Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Tomonari, Shigemura"'
Autor:
Tomonari Shigemura, Nahuel Perrot, Zimo Huang, Rupal S. Bhatt, Aseman Bagheri Sheshdeh, Nourhan El Ahmar, Fatme Ghandour, Sabina Signoretti, David F. McDermott, Gordon J. Freeman, Kathleen M. Mahoney
Publikováno v:
BMC Cancer, Vol 23, Iss 1, Pp 1-14 (2023)
Abstract Background The immune checkpoint HERV-H LTR-associating 2 (HHLA2) is expressed in kidney cancer and various other tumor types. Therapeutics targeting HHLA2 or its inhibitory receptor KIR3DL3 are being developed for solid tumors, including re
Externí odkaz:
https://doaj.org/article/85e734b4145c41299dfe482e37286e82
Autor:
Yusuke Azami, Naohiro Tsuyama, Yu Abe, Misaki Sugai-Takahashi, Ken-ichi Kudo, Akinobu Ota, Karnan Sivasundaram, Moe Muramatsu, Tomonari Shigemura, Megumi Sasatani, Yuko Hashimoto, Shigehira Saji, Kenji Kamiya, Ichiro Hanamura, Takayuki Ikezoe, Masafumi Onodera, Akira Sakai
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Multiple myeloma (MM) cells are derived from mature B cells based on immunoglobulin heavy chain (IgH) gene analysis. The onset of MM is often caused by a reciprocal chromosomal translocation (cTr) between chr 14 with IgH and chr 11 with CCND
Externí odkaz:
https://doaj.org/article/81747abd10d746a997909ec4057a1be8
Autor:
Etsushi Toyofuku, Kozue Takeshita, Hidenori Ohnishi, Yuko Kiridoshi, Hiroaki Masuoka, Tomonori Kadowaki, Ryuta Nishikomori, Kenichi Nishimura, Chie Kobayashi, Takasuke Ebato, Tomonari Shigemura, Yuzaburo Inoue, Wataru Suda, Masahira Hattori, Tomohiro Morio, Kenya Honda, Hirokazu Kanegane
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 11 (2022)
IntroductionHaploinsufficiency of A20 (HA20) is a form of inborn errors of immunity (IEI). IEIs are genetically occurring diseases, some of which cause intestinal dysbiosis. Due to the dysregulation of regulatory T cells (Tregs) observed in patients
Externí odkaz:
https://doaj.org/article/7def3c4cc537413ba58d2b7e13017a76
Autor:
Lika’a Fasih Y. Al-Kzayer, Hanadi Munaf H. Al-Aradi, Tomonari Shigemura, Kenji Sano, Miyuki Tanaka, Motoharu Hamada, Kenan Hussien Ali, Osamah Mohammed Aldaghir, Yozo Nakazawa, Yusuke Okuno
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Dedicator of cytokinesis 8 (DOCK8) deficiency (MIM #243700) is a rare disease, leads to a combined primary immunodeficiency (PID), and accounts for the autosomal recessive-hyper immunoglobulin E syndrome (AR-HIES). DOCK8 deficienc
Externí odkaz:
https://doaj.org/article/6e98f0ae7a2a455c8ceeb1783c571814
Autor:
Masakatsu Yanagimachi, Koji Kato, Akihiro Iguchi, Koji Sasaki, Chikako Kiyotani, Katsuyoshi Koh, Takashi Koike, Hideki Sano, Tomonari Shigemura, Hideki Muramatsu, Keiko Okada, Masami Inoue, Ken Tabuchi, Toyoki Nishimura, Tomoyuki Mizukami, Hiroyuki Nunoi, Kohsuke Imai, Masao Kobayashi, Tomohiro Morio
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Hematopoietic cell transplantation (HCT) is established as a curative treatment for severe chronic granulomatous disease (CGD). However, outcomes of HCT for CGD in Japan had not been precisely reported. We evaluated the outcome of HCT for CGD in Japa
Externí odkaz:
https://doaj.org/article/5ee250a523cb45debaca13a5242daa5e
Autor:
Koichi Hirabayashi, Mitsuho Takatsuki, Mitsuo Motobayashi, Takashi Kurata, Shoji Saito, Tomonari Shigemura, Yozo Nakazawa, Kazuo Sakashita, Satoshi Ishizone, Hiroyoshi Ota, Kenichi Koike
Publikováno v:
Pediatrics and Neonatology, Vol 58, Iss 1, Pp 81-84 (2017)
Nonocclusive mesenteric ischemia (NOMI) is induced by intestinal vasospasm without thromboembolic occlusion and is associated with high morbidity and mortality. The estimated overall incidence of autopsy-verified fatal NOMI is 2.0 cases/100,000 perso
Externí odkaz:
https://doaj.org/article/b8dbae6b881b40a49834d2d9b61a3051
Autor:
Shuzo Sato, Yuya Fujita, Tomonari Shigemura, Hisanori Matoba, Kazunaga Agematsu, Yuya Sumichika, Makiko Yashiro, Atsushi Ono, Yukihiko Kawasaki, Hiroko Kobayashi, Hiroshi Watanabe, Tomohiro Koga, Atsushi Kawakami, Kiyoshi Migita
Publikováno v:
Arthritis Research & Therapy, Vol 20, Iss 1, Pp 1-3 (2018)
Externí odkaz:
https://doaj.org/article/d39d32af79e44246935bd47a1ee3c5ac
Publikováno v:
Brazilian Journal of Infectious Diseases, Vol 22, Iss 1, Pp 60-62 (2018)
Herein we report the case of a 10-year-old boy with an autosomal mosaic mutation who developed bacteremia. The causative agent was identified as Moraxella osloensis by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and 1
Externí odkaz:
https://doaj.org/article/d8659be8e7924c75b9057904e257af87
Autor:
Lika'a Fasih Y. Al-Kzayer, Ahmed K. Yassin, Khalid Hama Salih, Tomonari Shigemura, Kenji Sano, Ruwaid Behnam Y. Al-Simaani, Miyuki Tanaka, Yozo Nakazawa, Yusuke Okuno
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare condition of primary immunodeficiency disorder. Interleukin-12 receptor β1 (IL12RB1) deficiency, is the most common genetic etiology of MSMD, which is characterized by the selective
Externí odkaz:
https://doaj.org/article/1b7237ceff6d4582b8d8b62eda0cd576
Autor:
McKenna Lamb, Yao Wei, Xiaoxin Ren, Rachel O'Connor, Austin Dulak, Matthew Rausch, Jamie Strand, Bijan Etemad-Gilbertson, Riale Gilligan, Scott Chappel, Tomonari Shigemura, David McDermott, Gordon Freeman, XingXing Zang
Publikováno v:
Regular and Young Investigator Award Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::037d05a19f16d43b5cedecb3b30274b4
https://doi.org/10.1136/jitc-2022-sitc2022.0489
https://doi.org/10.1136/jitc-2022-sitc2022.0489