Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Kenji Tokunaga"'
Autor:
Hiro Tatetsu, Miho Watanabe, Jun Liu, Kenji Tokunaga, Eisaku Iwanaga, Yoshihiro Komohara, Emily Thrash, Mahmoud A. Bassal, Masao Matsuoka, Daniel G. Tenen, Li Chai
Publikováno v:
Clinical and Translational Medicine, Vol 13, Iss 8, Pp n/a-n/a (2023)
Externí odkaz:
https://doaj.org/article/099f8f72f1da49b2a589a82379113b48
Autor:
Asuka Ono, Yuki Kitano, Katsunori Imai, Takashi Matsumoto, Shinya Endo, Kenji Tokunaga, Hiromitsu Hayashi, Yo-Ichi Yamashita, Masao Matsuoka, Hideo Baba
Publikováno v:
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Abstract Background Myeloid sarcoma (MS) is a rare disease, mostly found in conjunction with acute myelogenous leukemia or other diseases, and primary nonleukemic MS of the spleen is particularly rare. Case presentation We report a 57-year-old male w
Externí odkaz:
https://doaj.org/article/a44fa9c738b44f37a338db2d9ac46812
Autor:
Sho Kubota, Kenji Tokunaga, Tomohiro Umezu, Takako Yokomizo-Nakano, Yuqi Sun, Motohiko Oshima, Kar Tong Tan, Henry Yang, Akinori Kanai, Eisaku Iwanaga, Norio Asou, Takahiro Maeda, Naomi Nakagata, Atsushi Iwama, Kazuma Ohyashiki, Motomi Osato, Goro Sashida
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-16 (2019)
Translocation of (6;8)(p21;q24), a recurrent abnormality of blastic plasmacytoid dendritic cell neoplasm, involves adjacent MYC and RUNX2 regions. Here, the authors show that the RUNX2 super-enhancer is hijacked to activate MYC in addition to RUNX2 e
Externí odkaz:
https://doaj.org/article/b55f6237adba4583b97db796afe3c64f
Autor:
Sho Kubota, Kenji Tokunaga, Tomohiro Umezu, Takako Yokomizo-Nakano, Yuqi Sun, Motohiko Oshima, Kar Tong Tan, Henry Yang, Akinori Kanai, Eisaku Iwanaga, Norio Asou, Takahiro Maeda, Naomi Nakagata, Atsushi Iwama, Kazuma Ohyashiki, Motomi Osato, Goro Sashida
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://doaj.org/article/a9f5b6ded55344b394d22695b04a566d
Autor:
Hiro Tatetsu, Miho Watanabe, Jun Liu, Kenji Tokunaga, Eisaku Iwanaga, Yoshihiro Komohara, Emily Thrash, Matsuoka Masao, Daniel G. Tenen, Li Chai
Myelodysplastic syndrome (MDS) is a group of heterogeneous diseases characterized by cytologic dysplasia and cytopenias resulting from ineffective hematopoiesis. Oncofetal protein SALL4 is a known oncogene in MDS and its baseline expression level ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::507016bb21bb01e780992ae6248866e6
https://doi.org/10.1101/2022.12.05.518121
https://doi.org/10.1101/2022.12.05.518121
Autor:
Chelsia Qiuxia Wang, Motomi Osato, Sayed Hamada Madboly, Norio Asou, Kimi Araki, Eisaku Iwanaga, Masao Matsuoka, Naomi Nakagata, Takako Ideue, Kenji Tokunaga, Tomomasa Yokomizo, Mariko Morii, Vania Swee Imm Teoh, Abdellah Abosrie Ali Omar, Takako Yokomizo, Goro Sashida, Akiko Niibori-Nambu, Mohamed Gaber Abdallah, Sho Kubota, Mabrouk Mahmoud Aboelenin, Michelle Meng Huang Mok
Publikováno v:
Leukemia
Autor:
Tatsuya Morishima, Koichi Takahashi, Desmond Wai Loon Chin, Kenji Tokunaga, Yuichiro Arima, Masao Matsuoka, Toshio Suda, Hitoshi Takizawa
Publikováno v:
Blood. 140:3012-3013
Autor:
Yoshitaka Inoue, Kenji Tokunaga, Masao Matsuoka, Shinya Endo, Kouta Iwanaga, Yukiko Kimura, Yousuke Nagahata, Hiroshi Kawamoto, Eisaku Iwanaga, Kyoko Masuda
Publikováno v:
European Journal of Haematology. 106:327-339
Objectives CCAAT/enhancer-binding protein α (CEBPA) is an essential transcription factor for myeloid differentiation. Not only mutation of the CEBPA gene, but also promoter methylation, which results in silencing of CEBPA, contributes to the pathoge
Autor:
Shinya Endo, Hiromitsu Hayashi, Masao Matsuoka, Yuki Kitano, Takashi Matsumoto, Hideo Baba, Asuka Ono, Kenji Tokunaga, Yo-ichi Yamashita, Katsunori Imai
Publikováno v:
Surgical Case Reports
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Surgical Case Reports, Vol 7, Iss 1, Pp 1-5 (2021)
Background Myeloid sarcoma (MS) is a rare disease, mostly found in conjunction with acute myelogenous leukemia or other diseases, and primary nonleukemic MS of the spleen is particularly rare. Case presentation We report a 57-year-old male who presen
Autor:
Ayako Nakamura-Ishizu, Toshio Suda, Norio Asou, Kenji Tokunaga, Darren Qiancheng Tan, Touati Benoukraf, Takayoshi Matsumura, Tsukasa Okuda, Chelsia Qiuxia Wang, Siva Sai Naga Anurag Muddineni, Roberto Tirado-Magallanes, Motomi Osato, Masao Matsuoka, Stephanie Sian
Publikováno v:
Blood. 136(17)
RUNX1 is among the most frequently mutated genes in human leukemia, and the loss or dominant-negative suppression of RUNX1 function is found in myelodysplastic syndrome and acute myeloid leukemia (AML). How posttranslational modifications (PTMs) of R