Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome von Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki

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Effect of Genetic Polymorphism of OATP-C (SLCO1B1) on Lipid-Lowering Response to HMG-CoA Reductase Inhibitors von Tachibana-Iimori, Rieko, Tabara, Yasuharu, Kusuhara, Hiroyuki, Kohara, Katsuhiko, Kawamoto, Ryuichi, Nakura, Jun, Tokunaga, Katsushi, Kondo, Ikuko, Sugiyama, Yuichi, Miki, Tetsuro

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Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies von Komatsuzaki, Shoko, Aoki, Yoko, Niihori, Tetsuya, Okamoto, Nobuhiko, Hennekam, Raoul C M, Hopman, Saskia, Ohashi, Hirofumi, Mizuno, Seiji, Watanabe, Yoriko, Kamasaki, Hotaka, Kondo, Ikuko, Moriyama, Nobuko, Kurosawa, Kenji, Kawame, Hiroshi, Okuyama, Ryuhei, Imaizumi, Masue, Rikiishi, Takeshi, Tsuchiya, Shigeru, Kure, Shigeo, Matsubara, Yoichi

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Correction: Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome von Thijssen, Peter E., Ito, Yuya, Grillo, Giacomo, Wang, Jun, Velasco, Guillaume, Nitta, Hirohisa, Unoki, Motoko, Yoshihara, Minako, Suyama, Mikita, Sun, Yu, Lemmers, Richard J. L. F., de Greef, Jessica C., Gennery, Andrew, Picco, Paolo, Kloeckener-Gruissem, Barbara, Güngör, Tayfun, Reisli, Ismail, Picard, Capucine, Kebaili, Kamila, Roquelaure, Bertrand, Iwai, Tsuyako, Kondo, Ikuko, Kubota, Takeo, van Ostaijen-Ten Dam, Monique M., van Tol, Maarten J. D., Weemaes, Corry, Francastel, Claire, van der Maarel, Silvère M., Sasaki, Hiroyuki

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Home Blood Pressure Is a Better Predictor of Carotid Atherosclerosis than Office Blood Pressure in Community-Dwelling Subjects von TACHIBANA, Rieko, TABARA, Yasuharu, KONDO, Ikuko, MIKI, Tetsuro, KOHARA, Katsuhiko

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Polymorphism of the Monocyte Chemoattractant Protein (MCP-1) Gene Is Associated with the Plasma Level of MCP-1 But Not with Carotid Intima-Media Thickness von TABARA, Yasuharu, KOHARA, Katsuhiko, YAMAMOTO, Yoshikuni, IGASE, Michiya, NAKURA, Jun, KONDO, Ikuko, MIKI, Tetsuro

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Genetic polymorphism of paraoxonase 1 (PON1) and susceptibility to Parkinson's disease von Kondo, Ikuko, Yamamoto, Mitsutoshi

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Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by “dual-fluorescence labeled PCR-restriction fragment length analysis” von Lin, Jiang X., Ishikawa, Kinya, Sakamoto, Masaki, Tsunemi, Taiji, Ishiguro, Taro, Amino, Takeshi, Toru, Shuta, Kondo, Ikuko, Mizusawa, Hidehiro

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Orthostatic Systolic Hypotension and the Reflection Pressure Wave von Tabara, Yasuharu, Nakura, Jun, Kondo, Ikuko, Miki, Tetsuro, Kohara, Katsuhiko

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Hypotension Associated with Prone Body Position: A Possible Overlooked Postural Hypotension von Tabara, Yasuharu, Tachibana-Iimori, Rieko, Yamamoto, Miyuki, Abe, Michiko, Kondo, Ikuko, Miki, Tetsuro, Kohara, Katsuhiko

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Identification of hippocampus-related candidate genes for Alzheimer's disease von Taguchi, Keiko, Yamagata, Hidehisa D., Zhong, Wangtao, Kamino, Kouzin, Akatsu, Hiroyasu, Hata, Ryuji, Yamamoto, Takayuki, Kosaka, Kenji, Takeda, Masatoshi, Kondo, Ikuko, Miki, Tetsuro

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Classic Rett syndrome in a boy with R133C mutation of MECP2 von Masuyama, Tatsuo, Matsuo, Muneaki, Jing, Jin J., Tabara, Yasuharu, Kitsuki, Kyoko, Yamagata, Hidehisa, Kan, Yuka, Miki, Tetsuro, Ishii, Kiyohisa, Kondo, Ikuko

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Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome von Itaba-Matsumoto, Noriko, Maegawa, Shinji, Yamagata, Hidehisa, Kondo, Ikuko, Oshimura, Mitsuo, Nanba, Eiji

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Methyl-CpG binding protein 2 gene ( MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms von Fukuda, Takayuki, Yamashita, Yushiro, Nagamitsu, Shinichiro, Miyamoto, Kenichi, Jin, Jing-Ji, Ohmori, Iori, Ohtsuka, Yoko, Kuwajima, Katsuko, Endo, Shoichi, Iwai, Tsuyako, Yamagata, Hidehisa, Tabara, Yasuharu, Miki, Tetsuro, Matsuishi, Toyojiro, Kondo, Ikuko

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The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein von KOBAYASHI, K, SINASAC, D. S, CRACKOWER, M. A, KONDO, I, TSUI, L.-C, SCHERER, S. W, SAHEKI, T, IIJIMA, M, BORIGHT, A. P, BEGUM, L, LEE, J. R, YASUDA, T, IKEDA, S, HIRANO, R, TERAZONO, H

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Promoter polymorphism in fibroblast growth factor 1 gene increases risk of definite Alzheimer’s disease von Yamagata, Hidehisa, Chen, Yusen, Akatsu, Hiroyasu, Kamino, Kouzin, Ito, Jin-ichi, Yokoyama, Shinji, Yamamoto, Takayuki, Kosaka, Kenji, Miki, Tetsuro, Kondo, Ikuko

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Mutation analysis of the methyl-CpG-binding protein 2 gene ( MECP2) in Rett patients with preserved speech von Yamashita, Yushiro, Kondo, Ikuko, Fukuda, Takayuki, Morishima, Riyo, Kusaga, Akira, Iwanaga, Rikako, Matsuishi, Toyojiro

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Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans von Kitamura, Kunio, Yanazawa, Masako, Sugiyama, Noriyuki, Miura, Hirohito, Iizuka-Kogo, Akiko, Kusaka, Masatomo, Omichi, Kayo, Suzuki, Rika, Kato-Fukui, Yuko, Kamiirisa, Kyoko, Matsuo, Mina, Kamijo, Shin-ichi, Kasahara, Megumi, Yoshioka, Hidefumi, Ogata, Tsutomu, Fukuda, Takayuki, Kondo, Ikuko, Kato, Mitsuhiro, Dobyns, William B, Yokoyama, Minesuke, Morohashi, Ken-ichirou

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DELAYED REFLECTION PRESSURE WAVE: NEW ASPECTS FOR POSTPRANDIAL HYPOTENSION von Okuda, Yasuko, Tabara, Yasuharu, Kondo, Ikuko, Suyama, Keiko, Miki, Tetsuro, Kohara, Katsuhiko

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A novel alternative splice variant of nicastrin and its implication in Alzheimer disease von Mitsuda, Noriaki, Yamagata, Hidehisa D., Zhong, Wangtao, Aoto, Mamoru, Akatsu, Hiroyasu, Uekawa, Natsuko, Kamino, Kouzin, Taguchi, Keiko, Yamamoto, Takayuki, Maruyama, Mitsuo, Kosaka, Kenji, Takeda, Masatoshi, Kondo, Ikuko, Miki, Tetsuro

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