Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

M. Sakurai; H. Kasahara; K. Yoshida; A. Yoshimi; H. Kunimoto; N. Watanabe; Y. Shiraishi; K. Chiba; H. Tanaka; Y. Harada; H. Harada; T. Kawakita; M. Kurokawa; S. Miyano; S. Takahashi; S. Ogawa; S. Okamoto; H. Nakajima

doi:10.1038/bcj.2015.81

Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

M. Sakurai, H. Kasahara, K. Yoshida, A. Yoshimi, H. Kunimoto, N. Watanabe, Y. Shiraishi, K. Chiba, H. Tanaka, Y. Harada, H. Harada, T. Kawakita, M. Kurokawa, S. Miyano, S. Takahashi, S. Ogawa, S. Okamoto, H. Nakajima

Research output: Contribution to journal › Letter › peer-review

20 Citations (Scopus)

Original language	English
Article number	e392
Journal	Blood cancer journal
Volume	6
DOIs	https://doi.org/10.1038/bcj.2015.81
Publication status	Published - 2016 Feb 5

ASJC Scopus subject areas

Hematology
Oncology

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Sakurai, M., Kasahara, H., Yoshida, K., Yoshimi, A., Kunimoto, H., Watanabe, N., Shiraishi, Y., Chiba, K., Tanaka, H., Harada, Y., Harada, H., Kawakita, T., Kurokawa, M., Miyano, S., Takahashi, S., Ogawa, S., Okamoto, S., & Nakajima, H. (2016). Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele. Blood cancer journal, 6, [e392]. https://doi.org/10.1038/bcj.2015.81

Sakurai, M, Kasahara, H, Yoshida, K, Yoshimi, A, Kunimoto, H, Watanabe, N, Shiraishi, Y, Chiba, K, Tanaka, H, Harada, Y, Harada, H, Kawakita, T, Kurokawa, M, Miyano, S, Takahashi, S, Ogawa, S, Okamoto, S & Nakajima, H 2016, 'Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele', Blood cancer journal, vol. 6, e392. https://doi.org/10.1038/bcj.2015.81

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title = "Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele",

author = "M. Sakurai and H. Kasahara and K. Yoshida and A. Yoshimi and H. Kunimoto and N. Watanabe and Y. Shiraishi and K. Chiba and H. Tanaka and Y. Harada and H. Harada and T. Kawakita and M. Kurokawa and S. Miyano and S. Takahashi and S. Ogawa and S. Okamoto and H. Nakajima",

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AU - Sakurai, M.

AU - Kasahara, H.

AU - Yoshida, K.

AU - Yoshimi, A.

AU - Kunimoto, H.

AU - Watanabe, N.

AU - Shiraishi, Y.

AU - Chiba, K.

AU - Tanaka, H.

AU - Harada, Y.

AU - Harada, H.

AU - Kawakita, T.

AU - Kurokawa, M.

AU - Miyano, S.

AU - Takahashi, S.

AU - Ogawa, S.

AU - Okamoto, S.

AU - Nakajima, H.

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Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele

ASJC Scopus subject areas

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