Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Taichi Fujita"'
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Akademický článek
Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.
Autor: Katsuhiro Hosono, Chie Ishigami, Masayo Takahashi, Dong Ho Park, Yasuhiko Hirami, Hiroshi Nakanishi, Shinji Ueno, Tadashi Yokoi, Akiko Hikoya, Taichi Fujita, Yang Zhao, Sachiko Nishina, Jae Pil Shin, In Taek Kim, Shuichi Yamamoto, Noriyuki Azuma, Hiroko Terasaki, Miho Sato, Mineo Kondo, Shinsei Minoshima, Yoshihiro Hotta
Publikováno v: PLoS ONE, Vol 7, Iss 2, p e31036 (2012)
Retinitis pigmentosa (RP) is a highly heterogeneous genetic disease including autosomal recessive (ar), autosomal dominant (ad), and X-linked inheritance. Recently, arRP has been associated with mutations in EYS (Eyes shut homolog), which is a major
Externí odkaz: https://doaj.org/article/169e92ad12be4338a0b4893c40a96637
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3
Production Planning of Remanufactured Products with Inventory by Life-Cycle Simulation
Autor: Nobuyoshi Hashimoto, Taichi Fujita, Susumu Okumura
Publikováno v: Sustainable Production, Life Cycle Engineering and Management ISBN: 9789811567780
Manufacturers can reduce environmental impact and costs by introducing remanufacturing. In remanufacturing, inventory control of remanufactured and newly manufactured products should be considered for production planning. It is indispensable for pred
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5625b26e113bfbc401c3f37b0669bbd3
https://doi.org/10.1007/978-981-15-6779-7_16
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7
Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population
Autor: Hiroshi Nakanishi, Shuichi Yamamoto, Shinsei Minoshima, Hiroko Terasaki, Yang Zhao, Jae Pil Shin, Miho Sato, Yasuhiko Hirami, Akiko Hikoya, Mineo Kondo, Sachiko Nishina, Yoshihiro Hotta, Shinji Ueno, Tadashi Yokoi, Dong Ho Park, Noriyuki Azuma, In Taek Kim, Masayo Takahashi, Katsuhiro Hosono, Taichi Fujita, Chie Ishigami
Publikováno v: PLoS ONE
PLoS ONE, Vol 7, Iss 2, p e31036 (2012)
Retinitis pigmentosa (RP) is a highly heterogeneous genetic disease including autosomal recessive (ar), autosomal dominant (ad), and X-linked inheritance. Recently, arRP has been associated with mutations in EYS (Eyes shut homolog), which is a major
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07ec0ca88149892481328147f1fdc730
https://pubmed.ncbi.nlm.nih.gov/22363543
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Plný text Recenzováno Digitální knihovna AV ČR
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