Literature DB >> 24497566

Reply to "rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases". Haematologica 2014;99(2):e20-21.

Jason H Mendler1, Guido Marcucci, Clara D Bloomfield.   

Abstract

Entities:  

Keywords:  NPM1; RUNX1; acute myeloid leukemia; germline; mutational interrelationships

Mesh：

Substances：

Year:  2014        PMID： 24497566      PMCID： PMC3912980          DOI： 10.3324/haematol.2013.100669

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  2 in total

1.  In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline.

Authors:  Jason H Mendler; Kati Maharry; Heiko Becker; Ann-Kathrin Eisfeld; Leigha Senter; Krzysztof Mrózek; Jessica Kohlschmidt; Klaus H Metzeler; Sebastian Schwind; Susan P Whitman; Jihane Khalife; Michael A Caligiuri; Rebecca B Klisovic; Joseph O Moore; Thomas H Carter; Guido Marcucci; Clara D Bloomfield
Journal:  Haematologica       Date:  2013-06-10       Impact factor: 9.941

2.  Rare coincident NPM1 and RUNX1 mutations in intermediate risk acute myeloid leukemia display similar patterns to single mutated cases.

Authors:  Annette Fasan; Claudia Haferlach; Alexander Kohlmann; Frank Dicker; Christiane Eder; Wolfgang Kern; Torsten Haferlach; Susanne Schnittger
Journal:  Haematologica       Date:  2014-02       Impact factor: 9.941
  2 in total

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