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Cytogenetics Database CytoD 1.0

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Query: t(1;19)(q23;p13)

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t(1;19)(q23;p13)     Expression of identical E2A/PBX1 fusion transcripts occurs in both pre-B and early pre-B immunological subtypes of childhood acute lymphoblastic leukemia. Leukemia. 1993 Dec;7(12):2054-6.
t(1;19)(q23;p13)     Establishment and characterization of a childhood pre-B acute lymphoblastic leukemia cell line, PER-278, with chromosome translocations t(1;19) and t(1;9). Cancer Genet Cytogenet. 1990 Jun;46(2):201-8.
t(1;19)(q23;p13)     Heterogeneity of t(1;19)(q23;p13) acute leukaemias. French Haematological Cytology Group. Br J Haematol. 1995 Mar;89(3):516-26.
t(1;19)(q23;p13)     [E2A gene in t(1;19)-ALL] Nippon Rinsho. 1992 Jun;50(6):1369-73.
t(1;19)(q23;p13)     Characterization of two newly established EBV-containing lymphoblastoid cell lines from patients with myeloid leukemias. Leuk Res. 1990;14(4):309-20.
t(1;19)(q23;p13)     Human t(1;19)(q23;p13) pre-B acute lymphoblastic leukemia in mice with severe combined immunodeficiency. Blood. 1993 Jun 1;81(11):3052-62.
t(1;19)(q23;p13)     t(1;19)(q23;p13) in pre-B acute lymphocytic leukemia cell line 697. Cancer Genet Cytogenet. 1987 Apr;25(2):379-80.
t(1;19)(q23;p13)     Comment in: Genes Chromosomes Cancer. 1995 Feb;12(2):157-8. Genes Chromosomes Cancer. 1994 Jul;10(3):171-6.
t(1;19)(q23;p13)     Balanced and unbalanced 1;19 translocation-associated acute lymphoblastic leukemias. Cancer. 1986 Nov 15;58(10):2239-43.
t(1;19)(q23;p13)     Diagnosis and classification of the acute leukemias: recent advances and controversial issues. Hematopathol Mol Hematol. 1996;10(1-2):1-38.
t(1;19)(q23;p13)     Unexpected heterogeneity in E2A/PBX1 fusion messenger RNA detected by the polymerase chain reaction in pediatric patients with acute lymphoblastic leukemia. Blood. 1992 Sep 15;80(6):1413-7.
t(1;19)(q23;p13)     Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia. Leukemia. 1992 May;6(5):363-9.
t(1;19)(q23;p13)     Molecular analysis of the t(1;19)(q23;p13) translocation observed in adult leukemias. Int J Hematol. 1994 Dec;60(4):267-71.
t(1;19)(q23;p13)     Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia. Genes Chromosomes Cancer. 2004 Nov 12; [Epub ahead of print]
t(1;19)(q23;p13)     Acute lymphoblastic leukemia associated with a t(1;19)(q23;p13) in an adult. Intern Med. 1993 Jul;32(7):584-7.
t(1;19)(q23;p13)     Predictability of the t(1;19)(q23;p13) from surface antigen phenotype: implications for screening cases of childhood acute lymphoblastic leukemia for molecular analysis: a Pediatric Oncology Group study. Blood. 1993 Aug 15;82(4):1086-91.
t(1;19)(q23;p13)     T-cell acute lymphoblastic leukemia with translocation (1;18). Cancer Genet Cytogenet. 1988 Jan;30(1):165-9.
t(1;19)(q23;p13)     A case of mature B-cell ALL with coexistence of t(1;19) and t(14;18) and expression of the E2A/PBX1 fusion gene. Br J Haematol. 1996 Jul;94(1):133-5.
t(1;19)(q23;p13)     Childhood acute lymphoblastic leukemia with equivocal chromosome markers of the t(1;19) translocation. Genes Chromosomes Cancer. 1995 Jun;13(2):99-103.
t(1;19)(q23;p13)     Establishment of a new human pre-B acute lymphoblastic leukemia cell line (KMO-90) with 1;19 translocation carrying p53 gene alterations. Leukemia. 1993 Oct;7(10):1615-20.
t(1;19)(q23;p13)     Prognostic impact of karyotypic findings in childhood acute lymphoblastic leukaemia: a Nordic series comparing two treatment periods. For the Nordic Society of Paediatric Haematology and Oncology (NOPHO) Leukaemia Cytogenetic Study Group. Br J Haematol. 2000 Jul;110(1):147-53.
t(1;19)(q23;p13)     Identification of a novel fusion gene in a pre-B acute lymphoblastic leukemia with t(1;19)(q23;p13). Cancer Sci. 2004 Jun;95(6):503-7.
t(1;19)(q23;p13)     Translocation t(1;19)(q23;p13) in acute lymphoblastic leukemia. A report on six new cases and an unusual t(17;19)(q11;q13), with special reference to prognostic factors. Cancer Genet Cytogenet. 1989 Jan;37(1):9-17.
t(1;19)(q23;p13)     Establishment of a novel cell line (TS-2) of pre-B acute lymphoblastic leukemia with a t(1;19) not involving the E2A gene. Cancer Genet Cytogenet. 1998 Mar;101(2):95-102.
t(1;19)(q23;p13)     Different patterns of homozygous p16INK4A and p15INK4B deletions in childhood acute lymphoblastic leukemias containing distinct E2A translocations. Leukemia. 1998 Sep;12(9):1417-21.
t(1;19)(q23;p13.     Fifteen cases of t(1;19)(q23;p13.3) identified in an Australian series of 122 children and 80 adults with acute lymphoblastic leukemia. Cancer Genet Cytogenet. 2001 Jan 15;124(2):132-6.
t(1;19)(q23;p13)     Hyperdiploidy and E2A-PBX1 fusion in an adult with t(1;19)+ acute lymphoblastic leukemia: case report and review of the literature. Genes Chromosomes Cancer. 1997 Dec;20(4):392-8.
t(1;19)(q23;p13)     t(1;19)(q23;p13) in a case of acute monocytic leukemia. Cancer Genet Cytogenet. 1996 Mar;87(1):52-4.
t(1;19)(q23;p13)     Detection of E2A translocations in leukemias via fluorescence in situ hybridization. Leukemia. 2001 Jan;15(1):95-102.
t(1;19)(q23;p13)     E2A-PBX1 chimeric transcript status at end of consolidation is not predictive of treatment outcome in childhood acute lymphoblastic leukemias with a t(1;19)(q23;p13): a Pediatric Oncology Group study. Blood. 1998 Feb 1;91(3):1021-8.
t(1;19)(q23;p13)     Detection and clinical relevance of genetic abnormalities in pediatric acute lymphoblastic leukemia: a comparison between cytogenetic and polymerase chain reaction analyses. Leukemia. 1993 May;7(5):671-8.
t(1;19)(q23;p13)     Cytogenetic abnormalities in the leukemic phase of non-Hodgkin lymphoma. Cancer Genet Cytogenet. 1995 Aug;83(1):18-24.
t(1;19)(q23;p13)     Precursor B lymphoblastic leukemia with surface light chain immunoglobulin restriction: a report of 15 patients. Am J Clin Pathol. 2004 Apr;121(4):512-25.
t(1;19)(q23;p13.     A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL. Cell. 1990 Feb 23;60(4):547-55.
t(1;19)(q23;p13)     New E2A/PBX1 fusion transcript in a patient with t(1;19)(q23;p13) acute lymphoblastic leukemia. Leukemia. 1993 Sep;7(9):1441-4.
t(1;19)(q23;p13)     A t(1;19) chromosome translocation in three cases of human malignant melanoma. Cancer Res. 1986 Mar;46(3):1526-9.
t(1;19)(q23;p13.     Cytogenetic features and serum lactic dehydrogenase level predict a poor treatment outcome for children with pre-B-cell leukemia. Blood. 1986 Jun;67(6):1688-92.
t(1;19)(q23;p13)     Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. The NOPHO Leukemia Cytogenetic Study Group. Eur J Haematol. 2000 Mar;64(3):194-200.
t(1;19)(q23;p13.     Hypodiploidy is associated with a poor prognosis in childhood acute lymphoblastic leukemia. Blood. 1987 Jul;70(1):247-53.
t(1;19)(q23;p13)     The genetics of childhood acute lymphoblastic leukaemia. Baillieres Best Pract Res Clin Haematol. 2000 Sep;13(3):427-39.
t(1;19)(q23;p13)     Detection of BCR-ABL and E2A-PBX1 fusion genes by RT-PCR in acute lymphoblastic leukaemia with failed or normal cytogenetics. Br J Haematol. 1995 Feb;89(2):349-55.
t(1;19)(q23;p13)     Heterogeneity of hyperdiploid (51-67) childhood acute lymphoblastic leukemia. Leukemia. 1996 Feb;10(2):213-24.
t(1;19)(q23;p13)     Expression of the E2A-PBX1 fusion transcripts in t(1;19)(q23;p13) and der(19)t(1;19) at diagnosis and in remission of acute lymphoblastic leukemia with different B lineage immunophenotypes. Leukemia. 1995 May;9(5):821-5.
t(1;19)(q23;p13.     Fusion with E2A converts the Pbx1 homeodomain protein into a constitutive transcriptional activator in human leukemias carrying the t(1;19) translocation. Mol Cell Biol. 1994 Jun;14(6):3938-48.
t(1;19)(q23;p13)     Molecular variants of the 1;19 chromosomal translocation in pediatric acute lymphoblastic leukemia (ALL). Leukemia. 1994 Apr;8(4):554-9.
t(1;19)(q23;p13)     Poor prognosis of children with pre-B acute lymphoblastic leukemia is associated with the t(1;19)(q23;p13): a Pediatric Oncology Group study. Blood. 1990 Jul 1;76(1):117-22.
t(1;19)(q23;p13)     The gene for enhancer binding proteins E12/E47 lies at the t(1;19) breakpoint in acute leukemias. Science. 1989 Oct 20;246(4928):379-82.
t(1;19)(q23;p13)     Acute lymphoblastic leukaemia. Best Pract Res Clin Haematol. 2001 Sep;14(3):593-607.
t(1;19)(q23;p13)     The t(1;19)(q23;p13) results in consistent fusion of E2A and PBX1 coding sequences in acute lymphoblastic leukemias. Blood. 1991 Feb 15;77(4):687-93.
t(1;19)(q23;p13)     Acute lymphoblastic leukaemia: diagnosis and classification. Best Pract Res Clin Haematol. 2002 Dec;15(4):597-621.
t(1;19)(q23;p13.     Pbx1 is converted into a transcriptional activator upon acquiring the N-terminal region of E2A in pre-B-cell acute lymphoblastoid leukemia. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6061-5.
t(1;19)(q23;p13)     Molecular analysis of the t(1;19) breakpoint cluster region in pre-B cell acute lymphoblastic leukemias. Genes Chromosomes Cancer. 1990 Sep;2(3):239-47.
t(1;19)(q23;p13)     Biology and clinical significance of cytogenetic abnormalities in childhood acute lymphoblastic leukemia. Blood. 1990 Oct 15;76(8):1449-63.
t(1;19)(q23;p13.     Childhood acute lymphoblastic leukemia with both t(1;19) and t(9;22). Leukemia. 1992 Jun;6(6):535-40.
t(1;19)(q23;p13)     The detection and significance of chromosomal abnormalities in childhood acute lymphoblastic leukaemia. Blood Rev. 2001 Mar;15(1):49-59.
t(1;19)(q23;p13)     Isochromosomes in childhood acute lymphoblastic leukemia: a collaborative study of 83 cases. Blood. 1992 May 1;79(9):2384-91.
t(1;19)(q23;p13)     Mapping of translocation breakpoints on the short arm of chromosome 19 in acute leukemias by in situ hybridization. Genes Chromosomes Cancer. 1990 Nov;2(4):259-65.

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