Shinichi Misawa

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Publications in SciGraph latest 50 shown

  • 2001-02 Medical Cytogenetics in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1999-08 Distinct genetic involvement of the TP53 gene in therapy-related leukemia and myelodysplasia with chromosomal losses of Nos 5 and/or 7 and its possible relationship to replication error phenotype in LEUKEMIA
  • 1997-10 Internal tandem duplication of the FLT3 gene is preferentially seen in acute myeloid leukemia and myelodysplastic syndrome among various hematological malignancies. A study on a large series of patients and cell lines in LEUKEMIA
  • 1997-09 Tandem duplications of the FLT3 receptor gene are associated with leukemic transformation of myelodysplasia in LEUKEMIA
  • 1997-08 Mutation of CDKN2 is infrequently detected in myelodysplastic syndrome in LEUKEMIA
  • 1995 Neurofibromatosis 1 gene (NF1) mutation is a rare genetic event in myelodysplastic syndrome regardless of the disease progression. in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1995 Double mutations of the N-ras gene in a patient with acute myelomonocytic leukemia. in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1989-09 Rejoining between 9q+ and Philadelphia chromosomes results in normal-looking chromosomes 9 and 22 in Ph1-negative chronic myelocytic leukemia in HUMAN GENETICS
  • 1989-01 Acute nonlymphocytic leukemia (M2) with chromosome abnormality trisomy 4 developing eight years after radiation therapy for breast cancer in ANNALS OF HEMATOLOGY
  • 1988-12 DNA analysis using long-term preserved fixed cytogenetic preparations in JOURNAL OF HUMAN GENETICS
  • 1987-12 High resolution breakpoints of the Philadelphia translocation in patients with chronic myelogenous leukemia in JOURNAL OF HUMAN GENETICS
  • 1986-09 Determination of chromosomal area of double minute chromosomes and a homogeneously staining region in HL-60 human leukemia cells by the use of a color image analyzer in JOURNAL OF HUMAN GENETICS
  • 1979-03 Partial 18 trisomy syndrome resulting from paternal 6/18 reciprocal translocation in JOURNAL OF HUMAN GENETICS
  • 1977-06 18p− syndrome associated with hemivertebrae, fused ribs and micropenis in JOURNAL OF HUMAN GENETICS
  • 1977-06 Staining properties of a benzimidazol derivative “33258 hoechst” and a simplified staining method for chromosome banding in JOURNAL OF HUMAN GENETICS
  • 1975-09 Transmission of a t(13q22q) chromosome observed in three generations with segregation of the translocation D1-trisomy syndrome in HUMANGENETIK
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