Genetic analysis of TP53 in childhood myelodysplastic syndrome and juvenile myelomonocytic leukemia

Author:

Saito Shoji,Matsuda Kazuyuki,Taira Chiaki,Sano Kenji,Tanaka-Yanagisawa Miyuki,Yanagisawa Ryu,Nakazawa Yozo,Sakashita Kazuo,Shiohara Masaaki,Koike Kenichi

Publisher

Elsevier BV

Subject

Cancer Research,Oncology,Hematology

Reference28 articles.

1. P53 gene mutations in acute myeloid leukemia with 17p monosomy;Fenaux;Blood,1991

2. Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations;Lai;Leukemia,1995

3. Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype;Haferlach;Leukemia,2008

4. International prognostic scoring system and TP53 mutations are independent prognostic indicators for patients with myelodysplastic syndrome;Kita-Sasai;Br J Haematol,2001

5. Study Alliance Leukemia (SAL). The prognostic impact of 17p (p53) deletion in 2272 adults with acute myeloid leukemia;Seifert;Leukemia,2009

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