Less Time, Better Results.


Cytogenetics Database CytoD 1.0

Please enter your search karyotypes:    

Search Results:

Query: t(15;17)(q22;q21)

Search Results:

t(15;17)(q22;q21)     Comment in: Br J Haematol. 1997 Dec;99(3):711-2. Br J Haematol. 1997 Aug;98(2):440-3.
t(15;17)(q22;q21)     Genomic anatomy of the specific reciprocal translocation t(15;17) in acute promyelocytic leukemia. Genes Chromosomes Cancer. 2003 Feb;36(2):175-88.
t(15;17)(q22;q21)     Chronic myelomonocytic leukemia with trisomy 8 and a related clone with trisomy 8 and t(15;17). Cancer Genet Cytogenet. 1988 Jun;32(2):287-92.
t(15;17)(q22;q21)     Dendritic cells in acute promyelocytic leukaemia. Br J Haematol. 2001 Sep;114(4):830-3.
t(15;17)(q22;q21)     [A new variety of acute non-promyelocytic leukemia with t(15;17)] C R Seances Acad Sci D. 1979 Jan 8;288(1):177-9.
t(15;17)(q22;q21)     A new variant translocation in acute promyelocytic leukaemia: molecular characterization and clinical correlation. Leukemia. 1996 Apr;10(4):735-40.
t(15;17)(q22;q21)     The significance of trisomy 8 in de novo acute myeloid leukaemia: the accompanying chromosome aberrations determine the prognosis. German AML Cooperative Study Group. Br J Haematol. 1997 Dec;99(3):605-11.
t(15;17)(q22;q21)     Characterization of cryptic rearrangements and variant translocations in acute promyelocytic leukemia. Blood. 1997 Dec 15;90(12):4876-85.
t(15;17)(q22;q21)     Therapy-related acute myeloid leukemia with t(10;11)(q23;p15) following successful chemotherapy for acute promyelocytic leukemia with t(15;17)(q22;q21) Int J Hematol. 1999 Jun;69(4):270-1.
t(15;17)(q22;q21)     Interstitial insertion of retinoic acid receptor-alpha gene in acute promyelocytic leukemia with normal chromosomes 15 and 17. Blood. 1994 May 15;83(10):2946-51.
t(15;17)(q22;q21)     Diagnostic approaches to acute promyelocytic leukaemia. Leuk Lymphoma. 1999 Mar;33(1-2):53-63.
t(15;17)(q22;q21)     Two new 3' PML breakpoints in t(15;17)(q22;q21)-positive acute promyelocytic leukemia. Genes Chromosomes Cancer. 2000 Jan;27(1):35-43.
t(15;17)(q22;q21)     Additional chromosome aberrations in acute promyelocytic leukemia: characteristics and prognostic influence. Med Oncol. 2000 Nov;17(4):307-13.
t(15;17)(q22;q21)     Acute promyelocytic leukaemia with t(11;17)(q23;q12-21) and a good initial response to prolonged ATRA and combination chemotherapy. Br J Haematol. 1998 Feb;100(2):328-30.
t(15;17)(q22;q21)     The nerve growth factor receptor gene is at human chromosome region 17q12-17q22, distal to the chromosome 17 breakpoint in acute leukemias. Proc Natl Acad Sci U S A. 1986 Mar;83(5):1403-7.
t(15;17)(q22;q21)     Acute promyelocytic leukemia with apparently normal karyotype: molecular findings and response to all-trans retinoic acid. Leuk Lymphoma. 2001 Jun;42(1-2):151-61.
t(15;17)(q22;q21)     Variations on a theme: the alternate translocations in APL. Leukemia. 2002 Oct;16(10):1927-32.
t(15;17)(q22;q21)     Atypical blasts and bone marrow necrosis associated with near-triploid relapse of acute promyelocytic leukemia after arsenic trioxide treatment. Hum Pathol. 2002 Aug;33(8):849-51.
t(15;17)(q22;q21)     The t(15;17) breakpoint in acute promyelocytic leukemia cluster within two different sites of the myl gene: targets for the detection of minimal residual disease by the polymerase chain reaction. Blood. 1992 Feb 1;79(3):554-8.
t(15;17)(q22;q21)     Acute promyelocytic leukemia with additional chromosome abnormalities in a renal transplant case. Ann Hematol. 2001 Apr;80(4):246-50.
t(15;17)(q22;q21)     The significance of minimal residual disease in patients with t(15;17). Best Pract Res Clin Haematol. 2002 Mar;15(1):137-58.
t(15;17)(q22;q21-     The localization of the human myeloperoxidase gene is in close proximity to the translocation breakpoint in acute promyelocytic leukemia. Leukemia. 1987 May;1(5):458-62.
t(15;17)(q22;q21)     Incidence and implication of additional chromosome aberrations in acute promyelocytic leukaemia with translocation t(15;17)(q22;q21): a report on 50 patients. Br J Haematol. 1996 Sep;94(3):493-500.
t(15;17)(q22;q21)     Acute myeloblastic leukaemias of FAB types M6 and M4, with cryptic PML/RARalpha fusion gene formation, relapsing as acute promyelocytic leukaemia M3. Br J Haematol. 2001 Sep;114(3):551-6.
t(15;17)(q22;q21)     Rapid diagnosis and characterization of acute promyelocytic leukaemia in routine laboratory practice. Clin Lab Haematol. 2004 Apr;26(2):101-6.
t(15;17)(q22;q21)     PML, a growth suppressor disrupted in acute promyelocytic leukemia. Mol Cell Biol. 1994 Oct;14(10):6858-67.
t(15;17)(q22;q21)     Treatment of acute promyelocytic leukemia with ATRA and As2O3: a model of molecular target-based cancer therapy. Cancer Biol Ther. 2002 Nov-Dec;1(6):614-20.
t(15;17)(q22;q21)     Hypocellular acute promyelocytic leukemia with a tetraploid clone characterized by two t(15;17). Cancer Genet Cytogenet. 2003 Sep;145(2):169-71.
t(15;17)(q22;q21)     An eight-way variant t(15;17) in acute promyelocytic leukemia elucidated using fluorescence in situ hybridization. Cancer Genet Cytogenet. 1995 Sep;83(2):136-9.
t(15;17)(q22;q21)     Derivative (7)t(7;8)(q34;q21). a new additional cytogenetic abnormality in acute promyelocytic leukemia. Cancer Genet Cytogenet. 2003 Jan 1;140(1):78-81.
t(15;17)(q22;q21)     Rearrangement of one RAR-alpha gene in an acute promyelocytic leukemia case with t(15;17) and t(6;17) involving chromosomes 17 band q21. Cancer Genet Cytogenet. 1996 Apr;87(2):172-5.
t(15;17)(q22;q21)     Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in a case of acute monoblastic leukemia with tetrasomy 8. Cancer Genet Cytogenet. 1999 Aug;113(1):9-13.
t(15;17)(q22;q21.     Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17). Cancer Genet Cytogenet. 2002 Oct 1;138(1):17-21.
t(15;17)(q22;q21)     558-561, 1990). This result demonstrates that the two different types of
t(15;17)(q22;q21)     Tetraploid acute promyelocytic leukemia with double t(15;17) and PML/RARA rearrangements detected by fluorescence in situ hybridization analysis. Cancer Genet Cytogenet. 2003 Aug;145(1):49-53.
t(15;17)(q22;q21)     Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2. Cancer Res. 1992 May 1;52(9):2590-6.

Copyright © 2002-2004 Chang Bioscience, Inc. All rights reserved.