Torthaí cuardaigh - Sumiko Inoue

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  1. 1
    Oxidative DNA damage induced by simultaneous generation of nitric oxide and superoxide

    Oxidative DNA damage induced by simultaneous generation of nitric oxide and superoxide de réir Sumiko Inoue, Shosuke Kawanishi

    Foilsithe / Cruthaithe 1995
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  2. 2
    Mechanism of DNA cleavage induced by sodium chromate(VI) in the presence of hydrogen peroxide.

    Mechanism of DNA cleavage induced by sodium chromate(VI) in the presence of hydrogen peroxide. de réir Shosuke Kawanishi, Sumiko Inoue, Seiyo Sano

    Foilsithe / Cruthaithe 1986
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  3. 3
    8-Hydroxydeoxyguanosine formation at the 5' site of 5'-GG-3' sequences in double-stranded DNA by UV radiation with riboflavin

    8-Hydroxydeoxyguanosine formation at the 5' site of 5'-GG-3' sequences in double-stranded DNA by UV radiation with riboflavin de réir K. Ito, Sumiko Inoue, Kōji Yamamoto, Shosuke Kawanishi

    Foilsithe / Cruthaithe 1993
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  4. 4
    Distinct mechanisms of oxidative DNA damage induced by carcinogenic nickel subsulfide and nickel oxides.

    Distinct mechanisms of oxidative DNA damage induced by carcinogenic nickel subsulfide and nickel oxides. de réir Shosuke Kawanishi, Shinji Oikawa, Sumiko Inoue, Kohsuke Nishino

    Foilsithe / Cruthaithe 2002
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  5. 5
    Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan

    Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan de réir Miwako Dakeishi, Takanobu Shioya, Yasuhiko Wada, Tsutomu Shindo, Kousei Otaka, Motomu Manabe, Jun‐ichi Nozaki, Sumiko Inoue, Akio Koizumi

    Foilsithe / Cruthaithe 2002
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  6. 6
    Autosomal dominant moyamoya disease maps to chromosome 17q25.3

    Autosomal dominant moyamoya disease maps to chromosome 17q25.3 de réir Yohei Mineharu, W. Liu, K. Inoue, N Matsuura, Sumiko Inoue, Katsunobu Takenaka, Hidetoshi Ikeda, Kiyohiro Houkin, Yasushi Takagi, Ken‐ichiro Kikuta, Kazuhiko Nozaki, Nobuo Hashimoto, Akio Koizumi

    Foilsithe / Cruthaithe 2008
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  7. 7
    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients de réir Hatasu Kobayashi, M Brozman, Kateřina Kyselová, Daša Viszlayová, Takaaki Morimoto, Martin Roubec, David Školoudík, Andrea Petrovičová, Dominik Juskanič, Jozef Strauss, Marián Halaj, Peter Kurray, Marián Hranai, Kouji H. Harada, Sumiko Inoue, Yukako Yoshida, Toshiyuki Habu, Roman Herzig, Shohab Youssefian, Akio Koizumi

    Foilsithe / Cruthaithe 2016
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  8. 8
    Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

    Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder de réir Robert Kleta, Elisa Romeo, Zorica Ristic, Toshihiro Ohura, Caroline Stuart, Mauricio Arcos‐Burgos, Mital H. Dave, Carsten A. Wagner, Simone M. R. Camargo, Sumiko Inoue, Norio Matsuura, Amanda Helip‐Wooley, Detlef Böckenhauer, Richard Warth, Isa Bernardini, Gepke Visser, Thomas Eggermann, Philip Lee, Arthit Chairoungdua, Promsuk Jutabha, Ellappan Babu, Sirinun Nilwarangkoon, Naohiko Anzai, Yoshikatsu Kanai, François Verrey, William A. Gahl, Akio Koizumi

    Foilsithe / Cruthaithe 2004
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