Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yoko, Ohwada"'
Autor:
Takayuki Miyamoto, Yoshitaka Honda, Kazushi Izawa, Nobuo Kanazawa, Saori Kadowaki, Hidenori Ohnishi, Masakazu Fujimoto, Naotomo Kambe, Naoya Kase, Takeshi Shiba, Yasuo Nakagishi, Shuji Akizuki, Kosaku Murakami, Masahiro Bamba, Yutaka Nishida, Ayano Inui, Tomoo Fujisawa, Daisuke Nishida, Naomi Iwata, Yoshikazu Otsubo, Shingo Ishimori, Momoko Nishikori, Kiminobu Tanizawa, Tomoyuki Nakamura, Takeshi Ueda, Yoko Ohwada, Yu Tsuyusaki, Masaki Shimizu, Takasuke Ebato, Kousho Iwao, Akiharu Kubo, Toshinao Kawai, Tadashi Matsubayashi, Tatsuhiko Miyazaki, Tomohiro Kanayama, Masahiko Nishitani-Isa, Hiroshi Nihira, Junya Abe, Takayuki Tanaka, Eitaro Hiejima, Satoshi Okada, Osamu Ohara, Megumu K. Saito, Junko Takita, Ryuta Nishikomori, Takahiro Yasumi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
PurposeUpregulation of type I interferon (IFN) signaling has been increasingly detected in inflammatory diseases. Recently, upregulation of the IFN signature has been suggested as a potential biomarker of IFN-driven inflammatory diseases. Yet, it rem
Externí odkaz:
https://doaj.org/article/5700023cf0774dc68dac5c83825a3a61
Autor:
Xiaoyuan Jia, Tomohiko Yamamura, Rasheed Gbadegesin, Michelle T. McNulty, Kyuyong Song, China Nagano, Yuki Hitomi, Dongwon Lee, Yoshihiro Aiba, Seik-Soon Khor, Kazuko Ueno, Yosuke Kawai, Masao Nagasaki, Eisei Noiri, Tomoko Horinouchi, Hiroshi Kaito, Riku Hamada, Takayuki Okamoto, Koichi Kamei, Yoshitsugu Kaku, Rika Fujimaru, Ryojiro Tanaka, Yuko Shima, Jiwon Baek, Hee Gyung Kang, Il-Soo Ha, Kyoung Hee Han, Eun Mi Yang, Asiri Abeyagunawardena, Brandon Lane, Megan Chryst-Stangl, Christopher Esezobor, Adaobi Solarin, Claire Dossier, Georges Deschênes, Marina Vivarelli, Hanna Debiec, Kenji Ishikura, Masafumi Matsuo, Kandai Nozu, Pierre Ronco, Hae Il Cheong, Matthew G. Sampson, Katsushi Tokunaga, Kazumoto Iijima, Yoshinori Araki, Yoshinobu Nagaoka, Yasuyuki Sato, Asako Hayashi, Toshiyuki Takahashi, Hayato Aoyagi, Michihiko Ueno, Masanori Nakanishi, Nariaki Toita, Kimiaki Uetake, Norio Kobayashi, Shoji Fujita, Kazushi Tsuruga, Naonori Kumagai, Hiroki Kudo, Eriko Tanaka, Tae Omori, Mari Okada, Yoshiho Hatai, Tomohiro Udagawa, Yaeko Motoyoshi, Masao Ogura, Mai Sato, Yuji Kano, Motoshi Hattori, Kenichiro Miura, Yutaka Harita, Shoichiro Kanda, Emi Sawanobori, Anna Kobayashi, Manabu Kojika, Yoko Ohwada, Kunimasa Yan, Hiroshi Hataya, Chikako Terano, Ryoko Harada, Yuko Hamasaki, Junya Hashimoto, Shuichi Ito, Hiroyuki Machida, Aya Inaba, Takeshi Matsuyama, Miwa Goto, Masaki Shimizu, Kazuhide Ohta, Yohei Ikezumi, Takeshi Yamada, Toshiaki Suzuki, Soichi Tamamura, Yukiko Mori, Yoshihiko Hidaka, Daisuke Matsuoka, Tatsuya Kinoshita, Shunsuke Noda, Masashi Kitahara, Naoya Fujita, Satoshi Hibino, Shogo Minamikawa, Keita Nakanishi, Junya Fujimura, Nana Sakakibara, Yuya Aoto, Shinya Ishiko, Kyoko Kanda, Yosuke Inaguma, Yuya Hashimura, Shingo Ishimori, Naohiro Kamiyoshi, Takayuki Shibano, Yasuhiro Takeshima, Hiroaki Ueda, Akira Ashida, Hideki Matsumura, Takuo Kubota, Taichi Kitaoka, Yusuke Okuda, Toshihiro Sawai, Tomoyuki Sakai, Taketsugu Hama, Mikiya Fujieda, Masayuki Ishihara, Shigeru Itoh, Takuma Iwaki, Maki Shimizu, Koji Nagatani, Shoji Kagami, Maki Urushihara, Manao Nishimura, Miwa Yoshino, Ken Hatae, Maiko Hinokiyama, Rie Kuroki, Yasufumi Ohtsuka, Masafumi Oka, Shinji Nishimura, Tadashi Sato, Seiji Tanaka, Ayuko Zaitsu, Hitoshi Nakazato, Hiroshi Tamura, Koichi Nakanishi, Min Hyun Cho, Tae-Sun Ha, Ji Hyun Kim, Peong Gang Park, Myung Hyun Cho, Alejandro Quiroga, Asha Moudgil, Blanche Chavers, Charles Kwon, Corinna Bowers, Deb Gipson, Deepa Chand, Donald Jack Weaver, Elizabeth Abraham, Halima Janjua, Jen-Jar Lin, Larry Greenbaum, Mahmoud Kallash, Michelle Rheault, Nilka De Jeus Gonzalez, Patrick Brophy, Shashi Nagaraj, Susan Massengill, Tarak Srivastava, Tray Hunley, Yi Cai, Abiodun Omoloja, Cynthia Silva, Adebowale Adeyemo, Shenal Thalgahagoda, Jameela A. Kari, Sherif El Desoky, Mohammed Abdelhadi, Rachida Akil, Sonia Azib, Romain Basmaci, Gregoire Benoist, Philippe Bensaid, Philippe Blanc, Olivia Boyer, Julie Bucher, Anne Chace, Arnaud Chalvon, Marion Cheminee, Sandrine Chendjou, Patrick Daoud, Ossam Elias, Chantal Gagliadone, Vincent Gajdos, Aurélien Galerne, Evelyne Jacqz Aigrain, Lydie Joly Sanchez, Mohamed Khaled, Fatima Khelfaoui, Yacine Laoudi, Anis Larakeb, Tarek Limani, Fouad Mahdi, Alexis Mandelcwaijg, Stephanie Muller, Kacem Nacer, Sylvie Nathanson, Béatrice Pellegrino, Isabelle Pharaon, Véronica Roudault, Sébastien Rouget, Marc Saf, Tabassom Simon, Cedric Tahiri, Tim Ulinski, Férielle Zenkhri
Publikováno v:
Kidney International
Kidney International, Nature Publishing Group, 2020, ⟨10.1016/j.kint.2020.05.029⟩
Kidney Int
Kidney International, Nature Publishing Group, 2020, ⟨10.1016/j.kint.2020.05.029⟩
Kidney Int
To understand the genetics of steroid-sensitive nephrotic syndrome (SSNS), we conducted a genome-wide association study in 987 childhood SSNS patients and 3,206 healthy controls with Japanese ancestry. Beyond known associations in the HLA-DR/DQ regio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e9f498de3de6242760614976f35b3f9
https://hal.archives-ouvertes.fr/hal-02962717
https://hal.archives-ouvertes.fr/hal-02962717
Autor:
Xiaoyuan Jia, Seik-Soon Khor, Emi Sawanobori, Yuko Shima, Yusuke Okuda, Koichi Nakanishi, Tomoko Horinouchi, Kaname Kojima, Kazumoto Iijima, Kandai Nozu, Yuki Hitomi, Naonori Kumagai, Hitoshi Nakazato, Rika Fujimaru, Yosuke Kawai, Takayuki Okamoto, Katsushi Tokunaga, Koichi Kamei, Yoshitsugu Kaku, Kazuhide Ohta, Akemi Shono, Yasufumi Ohtsuka, Ryojiro Tanaka, Akira Ashida, Yoko Ohwada, Kenji Ishikura, Masao Nagasaki, Yosuke Omae, Ken Hatae
Publikováno v:
Journal of the American Society of Nephrology. 29:2189-2199
Background Nephrotic syndrome is the most common cause of chronic glomerular disease in children. Most of these patients develop steroid-sensitive nephrotic syndrome (SSNS), but the loci conferring susceptibility to childhood SSNS are mainly unknown.
Autor:
Ken Sakai, Junya Hashimoto, Mai Kubota, Yoko Ohwada, Yoshihiro Itabashi, Seiichiro Shishido, Naonori Kumagai, Yuko Hamasaki, T. Yanagisawa, Takeshi Kawamura, Masaki Muramatsu, Yusuke Takahashi
Publikováno v:
Nephrology (Carlton, Vic.). 24(4)
AIM Epstein syndrome is a hereditary disease characterized by macrothrombocytopaenia and progressive nephritis. The abnormality of the MYH9 gene has a strong relationship to the severity of the disease. Severe Epstein syndrome progresses to end-stage
Autor:
Xiaoyuan, Jia, Tomoko, Horinouchi, Yuki, Hitomi, Akemi, Shono, Seik-Soon, Khor, Yosuke, Omae, Kaname, Kojima, Yosuke, Kawai, Masao, Nagasaki, Yoshitsugu, Kaku, Takayuki, Okamoto, Yoko, Ohwada, Kazuhide, Ohta, Yusuke, Okuda, Rika, Fujimaru, Ken, Hatae, Naonori, Kumagai, Emi, Sawanobori, Hitoshi, Nakazato, Yasufumi, Ohtsuka, Koichi, Nakanishi, Yuko, Shima, Ryojiro, Tanaka, Akira, Ashida, Koichi, Kamei, Kenji, Ishikura, Kandai, Nozu, Katsushi, Tokunaga, Kazumoto, Iijima
Publikováno v:
Journal of the American Society of Nephrology : JASN. 29(8)
Background Nephrotic syndrome is the most common cause of chronic glomerular disease in children. Most of these patients develop steroid-sensitive nephrotic syndrome (SSNS), but the loci conferring susceptibility to childhood SSNS are mainly unknown.
Autor:
George, Imataka, Tatsuo, Tsuboi, Keiko, Tsukada, Yoshiyuki, Watabe, Susumu, Hagisawa, Yoko, Ohwada, Osamu, Arisaka
Publikováno v:
Dokkyo journal of medical sciences. 39(1):81-84
Trisomy 13 is a complication of various congenital abnormalities of the heart, brain, etc. Regarding the vitalprognosis, many die within a year from birth. We herein report on the case of a 7-year 1-month-old boywith mosaicism trisomy 13 with the two
Autor:
Kazumoto, Iijima, Mayumi, Sako, Mari Saito, Oba, Shuichi, Ito, Hiroshi, Hataya, Ryojiro, Tanaka, Yoko, Ohwada, Koichi, Kamei, Kenji, Ishikura, Nahoko, Yata, Kandai, Nozu, Masataka, Honda, Hidefumi, Nakamura, Michio, Nagata, Yasuo, Ohashi, Koichi, Nakanishi, Norishige, Yoshikawa, K, Nakanishi
Publikováno v:
Clinical journal of the American Society of Nephrology : CJASN. 9(2)
Summary Background and objectives An open-label, multicenter, randomized phase II trial was conducted from July 1, 2005 to March 29, 2011 to compare two protocols for treating children with frequently relapsing nephrotic syndrome using microemulsifie
Autor:
Toshiharu Furukawa, Setsuo Sugiyama, Yoshihiko Iwama, Mitsuoki Eguchi, Hitoshi Sakakibara, Akinori Kosaku, Yoko Ohwada, Kenichi Sugita, Hidemaru Kikushima
Publikováno v:
Experimental and molecular pathology. 59(3)
In order to determine whether there were any differences in distribution of nuclear DNA between acute lymphocytic leukemia (ALL) and acute myelogenous leukemia (AML), the localization of DNA in blasts from the bone marrow or buffy coat of 30 patients