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Nogawa Natsuko  野川 奈津子

ORCIDConnect your ORCID iD *help
Researcher Number 80757360
Other IDs
Affiliation (Current) 2025: 北海道大学, 歯学研究院, 専門研究員
Affiliation (based on the past Project Information) *help 2017 – 2021: 北海道大学, 大学病院, 医員
2016: 北海道大学, 歯学研究科, 専門研究員
Review Section/Research Field
Principal Investigator
Pediatrics
Keywords
Principal Investigator
免疫学 / 遺伝子 / PCR法 / SLC46A1 / HFM / deep intronic mutation / SLC46A1 / PCFT
  • Research Projects

    (1 results)
  • Research Products

    (1 results)
  • Co-Researchers

    (1 People)
  •  Hereditary folate malabsorption with a novel mutation in SLC46A1Principal Investigator

    • Principal Investigator
      Nogawa Natsuko
    • Project Period (FY)
      2016 – 2021
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Pediatrics
    • Research Institution
      Hokkaido University

All 2019

All Journal Article

  • [Journal Article] A deep intronic mutation of c.1166-285?T?>?G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM)2019

    • Author(s)
      Tozawa Yusuke、Abdrabou Shimaa Said Mohamed Ali、Nogawa-Chida Natsuko、Nishiuchi Ritsuo、Ishida Toshiaki、Suzuki Yuichi、Sano Hideki、Kobayashi Ryoji、Kishimoto Kenji、Ohara Osamu、Imai Kohsuke、Naruto Takuya、Kobayashi Kunihiko、Ariga Tadashi、Yamada Masafumi
    • Journal Title

      Clinical Immunology

      Volume: 208 Pages: 108256-108256

    • DOI

      10.1016/j.clim.2019.108256

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K07814, KAKENHI-PROJECT-18K07873, KAKENHI-PROJECT-16K20871
  • 1.  IMAI Kohsuke
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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