Art

J-GLOBAL ID：202002289053723555   Reference number：20A0207419

RUNX1 mutation in a patient with myelodysplastic syndrome and decreased erythrocyte expression of blood group A antigen

骨髄異形成症候群患者におけるRUNX1変異と血液型A抗原の赤血球発現減少【JST・京大機械翻訳】

Author (13)： Hayakawa Akira (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Sano Rie (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Takahashi Yoichiro (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Kubo Rieko (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Harada Megumi (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Omata Masato (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Yokohama Akihiko (Transfusion Service, Gunma University Hospital, Maebashi, Japan) ,  Handa Hiroshi (Department of Hematology, Gunma University Graduate School of Medicine, Maebashi, Japan) ,  Tsukada Junichi (Department of Hematology, University of Occupational and Environmental Health, Kitakyushu, Japan) ,  Takeshita Haruo (Department of Legal Medicine, Shimane University School of Medicine, Izumo, Japan) ,  Tsuneyama Hatsue (Japanese Red Cross Central Blood Institute, Tokyo, Japan) ,  Ogasawara Kenichi (Japanese Red Cross Central Blood Institute, Tokyo, Japan) ,  Kominato Yoshihiko (Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan)
Material： Transfusion
Volume： 60  Issue： 1  Page： 184-196  Publication year： 2020 
JST Material Number： T0063A  ISSN： 0041-1132  CODEN： TRANAT  Document type： Article
Article type： 原著論文  Country of issue： United States (USA)  Language： ENGLISH (EN)

Abstract/Point： BACKGROUND: Loss of blood grou...

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Thesaurus term： RT-PCR ,  dominance ,  mutation ,  peripheral blood ,  methylation ,  *antigen ,  *bone marrow ,  heredity ,  alternative splicing ,  cDNA ,  nucleotide sequence ,  *myelodysplastic syndrome ,  *erythrocyte ,  promoter(genetics) ,  protein

JST classification (5)： Gene expression  (EC02040Q) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Clinical hematology in general  (GK01030Y) ,  Structure and chemistry of genes  (EC02020U) ,  Blood cell tumors(=neoplasms)  (GK04000M)

Terms in the title (7)： 骨髄異形成症候群 ,  患者 ,  RUNX1 ,  変異 ,  血液型 ,  赤血球 ,  発現