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Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.
Shiba N, Yoshida K, Shiraishi Y, Okuno Y, Yamato G, Hara Y, Nagata Y, Chiba K, Tanaka H, Terui K, Kato M, Park MJ, Ohki K, Shimada A, Takita J, Tomizawa D, Kudo K, Arakawa H, Adachi S, Taga T, Tawa A, Ito E, Horibe K, Sanada M, Miyano S, Ogawa S, Hayashi Y. Shiba N, et al. Among authors: horibe k. Br J Haematol. 2016 Nov;175(3):476-489. doi: 10.1111/bjh.14247. Epub 2016 Jul 29. Br J Haematol. 2016. PMID: 27470916 Free article.
Etoposide-related acute promyelocytic leukemia.
Kudo K, Yoshida H, Kiyoi H, Numata S, Horibe K, Naoe T. Kudo K, et al. Among authors: horibe k. Leukemia. 1998 Aug;12(8):1171-5. doi: 10.1038/sj.leu.2401089. Leukemia. 1998. PMID: 9697869 Review.
Absence of mutations in the granulocyte colony-stimulating factor (G-CSF) receptor gene in patients with myelodysplastic syndrome/acute myeloblastic leukaemia occurring after treatment of aplastic anaemia with G-CSF.
Kudo K, Nagai H, Numata S, Ichihara M, Kinoshita T, Horibe K, Kato K, Matsuyama T, Kodera Y, Kojima S. Kudo K, et al. Among authors: horibe k. Br J Haematol. 2000 Nov;111(2):656-8. doi: 10.1046/j.1365-2141.2000.02370.x. Br J Haematol. 2000. PMID: 11122117 Free article.
417 results