Are PU.1 mutations frequent genetic events in acute myeloid leukemia (AML)?
Author:
Affiliation:
1. Correspondence: Docteur C. Preudhomme, UnitéINSERM U524 and Laboratoire d'Hématologie A, 1, Place de Verdun, 59037 Lille, France; e-mail:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/100/13/4680/1256820/h82402004676d.pdf
Reference5 articles.
1. Heterozygous PU.1 mutations are associated with acute myeloid leukemia.;Mueller;Blood.,2002
2. Proposals for the classification of acute leukemias, a report of the French-American-British Cooperative Group.;Benett;Br J Haematol.,1976
3. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction.;Orita;Genomics.,1989
4. C/EBPβ, C/EBPδ, PU.1, AML1 genes: mutational analysis in 381 samples of hematopoietic and solid malignancies.;Vegesna;Leukemia Res.,2002
5. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2αB gene associated with myeloblastic leukemias.;Osato;Blood.,1999
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