Heterozygous PU.1 mutations are associated with acute myeloid leukemia-Reference-Cited by-同舟云学术

Heterozygous PU.1 mutations are associated with acute myeloid leukemia

Published:2003-03-01 Issue:5 Volume:101 Page:2074-2074
ISSN:1528-0020
Container-title:Blood
language:en
Short-container-title:

Author:

Mueller Beatrice U.¹,Pabst Thomas¹,Osato Motomi¹,Asou Norio¹,Johansen Lisa M.¹,Minden Mark D.¹,Behre Gerhard¹,Hiddemann Wolfgang¹,Ito Yoshiaki¹,Tenen Daniel G.¹

Affiliation:

1. Correspondence: Daniel G. Tenen, Harvard Institutes of Medicine, Rm 954, 77 Avenue Louis Pasteur, Boston, MA 02115; e-mail:

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/101/5/2074/1262429/h80503002070f.pdf

Reference8 articles.

1. Are PU.1 mutations frequent genetic events in acute myeloid leukemia (AML)? [letter].;Lamandin;Blood.,2002

2. Heterozygous PU.1 mutations are associated with acute myeloid leukemia.;Mueller;Blood.,2002

3. Dominant negative mutations of CEBPA, encoding CCAAT/Enhancer Binding Protein alpha (C/EBP alpha), in acute myeloid leukemia.;Pabst;Nat Genet.,2001

4. Mutations in the gene encoding the transcription factor CCAAT/enhancer binding protein alpha in myelodysplastic syndromes and acute myeloid leukemias.;Gombart;Blood.,2002

5. Favorable prognostic significance of CEBPA mutations in patients with de novo acute myeloid leukemia: a study from the Acute Leukemia French Association (ALFA).;Preudhomme;Blood.,2002

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