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Genes, Chromosomes & Cancer|May 1, 2013
NUP98-NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemiaNorio Shiba, Hitoshi Ichikawa, Tomohiko Taki, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 12, 2011
Galectin-3 (Gal-3) induced by leukemia microenvironment promotes drug resistance and bone marrow lodgment in chronic myelogenous leukemiaMio Yamamoto-Sugitani, Junya Kuroda, Eishi Ashihara, et al.
British Journal of Haematology|July 22, 2014
Acute myeloid leukaemia with myelodysplastic features in children: a report of Japanese Paediatric Leukaemia/Lymphoma Study GroupAkitoshi Kinoshita, Hayato Miyachi, Hiromichi Matsushita, et al.
Human Genetics|April 1, 2003
Polymorphisms in the MLL breakpoint cluster region (BCR)Deborah R Echlin-Bell, Lydia L Smith, Loretta Li, et al.
Leukemia Research|July 2, 2013
CD56 expression is an independent prognostic factor for relapse in acute myeloid leukemia with t(8;21)Noriyoshi Iriyama, Yoshihiro Hatta, Jin Takeuchi, et al.
Pediatric Blood & Cancer|May 3, 2016
CXCR4 Overexpression is a Poor Prognostic Factor in Pediatric Acute Myeloid Leukemia With Low Risk: A Report From the Japanese Pediatric Leukemia/Lymphoma Study GroupHidemasa Matsuo, Naomi Nakamura, Daisuke Tomizawa, et al.
Pediatric Blood & Cancer|December 6, 2023
High IL2RA/CD25 expression is a prognostic stem cell biomarker for pediatric acute myeloid leukemia without a core-binding factorTakahiro Aoki, Norio Shiba, Shinichi Tsujimoto, et al.
Genes, Chromosomes & Cancer|January 8, 2017
Prognostic impact of specific molecular profiles in pediatric acute megakaryoblastic leukemia in non-Down syndromeYusuke Hara, Norio Shiba, Kentaro Ohki, et al.
Annals of Hematology|January 21, 2014
Normal karyotype acute myeloid leukemia with the CD7+ CD15+ CD34+ HLA-DR + immunophenotype is a clinically distinct entity with a favorable outcomeNoriyoshi Iriyama, Norio Asou, Yasushi Miyazaki, et al.
Blood|June 21, 2003
Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndromeGang Xu, Masumi Nagano, Rika Kanezaki, et al.
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