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Reduction of blood group A antigen on erythrocytes in a patient with myelodysplastic syndrome harboring somatic mutations in RUNX1 and GATA2.
Hayakawa, Akira; Sano, Rie; Takahashi, Yoichiro; Okawa, Takafumi; Kubo, Rieko; Harada, Megumi; Fukuda, Haruki; Yokohama, Akihiko; Handa, Hiroshi; Kawabata-Iwakawa, Reika; Tsuneyama, Hatsue; Tsukada, Junichi; Kominato, Yoshihiko.
Afiliação
  • Hayakawa A; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Sano R; Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
  • Takahashi Y; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Okawa T; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Kubo R; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Harada M; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Fukuda H; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Yokohama A; Department of Legal Medicine, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Handa H; Blood Transfusion Service, Gunma University Hospital, Maebashi, Japan.
  • Kawabata-Iwakawa R; Department of Hematology, Gunma University Graduate School of Medicine, Maebashi, Japan.
  • Tsuneyama H; Division of Integrated Oncology Research, Gunma University Initiative for Advanced Research, Maebashi, Japan.
  • Tsukada J; Kanto-Koshinetsu Block Blood Center, Japanese Red Cross Society, Tokyo, Japan.
  • Kominato Y; Department of Hematology, University of Occupational and Environmental Health, Kitakyushu, Japan.
Transfusion ; 62(2): 469-480, 2022 02.
Article em En | MEDLINE | ID: mdl-34918362

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Subunidade alfa 2 de Fator de Ligação ao Core Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Subunidade alfa 2 de Fator de Ligação ao Core Limite: Humans Idioma: En Revista: Transfusion Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Japão