Search Results - "Urata, Takayo"

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    The Nup98::Nsd1 fusion gene induces CD123 expression in 32D cells by Okamoto, Kenji, Imamura, Toshihiko, Tanaka, Seiji, Urata, Takayo, Yoshida, Hideki, Shiba, Norio, Iehara, Tomoko

    Published in International journal of hematology (01-08-2023)
    “…The NUP98::NSD1 fusion gene is associated with extremely poor prognosis in patients with acute myeloid leukemia (AML). NUP98::NSD1 induces self-renewal and…”
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    Journal Article
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    Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report by Urata, Takayo, Imamura, Toshihiko, Osone, Shinya, Muramatsu, Hideki, Takahashi, Yoshiyuki, Hosoi, Hajime

    Published in Journal of pediatric hematology/oncology (01-03-2022)
    “…Fanconi anemia (FA) is a rare genetic disorder that manifests as congenital abnormalities and bone marrow failure (BMF). Most patients with FA present with BMF…”
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    Journal Article
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    Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report by Urata, Takayo, Imamura, Toshihiko, Osone, Shinya, Muramatsu, Hideki, Takahashi, Yoshiyuki, Hosoi, Hajime

    Published in Journal of pediatric hematology/oncology (23-07-2021)
    “…Fanconi anemia (FA) is a rare genetic disorder that manifests as congenital abnormalities and bone marrow failure (BMF). Most patients with FA present with BMF…”
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    Journal Article
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    Allogeneic Hematopoietic Cell Transplantation for Dyskeratosis Congenita: A Report of 3 Cases by Tamura, Shinichi, Imamura, Toshihiko, Urata, Takayo, Kobayashi, Miki, Gen, Mari, Tomii, Toshihiro, Do, Junko, Osone, Shinya, Ishida, Hiroyuki, Hosoi, Hajime, Kuroda, Hiroshi

    Published in Journal of pediatric hematology/oncology (01-10-2017)
    “…Although bone marrow failure in patients with dyskeratosis congenita (DKC) can be successfully treated with allogeneic hematopoietic cell transplantation…”
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    Journal Article
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