DNA double strand break repair enzymes function at multiple steps in retroviral infection

per Agematsu Kazunaga, Komatsu Kenshi, Sakurai Yasuteru, Matsuoka Masao
Publicat 2009-12-01

DNA double strand break repair enzymes function at multiple steps in retroviral infection

per Sakurai, Yasuteru, Komatsu, Kenshi, Agematsu, Kazunaga, Matsuoka, Masao
Publicat 2009

A Case Report of Familial Mediterranean Fever Diagnosed Following the Total Knee Arthroplasty

per Kawamura, Sumito, Agematsu, Kazunaga, Kawamura, Daisuke, Kawamura, Goroh, Suzuki, Koji, Minami, Michio
Publicat a HSS J (2015)

Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease

per Shigemura, Tomonari, Kaneko, Naoe, Kobayashi, Norimoto, Kobayashi, Keiko, Takeuchi, Yusuke, Nakano, Naoko, Masumoto, Junya, Agematsu, Kazunaga
Publicat a RMD Open (2016)

Monitoring serum IL-18 levels is useful for treatment of a patient with systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome

per Shigemura, Tomonari, Yamazaki, Takashi, Hara, Yosuke, Ou, Jing-Ni, Stevens, Anne M, Ochs, Hans D, Koike, Kenichi, Agematsu, Kazunaga
Publicat 2011

DNA Cross-Link Repair Protein SNM1A Interacts with PIAS1 in Nuclear Focus Formation

per Ishiai, Masamichi, Kimura, Masayo, Namikoshi, Keiko, Yamazoe, Mitsuyoshi, Yamamoto, Kazuhiko, Arakawa, Hiroshi, Agematsu, Kazunaga, Matsushita, Nobuko, Takeda, Shunichi, Buerstedde, Jean-Marie, Takata, Minoru
Publicat 2004

Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome

per Minegishi, Yoshiyuki, Saito, Masako, Nagasawa, Masayuki, Takada, Hidetoshi, Hara, Toshiro, Tsuchiya, Shigeru, Agematsu, Kazunaga, Yamada, Masafumi, Kawamura, Nobuaki, Ariga, Tadashi, Tsuge, Ikuya, Karasuyama, Hajime
Publicat 2009

Serum Amyloid A Induces NLRP-3-Mediated IL-1β Secretion in Neutrophils

per Migita, Kiyoshi, Izumi, Yasumori, Jiuchi, Yuka, Kozuru, Hideko, Kawahara, Chieko, Nakamura, Minoru, Nakamura, Tadashi, Agematsu, Kazunaga, Masumoto, Junya, Yasunami, Michio, Kawakami, Atsushi, Eguchi, Katsumi
Publicat 2014

Defective IL-10 signaling in hyper-IgE syndrome results in impaired generation of tolerogenic dendritic cells and induced regulatory T cells

per Saito, Masako, Nagasawa, Masayuki, Takada, Hidetoshi, Hara, Toshiro, Tsuchiya, Shigeru, Agematsu, Kazunaga, Yamada, Masafumi, Kawamura, Nobuaki, Ariga, Tadashi, Tsuge, Ikuya, Nonoyama, Shigeaki, Karasuyama, Hajime, Minegishi, Yoshiyuki
Publicat 2011

Nod2-Nodosome in a Cell-Free System: Implications in Pathogenesis and Drug Discovery for Blau Syndrome and Early-Onset Sarcoidosis

per Iwasaki, Tomoyuki, Kaneko, Naoe, Ito, Yuki, Takeda, Hiroyuki, Sawasaki, Tatsuya, Heike, Toshio, Migita, Kiyoshi, Agematsu, Kazunaga, Kawakami, Atsushi, Morikawa, Shinnosuke, Mokuda, Sho, Kurata, Mie, Masumoto, Junya
Publicat a ScientificWorldJournal (2016)

Juvenile onset autoinflammatory disease due to a novel mutation in TNFAIP3 (A20)

per Sato, Shuzo, Fujita, Yuya, Shigemura, Tomonari, Matoba, Hisanori, Agematsu, Kazunaga, Sumichika, Yuya, Yashiro, Makiko, Ono, Atsushi, Kawasaki, Yukihiko, Kobayashi, Hiroko, Watanabe, Hiroshi, Koga, Tomohiro, Kawakami, Atsushi, Migita, Kiyoshi
Publicat a Arthritis Res Ther (2018)

KN3014, a piperidine-containing small compound, inhibits auto-secretion of IL-1β from PBMCs in a patient with Muckle–Wells syndrome

per Kaneko, Naoe, Kurata, Mie, Yamamoto, Toshihiro, Shigemura, Tomonari, Agematsu, Kazunaga, Yamazaki, Takashi, Takeda, Hiroyuki, Sawasaki, Tatsuya, Koga, Tomohiro, Kawakami, Atsushi, Yachie, Akihiro, Migita, Kiyoshi, Yoshiura, Koh-ichiro, Urano, Takeshi, Masumoto, Junya
Publicat a Sci Rep (2020)

Identification of Disease-Promoting HLA Class I and Protective Class II Modifiers in Japanese Patients with Familial Mediterranean Fever

per Yasunami, Michio, Nakamura, Hitomi, Agematsu, Kazunaga, Nakamura, Akinori, Yazaki, Masahide, Kishida, Dai, Yachie, Akihiro, Toma, Tomoko, Masumoto, Junya, Ida, Hiroaki, Koga, Tomohiro, Kawakami, Atsushi, Eguchi, Katsumi, Furukawa, Hiroshi, Nakamura, Tadashi, Nakamura, Minoru, Migita, Kiyoshi
Publicat a PLoS One (2015)

Multiple Serum Cytokine Profiling to Identify Combinational Diagnostic Biomarkers in Attacks of Familial Mediterranean Fever

per Koga, Tomohiro, Migita, Kiyoshi, Sato, Shuntaro, Umeda, Masataka, Nonaka, Fumiaki, Kawashiri, Shin-Ya, Iwamoto, Naoki, Ichinose, Kunihiro, Tamai, Mami, Nakamura, Hideki, Origuchi, Tomoki, Ueki, Yukitaka, Masumoto, Junya, Agematsu, Kazunaga, Yachie, Akihiro, Yoshiura, Koh-Ichiro, Eguchi, Katsumi, Kawakami, Atsushi
Publicat a Medicine (Baltimore) (2016)

The Contribution of SAA1 Polymorphisms to Familial Mediterranean Fever Susceptibility in the Japanese Population

per Migita, Kiyoshi, Agematsu, Kazunaga, Masumoto, Junya, Ida, Hiroaki, Honda, Seiyo, Jiuchi, Yuka, Izumi, Yasumori, Maeda, Yumi, Uehara, Ritei, Nakamura, Yoshikazu, Koga, Tomohiro, Kawakami, Atsushi, Nakashima, Munetoshi, Fujieda, Yuichiro, Nonaka, Fumiaki, Eguchi, Katsumi, Furukawa, Hiroshi, Nakamura, Tadashi, Nakamura, Minoru, Yasunami, Michio
Publicat 2013

Familial Mediterranean Fever: Genotype-Phenotype Correlations in Japanese Patients

per Migita, Kiyoshi, Agematsu, Kazunaga, Yazaki, Masahide, Nonaka, Fumiaki, Nakamura, Akinori, Toma, Tomoko, Kishida, Dai, Uehara, Ritei, Nakamura, Yoshikazu, Jiuchi, Yuka, Masumoto, Junya, Furukawa, Hiroshi, Ida, Hiroaki, Terai, Chihiro, Nakashima, Yoshikazu, Kawakami, Atsushi, Nakamura, Tadashi, Eguchi, Katsumi, Yasunami, Michio, Yachie, Akihiro
Publicat a Medicine (Baltimore) (2014)

Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia

per Cho, Kazutoshi, Yamada, Masafumi, Agematsu, Kazunaga, Kanegane, Hirokazu, Miyake, Noriko, Ueki, Masahiro, Akimoto, Takuma, Kobayashi, Norimoto, Ikemoto, Satoru, Tanino, Mishie, Fujita, Atsushi, Hayasaka, Itaru, Miyamoto, Satoshi, Tanaka-Kubota, Mari, Nakata, Koh, Shiina, Masaaki, Ogata, Kazuhiro, Minakami, Hisanori, Matsumoto, Naomichi, Ariga, Tadashi
Publicat a Am J Hum Genet (2018)

Familial Mediterranean fever is no longer a rare disease in Japan

per Migita, Kiyoshi, Izumi, Yasumori, Jiuchi, Yuka, Iwanaga, Nozomi, Kawahara, Chieko, Agematsu, Kazunaga, Yachie, Akihiro, Masumoto, Junya, Fujikawa, Keita, Yamasaki, Satoshi, Nakamura, Tadashi, Ubara, Yoshifumi, Koga, Tomohiro, Nakashima, Yoshikazu, Shimizu, Toshimasa, Umeda, Masataka, Nonaka, Fumiaki, Yasunami, Michio, Eguchi, Katsumi, Yoshiura, Koh-ichiro, Kawakami, Atsushi
Publicat a Arthritis Res Ther (2016)

Musculoskeletal manifestations occur predominantly in patients with later-onset familial Mediterranean fever: Data from a multicenter, prospective national cohort study in Japan

per Endo, Yushiro, Koga, Tomohiro, Ishida, Midori, Fujita, Yuya, Tsuji, Sosuke, Takatani, Ayuko, Shimizu, Toshimasa, Sumiyoshi, Remi, Igawa, Takashi, Umeda, Masataka, Fukui, Shoichi, Nishino, Ayako, Kawashiri, Shin-ya, Iwamoto, Naoki, Ichinose, Kunihiro, Tamai, Mami, Nakamura, Hideki, Origuchi, Tomoki, Agematsu, Kazunaga, Yachie, Akihiro, Masumoto, Junya, Migita, Kiyoshi, Kawakami, Atsushi
Publicat a Arthritis Res Ther (2018)