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
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J. Tchinda | E. Schröck | T. Ried | E. Hilgenfeld | T. Knutsen | W. Ludwig | C. Montagna | H. Serve | T. Büchner | J. Horst | W. Berdel | N. McNeil | H. Padilla-Nash
[1] O. Haas,et al. Felix Mitelman: Database of chromosome aberrations in cancer , 2002, Human Genetics.
[2] M. Slovak,et al. Twenty‐four‐color spectral karyotyping reveals chromosome aberrations in cytogenetically normal acute myeloid leukemia , 2000, Genes, chromosomes & cancer.
[3] H. Scherthan,et al. Double minutes and c-MYC amplification in acute myelogenous leukemia: Are they prognostic factors? , 2000, Cancer genetics and cytogenetics.
[4] Alex E. Lash,et al. A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome , 2000, Nature Genetics.
[5] S. Hiebert,et al. Role of the transcription factor AML-1 in acute leukemia and hematopoietic differentiation. , 2000, Gene.
[6] James R. Downing,et al. Expression of the AML-1 Oncogene Shortens the G1Phase of the Cell Cycle* , 2000, The Journal of Biological Chemistry.
[7] S. Glaser,et al. Acute Myeloid Leukemia , 2020, New England Journal of Medicine.
[8] N. Kakazu,et al. Combined spectral karyotyping and DAPI banding analysis of chromosome abnormalities in myelodysplastic syndrome , 1999, Genes, chromosomes & cancer.
[9] A. Friedman. Leukemogenesis by CBF oncoproteins , 1999, Leukemia.
[10] G Flandrin,et al. The World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues. Report of the Clinical Advisory Committee meeting, Airlie House, Virginia, November, 1997. , 1999, Annals of oncology : official journal of the European Society for Medical Oncology.
[11] L. Chan,et al. Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid leukemia and myelodysplastic syndrome. , 1999, Leukemia research.
[12] J. Rowley. The role of chromosome translocations in leukemogenesis. , 1999, Seminars in hematology.
[13] C. Morris,et al. Identification of amplified genes in a patient with acute myeloid leukemia and double minute chromosomes. , 1999, Cancer genetics and cytogenetics.
[14] W. Hiddemann,et al. Double induction strategy for acute myeloid leukemia: the effect of high-dose cytarabine with mitoxantrone instead of standard-dose cytarabine with daunorubicin and 6-thioguanine: a randomized trial by the German AML Cooperative Group. , 1999, Blood.
[15] H. Yamasaki,et al. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2alphaB gene associated with myeloblastic leukemias. , 1999, Blood.
[16] G. Evans,et al. Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation , 1999, Genes, chromosomes & cancer.
[17] M. Seto,et al. Amplification on double‐minute chromosomes and partial‐tandem duplication of the MILL gene in leukemic cells of a patient with acute myelogenous leukemia , 1998, Genes, chromosomes & cancer.
[18] A T Look,et al. Oncogenic transcription factors in the human acute leukemias. , 1997, Science.
[19] N. Zhao,et al. dic(5;17): A recurring abnormality in malignant myeloid disorders associated with mutations of TP53 , 1997, Genes, chromosomes & cancer.
[20] T. Veldman,et al. Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements , 1997, Histochemistry and Cell Biology.
[21] B. Johansson,et al. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia , 1997, Nature Genetics.
[22] Thomas Ried,et al. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping , 1997, Nature Genetics.
[23] T. Haferlach,et al. Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor. , 1996, Leukemia.
[24] D. Ledbetter,et al. Multicolor Spectral Karyotyping of Human Chromosomes , 1996, Science.
[25] D. Ward,et al. Karyotyping human chromosomes by combinatorial multi-fluor FISH , 1996, Nature Genetics.
[26] K. Tanaka,et al. Overexpression of the AML1 proto-oncoprotein in NIH3T3 cells leads to neoplastic transformation depending on the DNA-binding and transactivational potencies. , 1996, Oncogene.
[27] F. Mitelman. ISCN 1995 : an international system for human cytogenetic nomenclature (1995) : recommendations of the International Standing Committee on Human Cytogenetic Nomenclature : Memphis, Tennessee, USA, October 9-13, 1994 , 1995 .
[28] S. Shurtleff,et al. TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. , 1995, Leukemia.
[29] P. Jacobs,et al. Cytogenetic and molecular studies of Down syndrome individuals with leukemia. , 1995, American journal of human genetics.
[30] A. Hagemeijer,et al. Interphase cytogenetics of the t(8;21)(q22;q22) associated with acute myelogenous leukemia by two-color fluorescence in situ hybridization. , 1995, Cancer genetics and cytogenetics.
[31] R. Berger,et al. t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia , 1994, Genes, chromosomes & cancer.
[32] P. Pelicci,et al. Mapping of chromosome 17 breakpoints in acute myeloid leukemias. , 1990, Oncogene.
[33] G Flandrin,et al. Proposed revised criteria for the classification of acute myeloid leukemia. A report of the French-American-British Cooperative Group. , 1985, Annals of internal medicine.
[34] J. Westin,et al. Cytogenetic studies of bone marrow and extramedullary tissues and clinical course during metamorphosis of chronic myelocytic leukemia. , 1983, Cancer genetics and cytogenetics.
[35] M. Bernard,et al. Jumping translocation in acute leukemia of myelomonocytic lineage: a case report and review of the literature , 2000, Leukemia.
[36] U. Jäger,et al. Amplification of the MLL gene on double minutes, a homogeneously staining region, and ring chromosomes in five patients with acute myeloid leukemia or myelodysplastic syndrome. , 2000, Genes, chromosomes & cancer.
[37] 大里 元美. Biallelic and heterozygous point mutations in the runt domain of the AML1/PEBP2 α B gene associated with myeloblastic leukemias , 1999 .
[38] E. Estey,et al. Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes. , 1995, Leukemia.