教員紹介 - 大里　元美 | 熊本保健科学大学

オオサト　モトミ Osato Motomi
大里　元美

所属

保健科学部医学検査学科

職種教授

著書・論文等
論文	High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform. Nature Communications 14,281 (共著) 2023
論文	Independent origins of fetal liver haematopoietic stem and progenitor cells. Nature 609,779-784頁 (共著) 2022
論文	RUNX1-ETO (RUNX1-RUNX1T1) induces myeloid leukemia in mice in an age-dependent manner. Leukemia 35,2983-88頁 (共著) 2021
論文	Disruption of Runx1 and Runx3 leads to bone marrow failure and leukemia predisposition due to transcriptional and DNA repair defects. Cell Reports 8,767-82頁 (共著) 2014
論文	Requirement for Runx proteins in CD4 silencing at different stages of T lymphocyte development. Cell 111,621-33頁 (共著) 2002
論文	Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2aB associated with myeloblastic leukemias. Blood 93,1817-24頁 (共著) 1999
論文	Point Mutations in the RUNX1/AML1 Gene: Another Actor in RUNX Leukemia. Oncogene 23,4284-96頁 (単著) 2004
論文	Runx3 deficiency results in myeloproliferative disorder in aged mice Blood 122,562-66頁 (共著) 2013
論文	Lineage-specific RUNX2 super-enhancer activates MYC and promotes the development of blastic plasmacytoid dendritic cell neoplasm. Nature Communications 10,1653 (共著) 2019
著書	RUNX proteins in development and cancer (共著) 2017
著書	Animal Models 疾患モデルの作製と利用 (共著) 2012
著書	血液病学の進歩 -症例から研究へ- (共著) 1996
論文	An upstream RUNX3 enhancer, eR3 (-18m/-28h), regulates the development of gut-associated anti-tumorigenic CD8+CD103+ cytotoxic T lymphocytes in mouse and human. Genes to Cells (2025) 30,e70052 (共著) 2025
論文	Genetic analysis of cell-free DNA in follicular lymphoma in comparison with tissue-derived DNA. Leukemia & Lymphoma (2025) 66,2633-2643頁 (共著) 2025
論文	Super-silencer perturbation by EZH2 and REST inhibition leads to large loss of chromatin interactions and reduction in cancer growth. Nature Structural Molecular Biology (2025) 32,137-149頁 (共著) 2025
論文	Acquired Multidrug Resistance in AML Is Caused by Low Apoptotic Priming in Relapsed Myeloblasts. Blood Cancer Discovery (2024) 5,180-201頁 (共著) 2024
論文	Activation of NOTCH signaling impedes cell proliferation and survival in acute megakaryoblastic leukemia. Experimental Hematology (2024) 137,104255 (共著) 2024
論文	Chromatin modifier Hmga2 promotes adult hematopoietic stem cell function and blood regeneration in stress conditions. EMBO Journal (2024) 43,6236-6263頁 (共著) 2024
論文	Differential requirement for IL-2 and IL-23 in the differentiation and effector functions of Th17/ILC3-like cells in a human T cell line. Journal of Leukocyte Biology (2024) 115,1108-1117頁 (共著) 2024
論文	Expression pattern of Runt-related transcription factor (RUNX) family members and the role of RUNX1 during kidney development. Biochemical and Biophysical Research Communications (2024) 722,150155 (共著) 2024
論文	IGLL5 controlled by super-enhancer affects cell survival and MYC expression in mature B-cell lymphoma. Leukemia Research Reports (2024) 21,100451 (共著) 2024
論文	Integrin-α9 overexpression underlies the niche-independent maintenance of leukemia stem cells in acute myeloid leukemia. Gene (2024) 928,148761 (共著) 2024
論文	ZBTB48 is a priming factor regulating B-cell-specific CIITA expression. EMBO Journal (2024) 43,6236-6263頁 (共著) 2024
論文	Core-binding factor fusion downregulation of ADAR2 RNA editing contributes to AML leukemogenesis. Blood (2023) 141,3078-3090頁 (共著) 2023
論文	HEY1-NCOA2 expression modulates chondrogenic differentiation and induces mesenchymal chondrosarcoma in mice. JCI Insight (2023) 8,e160279 (共著) 2023
論文	Highly efficient Runx1 enhancer eR1-mediated genetic engineering for fetal, child and adult hematopoietic stem cells. Gene (2023) 851,147049 (共著) 2023
論文	（総説　英文）Childhood hematopoietic stem cells constitute the permissive window for RUNX1-ETO leukemogenesis. International Journal of Hematology (2023) 17,830-838頁 (共著) 2023
論文	（総説　英文）The RUNX Family, a Novel Multifaceted Guardian of the Genome. Cells (2023) 12,255 (共著) 2023
論文	（総説　邦文）AML1/RUNX1の発見と白血病(1)PEBP2/CBFの発見 Bio Clinica (2023) 38,229-233頁 (単著) 2023
論文	A Myb enhancer-guided analysis of basophil and mast cell differentiation. Nature Communications (2022) 13,7064 (共著) 2022
論文	A Point Mutation R122C in RUNX3 Promotes the Expansion of Isthmus Stem Cells and Inhibits Their Differentiation in the Stomach. Cellular and Molecular Gastroenterology and Hepatology (2022) 13,1317-1345頁 (共著) 2022
論文	A Runx1-enhancer Element eR1 Identified Lineage Restricted Mammary Luminal Stem Cells. Stem Cells (2022) 40,112-122頁 (共著) 2022
論文	Bone marrow-targetable Green Tea Catechin-Based Micellar Nanocomplex for synergistic therapy of Acute myeloid leukemia. Journal of Nanobiotechnology (2022) 20,481 (共著) 2022
論文	Hepatic leukemia factor-expressing paraxial mesoderm cells contribute to the developing brain vasculature. Biology Open (2022) 11,bio059510 (共著) 2022
論文	Leukopenia, macrocytosis, and thrombocytopenia occur in young adults with Down syndrome. Gene(2022) 835,146663 (共著) 2022
論文	Oncofetal protein IGF2BP1 regulates IQGAP3 expression to maintain stem cell potential in cancer. iScience (2022) 25,105194 (共著) 2022
論文	Self-Assembled Daunorubicin/Epigallocatechin Gallate Nanocomplex for Synergistic Reversal of Chemoresistance in Leukemia. International Journal of Molecular Sciences (2022) 24,381 (共著) 2022
論文	The acidic domain of Hmga2 and the domain's linker region are critical for driving self-renewal of hematopoietic stem cell. International Journal of Hematology (2022) 115,553-562頁 (共著) 2022
論文	Super-enhancers for RUNX3 are required for cell proliferation in EBV-infected B cell lines. Gene (2021) 774,145421 (共著) 2021
論文	Tocilizumab Induces IL-10-Mediated Immune Tolerance in Invasive Candidiasis. Journal of Fungi (2021) 7,656 (共著) 2021
論文	Trib1 promotes the development of acute myeloid leukemia in a Ts1Cje mouse model of Down syndrome. Leukemia (2021) 36,558 (共著) 2021
論文	ZNF143 mediates CTCF-bound promoter-enhancer loops required for murine hematopoietic stem and progenitor cell function. Nature Communications (2021) 12,43 (共著) 2021
論文	A two-pronged anti-leukemic agent based on hyaluronic acid-green tea catechin conjugate for inducing targeted cell death and terminal differentiation. Biomaterials Science(2020) 8,497-505頁 (共著) 2020
論文	ASLAN003, a potent dihydroorotate dehydrogenase inhibitor for differentiation of acute myeloid leukemia. Haematologica (2020) 105,2286-97頁 (共著) 2020
論文	EVI1 triggers metabolic reprogramming associated with leukemogenesis and increases sensitivity to L-asparaginase. Haematologica (2020) 105,2118-29頁 (共著) 2020
論文	Hematopoietic stem cells acquire survival advantage by loss of RUNX1 methylation identified in familial leukemia. Blood (2020) 136,1919-32頁 (共著) 2020
論文	Low prevalence of the BCR-ABL1 fusion gene in a normal population in southern Sarawak. International Journal of Hematology (2020) 111,217024 (共著) 2020
論文	Lysine acetyltransferase Tip60 is required for hematopoietic stem cell maintenance. Blood (2020) 136,1735-47頁 (共著) 2020
論文	Overexpression of RUNX3 Represses RUNX1 to Drive Transformation of Myelodysplastic Syndrome. Cancer Research (2020) 80,2523-36頁 (共著) 2020
論文	（総説　英文）Systematic Review of Normal Subjects Harbouring BCR-ABL1 Fusion Gene. Acta Haematologica(2020) 143,96-111頁 (共著) 2020
論文	（総説　英文）The RUNX1 enhancer element eR1: a versatile marker for adult stem cells. Molecules and Cells(2020) 43,121-125頁 (共著) 2020
論文	（総説　邦文）RUNX1変異による家族性白血病研究20年の成果と今後の課題臨床血液(2020) 61,687-696頁 (共著) 2020
論文	Hlf expression marks the developmental pathway for hematopoietic stem cells but not for erythroid-myeloid progenitors. Journal of Experimental Medicine (2019) 216,1599-1614頁 (共著) 2019
論文	Rap1 is a key regulator of stem cell survival, oncogenesis and response to chemotherapy. Nature Communications (2019) 10,5349 (共著) 2019
論文	TUBB1 dysfunction in inherited thrombocytopenia causes genome instability. British Journal of Haematologogy (2019) 185,888-902頁 (共著) 2019
論文	（総説　英文）Systematic review of pre-clinical chronic myeloid leukaemia. International Journal of Hematology (2018) 108,465-484頁 (共著) 2018
論文	A DNA contact map for the mouse Runx1 gene identifies novel hematopoietic enhancers. Scientific Reports (2017) 17,13347 (共著) 2017
論文	Aberrant Activation of the GIMAP Enhancer by the Oncogenic TAL1 Complex Contributes to T-cell Leukemogenesis. Leukemia (2017) 31,1798-1807頁 (共著) 2017
論文	Activation of EVI1 transcription by the LEF1/β-catenin complex with p53-alteration in myeloid blast crisis of chronic myeloid leukemia. Biochemical and Biophysical Research Communications (2017) 482,994-1000頁 (共著) 2017
論文	Identification of stem cells in the epithelium of the stomach corpus and antrum of mice. Gastroenterology (2017) 152,218-31頁 (共著) 2017
論文	Ikk2 regulates cytokinesis during vertebrate development. Scientific Reports 4 (2017) 14,8094 (共著) 2017
論文	In vivo generation of engraftable murine hematopoietic stem cells by Gfi1b, c-Fos and Gata2 overexpression within teratomas. Stem Cell Reports (2017) 9,1024-1033頁 (共著) 2017
論文	LIN28B Activation by PRL-3 Promotes Leukemogenesis and a Stem Cell-like Transcriptional Program in AML. Molecular Cancer Research (2017) 482,994-1000頁 (共著) 2017
論文	RUNX3 is oncogenic in natural killer/T-cell lymphoma and is transcriptionally regulated by MYC. Leukemia (2017) 31,2219-2227頁 (共著) 2017
論文	cyclin A2 regulates erythrocyte morphology and numbers. Cell Cycle(2016) 15,3070-3081頁 (共著) 2016
論文	DUSP10 regulates intestinal epithelial barrier function and colorectal tumorigenesis. Oncogene (2016) 35,206-217頁 (共著) 2016
論文	Lack of phenotypical and morphological evidences of endothelial to hematopoietic transition in the murine embryonic head during hematopoietic stem cell emergence. PLoS One (2016) 11,e0156427 (共著) 2016
論文	Runx1 haploinsufficiency results in granulocyte-colony stimulating factor hypersensitivity. Blood Cancer Journal (2016) 6,e379 (共著) 2016
論文	The artificial loss of Runx1 reduces the expression of quiescence-associated transcription factors in CD4+ T lymphocytes. Molecular Immunology (2016) 68,223-33頁 (共著) 2016
論文	Bimodal influence of Vitamin D in host response to candida infection – Vitamin D does matters. The Journal of Infectious Diseases, 2015 212,635-44頁 (共著) 2015
論文	Cbfb deficiency results in differentiation blocks and stem/progenitor cell expansion in murine hematopoiesis. Leukemia (2015) 29,753-57頁 (共著) 2015
論文	Hematopoiesis specific loss of Cdk2 and Cdk4 results in increased erythrocyte size and delayed platelet recovery following stress. Haematologica (2015) 100,431-38頁 (共著) 2015
論文	MYC regulates the core pre-mRNA splicing machinery as an essential step in lymphomagenesis. Nature (2015) 523,96-100頁 (共著) 2015
論文	RNA helicase DP103 and TAK1: a new connection in cancer. Molecular and Cellular Oncology (2015) 2,e985911 (共著) 2015
論文	（総説　英文）Hematopoietic stem cell enhancer: a powerful tool in stem cell biology. Histology and Histopathology (2015) 30,661-72頁 (共著) 2015
論文	（総説　英文）Mouse models for Core Binding Factor leukemia. Leukemia (2015) 29,1970-80頁 (共著) 2015
論文	Characterization of the Runx gene family in a jawless vertebrate, the Japanese lamprey (Lethenteron japonicum). PLoS One (2014) 9,e113445 (共著) 2014
論文	Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects. PLoS One (2014) 9,e89397 (共著) 2014
論文	Runx family genes in a cartilaginous fish, the elephant shark (Callorhinchus milii) PLoS One (2014) 9,e93816 (共著) 2014
論文	RUNX1 point mutations potentially identify a subset of ¬¬early immature T-cell acute lymphoblastic leukaemia that may originate from differentiated T-cells. Gene (2014) 545,111-16頁 (共著) 2014
論文	（総説　英文）An unsung runt 6e isoform for HSC expansion. Blood (2014) 123,3684-86頁 (単著) 2014
論文	Polyalanine repeat polymorphism in RUNX2 is associated with site-specific fracture in post-menopausal females. PLoS One (2013) 8,e72740 (共著) 2013
論文	Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia. Journal of Clinical Investigation(2013) 123,1123-37頁 (共著) 2013
論文	（総説　英文）Runx1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes. Leukemia(2013) 27,1793-802頁 (共著) 2013
論文	（総説　邦文）RUNXファミリー遺伝子と血液細胞分化臨床血液(2013) 54,1547-53頁 (共著) 2013
論文	Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivation. PLoS One (2012) 7,e42617 (共著) 2012
論文	In situ differentiation of CD8aa T cells from CD4 T cells in peripheral lymphoid tissues. Scientific Reports (2012) 2,642 (共著) 2012
論文	Isolation of undifferentiated female germline cells from adult Drosophila ovaries. Current Protocol in Stem Cell Biology (2012) 1 (SUPPL22),2E.3 (共著) 2012
論文	（総説　英文）Runx1: No longer just for leukemia. EMBO Journal (2012) 31,4098-99頁 (共著) 2012
論文	Rumba and Haus3 Are Essential Factors for Maintenance of Hematopoietic Stem/Progenitor Cells during Zebrafish Hematopoiesis. Development(2011) 138,619-29頁 (共著) 2011
論文	Runx3 is required for full activation of regulatory T cells to prevent colitis-associated tumor formation. Journal of Immunology (2011) 186,6515-20頁 (共著) 2011
論文	The ability of MLL to bind RUNX1 and methylate H3K4 at PU.1 regulatory regions is impaired by MDS/AML-associated RUNX1/AML1 mutations. Blood(2011) 118,6544-52頁 (共著) 2011
論文	Three-dimensional imaging of whole midgestation murine embryos show an intravascular localization for all hematopoietic clusters. Blood(2011) 117,6132-34頁 (共著) 2011
論文	A Runx1 intronic enhancer marks hemogenic endothelial cells and hematopoietic stem cells. Stem Cells (2010) 28,1869-81頁 (共著) 2010
論文	Requirement for Runx proteins in IgA class switching acting downstream of TGF-b1 and retinoic acid signaling. Journal of Immunology (2010) 184,2785 (共著) 2010
論文	Stem cell exhaustion due to Runx1 deficiency is prevented by Evi5 activation in leukemogenesis. Blood, 2010 115,1610-20頁 (共著) 2010
論文	（総説　英文）Runx family genes, niche, and stem cell quiescence. Blood Cells, Molecules and Diseases (2010) 44,275-86頁 (共著) 2010
論文	Expression profiling of a hemopoietic cell survival transcriptome implicates osteopontin as a functional prognostic factor in AML. Blood(2009) 114,4859-70頁 (共著) 2009
論文	（総説　英文）Stem cell exhaustion and leukemogenesis. Journal of Cellular Biochemistry(2009) 107,393-99頁 (共著) 2009
論文	Genetic evidence for PEBP2b-independent activation of Runx1 in the murine embryo. International Journal of Hematology (2008) 88,1373-78頁 (共著) 2008
論文	Identification of marker genes including RUNX3 (AML2) that discriminate between different myeloproliferative disorders and normal individuals. Leukemia (2008) 22,1773-78頁 (共著) 2008
論文	Integrative analysis of RUNX1 downstream pathways and target genes. BMC Genomics (2008) 9,363 (共著) 2008
論文	Runx1 is involved in murine primitive erythropoiesis. Blood (2008) 111,4075 (共著) 2008
論文	RUNX3 attenuates b-catenin/T cell factors in intestinal tumorigenesis. Cancer Cell (2008) 14,226-37頁 (共著) 2008
論文	（総説　英文）Retroviral integration sites (RIS) mark cis-regulatory elements. Current Cancer Therapy Review (2008) 4,188-95頁 (共著) 2008
論文	（総説　英文）Runx1/AML1 is a guardian of hematopoietic stem cells. Current Cancer Therapy Review (2008) 4,188-95頁 (共著) 2008
論文	cDNA cloning of Runx family genes from the pufferfish (Fugu rubripes). Gene (2007) 399,162-73頁 (共著) 2007
論文	Characterization of GATA-1+ hemangioblastic cells in the mouse embryo. EMBO Journal (2007) 26,184-96頁 (共著) 2007
論文	Concurrent transcriptional deregulation of RUNX1 and GATA factors by RUNX1-TRPS1 chimeric gene in t(8;21)(q24;q22) acute myeloid leukemia. Blood (2007) 109,4023-27頁 (共著) 2007
論文	Runx1 protects hematopoietic stem/progenitor cells from oncogenic insult. Stem Cells (2007) 25,2976-86頁 (共著) 2007
論文	The myeloid features of BXH2 leukemia might result from lack of one copy of repetitive sequence in long terminal repeat (LTR) viral enhancer. International Journal of Hematology (2007) 85,170-72頁 (共著) 2007
論文	The transcription factor Runx3 represses the neurotrophin receptor TrkB during lineage commitment of dorsal root ganglion neurons. Journal of Biological Chemistry (2007) 282,24175-84頁 (共著) 2007
論文	The zebrafish udu gene encodes a novel nuclear factor and is essential for primitive erythroid cell development. Blood (2007) 110,99-106頁 (共著) 2007
論文	PRL-3 initiates tumor angiogenesis by recruiting endothelial cells in vitro and in vivo. Cancer Research (2006) 66,9625-35頁 (共著) 2006
論文	Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukemogenesis in BXH2 mice. British Journal of Haematology (2005) 131,495-507頁 (共著) 2005
論文	Identification of cooperative genes for NUP98-HOXA9 in myeloid leukemogenesis using a mouse model. Blood (2005) 105,784-93頁 (共著) 2005
論文	Increased dosage of Runx1/AML1 acts as a positive modulator of myeloid leukemogenesis in BXH2 mice. Oncogene (2005) 24,4477-85頁 (共著) 2005
論文	（総説　英文）Increased dosage of the RUNX1/AML1 gene: a third mode of RUNX leukemia? Critical Reviews in Eukaryotic Gene Expression(2005) 15,217-28頁 (共著) 2005
論文	Molecular basis for a dominant inactivation of RUNX1/AML1 by the leukemogenic inversion 16 chimera. Blood (2004) 103,3200-07頁 (共著) 2004
論文	Dual mutations of the AML1 and FLT3 genes in patients with acute myeloblastic leukemia of the M0 subtypes. Leukemia (2003) 17,2492-99頁 (共著) 2003
論文	Heterozygous PU.1 mutations are associated with acute myeloid leukemia. Blood (2003) 101,2074 (共著) 2003
論文	（総説　英文）Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations. Blood Cells, Molecules and Diseases (2003) 30,184-93頁 (共著) 2003
論文	（総説　英文）Mutation analysis of the transcription factor PU.1 in younger adults (16 to 60 years) with acute myeloid leukemia: a study of the AML Study Group Ulm (AMLSG ULM). Blood (2003) 102,3850-51頁 (共著) 2003
論文	（総説　英文）Runx and cancer. Annals Academy of Medicine Singapore(2003) 32,6-7頁 (共著) 2003
論文	（総説　邦文）ポーカーゲーム仮説. 日経サイエンス(2003) 33,3 (単著) 2003
論文	Functional analysis of RUNX2 mutations in Japanese patients with Cleidocranial Dysplasia demonstrate novel genotype-phenotype correlations. American Journal of Human Genetics (2002) 71,724-38頁 (共著) 2002
論文	Heterozygous PU.1 mutations are associated with acute myeloid leukemia. Blood (2002) 100,998-1007頁 (共著) 2002
論文	In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukaemia: implications for mechanisms of pathogenesis. Blood (2002) 99,1364-72頁 (共著) 2002
論文	（総説　邦文）PEBP2b/ CBFb と白血病. 細胞工学(2002) 21,1212-13頁 (共著) 2002
論文	（総説　邦文）RUNX1 (AML1) とHaploinsufficiency. 分子細胞治療 (2002) 1,49-56頁 (共著) 2002
論文	（総説　邦文）RUNX1/AML1 と白血病. 細胞工学(2002) 21,1199-1200頁 (単著) 2002
論文	Requirement of Runx1/Aml1/PEBP2aB for the generation of haematopoietic cells from endothelial cells. Genes to Cells(2001) 5,1-12頁 (共著) 2001
論文	（総説　英文）Point mutations of the RUNX1/AML1 gene in sporadic and familial myeloid leukemias. International Journal of Hematology (2001) 74,245-25頁 (共著) 2001
論文	（総説　邦文）RUNX1/AML1と白血病. 血液・腫瘍科 (2001),98-107頁 (共著) 2001
論文	（総説　邦文）AML1/PEBPaB の機能消失と白血病原性. 蛋白質核酸酵素 (2000) 45,40-47頁 (共著) 2000
論文	（総説　邦文）RNase Cleavage Assay 法による点突然変異の検出. 血液・腫瘍科(2000) 40,376-80頁 (共著) 2000
論文	（総説　邦文）造血発生、血球分化とRUNX1 (AML1). 分子細胞治療(2000) 1,172-86頁 (共著) 2000
論文	Characterization of T-cell receptor b chain mRNA expression in IFN-a-responsive chronic myelogenous leukemia patients. British Journal of Hematology (1999) 105,173-80頁 (共著) 1999
論文	（総説　邦文）白血病細胞におけるAML1/PEBPaB遺伝子の点突然変異. 血液・腫瘍科 (1998) 36,69-76頁 (共著) 1999
論文	Acute Myelomonoblastic Leukemia Carrying the PEBP2b /MYH11 Fusion Gene. Leukemia & Lymphoma (1998) 31,81-91頁 (共著) 1998
論文	Induction of antitumor cytotoxic activity using CD34+ cord blood cell-derived and irradiated tumor cell-primed dendritic cells. International Journal of Hematology (1998) 68,169-82頁 (共著) 1998
論文	（総説　邦文）AML1 と白血病. 医学のあゆみ (1999) 190,318-22頁 (共著) 1998
論文	Myelomonoblastic leukaemia cells carrying the PEBP2b/MYH11 fusion gene are CD34+,c-KIT+ immature cells. British Journal of Haematology (1997) 97,656-58頁 (共著) 1997
論文	p53 gene mutation and loss of heterozygosity are associated with increased risk of disease progression in adult T-cell leukemia. British Journal of Haematology (1997) 97,656-58頁 (共著) 1997
論文	TEL/AML1 fusion gene resulting from a cryptic t(12;21) is uncommon in adult patients with B-cell lineage ALL and CML lymphoblastic transformation. International Journal of Hematology (1997) 66,213-18頁 (共著) 1997
論文	Lack of the expression of EBNA-2 and LMP-1 in T-cell neoplasms possessing Epstein-Barr-virus. Blood (1995) 85,480-86頁 (共著) 1995