Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Asuka, Shibamiya"'
Autor:
Arata Ishii, Shokichi Tsukamoto, Naoya Mimura, Yurie Miyamoto-Nagai, Yusuke Isshiki, Shinichiro Matsui, Sanshiro Nakao, Asuka Shibamiya, Yutaro Hino, Kensuke Kayamori, Nagisa Oshima-Hasegawa, Tomoya Muto, Yusuke Takeda, Tomoki Suichi, Sonoko Misawa, Chikako Ohwada, Koutaro Yokote, Satoshi Kuwabara, Chiaki Nakaseko, Hiroyuki Takamatsu, Emiko Sakaida
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein [M-protein], and skin changes) is a rare systemic disorder characterized by various symptoms caused by underlying plasma cell (PC) dyscrasia. Detection of monoc
Externí odkaz:
https://doaj.org/article/9b8f610b006b45589b8f86626a22aab6
Autor:
Ola Rizq, Naoya Mimura, Motohiko Oshima, Shuji Momose, Naoya Takayama, Naoki Itokawa, Shuhei Koide, Asuka Shibamiya, Yurie Miyamoto-Nagai, Mohamed Rizk, Yaeko Nakajima-Takagi, Kazumasa Aoyama, Changshan Wang, Atsunori Saraya, Masanori Seimiya, Mariko Watanabe, Satoshi Yamasaki, Tatsuhiro Shibata, Kiyoshi Yamaguchi, Yoichi Furukawa, Tetsuhiro Chiba, Emiko Sakaida, Chiaki Nakaseko, Jun-ichi Tamaru, Yu-Tzu Tai, Kenneth C. Anderson, Hiroaki Honda, Atsushi Iwama
Publikováno v:
Leukemia.
UTX/KDM6A, a histone H3K27 demethylase and a key component of the COMPASS complex, is frequently lost or mutated in cancer; however, its tumor suppressor function remains largely uncharacterized in multiple myeloma (MM). Here, we show that the condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::882fe5e65e35c9e8d7a3044d956c0f1e
https://doi.org/10.1038/s41375-023-01928-7
https://doi.org/10.1038/s41375-023-01928-7
Autor:
Asuka Shibamiya, Naoya Mimura, Yurie Miyamoto-Nagai, Shuhei Koide, Motohiko Oshima, Ola Rizq, Kazumasa Aoyama, Yaeko Nakajima-Takagi, Kensuke Kayamori, Yusuke Isshiki, Nagisa Oshima-Hasegawa, Tomoya Muto, Shokichi Tsukamoto, Yusuke Takeda, Ryo Koyama-Nasu, Tetsuhiro Chiba, Hiroaki Honda, Koutaro Yokote, Atsushi Iwama, Emiko Sakaida
Publikováno v:
Blood. 140:4240-4241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::313f27d8c453f3ea006764b91201a4c3
https://doi.org/10.1182/blood-2022-158111
https://doi.org/10.1182/blood-2022-158111
Autor:
Tomoya Muto, Nagisa Oshima-Hasegawa, Yusuke Takeda, Sonoko Misawa, Arata Ishii, Satoshi Kuwabara, Shokichi Tsukamoto, Naoya Mimura, Tatsuzo Mishina, Yutaro Hino, Yurie Nagai, Shio Mitsukawa, Emiko Sakaida, Asuka Shibamiya, Chikako Ohwada, Tohru Iseki, Kensuke Kayamori, Chiaki Nakaseko
Publikováno v:
Bone Marrow Transplantation. 56:517-520
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::712e407227f55652f26463d4c8781980
https://doi.org/10.1038/s41409-020-01024-9
https://doi.org/10.1038/s41409-020-01024-9
Autor:
Hirohumi Ohashi, Norihiro Mimura, Hirotoshi Kawashima, Makio Kawakami, Asuka Shibamiya, Masaki Hiraguri, Atsunari Utsugi, Ryota Hase, Takao Yanagisawa, Kazuma Iida
Publikováno v:
Immunologic Research. 67:99-107
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) and immunoglobulin G4-related diseases (IgG4-RD) are regarded as entirely different disease types with different etiological mechanisms. However, we experienced two cases that ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fddd5dbb914d1ea93fca6ada304cd49b
https://doi.org/10.1007/s12026-019-9070-7
https://doi.org/10.1007/s12026-019-9070-7
Autor:
Asuka, Shibamiya, Chikako, Ohwada, Arata, Ishii, Tatsuzo, Mishina, Yurie, Nagai, Yutaro, Hino, Kensuke, Kayamori, Nagisa, Oshima-Hasegawa, Tomoya, Muto, Shokichi, Tsukamoto, Yusuke, Takeda, Shio, Mitsukawa, Naoya, Mimura, Tohru, Iseki, Sonoko, Misawa, Satoshi, Kuwabara, Chiaki, Nakaseko, Emiko, Sakaida
Publikováno v:
Bone marrow transplantation. 56(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::12f0c814352dc0df602dd1cd7539648f
https://pubmed.ncbi.nlm.nih.gov/32778687
https://pubmed.ncbi.nlm.nih.gov/32778687
Autor:
Koutaro Yokote, Arata Ishii, Tomoki Suichi, Sonoko Misawa, Nagisa Oshima-Hasegawa, Hiroyuki Takamatsu, Shio Mitsukawa, Emiko Sakaida, Yurie Nagai, Naoya Mimura, Tomoya Muto, Shokichi Tsukamoto, Sanshiro Nakao, Kensuke Kayamori, Chiaki Nakaseko, Satoshi Kuwabara, Yutaro Hino, Shinichiro Matsui, Chikako Ohwada, Yusuke Takeda, Asuka Shibamiya
Publikováno v:
Blood. 138:2697-2697
Introduction POEMS syndrome is a rare systemic disorder characterized by various symptoms, including polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy (M-protein), and skin changes, which is based on the presence of monoclonal plasm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1571d801094e616ee259a0610804a711
https://doi.org/10.1182/blood-2021-150900
https://doi.org/10.1182/blood-2021-150900