Výsledky vyhledávání - Ueda, Yoshiyasu
- Zobrazuji výsledky 1 - 11 z 11
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Blocking Properdin Prevents Complement-Mediated Hemolytic Uremic Syndrome and Systemic Thrombophilia Autor Ueda, Yoshiyasu, Miwa, Takashi, Gullipalli, Damodar, Sato, Sayaka, Ito, Daisuke, Kim, Hangsoo, Palmer, Matthew, Song, Wen-Chao
Vydáno 2018Text -
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Antibody inhibition of properdin prevents complement-mediated intravascular and extravascular hemolysis(1) Autor Gullipalli, Damodar, Zhang, Fengkui, Sato, Sayaka, Ueda, Yoshiyasu, Kimura, Yuko, Golla, Mahdu, Miwa, Takashi, Wang, Jianxiang, Song, Wen-Chao
Vydáno 2018Text -
4
CREBH Determines the Severity of Sulpyrine-Induced Fatal Shock Autor Kamiyama, Naganori, Yamamoto, Masahiro, Saiga, Hiroyuki, Ma, Ji Su, Ohshima, Jun, Machimura, Sakaaki, Sasai, Miwa, Kimura, Taishi, Ueda, Yoshiyasu, Kayama, Hisako, Takeda, Kiyoshi
Vydáno 2013Text -
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Prevention of Fatal C3 Glomerulopathy by Recombinant Complement Receptor of the Ig Superfamily Autor Wang, Xiaoxu, Van Lookeren Campagne, Menno, Katschke, Kenneth J., Gullipalli, Damodar, Miwa, Takashi, Ueda, Yoshiyasu, Wang, Yuan, Palmer, Matthew, Xing, Guolan, Song, Wen-Chao
Vydáno 2018Text -
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Intestinal CX(3)C chemokine receptor 1(high) (CX(3)CR1(high)) myeloid cells prevent T-cell-dependent colitis Autor Kayama, Hisako, Ueda, Yoshiyasu, Sawa, Yukihisa, Jeon, Seong Gyu, Ma, Ji Su, Okumura, Ryu, Kubo, Atsuko, Ishii, Masaru, Okazaki, Taku, Murakami, Masaaki, Yamamoto, Masahiro, Yagita, Hideo, Takeda, Kiyoshi
Vydáno 2012Text -
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Complement Factor H Mutation W1206R Causes Retinal Thrombosis and Ischemic Retinopathy in Mice Autor Song, Delu, Ueda, Yoshiyasu, Bhuyan, Rupak, Mohammed, Imran, Miwa, Takashi, Gullipali, Damodar, Kim, Hangsoo, Zhou, Lin, Song, Ying, Schultz, Hannah, Bargoud, Albert, Dunaief, Joshua L., Song, Wen-Chao
Vydáno 2019Text -
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Probiotic Bifidobacterium breve Induces IL-10-Producing Tr1 Cells in the Colon Autor Jeon, Seong Gyu, Kayama, Hisako, Ueda, Yoshiyasu, Takahashi, Takuya, Asahara, Takashi, Tsuji, Hirokazu, Tsuji, Noriko M., Kiyono, Hiroshi, Ma, Ji Su, Kusu, Takashi, Okumura, Ryu, Hara, Hiromitsu, Yoshida, Hiroki, Yamamoto, Masahiro, Nomoto, Koji, Takeda, Kiyoshi
Vydáno 2012Text -
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Severe Osteomalacia with Dent Disease Caused by a Novel Intronic Mutation of the CLCN5 gene Autor Matsumoto, Ayumi, Matsui, Isao, Mori, Takayasu, Sakaguchi, Yusuke, Mizui, Masayuki, Ueda, Yoshiyasu, Takahashi, Atsushi, Doi, Yohei, Shimada, Karin, Yamaguchi, Satoshi, Kubota, Keiichi, Hashimoto, Nobuhiro, Oka, Tatsufumi, Takabatake, Yoshitsugu, Sohara, Eisei, Hamano, Takayuki, Uchida, Shinichi, Isaka, Yoshitaka
Vydáno 2018Text -
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Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation Autor Ueda, Yoshiyasu, Mohammed, Imran, Song, Delu, Gullipalli, Damodar, Zhou, Lin, Sato, Sayaka, Wang, Yuan, Gupta, Shuchi, Cheng, Zhongjian, Wang, Hong, Bao, Jialing, Mao, Yingying, Brass, Lawrence, Zheng, X. Long, Miwa, Takashi, Palmer, Matthew, Dunaief, Joshua, Song, Wen-Chao
Vydáno 2017Text -
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Ecto-Nucleoside Triphosphate Diphosphohydrolase 7 Controls Th17 Cell Responses through Regulation of Luminal ATP in the Small Intestine Autor Kusu, Takashi, Kayama, Hisako, Kinoshita, Makoto, Jeon, Seong Gyu, Ueda, Yoshiyasu, Goto, Yoshiyuki, Okumura, Ryu, Saiga, Hiroyuki, Kurakawa, Takashi, Ikeda, Kayo, Maeda, Yuichi, Nishimura, Jun-ichi, Arima, Yasunobu, Atarashi, Koji, Honda, Kenya, Murakami, Masaaki, Kunisawa, Jun, Kiyono, Hiroshi, Okumura, Meinoshin, Yamamoto, Masahiro, Takeda, Kiyoshi
Vydáno 2013Text