Genetic defects in pediatric-onset adrenal insufficiency in Japan von Amano, Naoko, Narumi, Satoshi, Hayashi, Mie, Takagi, Masaki, Imai, Kazuhide, Nakamura, Toshiro, Hachiya, Rumi, Sasaki, Goro, Homma, Keiko, Ishii, Tomohiro, Hasegawa, Tomonobu

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Knockdown of transmembrane protein 132A by RNA interference facilitates serum starvation-induced cell death in Neuro2a cells von Oh-hashi, Kentaro, Imai, Kazuhide, Koga, Hisashi, Hirata, Yoko, Kiuchi, Kazutoshi

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Involvement of the N-methyl-D-aspartate receptor GluN2D subunit in phencyclidine-induced motor impairment, gene expression, and increased Fos immunoreactivity von Yamamoto, Hideko, Kamegaya, Etsuko, Sawada, Wakako, Hasegawa, Ryota, Yamamoto, Toshifumi, Hagino, Yoko, Takamatsu, Yukio, Imai, Kazuhide, Koga, Hisashi, Mishina, Masayoshi, Ikeda, Kazutaka

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The subclassification of schizencephaly and its clinical characterization von Maeda, Tomoki, Akaishi, Mutsumi, Shimizu, Miki, Sekiguchi, Kazuhito, Anan, Aki, Takano, Tomoyuki, Imai, Kazuhide, Suenobu, So-ichi, Korematsu, Seigo, Izumi, Tatsuro

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A case of Fukuyama-type congenital muscular dystrophy with acute carnitine deficiency triggered by fever, vomiting, and gastrointestinal bleeding von Uchiyama, Shin-ichi, Korematsu, Seigo, Wasada, Rieko, Imai, Kazuhide, Uemura, Atsumi, Hiramatsu, Misako, Goto, Kazuya

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Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood von KASHIMADA, Ken-ichi, ONO, Makoto, ONISHI, Toshikazu, KOYAMA, Satimi, TOYOURA, Takio, IMAI, Kazuhide, SAISHO, Sumitaka, MIZUTANI, Shuki

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Microarray Analysis of Host Gene-Expression during Intracellular Nests Formation of Trypanosoma cruzi Amastigotes von Imai, Kazuhide, Mimori, Tatsuyuki, Kawai, Makoto, Koga, Hisashi

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Ph+ALL in a pediatric patient with neuroblastoma in infancy von Suenobu, So‐ichi, Handa, Yo‐suke, Kuga, Shuji, Kakiuchi, Tatsuo, Akiyoshi, Kensuke, Imai, Kazuhide, Izumi, Tatsuro

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Altered gene expression in the subdivisions of the amygdala of Fyn-deficient mice as revealed by laser capture microdissection and mKIAA cDNA array analysis von Kai, Nobuyuki, Iwase, Katsuro, Imai, Kazuhide, Nakahira, Eiko, Soma, Miho, Ohtsuka, Satoko, Yagi, Takeshi, Kobayashi, Kazuto, Koga, Hisashi, Takiguchi, Masaki, Yuasa, Shigeki

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Congenital neuromuscular disease with uniform type-1 fibers, presenting early stage dystrophic muscle pathology von Korematsu, Seigo, Imai, Kazuhide, Sato, Keisuke, Maeda, Tomoki, Suenobu, Souichi, Kojo, Masanobu, Izumi, Tatsuro

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A new method for gene discovery in large-scale microarray data von Yano, Kentaro, Imai, Kazuhide, Shimizu, Akifumi, Hanashita, Takao

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Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood von KEN-ICHI KASHIMADA, MAKOTO ONO, TOSHIKAZU ONISHI, SATIMI KOYAMA, TAKIO TOYOURA, KAZUHIDE IMAI, SUMITAKA SAISHO, SHUKI MIZUTANI

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Repeated Methamphetamine Administration Alters Expression of the NMDA Receptor Channel epsilon 2 Subunit and Kinesins in the Mouse Brain von Yamamoto, Hideko, Imai, Kazuhide, Kamegaya, Etsuko, Takamatsu, Yukio, Irago, Masashi, Hagino, Yoko, Kasai, Sinya, Shimada, Kiyo, Yamamoto, Toshifumi, Sora, Ichiro, Koga, Hisashi, Ikeda, Kazutaka

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Genetic deletion of vesicular monoamine transporter-2 (VMAT2) reduces dopamine transporter activity in mesencephalic neurons in primary culture von Yamamoto, Hideko, Kamegaya, Etsuko, Hagino, Yoko, Imai, Kazuhide, Fujikawa, Akihiro, Tamura, Kohei, Enokiya, Tomoyuki, Yamamoto, Toshifumi, Takeshima, Takao, Koga, Hisashi, Uhl, George R., Ikeda, Kazutaka, Sora, Ichiro

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A novel SNP detection technique utilizing a multiple primer extension (MPEX) on a phospholipid polymer-coated surface von Imai, Kazuhide, Ogai, Yasukazu, Nishizawa, Daisuke, Kasai, Shinya, Ikeda, Kazutaka, Koga, Hisashi

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Temporal change in mKIAA gene expression during the early stage of retinoic acid-induced neurite outgrowth von Imai, Kazuhide, Kawai, Makoto, Tada, Mitsuhiro, Nagase, Takahiro, Ohara, Osamu, Koga, Hisashi

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PRINTED WIRING BOARD von IMAI KAZUHIDE

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Repeated Methamphetamine Administration Alters Expression of the NMDA Receptor Channel ɛ2 Subunit and Kinesins in the Mouse Brain von YAMAMOTO, HIDEKO, IMAI, KAZUHIDE, KAMEGAYA, ETSUKO, TAKAMATSU, YUKIO, IRAGO, MASASHI, HAGINO, YOKO, KASAI, SINYA, SHIMADA, KIYO, YAMAMOTO, TOSHIFUMI, SORA, ICHIRO, KOGA, HISASHI, IKEDA, KAZUTAKA

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Repeated methamphetamine administration alters expression of the NMDA receptor channel epsilon2 subunit and kinesins in the mouse brain von Yamamoto, Hideko, Imai, Kazuhide, Kamegaya, Etsuko, Takamatsu, Yukio, Irago, Masashi, Hagino, Yoko, Kasai, Sinya, Shimada, Kiyo, Yamamoto, Toshifumi, Sora, Ichiro, Koga, Hisashi, Ikeda, Kazutaka

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Altered gene expression in the subdivisions of the amygdala of Fyn-deficient mice as revealed by laser capture microdissection and mKIAA cDNA array analysis von KAI, Nobuyuki, IWASE, Katsuro, YUASA, Shigeki, IMAI, Kazuhide, NAKAHIRA, Eiko, SOMA, Miho, OHTSUKA, Satoko, YAGI, Takeshi, KOBAYASHI, Kazuto, KOGA, Hisashi, TAKIGUCHI, Masaki

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