Tatsuo Abe

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Publications in SciGraph latest 50 shown

  • 2006-07 Osteoblast differentiation is impaired in SOCS-1-deficient mice in JOURNAL OF BONE AND MINERAL METABOLISM
  • 2002-11 Differential gene expression profiles of gastric cancer cells established from primary tumour and malignant ascites in BRITISH JOURNAL OF CANCER
  • 2002-11 Acute Myeloid Leukemia (FAB-M2) with a Masked Type of t(8;21) Translocation Revealed by Spectral Karyotyping in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2001-07 Involvement of the NUP98 Gene in a Chromosomal Translocation t(11;20)(p15;q11.2) in a Patient With Acute Monocytic Leukemia (FAB-M5b) in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2001-07 A Variant Form of Myelodysplastic Syndrome With Ph− Minor-BCR/ABL Transcript in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 2001-04 Agranular CD4+CD56+ blastic natural killer leukemia/lymphoma in ANNALS OF HEMATOLOGY
  • 2001-01 Fusion of MOZ and p300 histone acetyltransferases in acute monocytic leukemia with a t(8;22)(p11;q13) chromosome translocation in LEUKEMIA
  • 2001 Tumour-amplified kinase BTAK is amplified and overexpressed in gastric cancers with possible involvement in aneuploid formation in BRITISH JOURNAL OF CANCER
  • 2000-09 Aggressive natural killer cell leukemia/lymphoma: a comprehensive cytogenetic study by spectral karyotyping in ANNALS OF HEMATOLOGY
  • 2000-09 c-myc overexpression is not mandatory in aggressive-phase multiple myeloma with Burkitt's type translocation in ANNALS OF HEMATOLOGY
  • 2000-03 Reply to Ian Morison in LEUKEMIA
  • 1999-08 Chromosomal aberrations in human hepatocellular carcinomas associated with hepatitis C virus infection detected by comparative genomic hybridization in BRITISH JOURNAL OF CANCER
  • 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
  • 1999-07 Interleukin-11 (IL-11) enhances clonal proliferation of acute myelogenous leukemia cells with strong expression of the IL-11 receptor α chain and signal transducing gp130 in LEUKEMIA
  • 1998-05 Human cord blood-derived primitive progenitors are enriched in CD34+c-kit− cells: correlation between long-term culture-initiating cells and telomerase expression in LEUKEMIA
  • 1998-01 Analysis of histological therapeutic effect, apoptosis rate and p53 status after combined treatment with radiation, hyperthermia and 5-fluorouracil suppositories for advanced rectal cancers in BRITISH JOURNAL OF CANCER
  • 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 Increased apoptosis rate by hyperthermochemoradiotherapy for advanced rectal cancers in SURGERY TODAY
  • 1996-08 Precise localization of the human gene encoding cell adhesion kinase β (CAKβ/PYK2) to chromosome 8 at p21.1 by fluorescence in situ hybridization in HUMAN GENETICS
  • 1996 Philadelphia chromosome-negative cells with trisomy 8 after busulfan and interferon treatment of Ph1-positive chronic myelogenous leukemia. in INTERNATIONAL JOURNAL OF HEMATOLOGY
  • 1994-09 Fluorescencein situ hybridization analysis of chromosomal localization of three human cytochrome P450 2C genes (CYP2C8, 2C9, and 2C10) at 10q24.1 in JOURNAL OF HUMAN GENETICS
  • 1992-06 Assignment of the human cytochrome P-450 nifedipine oxidase gene (CYP3A4) to chromosome 7 at band q22.1 by fluorescencein situ hybridization in JOURNAL OF HUMAN GENETICS
  • 1991-10 Clinical effect of recombinant human granulocyte colony-stimulating factor (rhG-CSF) on various types of neutropenia including cyclic neutropenia in BIOTHERAPY
  • 1991 Chromosomes and Clinical Features in 6 Cases of Gliomas in BIOLOGICAL ASPECTS OF BRAIN TUMORS
  • 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
  • 1989-09 A case of incomplete DiGeorge syndrome associated with partial monosomy 22q11.1 due to maternal 14;22 translocation in JOURNAL OF 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
  • 1985-04 Human renal cell carcinoma: Establishment and characterization of a new cell line (OS-RC-2) in IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY
  • 1981-09 Activation of cyclophosphamide using perfused rat liver system and induction of sister chromatid exchanges in vitro in HUMAN GENETICS
  • 1979-03 Partial 18 trisomy syndrome resulting from paternal 6/18 reciprocal translocation in JOURNAL OF HUMAN GENETICS
  • 1977-06 Trisomy for the long arm of the chromosome 18 due tode novo 18/21 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
  • 1974-06 Possible complex translocation t(9; 14; 13)(q12;pl?;q31) in mother of a child with 9p-trisomy syndrome in HUMANGENETIK
  • 1968-06 Kongenitale nichtsphärozytäre hämolytische Anämien durch Mangel an Glucose-6-Phosphat-Dehydrogenase der Erythrozyten in einer japanischen Familie in ANNALS OF HEMATOLOGY
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