Reply to Walsh et al

gan Kawai, Tomoki, Hiejima, Eitaro, Oda, Hirotsugu, Izawa, Kazushi, Yasumi, Takahiro, Nishikomori, Ryuta, Okamoto, Shinya, Heike, Toshio
Cyhoeddwyd yn Eur J Hum Genet (2017)

Direct activation of natural killer T cells induces airway hyperreactivity in nonhuman primates

gan Matangkasombut, Ponpan, Pichavant, Muriel, Yasumi, Takahiro, Hendricks, Carrie, Savage, Paul B., DeKruyff, Rosemarie H., Umetsu, Dale T.
Cyhoeddwyd 2008

Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis

gan Iwatani, Sota, Uemura, Kazuya, Mizobuchi, Masami, Yoshimoto, Seiji, Kawasaki, Keiichiro, Kosaka, Yoshiyuki, Hori, Masayuki, Yasumi, Takahiro, Nakao, Hideto
Cyhoeddwyd yn AJP Rep (2015)

Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq

gan Nakayama, Manabu, Oda, Hirotsugu, Nakagawa, Kenji, Yasumi, Takahiro, Kawai, Tomoki, Izawa, Kazushi, Nishikomori, Ryuta, Heike, Toshio, Ohara, Osamu
Cyhoeddwyd yn Biochem Biophys Rep (2016)

Activation of Nonclassical CD1d-Restricted NK T Cells Induces Airway Hyperreactivity in β(2)-Microglobulin-Deficient Mice()

gan Koh, Youngil I., Kim, Hye Young, Meyer, Everett H., Pichavant, Muriel, Akbari, Omid, Yasumi, Takahiro, Savage, Paul B., DeKruyff, Rosemarie H., Umetsu, Dale T.
Cyhoeddwyd yn J Immunol (2008)

Plasma infliximab monitoring contributes to optimize Takayasu arteritis treatment: a case report

gan Masui, Sho, Yonezawa, Atsushi, Izawa, Kazushi, Hayakari, Makoto, Asakura, Kayoko, Taniguchi, Risa, Isa, Masahiko, Shibata, Hirofumi, Yasumi, Takahiro, Nishikomori, Ryuta, Takita, Junko, Matsubara, Kazuo
Cyhoeddwyd yn J Pharm Health Care Sci (2019)

Detection of Base Substitution-Type Somatic Mosaicism of the NLRP3 Gene with >99.9% Statistical Confidence by Massively Parallel Sequencing

gan Izawa, Kazushi, Hijikata, Atsushi, Tanaka, Naoko, Kawai, Tomoki, Saito, Megumu K, Goldbach-Mansky, Raphaela, Aksentijevich, Ivona, Yasumi, Takahiro, Nakahata, Tatsutoshi, Heike, Toshio, Nishikomori, Ryuta, Ohara, Osamu
Cyhoeddwyd 2012

Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report

gan Hiejima, Eitaro, Yasumi, Takahiro, Nakase, Hiroshi, Matsuura, Minoru, Honzawa, Yusuke, Higuchi, Hirokazu, Okafuji, Ikuo, Yorifuji, Tohru, Tanaka, Takayuki, Izawa, Kazushi, Kawai, Tomoki, Nishikomori, Ryuta, Heike, Toshio
Cyhoeddwyd yn Medicine (Baltimore) (2017)

Subtypes of Familial Hemophagocytic Lymphohistiocytosis in Japan Based on Genetic and Functional Analyses of Cytotoxic T Lymphocytes

gan Nagai, Kozo, Yamamoto, Ken, Fujiwara, Hiroshi, An, Jun, Ochi, Toshiki, Suemori, Koichiro, Yasumi, Takahiro, Tauchi, Hisamichi, Koh, Katsuyoshi, Sato, Maho, Morimoto, Akira, Heike, Toshio, Ishii, Eiichi, Yasukawa, Masaki
Cyhoeddwyd 2010

Natural Killer T Cells in the Lungs of Patients with Asthma

gan Matangkasombut, Ponpan, Marigowda, Gautham, Ervine, Aaron, Idris, Luaie, Pichavant, Muriel, Kim, Hye Young, Yasumi, Takahiro, Wilson, S. Brian, DeKruyff, Rosemarie H., Faul, John L., Israel, Elliot, Akbari, Omid, Umetsu, Dale T.
Cyhoeddwyd 2009

Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations

gan Oda, Hirotsugu, Nakagawa, Kenji, Abe, Junya, Awaya, Tomonari, Funabiki, Masahide, Hijikata, Atsushi, Nishikomori, Ryuta, Funatsuka, Makoto, Ohshima, Yusei, Sugawara, Yuji, Yasumi, Takahiro, Kato, Hiroki, Shirai, Tsuyoshi, Ohara, Osamu, Fujita, Takashi, Heike, Toshio
Cyhoeddwyd 2014

Tocilizumab modifies clinical and laboratory features of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis

gan Shimizu, Masaki, Mizuta, Mao, Okamoto, Nami, Yasumi, Takahiro, Iwata, Naomi, Umebayashi, Hiroaki, Okura, Yuka, Kinjo, Noriko, Kubota, Tomohiro, Nakagishi, Yasuo, Nishimura, Kenichi, Mohri, Mariko, Yashiro, Masato, Yasumura, Junko, Wakiguchi, Hiroyuki, Mori, Masaaki
Cyhoeddwyd yn Pediatr Rheumatol Online J (2020)

Robust and Highly-Efficient Differentiation of Functional Monocytic Cells from Human Pluripotent Stem Cells under Serum- and Feeder Cell-Free Conditions

gan Yanagimachi, Masakatsu D., Niwa, Akira, Tanaka, Takayuki, Honda-Ozaki, Fumiko, Nishimoto, Seiko, Murata, Yuuki, Yasumi, Takahiro, Ito, Jun, Tomida, Shota, Oshima, Koichi, Asaka, Isao, Goto, Hiroaki, Heike, Toshio, Nakahata, Tatsutoshi, Saito, Megumu K.
Cyhoeddwyd 2013

Clinical features and characteristics of uveitis associated with juvenile idiopathic arthritis in Japan: first report of the pediatric rheumatology association of Japan (PRAJ)

gan Yasumura, Junko, Yashiro, Masato, Okamoto, Nami, Shabana, Kosuke, Umebayashi, Hiroaki, Iwata, Naomi, Okura, Yuka, Kubota, Tomohiro, Shimizu, Masaki, Tomiita, Minako, Nakagishi, Yasuo, Nishimura, Kenichi, Hara, Ryoki, Mizuta, Mao, Yasumi, Takahiro, Yamaide, Fumiya, Wakiguchi, Hiroyuki, Kobayashi, Masao, Mori, Masaaki
Cyhoeddwyd yn Pediatr Rheumatol Online J (2019)

Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function

gan Oda, Hirotsugu, Sato, Tatsuhiro, Kunishima, Shinji, Nakagawa, Kenji, Izawa, Kazushi, Hiejima, Eitaro, Kawai, Tomoki, Yasumi, Takahiro, Doi, Hiraku, Katamura, Kenji, Numabe, Hironao, Okamoto, Shinya, Nakase, Hiroshi, Hijikata, Atsushi, Ohara, Osamu, Suzuki, Hidenori, Morisaki, Hiroko, Morisaki, Takayuki, Nunoi, Hiroyuki, Hattori, Seisuke, Nishikomori, Ryuta, Heike, Toshio
Cyhoeddwyd yn Eur J Hum Genet (2016)

Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease

gan Tsumura, Miyuki, Okada, Satoshi, Sakai, Hidemasa, Yasunaga, Shin’ichiro, Ohtsubo, Motoaki, Murata, Takuji, Obata, Hideto, Yasumi, Takahiro, Kong, Xiao-Fei, Abhyankar, Avinash, Heike, Toshio, Nakahata, Tatsutoshi, Nishikomori, Ryuta, Al-Muhsen, Saleh, Boisson-Dupuis, Stéphanie, Casanova, Jean-Laurent, AlZahrani, Mofareh, Shehri, Mohammed Al, ElGhazali, Geyhad, Takihara, Yoshihiro, Kobayashi, Masao
Cyhoeddwyd 2012

High Incidence of NLRP3 Somatic Mosaicism in Patients With Chronic Infantile Neurologic, Cutaneous, Articular Syndrome: Results of an International Multicenter Collaborative Study

gan Tanaka, Naoko, Izawa, Kazushi, Saito, Megumu K., Sakuma, Mio, Oshima, Koichi, Ohara, Osamu, Nishikomori, Ryuta, Morimoto, Takeshi, Kambe, Naotomo, Goldbach-Mansky, Raphaela, Aksentijevich, Ivona, de Saint Basile, Geneviève, Neven, Bénédicte, van Gijn, Mariëlle, Frenkel, Joost, Aróstegui, Juan I., Yagüe, Jordi, Merino, Rosa, Ibañez, Mercedes, Pontillo, Alessandra, Takada, Hidetoshi, Imagawa, Tomoyuki, Kawai, Tomoki, Yasumi, Takahiro, Nakahata, Tatsutoshi, Heike, Toshio
Cyhoeddwyd 2011

Rescue of recurrent deep intronic mutation underlying cell type–dependent quantitative NEMO deficiency

gan Boisson, Bertrand, Honda, Yoshitaka, Ajiro, Masahiko, Bustamante, Jacinta, Bendavid, Matthieu, Gennery, Andrew R., Kawasaki, Yuri, Ichishima, Jose, Osawa, Mitsujiro, Nihira, Hiroshi, Shiba, Takeshi, Tanaka, Takayuki, Chrabieh, Maya, Bigio, Benedetta, Hur, Hong, Itan, Yuval, Liang, Yupu, Okada, Satoshi, Izawa, Kazushi, Nishikomori, Ryuta, Ohara, Osamu, Heike, Toshio, Abel, Laurent, Puel, Anne, Saito, Megumu K., Casanova, Jean-Laurent, Hagiwara, Masatoshi, Yasumi, Takahiro
Cyhoeddwyd yn J Clin Invest (2018)