The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism von Marui, T., Funatogawa, I., Koishi, S., Yamamoto, K., Matsumoto, H., Hashimoto, O., Jinde, S., Nishida, H., Sugiyama, T., Kasai, K., Watanabe, K., Kano, Y., Kato, N.

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Rb-substitution effect on the metal-insulator transition of hollandite vanadate, K2V8O16 von Isobe, M, Koishi, S, Ueda, Y

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Molecular Cloning of a Putative Ca2+-Sensing Receptor cDNA from Human Kidney von Aida, K., Koishi, S., Tawata, M., Onaya, T.

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Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism – Corrigendum von Marui, T., Funatogawa, I., Koishi, S., Yamamoto, K., Matsumoto, H., Hashimoto, O., Nanba, E., Nishida, H., Sugiyama, T., Kasai, K., Watanabe, K., Kano, Y., Kato, N.

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Expansion of Oropouche virus in non-endemic Brazilian regions: analysis of genomic characterisation and ecological drivers von Gräf, Tiago, Delatorre, Edson, do Nascimento Ferreira, Caroline, Rossi, Agata, Santos, Hellen Geremias Gatica, Pizzato, Bianca Ribeiro, Nascimento, Valdinete, Souza, Victor, de Lima, Gustavo Barbosa, Dezordi, Filipe Zimmer, da Silva, Alexandre Freitas, de Morais, Clarice Neuenschwander Lins, Arantes, Ighor, Machado, Mariza Hoffmann, Rovaris, Darcita Buerger, Presibella, Mayra Marinho, Marques, Nelson Fernando Quallio, Pouzato, Emanuelle Gemin, Stadinicki, Jucelia, Ribeiro-Rodrigues, Rodrigo, de Jesus Sousa, Thiago, Cavalcanti, Andréa Cony, Camargo, Adriana Cardoso, e Silva, Keilla Maria Paz, de Oliveira Marques da Costa, Mayara Matias, de Bruycker-Nogueira, Fernanda, Zanluca, Camila, de Filippis, Ana Maria Bispo, dos Santos, Claudia Nunes Duarte, Wallau, Gabriel Luz, Bello, Gonzalo, Naveca, Felipe Gomes, Gonçalves, Sabrina, Araújo, Sofia Isabel Rótulo, Belettini, Senele Ana de Alcantara, de Castilhos, Marília de Melo Santos, Pimentel, Jociene Santana, da Silva, Aparecida Martins, de Moraes, Raquel Monteiro, da Silva, Gabriela Mayoral Pedroso, Koishi, Andrea Cristine, Romancini, Nicole Tanuri, Ferreira, Carla Elizabeth de Oliveira, Gruber Dorl, Gisiane, Goulart, Jaqueline Pegoretti, Nodari, Joana Zorzal, de Mendonça, Gabriela Colombo, Gatti, Felipe Donateli, Vaz, Maria Carmelita dos Santos, de Souza, Leandro Magalhães, Mejía, Matilde, Nascimento, Fernanda, Silva, Dejanane, Damasceno, Cintia, Santos, Carolina, Falcão, Diego Arruda, Vasconcelos, Andreza Pâmela, da Silva, Clintiano Curvêlo, da Silva, Veronica Gomes, Azevedo, Elisa de Almeida Neves, Acioli-Santos, Bartolomeu, Bezerra, Matheus Filgueira, Paiva, Marcelo Henrique Santos, Campos, Tulio de Lima

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A new design of the gaseous imaging detector: Micro Pixel Chamber von Ochi, Atsuhiko, Nagayoshi, Tsutomu, Koishi, Satoshi, Tanimori, Toru, Nagae, Tomofumi, Nakamura, Mirei

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Observation of large CP violation in the neutral B meson system von Abe, K, Abe, K, Abe, R, Adachi, I, Ahn, B S, Aihara, H, Akatsu, M, Alimonti, G, Asai, K, Asai, M, Asano, Y, Aso, T, Aulchenko, V, Aushev, T, Bakich, A M, Banas, E, Behari, S, Behera, P K, Beiline, D, Bondar, A, Bozek, A, Browder, T E, Casey, B C, Chang, P, Chao, Y, Chen, K F, Cheon, B G, Chistov, R, Choi, S K, Choi, Y, Dong, L Y, Dragic, J, Drutskoy, A, Eidelman, S, Eiges, V, Enari, Y, Enomoto, R, Everton, C W, Fang, F, Fujii, H, Fukunaga, C, Fukushima, M, Gabyshev, N, Garmash, A, Gershon, T J, Gordon, A, Gotow, K, Guler, H, Guo, R, Haba, J, Hamasaki, H, Hanagaki, K, Handa, F, Hara, K, Hara, T, Hastings, N C, Hayashii, H, Hazumi, M, Heenan, E M, Higasino, Y, Higuchi, I, Higuchi, T, Hirai, T, Hirano, H, Hojo, T, Hokuue, T, Hoshi, Y, Hoshina, K, Hou, S R, Hou, W S, Hsu, S C, Huang, H C, Igarashi, Y, Iijima, T, Ikeda, H, Ikeda, K, Inami, K, Ishikawa, A, Ishino, H, Itoh, R, Iwai, G, Iwasaki, H, Iwasaki, Y, Jackson, D J, Jalocha, P, Jang, H K, Jones, M, Kagan, R, Kakuno, H, Kaneko, J, Kang, J H, Kang, J S, Kapusta, P, Katayama, N, Kawai, H, Kawakami, Y, Kawamura, N, Kawasaki, T, Kichimi, H

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Polymorphism of the human Ca(2+)-sensing receptor gene in Japanese individuals: no relation to non-insulin dependent diabetes mellitus von Koishi, S, Aida, K, Tawata, M, Onaya, T

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Polymorphism of the Human Ca2+-Sensing Receptor Gene in Japanese Individuals: No Relation to Non-Insulin Dependent Diabetes Mellitus von Koishi, S., Aida, K., Tawata, M., Onaya, T.

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Prospective study of mutant frequencies at the hprt and T-cell receptor gene loci in pediatric cancer patients during chemotherapy von Sawada, M, Kubota, M, Lin, Y W, Watanabe, K, Koishi, S, Usami, I, Akiyama, Y, Matsumura, T, Furusho, K

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Serotonin transporter gene promoter polymorphism and autism: A family-based genetic association study in Japanese population von Koishi, Shinko, Yamamoto, Kenji, Matsumoto, Hideo, Koishi, Seiji, Enseki, Youichi, Oya, Akitoshi, Asakura, Arata, Aoki, Yutaka, Atsumi, Mariko, Iga, Tomiei, Inomata, Jyoji, Inoko, Hidetoshi, Sasaki, Tsukasa, Nanba, Eiji, Kato, Nobumasa, Ishii, Tetsuo, Yamazaki, Kosuke

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Molecular cloning of a putative Ca(2+)-sensing receptor cDNA from human kidney von Aida, K, Koishi, S, Tawata, M, Onaya, T

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Maternal clinic and home blood pressure measurements during pregnancy and infant birth weight: the BOSHI study von Iwama, Noriyuki, Metoki, Hirohito, Ohkubo, Takayoshi, Ishikuro, Mami, Obara, Taku, Kikuya, Masahiro, Yagihashi, Katsuyo, Nishigori, Hidekazu, Sugiyama, Takashi, Sugawara, Junichi, Yaegashi, Nobuo, Hoshi, Kazuhiko, Suzuki, Masakuni, Kuriyama, Shinichi, Imai, Yutaka

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Development of micro pixel chamber von Ochi, Atsuhiko, Nagayoshi, Tsutomu, Koishi, Satoshi, Tanimori, Toru, Nagae, Tomofumi, Nakamura, Mirei

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No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population von Marui, Tetsuya, Koishi, Shinko, Funatogawa, Ikuko, Yamamoto, Kenji, Matsumoto, Hideo, Hashimoto, Ohiko, Nanba, Eiji, Kato, Chieko, Ishijima, Michiko, Watanabe, Keiichiro, Kasai, Kiyoto, Kato, Nobumasa, Sasaki, Tsukasa

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Myelodysplasia in a child with Beckwith-Wiedemann syndrome previously treated for hepatoblastoma with multi-agent chemotherapy von Koishi, S, Kubota, M, Taniguchi, Y, Takei, N, Mamada, M, Akiyama, Y, Furusho, K, Hayashidera, T

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Rb-substitution effect on the metal-insulator transition of hollandite vanadate, K 2 V 8 O 16 von Isobe, M, Koishi, S, Ueda, Y

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Myelodysplastic syndrome presenting as third malignancy after non-Hodgkin's lymphoma and osteosarcoma von KUBOTA, M, SAWADA, M, WATANABE, K, KOISHI, S, KATAOKA, A, USAMI, I, LIN, Y. W, OKUDA, A, AKIYAMA, Y, FURUSHO, K

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Cancer chemotherapy and somatic cell mutation von Kubota, Masaru, Lin, Ying-Wei, Hamahata, Keigo, Sawada, Machiko, Koishi, Seiji, Hirota, Haruyo, Wakazono, Yoshihiro

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Notch4 gene polymorphisms are not associated with autism in Japanese population von Koishi, Shinko, Yamazaki, Kosuke, Yamamoto, Kenji, Koishi, Seiji, Enseki, Youichi, Nakamura, Yuri, Oya, Akitoshi, Yasueda, Mitsuaki, Asakura, Arata, Aoki, Yutaka, Atsumi, Mariko, Inomata, Jyoji, Inoko, Hidetoshi, Matsumoto, Hideo

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