anticoagulant effects of retinoic acids on leukemia cells;Blood;1996-01-15
5. The Biologic Function of PML and its Role in Acute Promyelocytic Leukemia;Leukemia & Lymphoma;1996-01
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