Activities of daily living in patients with Hunter syndrome: Impact of enzyme replacement therapy and hematopoietic stem cell transplantation von Tanjuakio, Julian, Suzuki, Yasuyuki, Patel, Pravin, Yasuda, Eriko, Kubaski, Francyne, Tanaka, Akemi, Yabe, Hiromasa, Mason, Robert W., Montaño, Adriana M., Orii, Kenji E., Orii, Koji O., Fukao, Toshiyuki, Orii, Tadao, Tomatsu, Shunji

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Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation von Honda, Shozo, Orii, Koji O, Kobayashi, Junya, Hayashi, Shin, Imamura, Atsushi, Imoto, Issei, Nakagawa, Eiji, Goto, Yu-ichi, Inazawa, Johji

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Severe upper airway stenosis in a boy with partial monosomy 16p13.3pter and partial trisomy 16q22qter von Yamada, Keitaro, Uchiyama, Atsushi, Arai, Mayuki, Kubodera, Kuniko, Yamamoto, Yutaka, Orii, Koji O., Nagasawa, Hiroyuki, Masuno, Mitsuo, Kohno, Yoshinori

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Missense Models [Gustm(E536A)Sly, Gustm(E536Q)Sly, and Gustm(L175F)Sly] of Murine Mucopolysaccharidosis Type VII Produced by Targeted Mutagenesis von Tomatsu, Shunji, Orii, Koji O., Vogler, Carole, Grubb, Jeffrey H., Snella, Elizabeth M., Gutierrez, Monica A., Dieter, Tatiana, Sukegawa, Kazuko, Orii, Tadao, Kondo, Naomi, Sly, William S.

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Development of MPS IVA mouse (Galnstm(hC79S·mC76S)slu) tolerant to human N-acetylgalactosamine-6-sulfate sulfatase von Tomatsu, Shunji, Gutierrez, Monica, Nishioka, Tatsuo, Yamada, Masamichi, Yamada, Mana, Tosaka, Yasuhiro, Grubb, Jeffrey H., Montaño, Adriana M., Vieira, Matheus B., Trandafirescu, Georgeta G., Peña, Olga M., Yamaguchi, Seiji, Orii, Koji O., Orii, Tadao, Noguchi, Akihiko, Laybauer, Leticia

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Defining the Pathway for Tat-mediated Delivery of β-Glucuronidase in Cultured Cells and MPS VII Mice von Orii, Koji O, Grubb, Jeffrey H, Vogler, Carole, Levy, Beth, Tan, Yun, Markova, Kamelia, Davidson, Beverly L, Mao, Q, Orii, Tadao, Kondo, Naomi, Sly, William S

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Mucopolysaccharidosis IVA (Morquio A): Identification of novel common mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene in Italian patients von Tomatsu, Shunji, Filocamo, Mirella, Orii, Koji O., Sly, William S., Gutierrez, Monica A., Nishioka, Tatsuo, Serrato, Olga Peña, Natale, Paola Di, Montaño, Adriana Maria, Yamaguchi, Seiji, Kondo, Naomi, Orii, Tadao, Noguchi, Akihiko

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BLM (the Causative Gene of Bloom Syndrome) Protein Translocation into the Nucleus by a Nuclear Localization Signal von Kaneko, Hideo, Orii, Koji O, Matsui, Eiko, Shimozawa, Nobuyuki, Fukao, Toshiyuki, Matsumoto, Takehisa, Shimamoto, Akira, Furuichi, Yasuhiro, Hayakawa, Seiro, Kasahara, Kimiko, Kondo, Naomi

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Molecular characterization of the mouse very-long-chain acyl-CoA dehydrogenase gene von Orii, K O, Aoyama, T, Saito-Ohara, F, Ikeuchi, T, Orii, T, Kondo, N, Hashimoto, T

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Defining the Pathway for Tat-mediated Delivery of [beta]-Glucuronidase in Cultured Cells and MPS VII Mice von Orii, Koji O, Grubb, Jeffrey H, Vogler, Carole, Levy, Beth, Tan, Yun, Markova, Kamelia, Davidson, Beverly L, Mao, Q, Orii, Tadao, Kondo, Naomi, Sly, William S

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Mucopolysaccharidosis IVA (Morquio A): Identification of novel common mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene in Italian patients: MUTATIONS IN BRIE... von Tomatsu, Shunji, Filocamo, Mirella, Orii, Koji O., Sly, William S., Gutierrez, Monica A., Nishioka, Tatsuo, Serrato, Olga Peña, Natale, Paola Di, Montaño, Adriana Maria, Yamaguchi, Seiji, Kondo, Naomi, Orii, Tadao, Noguchi, Akihiko

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Genes for the human mitochondrial trifunctional protein α- and β-subunits are divergently transcribed from a common promoter region von Orii, Kenji E., Orii, Koji O., Souri, Masayoshi, Orii, Tadao, Kondo, Naomi, Hashimoto, Takashi, Aoyama, Toshifumi

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Formation of the Enzyme Complex in Mitochondria Is Required for Function of Trifunctional β-Oxidation Protein von Orii, Kenji E., Aoyama, Toshifumi, Souri, Masayoshi, Jiang, Ling Ling, Orii, Koji O., Hayashi, Shuhei, Yamaguchi, Seiji, Kondo, Naomi, Orii, Tadao, Hashimoto, Takashi

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Assignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase gene (LCACD) to 17p13 by in situ hybridization von AOYAMA, T, WAKUI, K, FUKUSHIMA, Y, ORII, K. O, HASHIMOTO, T

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Assignment of the Human Mitochondrial Very-Long-Chain Acyl-CoA Dehydrogenase Gene (LCACD) to 17p13 byin SituHybridization von Aoyama, Toshifumi, Wakui, Keiko, Fukushima, Yoshimitsu, Orii, Koji O., Hashimoto, Takashi

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METHOD FOR PRODUCING DI(ARYLAMINO)ARYL COMPOUND, AND SYNTHETIC INTERMEDIATE THEREFOR von KOJI KOBAYASHI, RYOKI ORII, KAZUYOSHI OBITSU, SHUN HIRASAWA, YUJI TAKAHAMA, TAKAHIRO AKIBA, KAZUHIRO TAKEGUCHI, YUTAKA KONDOH

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