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

od Agematsu Kazunaga, Komatsu Kenshi, Sakurai Yasuteru, Matsuoka Masao
Izdano 2009-12-01

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

od Sakurai, Yasuteru, Komatsu, Kenshi, Agematsu, Kazunaga, Matsuoka, Masao
Izdano 2009

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

od Kawamura, Sumito, Agematsu, Kazunaga, Kawamura, Daisuke, Kawamura, Goroh, Suzuki, Koji, Minami, Michio
Izdano u HSS J (2015)

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

od Shigemura, Tomonari, Kaneko, Naoe, Kobayashi, Norimoto, Kobayashi, Keiko, Takeuchi, Yusuke, Nakano, Naoko, Masumoto, Junya, Agematsu, Kazunaga
Izdano u 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

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

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

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

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

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

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

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

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

od 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
Izdano 2011

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

od 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
Izdano u ScientificWorldJournal (2016)

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

od 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
Izdano u 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

od 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
Izdano u Sci Rep (2020)

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

od 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
Izdano u PLoS One (2015)

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

od 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
Izdano u Medicine (Baltimore) (2016)

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

od 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
Izdano 2013

Familial Mediterranean Fever: Genotype-Phenotype Correlations in Japanese Patients

od 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
Izdano u Medicine (Baltimore) (2014)

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

od 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
Izdano u Am J Hum Genet (2018)

Familial Mediterranean fever is no longer a rare disease in Japan

od 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
Izdano u 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

od 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
Izdano u Arthritis Res Ther (2018)