Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Hisayuki, Matsumoto"'
Autor:
Aki Inase, Yimamu Maimaitili, Shiro Kimbara, Yu Mizutani, Yoshiharu Miyata, Shinya Ohata, Hisayuki Matsumoto, Akihito Kitao, Rina Sakai, Koji Kawaguchi, Ako Higashime, Shigeki Nagao, Keiji Kurata, Hideaki Goto, Shinichiro Kawamoto, Kimikazu Yakushijin, Hironobu Minami, Hiroshi Matsuoka
Publikováno v:
eJHaem, Vol 4, Iss 1, Pp 153-164 (2023)
Abstract In acute myeloid leukemia (AML), the heterogeneity of genetic and epigenetic characteristics makes treatment difficult. The prognosis for AML is therefore poor, and there is an urgent need for new treatments for this condition. Gemtuzumab oz
Externí odkaz:
https://doaj.org/article/46ed2f3d177c4823ba6643c7ae758cc7
Autor:
Yohei Funakoshi, Goh Ohji, Kimikazu Yakushijin, Kei Ebisawa, Yu Arakawa, Jun Saegusa, Hisayuki Matsumoto, Takamitsu Imanishi, Eriko Fukuda, Takaji Matsutani, Yasuko Mori, Kentaro Iwata, Hironobu Minami
Publikováno v:
Heliyon, Vol 7, Iss 8, Pp e07748- (2021)
Background: Antibody production is one of the primary mechanisms for recovery from coronavirus disease 2019 (COVID-19). It is speculated that massive clonal expansion of B cells, which can produce clinically meaningful neutralizing antibodies, occurs
Externí odkaz:
https://doaj.org/article/8b33ab3692df44f9b5d9e79c219d5924
Autor:
Hideaki Goto, Kimikazu Yakushijin, Yoko Adachi, Hisayuki Matsumoto, Katsuya Yamamoto, Sakuya Matsumoto, Tomoe Yamashita, Ako Higashime, Koji Kawaguchi, Keiji Kurata, Hiroshi Matsuoka, Hironobu Minami
Publikováno v:
Internal Medicine. 62:1329-1334
Autor:
Katsuya Yamamoto, Hisayuki Matsumoto, Sakuya Matsumoto, Rina Sakai, Akihito Kitao, Marika Watanabe, Hideaki Goto, Takeshi Sugimoto, Yoshihiko Yano, Kimikazu Yakushijin, Hironobu Minami
Publikováno v:
Cancer Genetics. :41-46
Autor:
Aki Inase, Yimamu Maimaitili, Shiro Kimbara, Yu Mizutani, Yoshiharu Miyata, Shinya Ohata, Hisayuki Matsumoto, Akihito Kitao, Rina Sakai, Koji Kawaguchi, Ako Higashime, Shigeki Nagao, Keiji Kurata, Hideaki Goto, Shinichiro Kawamoto, Kimikazu Yakushijin, Hironobu Minami, Hiroshi Matsuoka
Publikováno v:
eJHaem. 4:153-164
Autor:
Hideaki, Goto, Kimikazu, Yakushijin, Yoko, Adachi, Hisayuki, Matsumoto, Katsuya, Yamamoto, Sakuya, Matsumoto, Tomoe, Yamashita, Ako, Higashime, Koji, Kawaguchi, Keiji, Kurata, Hiroshi, Matsuoka, Hironobu, Minami
Publikováno v:
Internal medicine (Tokyo, Japan).
An acute promyelocytic leukemia (APL) patient not demonstrating the retinoic acid receptor α (RARA) translocation is rare. A 76-year-old man was diagnosed with myelodysplastic syndrome (MDS). After a year, abnormal promyelocytes were detected with p
Autor:
Hisayuki Matsumoto, Kimikazu Yakushijin, Yu Mizutani, Marika Okuni-Watanabe, Hironobu Minami, Hiroshi Matsuoka, Katsuya Yamamoto, Yoshiharu Miyata, Akihito Kitao, Jun Saegusa, Hideaki Goto, Ako Higashime
Publikováno v:
Cancer Genetics. 254:92-97
The t(1;11)(p32;q23) translocation is a rare but recurrent cytogenetic aberration in acute myeloid leukemia (AML) and B-cell acute lymphoblastic leukemia (B-ALL). This translocation was initially shown to form a fusion gene between KMT2A exon 8 at 11
Autor:
Masayuki Akita, Yoshihiro Kakeji, Yoh Zen, Hisayuki Matsumoto, Masato Komatsu, Jun Saegusa, Kohei Fujikura, Ryuichiro Sawada, Tomoo Itoh, Sonoko Ishida
Publikováno v:
Human Pathology. 110:1-10
Summary The gene mutation profiles of gastric neuroendocrine neoplasms are incompletely understood. The purpose of this study was to characterize the molecular pathology of poorly differentiated neuroendocrine carcinoma (NEC) and mixed neuroendocrine
Autor:
Satoshi Takada, Yasuko Takagi, Mio Nishimura, Takeshi Kato, Masami Mizobuchi, Hiroaki Nagase, Masashi Nagai, Hisayuki Matsumoto, Tomoko Horinouchi, Sachiyo Fukushima, Noriyuki Nishimura, Kazumichi Fujioka, Yuka Okada, Jun Saegusa, Kazumi Tomioka, Mieko Yoshioka, Yoko Kawasaki, Yuji Nakamachi, Kandai Nozu, Kazumoto Iijima, Kaori Maeyama
Publikováno v:
Journal of Autism and Developmental Disorders. 52:483-489
Neonatal jaundice has been suggested as a perinatal risk factor for autism spectrum disorder (ASD). We examined UGT1A1 polymorphisms to assess the potential of neonatal jaundice as a risk factor for ASD in children by using DNA extracted from preserv
Autor:
Yoriko Noguchi, Ryosuke Bo, Hisahide Nishio, Hisayuki Matsumoto, Keiji Matsui, Yoshihiko Yano, Masami Sugawara, Go Ueda, Yogik Onky Silvana Wijaya, Emma Tabe Eko Niba, Masakazu Shinohara, Yoshihiro Bouike, Atsuko Takeuchi, Kentaro Okamoto, Toshio Saito, Hideki Shimomura, Tomoko Lee, Yasuhiro Takeshima, Kazumoto Iijima, Kandai Nozu, Hiroyuki Awano
Publikováno v:
Genes. 14:759
The authors wish to make the following correction to this paper [...]