Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kanako Mitsui"'
Autor:
Kunihiko Moriya, Kanako Mitsui-Sekinaka, Yujin Sekinaka, Akifumi Endo, Hirokazu Kanegane, Tomohiro Morio, Kohsuke Imai, Shigeaki Nonoyama
Publikováno v:
Immunological Medicine, Vol 46, Iss 4, Pp 153-157 (2023)
AbstractActivated phosphatidyl inositol 3-kinase-delta syndrome (APDS) due to gain-of-function variant in the class IA PI3K catalytic subunit p110δ (responsible gene: PIK3CD) was described in 2013. The disease is characterized by recurrent airway in
Externí odkaz:
https://doaj.org/article/f9f8fcf3a735433e9c853e54072fe3d6
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
The Primary Immunodeficiency Database in Japan (PIDJ) is a registry of primary immunodeficiency diseases (PIDs) that was established in 2007. The database is a joint research project with research groups associated with the Ministry of Health, Labor
Externí odkaz:
https://doaj.org/article/ccd956b9de3a4ff384cc0bba90f63465
Autor:
Akihiro Hoshino, Etsushi Toyofuku, Noriko Mitsuiki, Motoi Yamashita, Keisuke Okamoto, Michio Yamamoto, Kenji Kanda, Genki Yamato, Dai Keino, Yuri Yoshimoto-Suzuki, Junji Kamizono, Yasuhiro Onoe, Takuya Ichimura, Mika Nagao, Masaru Yoshimura, Koji Tsugawa, Toru Igarashi, Kanako Mitsui-Sekinaka, Yujin Sekinaka, Takehiko Doi, Takahiro Yasumi, Yozo Nakazawa, Masatoshi Takagi, Kohsuke Imai, Shigeaki Nonoyama, Tomohiro Morio, Sylvain Latour, Hirokazu Kanegane
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
IKAROS and CTLA4 deficiencies are inborn errors of immunity and show similar clinical phenotypes, including hypogammaglobulinemia and autoimmune diseases (ADs). However, the differences in clinical features and pathogenesis of these are not fully und
Externí odkaz:
https://doaj.org/article/64b1507f6deb42d5adb37948dc93e58e
Autor:
Osamu Ohara, Kohsuke Imai, Taizo Wada, Kunio Hashimoto, Akira Shimada, Kanako Mitsui-Sekinaka, Tzu-Wen Yeh, Takaki Asano, Youjiro Ichinose
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Activated PI3Kδ syndrome (APDS) is a primary immunodeficiency characterized by recurrent respiratory tract infections, lymphoproliferation, and defective IgG production. Heterozygous mutations in PIK3CD, PIK3R1, or PTEN, which are related to the hyp
Externí odkaz:
https://doaj.org/article/6ada6c9333d2423db340754668339554
Autor:
Kunihiko Moriya, Kanako Mitsui-Sekinaka, Yujin Sekinaka, Akifumi Endo, Hirokazu Kanegane, Tomohiro Morio, Kohsuke Imai, Shigeaki Nonoyama
Publikováno v:
Immunological Medicine; Dec2023, Vol. 46 Issue 4, p153-157, 5p
Autor:
Fumiaki Sakura, Kosuke Noma, Takaki Asano, Kay Tanita, Etsushi Toyofuku, Kentaro Kato, Miyuki Tsumura, Hiroshi Nihira, Kazushi Izawa, Kanako Mitsui-Sekinaka, Ryo Konno, Yusuke Kawashima, Yoko Mizoguchi, Shuhei Karakawa, Seiichi Hayakawa, Hiroshi Kawaguchi, Kohsuke Imai, Shigeaki Nonoyama, Takahiro Yasumi, Hidenori Ohnishi, Hirokazu Kanegane, Osamu Ohara, Satoshi Okada
Publikováno v:
PNAS Nexus. 2
Advances in next-generation sequencing technology have identified many genes responsible for inborn errors of immunity (IEI). However, there is still room for improvement in the efficiency of genetic diagnosis. Recently, RNA sequencing and proteomics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::993b36867281f2ee01343bfdd988374e
https://doi.org/10.1093/pnasnexus/pgad104
https://doi.org/10.1093/pnasnexus/pgad104
Autor:
Hirohito Shima, Yusuke Yoshida, Naoko Amano, Kenji Uematsu, Tomonobu Hasegawa, Kanako Mitsui-Sekinaka, Yujin Sekinaka, Shigeaki Nonoyama, Satoshi Narumi
Publikováno v:
Journal of Clinical Immunology. 41:709-711
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76fe211fe20cf7ee1d1166834e1da047
https://doi.org/10.1007/s10875-020-00964-7
https://doi.org/10.1007/s10875-020-00964-7
Autor:
Tomohiro Morio, Tsubasa Okano, Yujin Sekinaka, Eri Endo, Katsuyuki Hanabusa, Ikuya Tsuge, Shiann Tarng Jou, Masataka Ishimura, Hsin-Hui Yu, Yoshihiro Maruo, Tomiko Kimoto, Tomoaki Kunitsu, Hiroshi Yagasaki, Masami Inoue, Kenichi Yoshida, Yuki Tsujita, Taizo Wada, Kohsuke Imai, Kyoko Suzuki, Seiji Kojima, Sven Kracker, Tetsuzo Tauchi, Yuko Hashimoto, Takehiro Takashima, Yuzaburo Inoue, Toru Uchiyama, Hidetoshi Takada, Kenichi Honma, Motohiro Kato, Masakazu Nagahori, Takashi Kaneko, Yoshiaki Shikama, Naohiko Moriguchi, Tomoko Waragai, Daiei Kojima, Haruka Hiroki, Tamaki Kato, Kanako Mitsui-Sekinaka, Keisuke Tanaka, Anne Durandy, Yuki Bando, Hideki Muramatsu, Kazuhiro Tasaki, Seishi Ogawa, Hirokazu Kanegane, Fuminori Iwasaki, Shigeaki Nonoyama, Tzu Wen Yeh, Chikako Kamae, Toshihiko Shirakawa, Osamu Suzuki, Tomoyo Matsubara, Hideki Sano, Yuki Yuza, Osamu Ohara, Noriko Mitsuiki
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:266-275
Background Activated phosphatidylinositol-3-OH kinase δ syndrome type 1 (APDS1) is a recently described primary immunodeficiency syndrome characterized by recurrent respiratory tract infections, lymphoid hyperplasia, and Herpesviridae infections cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bb44153e5e8d631309e74864a023dc5
https://doi.org/10.1016/j.jaci.2018.04.032
https://doi.org/10.1016/j.jaci.2018.04.032
Autor:
Yujin Sekinaka, Ryo Ohyama, Chigusa Oyama, Mamoru Honda, Kiyotaka Isobe, Kanako Mitsui-Sekinaka, Makiko Mori, Hiroyuki Kawaguchi, Katsuyoshi Koh, Ryoji Hanada, Yumi Ogura, Shigeaki Nonoyama, Yuki Arakawa
Publikováno v:
Leukemia & Lymphoma. 59:1511-1513
Approximately 20% of the pediatric acute myeloid leukemia (AML) cases show normal karyotypes without any recognizable cytogenetic alteration on conventional cytogenetic analysis. Recent state-of-th...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b00f895e99fc99dc1111890a6297bef5
https://doi.org/10.1080/10428194.2017.1387901
https://doi.org/10.1080/10428194.2017.1387901
Autor:
Kunio Hashimoto, Kohsuke Imai, Youjiro Ichinose, Shigeaki Nonoyama, Takaki Asano, Taizo Wada, Tomohiro Morio, Akira Shimada, Osamu Ohara, Kanako Mitsui-Sekinaka, Yuki Tsujita, Masao Kobayashi, Tzu Wen Yeh, Miyuki Tsumura, Satoshi Okada
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Vol 9 (2018)
Frontiers in Immunology, Vol 9 (2018)
Activated PI3Kδ syndrome (APDS) is a primary immunodeficiency characterized by recurrent respiratory tract infections, lymphoproliferation, and defective IgG production. Heterozygous mutations in PIK3CD, PIK3R1, or PTEN, which are related to the hyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d78887472fd5616730dfca39afe4c91e
http://ir.lib.hiroshima-u.ac.jp/00045835
http://ir.lib.hiroshima-u.ac.jp/00045835
