Fusion of the dominant negative transcription regulator CHOP with a novel gene FUS by translocation t(12;16) in malignant liposarcoma
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R. Larson | T. Rabbitts | A. Forster | R. Larson | P. Nathan
[1] M. Ohki,et al. The t(8;21) translocation in acute myeloid leukemia results in production of an AML1‐MTG8 fusion transcript. , 1993, The EMBO journal.
[2] J. Biegel,et al. Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma , 1993, Nature Genetics.
[3] P. Meltzer,et al. The last shall be first , 1993, Nature Genetics.
[4] F. Mitelman,et al. Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11) , 1992, Genes, chromosomes & cancer.
[5] H. Drabkin,et al. Identification of breakpoints in t(8;21) acute myelogenous leukemia and isolation of a fusion transcript, AML1/ETO, with similarity to Drosophila segmentation gene, runt. , 1992, Blood.
[6] G. Thomas,et al. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours , 1992, Nature.
[7] J. Fargnoli,et al. Isolation, characterization and chromosomal localization of the human GADD153 gene. , 1992, Gene.
[8] M. Fornerod,et al. The translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNA , 1992, Molecular and cellular biology.
[9] D. Ron,et al. CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. , 1992, Genes & development.
[10] S. Kamel‐Reid,et al. A novel human homeobox gene lies at the chromosome 10 breakpoint in lymphoid neoplasias with chromosomal translocation t(10;14) , 1991 .
[11] T. Rabbitts. Translocations, master genes, and differences between the origins of acute and chronic leukemias , 1991, Cell.
[12] T. Rabbitts,et al. HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[13] M. Lu,et al. The tcl‐3 proto‐oncogene altered by chromosomal translocation in T‐cell leukemia codes for a homeobox protein. , 1991, The EMBO journal.
[14] M. Cleary. Oncogenic conversion of transcription factors by chromosomal translocations , 1991, Cell.
[15] S. Korsmeyer,et al. Deregulation of a homeobox gene, HOX11, by the t(10;14) in T cell leukemia. , 1991, Science.
[16] N. Spurr,et al. Confirmation of the assignment of the vitronectin (VNRA) and fibronectin (FNRA) receptor α‐subunits , 1991 .
[17] P. Pandolfi,et al. Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[18] T. Rabbitts,et al. Structural and functional chimerism results from chromosomal translocation in lymphoid tumors. , 1991, Advances in immunology.
[19] Christine Chomienne,et al. The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus , 1990, Nature.
[20] D. Sheer,et al. Molecular analysis of acute promyelocytic leukemia breakpoint cluster region on chromosome 17. , 1990, Science.
[21] F. Mitelman,et al. Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2. , 1990, Cancer genetics and cytogenetics.
[22] David Baltimore,et al. A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B all , 1990, Cell.
[23] Michael L. Cleary,et al. Chromosomal translocation t(1;19) results in synthesis of a homeobox fusion mRNA that codes for a potential chimeric transcription factor , 1990, Cell.
[24] R. Tjian,et al. Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins. , 1989, Science.
[25] M. Rieger,et al. Identification of an orthologous mammalian cytokeratin gene. High degree of intron sequence conservation during evolution of human cytokeratin 10. , 1988, Journal of molecular biology.
[26] S. Latt,et al. A novel alteration in the structure of an activated c-myc gene in a variant t(2;8) burkitt lymphoma , 1984, Cell.
[27] T. Rabbitts,et al. Chromosome translocation can occur on either side of the c-myc oncogene in Burkitt lymphoma cells , 1984, Nature.
[28] J. Stephenson,et al. Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22 , 1984, Cell.
[29] J. Stephenson,et al. Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia , 1983, Nature.
[30] F. Mitelman,et al. Catalog of Chromosome Aberrations in Cancer , 1996, British Journal of Cancer.
[31] P. Nowell,et al. Transcriptional activation of an unrearranged and untranslocated c-myc oncogene by translocation of a C lambda locus in Burkitt. , 1983, Proceedings of the National Academy of Sciences of the United States of America.
[32] T. Rabbitts,et al. Translocation joins c-myc and immunoglobulin γ1 genes in a Burkitt lymphoma revealing a third exon in the c-myc oncogene , 1983, Nature.
[33] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[34] J. Stephenson,et al. A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia , 1982, Nature.
[35] C. Croce,et al. Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[36] P. Leder,et al. Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[37] P. Thomas,et al. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. , 1980, Proceedings of the National Academy of Sciences of the United States of America.
[38] S. Povey,et al. Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16 , 1980, Annals of human genetics.
[39] E. Southern. Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.
[40] P. Nowell,et al. A minute chromosome in human chronic granulocytic leukemia , 1960 .