Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yoko, Ueki"'
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionBlau syndrome is a rare autosomal dominant autoinflammatory granulomatous disease caused by a mutation in the NOD2 gene. It is characterized by a clinical trial of granulomatous dermatitis, arthritis, and uveitis. Tofacitinib is a pan Jan
Externí odkaz:
https://doaj.org/article/63e22e968a1540e1a1ce71ed3631fbbe
Autor:
Tomoko Matsuda, Naotomo Kambe, Riko Takimoto-Ito, Yoko Ueki, Satoshi Nakamizo, Megumu K. Saito, Syuji Takei, Nobuo Kanazawa
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Blau syndrome is a systemic autoinflammatory granulomatous disease caused by mutations in the nucleotide-binding oligomerization domain 2 (NOD2) gene. NOD2 is an intracellular pathogen recognition receptor. Upon binding to muramyl dipeptide (MDP), NO
Externí odkaz:
https://doaj.org/article/2533f05b4c0b415c9e65a5d3e36ccc1b
Autor:
Izumi Kishimoto, Chuyen Thi Hong Nguyen, Naotomo Kambe, Nhung Thi My Ly, Yoko Ueki, Ikuko Ueda-Hayakawa, Hiroyuki Okamoto
Publikováno v:
Allergology International, Vol 69, Iss 2, Pp 310-312 (2020)
Externí odkaz:
https://doaj.org/article/2af5af08af1a40c1a3e79c4dd890bc13
Autor:
Yoshihiko Sakurai, Satoshi Okada, Masato Yashiro, Nami Okamoto, Tomoko Matsuda, Hiroshi Fujii, Ryuta Nishikomori, Yuzaburo Inoue, Ikuo Okafuji, Naotomo Kambe, Yoko Ueki, Utako Kaneko, Masami Inoue, Mototsugu Doi, Naoki Kato, Nobuo Kanazawa, Hiroko Kobayashi, Junichi Hosokawa, Ichiro Kobayashi, Shuichi Ito, Syuji Takei, Kyoko Tonomura, Yasuhiro Kondo, Yoshikazu Otsubo, Atsushi Kawakami, Kazushi Izawa, Megumu K. Saito, Naomi Iwata, Teruhiko Makino, Osamu Ohara, Yuta Maruyama, Yoshitaka Honda, Shusaku Ito
Publikováno v:
Annals of the Rheumatic Diseases. 79:1492-1499
ObjectivesTo collect clinical information and NOD2 mutation data on patients with Blau syndrome and to evaluate their prognosis.MethodsFifty patients with NOD2 mutations were analysed. The activity of each NOD2 mutant was evaluated in HEK293 cells by
Publikováno v:
The Journal of dermatology. 47(7)
Autor:
Tomoko, Matsuda, Naotomo, Kambe, Yoko, Ueki, Nobuo, Kanazawa, Kazushi, Izawa, Yoshitaka, Honda, Atsushi, Kawakami, Syuji, Takei, Kyoko, Tonomura, Masami, Inoue, Hiroko, Kobayashi, Ikuo, Okafuji, Yoshihiko, Sakurai, Naoki, Kato, Yuta, Maruyama, Yuzaburo, Inoue, Yoshikazu, Otsubo, Teruhiko, Makino, Satoshi, Okada, Ichiro, Kobayashi, Masato, Yashiro, Shusaku, Ito, Hiroshi, Fujii, Yasuhiro, Kondo, Nami, Okamoto, Shuichi, Ito, Naomi, Iwata, Utako, Kaneko, Mototsugu, Doi, Junichi, Hosokawa, Osamu, Ohara, Megumu K, Saito, Ryuta, Nishikomori, Taizo, Wada
Publikováno v:
Annals of the rheumatic diseases. 79(11)
To collect clinical information andFifty patients withThe study population comprised 26 males and 24 females aged 0-61 years. Thirty-two cases were sporadic, and 18 were familial from 9 unrelated families. Fifteen different mutations inIn patients wi
Publikováno v:
The Journal of Dermatology. 45:109-110
Publikováno v:
The Journal of Dermatology. 44:845-846
Publikováno v:
The Journal of Dermatology. 44:726-727