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Genetic basis of myeloid transformation in familial platelet disorder/acute myeloid leukemia patients with haploinsufficient RUNX1 allele.
Sakurai, M; Kasahara, H; Yoshida, K; Yoshimi, A; Kunimoto, H; Watanabe, N; Shiraishi, Y; Chiba, K; Tanaka, H; Harada, Y; Harada, H; Kawakita, T; Kurokawa, M; Miyano, S; Takahashi, S; Ogawa, S; Okamoto, S; Nakajima, H.
Afiliación
  • Sakurai M; Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Kasahara H; Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Yoshida K; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Yoshimi A; Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Kunimoto H; Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
  • Watanabe N; Department of Transfusion Medicine & Cell Therapy, Keio University School of Medicine, Tokyo, Japan.
  • Shiraishi Y; Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Chiba K; Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Tanaka H; Laboratory of Sequence Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Harada Y; Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.
  • Harada H; Department of Hematology, Juntendo University School of Medicine, Tokyo, Japan.
  • Kawakita T; Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Kurokawa M; Department of Hematology and Oncology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Miyano S; Laboratory of DNA Information Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Takahashi S; Laboratory of Sequence Analysis, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Ogawa S; Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
  • Okamoto S; Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Nakajima H; Division of Hematology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Blood Cancer J ; 6: e392, 2016 Feb 05.
Article en En | MEDLINE | ID: mdl-26849013
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de las Plaquetas Sanguíneas / Leucemia Mieloide Aguda / Transformación Celular Neoplásica / Predisposición Genética a la Enfermedad / Alelos / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Haploinsuficiencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Cancer J Año: 2016 Tipo del documento: Article País de afiliación: Japón
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de las Plaquetas Sanguíneas / Leucemia Mieloide Aguda / Transformación Celular Neoplásica / Predisposición Genética a la Enfermedad / Alelos / Subunidad alfa 2 del Factor de Unión al Sitio Principal / Haploinsuficiencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Cancer J Año: 2016 Tipo del documento: Article País de afiliación: Japón