Aberrant serine protease activities in atopic dermatitis von Morizane, Shin, Sunagawa, Ko, Nomura, Hayato, Ouchida, Mamoru

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Uncovering Direct Targets of MiR-19a Involved in Lung Cancer Progression von Yamamoto, Kumiko, Ito, Sachio, Hanafusa, Hiroko, Shimizu, Kenji, Ouchida, Mamoru

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Thioredoxin deficiency increases oxidative stress and causes bilateral symmetrical degeneration in rat midbrain von Ohmori, Iori, Ouchida, Mamoru, Imai, Hirohiko, Ishida, Saeko, Toyokuni, Shinya, Mashimo, Tomoji

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VLX1570 induces apoptosis through the generation of ROS and induction of ER stress on leukemia cell lines von Kurozumi, Nami, Tsujioka, Takayuki, Ouchida, Mamoru, Sakakibara, Kanae, Nakahara, Takako, Suemori, Shin‐ichiro, Takeuchi, Masaki, Kitanaka, Akira, Shibakura, Misako, Tohyama, Kaoru

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“Input/output cytokines” in epidermal keratinocytes and the involvement in inflammatory skin diseases von Morizane, Shin, Mukai, Tomoyuki, Sunagawa, Ko, Tachibana, Kota, Kawakami, Yoshio, Ouchida, Mamoru

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Novel direct targets of miR-19a identified in breast cancer cells by a quantitative proteomic approach von Ouchida, Mamoru, Kanzaki, Hirotaka, Ito, Sachio, Hanafusa, Hiroko, Jitsumori, Yoshimi, Tamaru, Seiji, Shimizu, Kenji

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REPAIR FROM NEURONAL DEATH OCCURS SPONTANEOUSLY WITHIN 4 WEEKS IN TXN1 MUTANT RATS von Ohmori, Iori, Ouchida, Mamoru, Imai, Hirohiko, Ishida, Saeko, Toyokuni, Shinya, Mashimo, Tomoji

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CACNA1A variants may modify the epileptic phenotype of Dravet syndrome von Ohmori, Iori, Ouchida, Mamoru, Kobayashi, Katsuhiro, Jitsumori, Yoshimi, Mori, Akiko, Michiue, Hiroyuki, Nishiki, Teiichi, Ohtsuka, Yoko, Matsui, Hideki

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Detection of EGFR Gene Mutation in Lung Cancer by Mutant-Enriched Polymerase Chain Reaction Assay von ASANO, Hiroaki, TOYOOKA, Shinichi, HIRAKI, Akio, SUGI, Kazuro, KIURA, Katsuyuki, DATE, Hiroshi, SHIMIZU, Nobuyoshi, TOKUMO, Masaki, ICHIMURA, Kouichi, AOE, Keisuke, ITO, Sachio, TSUKUDA, Kazunori, OUCHIDA, Mamoru, AOE, Motoi, KATAYAMA, Hideki

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A Screening test for the prediction of Dravet syndrome before one year of age von Hattori, Junri, Ouchida, Mamoru, Ono, Junko, Miyake, Susumu, Maniwa, Satoshi, Mimaki, Nobuyoshi, Ohtsuka, Yoko, Ohmori, Iori

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Five-aza-2′-deoxycytidine-induced hypomethylation of cholesterol 25-hydroxylase gene is responsible for cell death of myelodysplasia/leukemia cells von Tsujioka, Takayuki, Yokoi, Akira, Itano, Yoshitaro, Takahashi, Kentaro, Ouchida, Mamoru, Okamoto, Shuichiro, Kondo, Toshinori, Suemori, Shin-ichiro, Tohyama, Yumi, Tohyama, Kaoru

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Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy von Ohmori, Iori, Ouchida, Mamoru, Ohtsuka, Yoko, Oka, Eiji, Shimizu, Kenji

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Analysis of All 34 Exons of the SPINK5 Gene in Japanese Atopic Dermatitis Patients von Morizane, Shin, Ouchida, Mamoru, Sunagawa, Ko, Sugimoto, Saeko, Kobashi, Mina, Sugihara, Satoru, Nomura, Hayato, Tsuji, Kazuhide, Sato, Atsushi, Miura, Yoshihiro, Hattori, Hiroaki, Tada, Kotaro, Huh, Wook-Kang, Seno, Akemi, Iwatsuki, Keiji

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A missense mutation of the gene encoding voltage-dependent sodium channel (Nav1.1) confers susceptibility to febrile seizures in rats von Mashimo, Tomoji, Ohmori, Iori, Ouchida, Mamoru, Ohno, Yukihiro, Tsurumi, Toshiko, Miki, Takafumi, Wakamori, Minoru, Ishihara, Shizuka, Yoshida, Takashi, Takizawa, Akiko, Kato, Megumi, Hirabayashi, Masumi, Sasa, Masashi, Mori, Yasuo, Serikawa, Tadao

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Identification of direct targets for the miR-17-92 cluster by proteomic analysis von Kanzaki, Hirotaka, Ito, Sachio, Hanafusa, Hiroko, Jitsumori, Yoshimi, Tamaru, Seiji, Shimizu, Kenji, Ouchida, Mamoru

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A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data von Kobayashi, Yoshinori, Hanaoka, Yoshiyuki, Akiayma, Tomoyuki, Ohmori, Iori, Ouchida, Mamoru, Yamamoto, Toshiyuki, Oka, Makio, Yoshinaga, Harumi, Kobayashi, Katsuhiro

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Methylphenidate improves learning impairments and hyperthermia‐induced seizures caused by an Scn1a mutation von Ohmori, Iori, Kawakami, Nozomi, Liu, Sumei, Wang, Haijiao, Miyazaki, Ikuko, Asanuma, Masato, Michiue, Hiroyuki, Matsui, Hideki, Mashimo, Tomoji, Ouchida, Mamoru

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Human RAD 17 Polymorphism at Codon 546 Is Associated with the Risk of Colorectal Cancer von Yasuda, Yukiko, Sakai, Akiko, Ito, Sachio, Sasai, Kaori, Yamamoto, Hiromasa, Matsubara, Nagahide, Ouchida, Mamoru, Katayama, Hiroshi, Shimizu, Kenji

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Allelic loss and reduced expression of the ING3, a candidate tumor suppressor gene at 7q31, in human head and neck cancers von GUNDUZ, Mehmet, OUCHIDA, Mamoru, FUKUSHIMA, Kunihiro, ITO, Sachio, JITSUMORI, Yoshimi, NAKASHIMA, Tomoko, NAGAI, Noriyuki, NISHIZAKI, Kazunori, SHIMIZU, Kenji

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Truncated SSX protein suppresses synovial sarcoma cell proliferation by inhibiting the localization of SS18-SSX fusion protein von Yoneda, Yasushi, Ito, Sachio, Kunisada, Toshiyuki, Morimoto, Yuki, Kanzaki, Hirotaka, Yoshida, Aki, Shimizu, Kenji, Ozaki, Toshifumi, Ouchida, Mamoru

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