THREE-DIMENSIONAL MODEL GENERATION DEVICE BASED ON THREE-DIMENSIONAL POINT GROUP DATA von TANAKA SHIGENORI, MARUYAMA AKIRA, TSUJI MITSUHIRO, YAMAKAWA JUNZO, GOTO KANA, OTSUKI SHOJI, YAMAZAKI FUMIAKI, KUBOTA SATOSHI, INOUE HARUYOSHI, AIDA TAKASHI, TOGUCHI SHINZO, ITO TOSHIHIDE, IMAI RYUICHI, SHIMIZU TOSHIHIRO, YASUI YOSHIFUMI, IWASA KOICHI, KIMURA TAIZO, MATSUDA KATSUMI, NAKAYAMA TADAMASA, KIKUCHI HIDEKAZU, UEDA MAYUMI, KAGEYAMA MASAHIRO, SONODA NAOKI, SATO RYUTA, NAKAMURA KENJI, NISHIKAWA KEIICHI, SHIMOJO TAKAHIRO, KITADA TOSHIHARU, JIANG WENYUAN, FUKUZUMI KEN, NISHIMURA OSAMU, UMEHARA YOSHIMASA, KAMIYA DAISUKE, MIKAMI TAKU, NAKAJIMA SHINSUKE, HIRAMI KATSUHIRO, FUJIWARA TOSHIHIRO, BABA AKIFUMI, OKUHIRA TORU, NARUO TAKESHI, MIURA YASUO, TSUKADA YOSHINORI, HIRANO YORITOSHI, YAMAMOTO YUHEI

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PANEL POINT STRUCTURE OF STEEL TRUSS WEB PRESTRESSED CONCRETE BRIDGE von HIRAMI KATSUHIRO, HONMA JUNJI, TERADA NORIO, TAKENAKA HIROFUMI

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Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population von Hosono, Katsuhiro, Ishigami, Chie, Takahashi, Masayo, Park, Dong Ho, Hirami, Yasuhiko, Nakanishi, Hiroshi, Ueno, Shinji, Yokoi, Tadashi, Hikoya, Akiko, Fujita, Taichi, Zhao, Yang, Nishina, Sachiko, Shin, Jae Pil, Kim, In Taek, Yamamoto, Shuichi, Azuma, Noriyuki, Terasaki, Hiroko, Sato, Miho, Kondo, Mineo, Minoshima, Shinsei, Hotta, Yoshihiro

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The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in C... von Zhao, Yang, Hosono, Katsuhiro, Suto, Kimiko, Ishigami, Chie, Arai, Yuuki, Hikoya, Akiko, Hirami, Yasuhiko, Ohtsubo, Masafumi, Ueno, Shinji, Terasaki, Hiroko, Sato, Miho, Nakanishi, Hiroshi, Endo, Shiori, Mizuta, Kunihiro, Mineta, Hiroyuki, Kondo, Mineo, Takahashi, Masayo, Minoshima, Shinsei, Hotta, Yoshihiro

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