BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 8706171)

  • 1. [Detection of trisomy 3 in angioimmunoblastic lymphadenopathy with dysproteinemia by fluorescence in situ hybridization].
    Zhang Y; Brigitte S
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Oct; 17(5):359-64. PubMed ID: 8706171
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Detection of chromosome aberrations in peripheral T-cell lymphomas by fluorescence in situ hybridization].
    Zhang Y
    Zhonghua Zhong Liu Za Zhi; 1995 May; 17(3):187-90. PubMed ID: 7656822
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of aberrant clones in nearly all cases of angioimmunoblastic lymphadenopathy with dysproteinemia-type T-cell lymphoma by combined interphase and metaphase cytogenetics.
    Schlegelberger B; Zhang Y; Weber-Matthiesen K; Grote W
    Blood; 1994 Oct; 84(8):2640-8. PubMed ID: 7919378
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clonal identification of trisomies 3, 5 and X in angioimmunoblastic lymphadenopathy with dysproteinemia by fluorescence in situ hybridization.
    Kumaravel TS; Tanaka K; Arif M; Ohshima K; Ohgami A; Takeshita M; Kikuchi M; Kamada N
    Leuk Lymphoma; 1997 Feb; 24(5-6):523-32. PubMed ID: 9086442
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Angioimmunoblastic lymphadenopathy with trisomy 3: the cells of the malignant clone are T cells.
    Schlegelberger B; Nölle I; Feller AC; Bauer E; Grote W
    Hematol Pathol; 1990; 4(4):179-83. PubMed ID: 2074259
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
    Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fluorescence in situ hybridization improves the detection of 5q31 deletion in myelodysplastic syndromes without cytogenetic evidence of 5q-.
    Mallo M; Arenillas L; Espinet B; Salido M; Hernández JM; Lumbreras E; del Rey M; Arranz E; Ramiro S; Font P; González O; Renedo M; Cervera J; Such E; Sanz GF; Luño E; Sanzo C; González M; Calasanz MJ; Mayans J; García-Ballesteros C; Amigo V; Collado R; Oliver I; Carbonell F; Bureo E; Insunza A; Yañez L; Muruzabal MJ; Gómez-Beltrán E; Andreu R; León P; Gómez V; Sanz A; Casasola N; Moreno E; Alegre A; Martín ML; Pedro C; Serrano S; Florensa L; Solé F
    Haematologica; 2008 Jul; 93(7):1001-8. PubMed ID: 18591625
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Common karyotypic pattern in angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) and malignant lymphoma of peripheral T-cell origin with AILD features.
    Kaneko Y
    Nihon Ketsueki Gakkai Zasshi; 1987 Dec; 50(8):1677-8. PubMed ID: 3502312
    [No Abstract]   [Full Text] [Related]  

  • 9. [Cytogenetic study of 121 patients suffering from various hematologic neoplasms using the in situ hybridization technique].
    Pérez Losada A; Solé F; Woessner S; Florensa L; Besses C; Espinet B; Caballín MR; García Eroles L; Sans-Sabrafén J
    Sangre (Barc); 1996 Jun; 41(3):201-9. PubMed ID: 8755208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
    Yang K; Huang L
    Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Detection of trisomy 8 with interphase fluorescence in situ hybridization in myelodysplastic syndromes].
    Li J; Pan J; Xue Y; Wu C; Xie X; Guo Y; Ruan C
    Zhonghua Xue Ye Xue Za Zhi; 2000 Apr; 21(4):179-81. PubMed ID: 11876976
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.
    Cuneo A; Bigoni R; Roberti MG; Bardi A; Rigolin GM; Piva N; Mancini M; Nanni M; Alimena G; Mecucci C; Matteucci C; La Starza R; Bernasconi P; Cavigliano P; Genini E; Zaccaria A; Testoni N; Carboni C; Castoldi G
    Haematologica; 1998 Jan; 83(1):21-6. PubMed ID: 9542319
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of trisomy 12 by fluorescence in situ hybridization in peripheral blood, bone marrow and lymph nodes of patients with B-cell chronic lymphocytic leukemia.
    Liso V; Capalbo S; Lapietra A; Pavone V; Guarini A; Specchia G
    Haematologica; 1999 Mar; 84(3):212-7. PubMed ID: 10189384
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impact of trisomy 12, del(13q), del(17p), and del(11q) on the immunophenotype, DNA ploidy status, and proliferative rate of leukemic B-cells in chronic lymphocytic leukemia.
    Quijano S; López A; Rasillo A; Sayagués JM; Barrena S; Sánchez ML; Teodosio C; Giraldo P; Giralt M; Pérez MC; Romero M; Perdiguer L; Orfao A
    Cytometry B Clin Cytom; 2008 May; 74(3):139-49. PubMed ID: 18061951
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Detection of abnormal numbers of chromosome 8 with interphase fluorescence in situ hybridization in hematologic malignancies].
    Wang HP; Li GX; Qiao ZH; Wang HW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):395-7. PubMed ID: 15300644
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia.
    Rasillo A; Tabernero MD; Sánchez ML; Pérez de Andrés M; Martín Ayuso M; Hernández J; Moro MJ; Fernández-Calvo J; Sayagués JM; Bortoluci A; San Miguel JF; Orfao A
    Cancer; 2003 Feb; 97(3):601-9. PubMed ID: 12548602
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular cytogenetic characteristics of chronic lymphocytic leukemia].
    Xu W; Li JY; Pan JL; Qiu HR; Shen YF; Xiao B; Chen LJ; Wu YF; Sheng RL; Xue YQ
    Zhonghua Zhong Liu Za Zhi; 2006 May; 28(5):349-52. PubMed ID: 17044998
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Detection of extra chromosomes 12 by fluorescent in situ hybridization (FISH) in ovarian stromal tumors. Study of 12 cases and review of the literature].
    Gancberg D; Scourneau M; Verdebout JM; Larsimont D; Verhest A
    Ann Pathol; 2001 Oct; 21(5):393-8. PubMed ID: 11852357
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Significance of trisomy 7 and 12 in thyroid lesions with follicular differentiation: a cytogenetic and in situ hybridization study.
    Roque L; Serpa A; Clode A; Castedo S; Soares J
    Lab Invest; 1999 Apr; 79(4):369-78. PubMed ID: 10211989
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In situ hybridization and flow cytometric analysis of colorectal tumours suggests two routes of tumourigenesis characterized by gain of chromosome 7 or loss of chromosomes 17 and 18.
    Herbergs J; Hopman AH; De Bruïne AP; Ramaekers FC; Arends JW
    J Pathol; 1996 Jul; 179(3):243-7. PubMed ID: 8774477
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.