BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

265 related articles for article (PubMed ID: 10870117)

  • 1. Application of cross-species color banding (RxFISH) in the study of T-prolymphocytic leukemia.
    Espinet B; Solé F; Salido M; Lloveras E; Abella E; Besses C; Serrano S; Woessner S; Florensa L
    Haematologica; 2000 Jun; 85(6):607-12. PubMed ID: 10870117
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic characterization of Sézary's syndrome by conventional cytogenetics and cross-species color banding fluorescent in situhybridization.
    Espinet B; Salido M; Pujol RM; Florensa L; Gallardo F; Domingo A; Servitje O; Estrach T; Garcìa-Muret P; Woessner S; Serrano S; Solé F
    Haematologica; 2004 Feb; 89(2):165-73. PubMed ID: 15003891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cross-species color banding characterization of chromosomal rearrangements in leukemias with incomplete G-band karyotypes.
    Teixeira MR; Micci F; Dietrich CU; Heim S
    Genes Chromosomes Cancer; 1999 Sep; 26(1):13-9. PubMed ID: 10441000
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
    Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
    Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Abnormalities of chromosomes 8, 11, 14, and X in T-prolymphocytic leukemia studied by fluorescence in situ hybridization.
    Maljaei SH; Brito-Babapulle V; Hiorns LR; Catovsky D
    Cancer Genet Cytogenet; 1998 Jun; 103(2):110-6. PubMed ID: 9614908
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New t(11;12)(q12;q11) characterized by RxFISH in a patient with T-cell large granular lymphocyte leukemia.
    Salido M; Solé F; Espinet B; Zamora L; Woessner S; Florensa L
    Cancer Genet Cytogenet; 2001 Feb; 125(1):70-3. PubMed ID: 11297771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Combined RxFISH/G-banding allows refined karyotyping of solid tumors.
    Micci F; Teixeira MR; Dietrich CU; Saeter G; Bjerkehagen B; Heim S
    Hum Genet; 1999 May; 104(5):370-5. PubMed ID: 10394927
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
    Soulier J; Pierron G; Vecchione D; Garand R; Brizard F; Sigaux F; Stern MH; Aurias A
    Genes Chromosomes Cancer; 2001 Jul; 31(3):248-54. PubMed ID: 11391795
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
    Fröhling S; Kayser S; Mayer C; Miller S; Wieland C; Skelin S; Schlenk RF; Döhner H; Döhner K;
    Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
    Dürig J; Bug S; Klein-Hitpass L; Boes T; Jöns T; Martin-Subero JI; Harder L; Baudis M; Dührsen U; Siebert R
    Leukemia; 2007 Oct; 21(10):2153-63. PubMed ID: 17713554
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enhanced detection of chromosomal abnormalities with the use of RxFISH multicolor banding technique.
    Zhao L; Hayes K; Glassman A
    Cancer Genet Cytogenet; 2000 Apr; 118(2):108-11. PubMed ID: 10748290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. G-banding and molecular cytogenetic analyses of marginal zone lymphoma.
    Aamot HV; Micci F; Holte H; Delabie J; Heim S
    Br J Haematol; 2005 Sep; 130(6):890-901. PubMed ID: 16156859
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The application of fluorescence in situ hybridization in detecting chronic myeloid leukemia].
    Qiu HR; Miao KR; Wang R; Qiao C; Zhang JF; Zhang SJ; Qian SX; Xu W; Li JY
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):207-10. PubMed ID: 19350518
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
    Karst C; Gross M; Haase D; Wedding U; Höffken K; Liehr T; Mkrtchyan H
    Int J Oncol; 2006 Apr; 28(4):891-7. PubMed ID: 16525638
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Splenic marginal zone B-cell lymphomas: two cytogenetic subtypes, one with gain of 3q and the other with loss of 7q.
    Solé F; Salido M; Espinet B; Garcia JL; Martinez Climent JA; Granada I; Hernández JM; Benet I; Piris MA; Mollejo M; Martinez P; Vallespí T; Domingo A; Serrano S; Woessner S; Florensa L
    Haematologica; 2001 Jan; 86(1):71-7. PubMed ID: 11146574
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.
    Mrózek K; Heinonen K; Theil KS; Bloomfield CD
    Genes Chromosomes Cancer; 2002 Jun; 34(2):137-53. PubMed ID: 11979548
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
    Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
    Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark.
    Christensen JH; Abildgaard N; Plesner T; Nibe A; Nielsen O; Sørensen AG; Kerndrup GB;
    Cancer Genet Cytogenet; 2007 Apr; 174(2):89-99. PubMed ID: 17452249
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.