書籍詳細

1. 細胞形態、細胞化学に基づく診断

P.6 掲載の参考文献

• 1) Bennett JM et al:Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 33(4):451, 1976
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• 2) Shafer JA:Preparation of blood films for examination. in Clinical hematology Principles, procedures, correlations, Lippincott, Philadelphia, 1998

2. 遺伝子診断法

P.12 掲載の参考文献

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• 6) Takeuchi S et al:TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia. Leukemia 11:1220, 1997
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• 7) Korsmeyer SJ:Chromosomal translocations in lymphoid malignancies reveal novel proto-oncogenes. Ann Rev Immunol 10:785, 1992

• 8) van Dongen JJ et al:Arialysis of immunoglobulin and T-cell receptor genes. Part Basic and technical aspects. Clin Chim Acta 198:1, 1991

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• 17) Sparkman DR:Paraffin wax as a vapor banier for the PCR. PCR Methods 2(2):180, 1992

• 18) Don RH et al:'Touchdown' PCR to circumvent spurious priming during gene amplification. Nucleic Acids Res 19(14):4008, 1991

• 19) Cheng S et al:Long PCR. Natllre 69:684, 1994

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• 21) Kawasaki ES et al:Diagnosis of chronic myeloid and acute lymphocytic leukemias by detection of leukemia-specific mRNA sequences amplified vitro. Proc Natl Acad Sci USA 85(15):5698, 1988
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• 22) Miyoshi H et al:The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 12(7):2715, 1993

• 23) Kakizuka A et al:Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RAR alpha with a novel putative transcription factor, PML. Cell 66(4):663, 1991
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• 24) Inoue K et al:WT1 as a new prognostic factor and a new marker for the detection of minimal residual disease in acute leukemia. Blood 84(9):3071, 1994

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• 28) Akasaka T et al:Molecular and clinical features of non-Burkitt's, diffuse large-cell lymphoma of B-cell type associated with the c-MYC/immuboglobulin heavy-chain fusion gene. J Clin Oncol 18(3):510, 2000

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• 30) Borrensen AL et al:Constant denaturing gel electrophoresis as a rapid screening technique for p53 mutations. Proc Natl Acad Sci 88:8405, 1991

• 31) Nedergaard T et al:A one-step DGGE scanning method for detection of mutations in the K-, N-, and H-ras oncogenes:mutations at codons 12, 13 and 61 are rare in B-cell non-Hodgkin's lymphoma. Int J Cancer 71:364, 1997

• 32) Pongers-Willemse MJ et al:Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets. Leukernia 13:110, 1999

• 33) Briet TM et al:Human T cell leukemias with continuous V(D)J recombinase activity for TCR-δ gene deletion. J Immunol 159:4341, 1997

• 34) Beishuizen A et al:Heterogeneity in junctional regions of immunoglobulin kappa deleting element rearrangements in B cell leukemias:a new molecular target for detection of minimal residual disease. Leukemia 11:2200, 1997

• 35) Breit TM et al:Extensive junctional diversity of γδ T-cell receptors expressed by T-cell acute lymphoblastic leukemia:implications for the detection of minimal residual disease. Leukemia 5:1076, 1991

• 36) Bottaro M et al:Heteroduplex analysis of T cell receptor γ gene rearrangements for diagnosis and monitoring of cutaneous T cell lymphomas. Blood 83:3271, 1994

• 37) Kneba M et al:Analysis of rearranged T-cell receptor β-chain genes by polymerase chain reaction (PCR) DNA sequencing and automated high resolution PCR fragment analysis. Blood 86:3930, 1995

• 38) Wang AM et al:Quantitation of mRNA by the polymerase chain reaction. Proc Natl Acad Sci USA 86:9717, 1989
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• 46) Tchirkov A et al:Interphase cytogenetics and competitive RT-PCR for residual disease monitoring in patients with chronic myeloid leukemia during interferon-α therapy. Br J Haematol 101:552, 1998

• 47) Tchirkov A et al:Molecular detection of a late-appearing BCR-ABL gene in a child with T-cell acute lymphoblastic leukemia. Ann Hematol 77:55, 1998

• 48) Kuhr T et al:Detection and quantitation of genetically marked acute myeloid leukemia by competitive polymerase chain reaction after autologous bone marrow transplantation. Experimental Hematology 27:266, 1999
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• 49) Hosler GA et al:Development and validation of a quantitative polymerase chain reaction assay to evaluate minimal residual disease for T-cell acute lymphoblastic leukemia and follicular lymphoma. Am J pathol 154:lo23, 1999

• 50) Freeman WM et al:Quantitative RT-PCR:Pitfalls and Potential. BioTechniques 26:112, 1999
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• 51) Taniguchi T et al:Cyclin D1 overexpression detected by a simple competitive reverse transcription-polymerase chain reaction assay for Lymphoid Malignancies. Jpn J Cancer Res 89:159, 1998
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• 52) 島田 敦ほか:急性リンパ性白血病患者におけるcompetitive RT-PCR法を用いたWT1遺伝子mRNAの定量, 日本臨床血液学会, 第38回総会, 演題番号261, 1996

• 53) 島田 敦ほか:急性白血病患者における競合RT-PCR法を用いたflt3 mRNAの定量, 日本臨床血液学会, 第39回総会, 演題番号83, 1997

• 54) 島田 敦ほか:BCR/ABLキメラmRNAの次世代遺伝子検出システムによる定量, 日本血液学会, 第60回総会, 演題番号222, 1998

• 55) Hochhaus A et al:Molecular heterogeneity in complete cytogenetic responders after interferon-α therapy for chronic myelogenous leukemia. Blood 95(1):62, 2000

• 56) Tobal K et al:Molecular quantitation of minimal residual disease in acute myeloid leukemia with t(8;21) can identify patients in durable remission and predict clinical relapse. Blood 95(3):815, 2000

• 57) Wattjes MP et al:Comparison of nested competitive RT-PCR and real-time RT-PCR for detection and quantification of AML1/MTG8 fusion transcripts in t(8;21) positive acute myelogenous leukemia. Leukemia 14:329, 2000

• 58) Campanini F et al:Competitive polymerase chain reaction as a method to detect the amplification of bcr-abl gene of chronic myeloid leukemia. Haematologica 86(2):167, 2001
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• 59) Higuchi R et al:Kinetic PCR;Real time monitering of DNA amplification reaction. Biotechnology 11:1026, 1993

• 60) Heid CA et al:Real time quantitative PCR. Genome Res 6:986, 1996
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• 61) Kreuzer KA et al:Light Cycler technology for the quantitation of bcr/abl fusion transcripts. Cancer Res 59:3171, 1999

• 62) Kawai S et al:Quantification of hepatitis C Virus by TaqMan PCR;comparison with HCV amplicor moniter assay. J Med Virol 58:121, 1999

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• 64) Ross AA:Minimual residual disease in solid tumor malignancies;a review. J Hematother 7:9, 1998

• 65) Leung W et al:Frequent detection of tumor cells in hematopoietic grafts in neuroblastoma and Ewing's sarcoma. Bone Marrow Transplant 22:971, 1998

• 66) Naito H et al:Detection of tyrosine Hydroxylase mRNA and minimal neuroblastoma cells by the reverse transcription-polymerase chain reaction. Eur J Cancer 27:762, 1991
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• 67) Mattano LA Jr et al:Sensitive detection of rare circulating neuroblastoma cells by the reverse transcriptase-polymerase chain reaction. Cancer Res 52:4701, 1992
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• 68) Burchill SA et al:Minimal residual disease at the time of peripheral blood stem cell harvest in patients with advanced neuroblastoma. Med Pediatr Oncol 36:213, 2001
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• 69) Horibe K et al:Outcome prediction by molecular detection of minimal residual disease in bone marrow for advanced neuroblastoma. Med Pediatr Oncol 36:203, 2001
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• 70) Cheung VG et al:Making and reading microarrays. Nat Genet 21:15, 1999
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• 71) Duggan DJ et al:Expression profiling using cDNA microarrays. Nat Genet 21:10, 1999
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• 72) Lipshutz RJ et al:High density synthetic oligonucleotide arrays. Nat Genet 21:20, 1999
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• 73) Chee M et al:Accessing genetic inforrnation with high-density DNA arrays. Science 274:610, 1996

3. 腫瘍の遺伝子検査と倫理

P.78 掲載の参考文献

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• 2) Hook EB:Exclusion of chromosomal mosaicism:table of 90%, 95% and 99% confidence limits and comments on use. Am J Hum Genet 29:94, 1977

• 3) Bauman JG et al:A new method for fluorescence microscopical localization of DNA sequences by in situ hybridizatuion of fluorochromelabelled RNA. Exp Cell Res 128:485, 1980
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• 4) Pinkel D et al:Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 83:2934, 1986
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• 7) Mark HFL et al:Sequential flow cytometry and fluorescence in situ hybridization for the study of formalin-fixed, paraffin-embedded breast cancer cells. Cancer Genet Cytogenet 100:129, 1998

• 8) Schrock E et al:Multicolor spectral karyotyping of human chromosomes. Science 273:494, 1996
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• 9) Kakazu N et al:Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome. Genes Chromosomes & Cancer 26:336, 1999
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• 10) Hilgenfeld E et al:Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2. Br J Haematol 113:305, 2001
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5. 細胞免疫学的診断法

P.96 掲載の参考文献

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• 2) Sun T:Color atlas-Text of flow cytometric analysis of hematologic neoplasms, New York, IGAKU-SHOIN, 1993

• 3) Rothe G, Schmitz G for the Working Group on Flow Cytometry and Image Analysis:Consensus protocol for the flow cytometric immunophenotyping of hematopoietic malignancies. Leukemia 10:877, 1996

• 4) Jennings CD et al:Recent advances in flow cytometry:Application to the diagnosis of hematologic malignancy. Blood 90:2863, 1997

• 5) Inaba T et al:CD45-negative acute leukemia in adulthood. Eur J Haematol 64:66, 2000
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• 6) Inaba T et al:T-cell associated antigen-positive B-cell lymphoma. Leuk Lymphoma 42:1161, 2001

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• 9) Yakura H:The role of protein tyrosine phosphatase in lymphocyte activation and differentiation. Critical ReViews in Immunology 14:311, 1994
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• 10) Sun T et al:Gating strategy for immunophenotyping of leukemia and lymphoma. Am J Clin Pathol 108:152, 1997
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6. タンパク分析法

P.110 掲載の参考文献

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• 2) Towbin H et al:Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets:procedure and some applications. Proc Natl Acad Sci USA 76:4350, 1979
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7. 検査用検体の処理と保存

P.118 掲載の参考文献

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8. 腫瘍の遺伝子・免疫学的診断と臨床的意義

P.140 掲載の参考文献

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9. 遺伝子・免疫学的検査の治療への応用

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