Zobrazeno 21 - 30
of 251
pro vyhledávání: '"Norio Asou"'
Autor:
Chie Asou, Tomoya Maeda, Maho Ishikawa, Daisuke Okamura, Mika Kohri, Naoki Takahashi, Kunihiro Tsukasaki, Hirozo Sakaguchi, Tsugumi Satoh, Hidekazu Kayano, Akira Matsuda, Norio Asou
Publikováno v:
International journal of hematology. 115(6)
We present the case of a 56-year-old male patient with paravertebral extramedullary hematopoiesis (EMH) secondary to myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia. In a routine health checkup over 5 years prior, he presen
Autor:
Hideyuki Honda, Yasuhiro Nakashima, Yasushi Miyazaki, Takahiro Yamauchi, Courtney D. DiNardo, Norio Asou, M. Kurokawa, Ying Zhou, Jalaja Potluri, Jiuhong Zha, Kenichi Ishizawa, Keith W. Pratz, Itaru Matsumura, Ilseung Choi, Atsushi Shinagawa, Sumiko Okubo, Kazuhito Yamamoto, Noboru Asada, Norio Komatsu, Noriko Fukuhara, Kensuke Usuki, Chikashi Yoshida, Toshihiro Miyamoto
Publikováno v:
Japanese journal of clinical oncology. 52(1)
Background The phase 3 VIALE-A trial (NCT02993523) reported that venetoclax-azacitidine significantly prolonged overall survival compared with placebo-azacitidine in patients with newly diagnosed acute myeloid leukemia ineligible for intensive chemot
Autor:
Masashi Sanada, Asao Hirose, Tomomi Yamada, Tohru Murayama, Yasuhito Nannya, Yasushi Miyazaki, Yukinori Nakamura, Norio Asou, Rieko Nishimura, Shinya Kojima, Hitoshi Kiyoi, Emiko Sakaida, Yoshihiro Hatta, Masahito Kawazu, Shinya Sato, Yuna Katsuoka, Yuichi Shiraishi, Eisuke Iwamoto, Masahiko Sumi, Takahiko Yasuda, Toyotaka Kawamata, Shinobu Tsuzuki, Seishi Ogawa, Hiroyuki Mano, Keizo Horibe, Fumihiko Hayakawa, Satoru Takada, Yuka Iijima-Yamashita, Nobuaki Dobashi, Takashi Kanamori, Shuichi Ota, Etsuko Yamazaki, Masatsugu Tanaka, Tomoki Naoe, Naoyuki Tange, Yachiyo Kuwatsuka, Hiroo Ueno, Itaru Matsumura, Hiroatsu Iida, Masafumi Taniwaki
Publikováno v:
Blood. 139(12)
The genetic basis of leukemogenesis in adults with B-cell acute lymphoblastic leukemia (B-ALL) is largely unclear, and its clinical outcome remains unsatisfactory. This study aimed to advance the understanding of biological characteristics, improve d
Autor:
Masao Matsuoka, Takayoshi Matsumura, Toshio Suda, Siva Sai Naga Anurag Muddineni, Chelsia Qiuxia Wang, Mineo Kurokawa, Makoto Kawakita, Norio Asou, Ayako Nakamura-Ishizu, Hiroaki Maki, Hitoshi Suzushima, Kensuke Takaoka, Motomi Osato
Publikováno v:
British Journal of Haematology. 185:888-902
Inherited thrombocytopenia is a genetically heterogeneous disease characterized by varying degrees of thrombocytopenia and risk of haematological malignancy, and the genetic cause of many cases remains unknown. We performed whole-exome sequencing of
Autor:
Chie Asou, Norio Asou, Kunihiro Tsukasaki, Masami Bessho, Nobutaka Kawai, Mika Kohri, Daisuke Okamura, Naoki Takahashi, Akira Matsuda, Tomoya Maeda, Ken Tanae, Maho Ishikawa
Publikováno v:
Leukemia Research Reports, Vol 15, Iss, Pp 100231-(2021)
To determine the impact of peripheral blood (PB) Wilms’ tumour 1 (WT-1) mRNA levels in patients with primary myelodysplastic syndromes (MDS), we analysed the relationships between several clinical variables at the time of diagnosis and the haematol
Autor:
Tomoya, Maeda, Akira, Matsuda, Chie, Asou, Daisuke, Okamura, Ken, Tanae, Mika, Kohri, Maho, Ishikawa, Naoki, Takahashi, Kunihiro, Tsukasaki, Nobutaka, Kawai, Norio, Asou, Masami, Bessho
Publikováno v:
Leukemia Research Reports
To determine the impact of peripheral blood (PB) Wilms’ tumour 1 (WT-1) mRNA levels in patients with primary myelodysplastic syndromes (MDS), we analysed the relationships between several clinical variables at the time of diagnosis and the haematol
Autor:
Shigehisa Tamaki, Akihiro Takeshita, Hitoshi Minamiguchi, Katsumichi Fujimaki, Hiroyuki Fujita, Masako Iwanaga, Yasushi Miyazaki, Yoshiko Atsuta, Yasunori Ueda, Akihiro Tomita, Toru Sakura, Masashi Sawa, Maki Hagihara, Itaru Matsumura, Masamitsu Yanada, Yoshihito Uchino, Nobuaki Dobashi, Yukio Kobayashi, Norio Asou, Yasuhiro Taniguchi, Hitoshi Kiyoi, Noriko Usui, Tomoki Naoe, Yoshinobu Maeda, Shigeki Ohtake, Rikio Suzuki
Publikováno v:
Annals of hematology. 99(12)
Significant advancements have been achieved with regard to the outcomes of acute promyelocytic leukemia (APL) patients through the introduction of all-trans retinoic acid; however, early hemorrhagic death and differentiation syndrome remain the major
Autor:
Nobuaki Dobashi, Yasushi Miyazaki, Shigeki Ohtake, Akihiro Takeshita, Yukako Obata, Noriko Usui, Toru Sakura, Hiroaki Furumaki, Yoshinobu Maeda, Rikio Suzuki, Masashi Sawa, Itaru Matsumura, Masamitsu Yanada, Masaru Nakagawa, Shigehisa Tamaki, Norio Asou, Yoshiko Atsuta, Maki Hagihara, Yasunori Ueda, Hitoshi Kiyoi, Tomoki Naoe, Hiroyuki Fujita, Yasuhiro Taniguchi, Katsumichi Fujimaki, Yukio Kobayashi
Publikováno v:
Leukemia. 33:358-370
Between April 2004 and December 2010, we conducted a prospective randomized controlled study comparing tamibarotene with all-trans retinoic acid (ATRA) in the maintenance therapy of newly diagnosed acute promyelocytic leukemia (APL), and here report
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
Autor:
Akira Matsuda, Mika Kohri, Ken Tanae, Shin Arai, Kunihiro Tsukasaki, Tsuyoshi Saeki, Norio Asou, Daisuke Okamura, Yu Akuzawa, Nobutaka Kawai, Eiichi Arai, Maho Ishikawa, Naoki Takahashi, Tomoya Maeda
Publikováno v:
Leukemia research. 91
The 2017 WHO classification includes a new provisional entity of indolent T-lymphoproliferative disorders of the gastrointestinal tract (ITLPD-GIT). We investigated GI involvement of peripheral T-cell lymphoma (PTCL). Eighty-two patients were diagnos