These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 10706457)

  • 1. Cytogenetic analysis of non Hodgkin's lymphomas by ratio-painting and comparative genomic hybridization reveals unsuspected chromosomal abnormalities.
    Alqahtani MH; Hammond DW; Goepel JR; Goyns MH
    Leuk Lymphoma; 1999 Oct; 35(3-4):325-37. PubMed ID: 10706457
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of 14q+ derivative chromosomes in non-Hodgkin's lymphomas by fluorescence in-situ hybridization.
    Hammond DW; Hancock BW; Goyns MH
    Leuk Lymphoma; 1995 Dec; 20(1-2):111-7. PubMed ID: 8750631
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome analysis of non-Hodgkin's lymphomas by fluorescence in situ hybridization.
    Hammond DW; Hancock BW; Goyns MH
    Ann Oncol; 1994; 5 Suppl 1():51-4. PubMed ID: 8172818
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic analysis of 147 cases of non-Hodgkin's lymphoma: non-random chromosomal abnormalities and histological correlations.
    Juneja S; Lukeis R; Tan L; Cooper I; Szelag G; Parkin JD; Ironside P; Garson OM
    Br J Haematol; 1990 Oct; 76(2):231-7. PubMed ID: 2094325
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Chromosome painting as a supplement to cytogenetic banding analysis in non-Hodgkin's lymphoma.
    Bajalica S; Sørensen AG; Pedersen NT; Heim S; Brøndum-Nielsen K
    Genes Chromosomes Cancer; 1993 Aug; 7(4):231-9. PubMed ID: 7692950
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New chromosomal breakpoints in non-Hodgkin's lymphomas revealed by spectral karyotyping and G-banding.
    Nordgren A; Sørensen AG; Tinggaard-Pedersen N; Blennow E; Larsson C; Lagercrantz S
    Int J Mol Med; 2000 May; 5(5):485-92. PubMed ID: 10762651
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.
    Micci F; Teixeira MR; Heim S
    Cancer Genet Cytogenet; 2001 Nov; 131(1):25-30. PubMed ID: 11734314
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomas.
    Renedo M; Martinez-Delgado B; Arranz E; Garcia M; Urioste M; Martinez-Ramirez A; Rivas C; Cigudosa JC; Benitez I
    Leukemia; 2001 Oct; 15(10):1627-32. PubMed ID: 11587222
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polysomy of chromosome 12 in 60 patients with non-Hodgkin's lymphoma assessed by fluorescence in situ hybridization: differences between follicular and diffuse large cell lymphoma.
    Younes A; Pugh W; Goodacre A; Katz R; Rodriguez MA; Hill D; Cabanillas F; Andreeff M
    Genes Chromosomes Cancer; 1994 Mar; 9(3):161-7. PubMed ID: 7515657
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic analysis of 434 consecutively ascertained specimens of non-Hodgkin's lymphoma: correlations between recurrent aberrations, histology, and exposure to cytotoxic treatment.
    Offit K; Jhanwar SC; Ladanyi M; Filippa DA; Chaganti RS
    Genes Chromosomes Cancer; 1991 May; 3(3):189-201. PubMed ID: 1868033
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a subclass of double minute chromosomes containing centromere-associated DNA.
    Hammond DW; Hancock BW; Goyns MH
    Genes Chromosomes Cancer; 1994 Jun; 10(2):139-42. PubMed ID: 7520268
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of hematologic diseases using conventional karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH).
    Wilkens L; Tchinda J; Burkhardt D; Nolte M; Werner M; Georgii A
    Hum Pathol; 1998 Aug; 29(8):833-9. PubMed ID: 9712425
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic imbalances in primary gastric diffuse large B-cell lymphomas: comparison of comparative genomic hybridization, microsatellite, and cytogenetic analysis.
    Peters K; Zettl A; Starostik P; Greiner A; Rosenwald A; Katzenberger T; Ott G; Müller-Hermelink HK
    Diagn Mol Pathol; 2000 Mar; 9(1):58-65. PubMed ID: 10718214
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular cytogenetic analysis of a nontumorigenic human breast epithelial cell line that eventually turns tumorigenic: validation of an analytical approach combining karyotyping, comparative genomic hybridization, chromosome painting, and single-locus fluorescence in situ hybridization.
    Nielsen KV; Niebuhr E; Ejlertsen B; Holstebroe S; Madsen MW; Briand P; Mouridsen HT; Bolund L
    Genes Chromosomes Cancer; 1997 Sep; 20(1):30-7. PubMed ID: 9290951
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular cytogenetic analysis of chemoresistant non-Hodgkin's lymphoma patients with p53 abnormalities using fluorescence in situ hybridisation and comparative genomic hybridisation.
    Foroutan B; Zitzelsberger H; Bauer V; Ruf AA; Baumgartner A; Anderson D
    Arch Iran Med; 2011 Sep; 14(5):321-6. PubMed ID: 21888455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
    Naus NC; van Drunen E; de Klein A; Luyten GP; Paridaens DA; Alers JC; Ksander BR; Beverloo HB; Slater RM
    Genes Chromosomes Cancer; 2001 Mar; 30(3):267-73. PubMed ID: 11170284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clusters of chromosome 9 aberrations are associated with clinico-pathologic subsets of non-Hodgkin's lymphoma.
    Offit K; Parsa NZ; Jhanwar SC; Filippa D; Wachtel M; Chaganti RS
    Genes Chromosomes Cancer; 1993 May; 7(1):1-7. PubMed ID: 7688550
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of double minute chromosomes' DNA content in a human high grade astrocytoma cell line by using comparative genomic hybridization and fluorescence in situ hybridization.
    Giollant M; Bertrand S; Verrelle P; Tchirkov A; du Manoir S; Ried T; Mornex F; Doré JF; Cremer T; Malet P
    Hum Genet; 1996 Sep; 98(3):265-70. PubMed ID: 8707292
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of genetic imbalances in malignant lymphoma using comparative genomic hybridization.
    Bentz M; Döhner H; Werner CA; Huck K; Baudis M; Joos S; Schlegelberger B; Trümper LH; Feller AC; Pfreundschuh M
    Stem Cells; 1995 Dec; 13 Suppl 3():83-7. PubMed ID: 8747993
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping.
    Veldman T; Vignon C; Schröck E; Rowley JD; Ried T
    Nat Genet; 1997 Apr; 15(4):406-10. PubMed ID: 9090389
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.