Reply to Walsh et al

Por Kawai, Tomoki, Hiejima, Eitaro, Oda, Hirotsugu, Izawa, Kazushi, Yasumi, Takahiro, Nishikomori, Ryuta, Okamoto, Shinya, Heike, Toshio
Publicado no Eur J Hum Genet (2017)

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

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

Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis

Por Iwatani, Sota, Uemura, Kazuya, Mizobuchi, Masami, Yoshimoto, Seiji, Kawasaki, Keiichiro, Kosaka, Yoshiyuki, Hori, Masayuki, Yasumi, Takahiro, Nakao, Hideto
Publicado no AJP Rep (2015)

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

Por Nakayama, Manabu, Oda, Hirotsugu, Nakagawa, Kenji, Yasumi, Takahiro, Kawai, Tomoki, Izawa, Kazushi, Nishikomori, Ryuta, Heike, Toshio, Ohara, Osamu
Publicado no Biochem Biophys Rep (2016)

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

Por Koh, Youngil I., Kim, Hye Young, Meyer, Everett H., Pichavant, Muriel, Akbari, Omid, Yasumi, Takahiro, Savage, Paul B., DeKruyff, Rosemarie H., Umetsu, Dale T.
Publicado no J Immunol (2008)

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

Por Masui, Sho, Yonezawa, Atsushi, Izawa, Kazushi, Hayakari, Makoto, Asakura, Kayoko, Taniguchi, Risa, Isa, Masahiko, Shibata, Hirofumi, Yasumi, Takahiro, Nishikomori, Ryuta, Takita, Junko, Matsubara, Kazuo
Publicado no 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

Por 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
Publicado em 2012

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

Por 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
Publicado no Medicine (Baltimore) (2017)

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

Por 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
Publicado em 2010

Natural Killer T Cells in the Lungs of Patients with Asthma

Por 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.
Publicado em 2009

Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations

Por 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
Publicado em 2014

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

Por 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
Publicado no 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

Por 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.
Publicado em 2013

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

Por 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
Publicado no Pediatr Rheumatol Online J (2019)

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

Por 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
Publicado no Eur J Hum Genet (2016)

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

Por 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
Publicado em 2012

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

Por 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
Publicado em 2011

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

Por 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
Publicado no J Clin Invest (2018)