Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Takeshi Shiba"'
Autor:
Takayuki Miyamoto, Yoshitaka Honda, Kazushi Izawa, Nobuo Kanazawa, Saori Kadowaki, Hidenori Ohnishi, Masakazu Fujimoto, Naotomo Kambe, Naoya Kase, Takeshi Shiba, Yasuo Nakagishi, Shuji Akizuki, Kosaku Murakami, Masahiro Bamba, Yutaka Nishida, Ayano Inui, Tomoo Fujisawa, Daisuke Nishida, Naomi Iwata, Yoshikazu Otsubo, Shingo Ishimori, Momoko Nishikori, Kiminobu Tanizawa, Tomoyuki Nakamura, Takeshi Ueda, Yoko Ohwada, Yu Tsuyusaki, Masaki Shimizu, Takasuke Ebato, Kousho Iwao, Akiharu Kubo, Toshinao Kawai, Tadashi Matsubayashi, Tatsuhiko Miyazaki, Tomohiro Kanayama, Masahiko Nishitani-Isa, Hiroshi Nihira, Junya Abe, Takayuki Tanaka, Eitaro Hiejima, Satoshi Okada, Osamu Ohara, Megumu K. Saito, Junko Takita, Ryuta Nishikomori, Takahiro Yasumi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
PurposeUpregulation of type I interferon (IFN) signaling has been increasingly detected in inflammatory diseases. Recently, upregulation of the IFN signature has been suggested as a potential biomarker of IFN-driven inflammatory diseases. Yet, it rem
Externí odkaz:
https://doaj.org/article/5700023cf0774dc68dac5c83825a3a61
Autor:
Mariko Aoki, Kazushi Izawa, Takayuki Tanaka, Yoshitaka Honda, Takeshi Shiba, Yukako Maeda, Takayuki Miyamoto, Keisuke Okamoto, Masahiko Nishitani-Isa, Hiroshi Nihira, Kohsuke Imai, Junko Takita, Ryuta Nishikomori, Eitaro Hiejima, Takahiro Yasumi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Familial Mediterranean fever (FMF) is a hereditary, autoinflammatory disease that causes recurrent fever, arthritis, and serositis. The diagnosis of FMF is based on the presentation of typical clinical symptoms and the Mediterranean fever gene (MEFV)
Externí odkaz:
https://doaj.org/article/de636ce9fe18427db2a7afcc9eaf72bd
Autor:
Takayuki Tanaka, Takeshi Shiba, Yoshitaka Honda, Kazushi Izawa, Takahiro Yasumi, Megumu K. Saito, Ryuta Nishikomori
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The concept of autoinflammation, first proposed in 1999, refers to a seemingly unprovoked episode of sterile inflammation manifesting as unexplained fever, skin rashes, and arthralgia. Autoinflammatory diseases are caused mainly by hereditary abnorma
Externí odkaz:
https://doaj.org/article/a913a44a94924da998ce46e3eae35517
Autor:
Takahiro Yasumi, Ryuta Nishikomori, Osamu Ohara, Yusuke Kawashima, Tomohiro Morio, Kosaku Murakami, Syuji Takei, Tomohiro Kubota, Toshio Heike, Makio Takahashi, Hirokazu Kanegane, Hidetoshi Takada, Masahiko Isa-Nishitani, Atsushi Hijikata, Moeko Ito, Takeshi Shiba, Shunsuke Kajikawa, Tadateru Yasu, Naoko Nakano, Shouichi Ohga, Tsubasa Okano, Hiroaki Umebayashi, Junko Takita, Yoshinori Hasegawa, Dai Keino, Sachiko Iwaki-Egawa, Etsuro Nanishi, Hiroshi Nihira, Kazushi Izawa, Yoji Sasahara, Yoshitaka Honda
Publikováno v:
Journal of Allergy and Clinical Immunology. 148:550-562
Background Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive inflammatory disease caused by loss-of-function mutations in both alleles of the ADA2 gene. Most patients with DADA2 exhibit systemic vasculopathy consistent with polyar
Autor:
Hiroki Mukoyama, Junko Takita, Takayuki Miyamoto, Takayuki Tanaka, Osamu Ohara, Yoshitaka Honda, Haruna Nakaseko, Takeshi Shiba, Keisuke Nishimura, Masahiko Isa-Nishitani, Hirofumi Shibata, Eitaro Hiejima, Yukako Maeda, Kazushi Izawa, Hiroshi Nihira, Takahiro Yasumi, Ryuta Nishikomori
Publikováno v:
Journal of Clinical Immunology. 41:1187-1197
Pathogenic MEFV variants cause pyrin-associated autoinflammatory diseases (PAADs), which include familial Mediterranean fever (FMF), FMF-like disease, and pyrin-associated autoinflammation with neutrophilic dermatosis (PAAND). The diagnosis of PAADs
Publikováno v:
Heart and Vessels. 36:155-162
In 2013, a drug-coated balloon catheter (DCB) (SeQuent Please) for the treatment of coronary in-stent restenosis (ISR) was approved in Japan. The pre-marketing Japan domestic NP001 study demonstrated better outcomes of the DCB (n = 138) compared to p
Autor:
Maya Chrabieh, Anne Puel, Yuri Kawasaki, Hong Hur, Kazushi Izawa, Bertrand Boisson, Osamu Ohara, Takahiro Yasumi, Mitsujiro Osawa, Matthieu Bendavid, Ryuta Nishikomori, Benedetta Bigio, Masatoshi Hagiwara, Yuval Itan, Masahiko Ajiro, Hiroshi Nihira, Toshio Heike, Andrew R. Gennery, Megumu K. Saito, Jacinta Bustamante, Jean-Laurent Casanova, Takayuki Tanaka, Jose Ichishima, Satoshi Okada, Yupu Liang, Laurent Abel, Yoshitaka Honda, Takeshi Shiba
Publikováno v:
Journal of Clinical Investigation. 129:583-597
X-linked dominant incontinentia pigmenti (IP) and X-linked recessive anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) are caused by loss-of-function and hypomorphic IKBKG (also known as NEMO) mutations, respectively. We describe a Europ
Autor:
Yoshitaka, Honda, Yukako, Maeda, Kazushi, Izawa, Takeshi, Shiba, Takayuki, Tanaka, Haruna, Nakaseko, Keisuke, Nishimura, Hiroki, Mukoyama, Masahiko, Isa-Nishitani, Takayuki, Miyamoto, Hiroshi, Nihira, Hirofumi, Shibata, Eitaro, Hiejima, Osamu, Ohara, Junko, Takita, Takahiro, Yasumi, Ryuta, Nishikomori
Publikováno v:
Journal of clinical immunology. 41(6)
Pathogenic MEFV variants cause pyrin-associated autoinflammatory diseases (PAADs), which include familial Mediterranean fever (FMF), FMF-like disease, and pyrin-associated autoinflammation with neutrophilic dermatosis (PAAND). The diagnosis of PAADs
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 63(8)
Autor:
Naoki Miki, Mitshuhiko Nambu, Takeshi Shiba, Hiraku Doi, Takeshi Iwasaki, Masahiro Fukushima, Shinichiro Yoshimura
Publikováno v:
Tenri Medical Bulletin. 20:38-43