Search Results - "ITO, Shiro"

Mutations of the RNA-Specific Adenosine Deaminase Gene (DSRAD) Are Involved in Dyschromatosis Symmetrica Hereditaria by Miyamura, Yoshinori, Suzuki, Tamio, Kono, Michihiro, Inagaki, Katsuhiko, Ito, Shiro, Suzuki, Noriyuki, Tomita, Yasushi

“…Dyschromatosis symmetrica hereditaria (DSH) (also called “reticulate acropigmentation of Dohi”) is a pigmentary genodermatosis of autosomal dominant…”
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Dyschromatosis symmetrica hereditaria associated with neurological disorders by KONDO, Taisuke, SUZUKI, Tamio, ITO, Shiro, KONO, Michihiro, NEGORO, Tamiko, TOMITA, Yasushi

“…ABSTRACT Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal dominant inheritance caused by a mutation of adenosine…”
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Oculocutaneous Albinism Type 4 Is One of the Most Common Types of Albinism in Japan by Inagaki, Katsuhiko, Suzuki, Tamio, Shimizu, Hiroshi, Ishii, Norihisa, Umezawa, Yoshinori, Tada, Joji, Kikuchi, Noriaki, Takata, Minoru, Takamori, Kenji, Kishibe, Mari, Tanaka, Michi, Miyamura, Yoshinori, Ito, Shiro, Tomita, Yasushi

“…Oculocutaneous albinism (OCA) is a complex genetic disease with great clinical heterogeneity. Four different types of OCA have been reported to date (OCA1,…”
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Mutation Analysis of the ADAR1 Gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis by Suzuki, Noriyuki, Suzuki, Tamio, Inagaki, Katsuhiko, Ito, Shiro, Kono, Michihiro, Fukai, Kazuyoshi, Takama, Hiromichi, Sato, Kenji, Ishikawa, Osamu, Abe, Masatoshi, Shimizu, Hiroshi, Kawai, Masaaki, Horikawa, Tatsuya, Yoshida, Kunihiro, Matsumoto, Kazuhiko, Terui, Tadashi, Tsujioka, Kaoru, Tomita, Yasushi

“…Dyschromatosis symmetrica hereditaria (DSH) (also called “reticulate acropigmentation of Dohi”) is a pigmentary genodermatosis of autosomal dominant…”
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Enhancing shitsuke: a planned change intervention model for convenience stores in Japan by Ito, Shiro

“…Purpose The purpose of this paper is to emphasize the importance of good management and well-disciplined workforce in convenience store operations as well as…”
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Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes by KONDO, Taisuke, SUZUKI, Tamio, MITSUHASHI, Yoshihiko, ITO, Shiro, KONO, Michihiro, KOMINE, Mayumi, AKITA, Hirotaka, TOMITA, Yasushi

“…ABSTRACT Dyschromatosis symmetrica hereditaria (DSH), is a pigmentary genodermatosis of autosomal dominant inheritance. Since we clarified that the disease is…”
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Two novel mutations detected in Japanese patients with oculocutaneous albinism by Ito, Shiro, Suzuki, Tamio, Inagaki, Katsuhiko, Suzuki, Noriyuki, Kono, Michihiro, Tomita, Yasushi, Iwamoto, Takao, Mochizuki, Narutaka

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Ultrastructural Features of Trafficking Defects Are Pronounced in Melanocytic Nevus in Hermansky–Pudlak Syndrome Type 1 by Natsuga, Ken, Akiyama, Masashi, Shimizu, Tadamichi, Suzuki, Tamio, Ito, Shiro, Tomita, Yasushi, Tanaka, Junji, Shimizu, Hiroshi

“…Hermansky–Pudlak syndrome (HPS) is an autosomal recessive disorder characterized by oculocutaneous albinism, a bleeding disorder, and ceroid lipofuscinosis in…”
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Stocking effectiveness of hatchery-released kuruma prawns estimated by two-stage sampling of commercial catch in Ariake Sound, Japan by Yamaguchi, T.(Saga-ken. Ariake Fisheries Research and Development Center, Ogi (Japan)), Ito, S, Hamasaki, K, Kitada, S

“…To evaluate the stocking effectiveness of the kuruma prawn Penaeus japonicus, a two‐stage sampling survey of Gensiki bottom‐drift‐netters was carried out in…”
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Investigation on the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky–Pudlak syndrome by Suzuki, Tamio, Ito, Shiro, Inagaki, Katsuhiko, Suzuki, Noriyuki, Tomita, Yasushi, Yoshino, Makoto, Hashimoto, Takashi

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Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria by Suzuki, Noriyuki, Suzuki, Tamio, Inagaki, Katsuhiko, Ito, Shiro, Kono, Michihiro, Horikawa, Tatsuya, Fujiwara, Sakuhei, Ishiko, Akira, Matsunaga, Kayoko, Aoyama, Yumi, Tosaki-Ichikawa, Hiroko, Tomita, Yasushi

“…Dyschromatosis symmetrica hereditaria (DSH) is a pigmentary genodermatosis of autosomal-dominant inheritance. We have reported 20 different mutations of the…”
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Amplification of Both c‐myc and c‐raf‐1 Oncogenes in a Human Osteosarcoma by Ikeda, Shogo, Sumii, Hiroshi, Akiyama, Kosuke, Watanabe, Sekiko, Ito, Shiro, Inoue, Hajime, Takechi, Hideo, Tanabe, Gozo, Oda, Takuzo

“…Fourteen human bone and soft part tumor tissues were screened by Southern blot hybridization using five oncogene probes (c‐myc, c‐K‐ras, c‐fos, c‐raf‐l, and…”
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High Frequency of Hermansky–Pudlak Syndrome Type 1 (HPS1) Among Japanese Albinism Patients and Functional Analysis of HPS1 Mutant Protein by Ito, Shiro, Suzuki, Tamio, Inagaki, Katsuhiko, Suzuki, Noriyuki, Takamori, Kenji, Yamada, Tomoko, Nakazawa, Mitsuru, Hatano, Michihiro, Takiwaki, Hirotsugu, Kakuta, Yumi, Spritz, Richard A., Tomita, Yasushi

“…Hermansky–Pudlak syndrome (HPS) is an autosomal recessive disorder characterized by oculocutaneous albinism (OCA), bleeding tendency, and lysosomal…”
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OCA4: evidence for a founder effect for the p.D157N mutation of the MATP gene in Japanese and Korean by Inagaki, Katsuhiko, Suzuki, Tamio, Ito, Shiro, Suzuki, Noriyuki, Fukai, Kazuyoshi, Horiuchi, Toshiyuki, Tanaka, Toshihiko, Manabe, Etsuko, Tomita, Yasushi

“…Summary Oculocutaneous albinism type 4 (OCA4) was identified as a rare form of human OCA among a group of autosomal recessive hypopigmentary disorders. Little…”
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Virus-like particles associated with mass mortalities of the pen shell Atrina pectinata in Japan by MAENO, Yukio, YURIMOTO, Tatsuya, NASU, Hiroshi, ITO, Shiro, AISHIMA, Noboru, MATSUYAMA, Tomomasa, KAMAISHI, Takashi, OSEKO, Norihisa, WATANABE, Yasunori

“…Mass mortalities of the pen shell Atrina pectinata occurred in the fishing grounds of Ariake Bay, in southwestern Japan, during late spring and summer in 2003…”
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Medical pots of Yakushi Buddha in Japan by Okuda, Jun, Noro, Yukio, Ito, Shiro

“…The origin of Yakushi buddha (Bhaisajyaguru in Sanscrit, buddha of healing) is not clearly known. It has been proposed the original statue of Yakushi buddha…”
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A patient with subclinical oculocutaneous albinism type 2 diagnosed on getting severely sunburned by Kawai, Masahiro, Suzuki, Tamio, Ito, Shiro, Inagaki, Katsuhiko, Suzuki, Noriyuki, Tomita, Yasushi

“…P-gene-related oculocutaneous albinism (OCA2) is an autosomal recessive disorder. The phenotype is typically somewhat less severe than that of the…”
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Studies on the Conpression of Powder-like Materials. IV. : Some Consideration of Repeating Compression by BESSHO, SADAO, TOMIOKA, SUIICHI, ITO, SHIRO

“…As one of the methods for effectively carrying out the compression of powder granules (granular powders), repeated compression is reported. In order to examine…”
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STUDIES ON ATP DEAMINASE by CHUNG, SHIAU-TA, ITO, SHIRO, AIDA, KO, UEMURA, TEIJIRO

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STUDIES ON ATP DEAMINASE: V. A RELATIONSHIP BETWEEN DEAMINATION AND DECHLORINATION ACTIVITIES OF ATP DEAMINASE, ADP-DEAMINATING ENZYME AND AMP DEAMINASE by CHUNG, SHIAU-TA, ITO, SHIRO, AIDA, KO, UEMURA, TEIJIRO

“…Both ATP deaminase from Microsporum audouini and acid ADP-deaminating enzyme from Aspergillus melleus were found to catalyze the dechlorination of…”
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