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Journal Abstract Search

896 related items for PubMed ID: 10702812

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  • 3. [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
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  • 4. Epstein-Barr virus integrates frequently into chromosome 4q, 2q, 1q and 7q of Burkitt's lymphoma cell line (Raji).
    Gao J, Luo X, Tang K, Li X, Li G.
    J Virol Methods; 2006 Sep; 136(1-2):193-9. PubMed ID: 16806502
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  • 5. Genotypic analysis of esophageal squamous cell carcinoma by molecular cytogenetics and real-time quantitative polymerase chain reaction.
    Yen CC, Chen YJ, Lu KH, Hsia JY, Chen JT, Hu CP, Chen PM, Liu JH, Chiou TJ, Wang WS, Yang MH, Chao TC, Lin CH.
    Int J Oncol; 2003 Oct; 23(4):871-81. PubMed ID: 12963965
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  • 8. Chromosomal imbalances revealed in primary rhabdomyo-sarcomas by comparative genomic hybridization.
    Li QX, Liu CX, Chun CP, Qi Y, Chang B, Li XX, Chen YZ, Nong WX, Li HA, Li F.
    Chin Med J (Engl); 2009 Jun 05; 122(11):1277-82. PubMed ID: 19567137
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  • 9. Homogeneous immunophenotype and paucity of secondary genomic aberrations are distinctive features of endemic but not of sporadic Burkitt's lymphoma and diffuse large B-cell lymphoma with MYC rearrangement.
    Barth TF, Müller S, Pawlita M, Siebert R, Rother JU, Mechtersheimer G, Kitinya J, Bentz M, Möller P.
    J Pathol; 2004 Aug 05; 203(4):940-5. PubMed ID: 15258997
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  • 10. DNA in situ hybridization (interphase cytogenetics) versus comparative genomic hybridization (CGH) in human cancer: detection of numerical and structural chromosome aberrations.
    Van Dekken H, Krijtenburg PJ, Alers JC.
    Acta Histochem; 2000 Feb 05; 102(1):85-94. PubMed ID: 10726167
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  • 11. 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 01; 97(3):601-9. PubMed ID: 12548602
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  • 12. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
    van Gils W, Kilic E, Brüggenwirth HT, Vaarwater J, Verbiest MM, Beverloo B, van Til-Berg ME, Paridaens D, Luyten GP, de Klein A.
    Melanoma Res; 2008 Feb 01; 18(1):10-5. PubMed ID: 18227702
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  • 13. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
    Lau CC, Harris CP, Lu XY, Perlaky L, Gogineni S, Chintagumpala M, Hicks J, Johnson ME, Davino NA, Huvos AG, Meyers PA, Healy JH, Gorlick R, Rao PH.
    Genes Chromosomes Cancer; 2004 Jan 01; 39(1):11-21. PubMed ID: 14603437
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  • 14. Genomic imbalances in AIDS-related lymphomas: relation with tumoral Epstein-Barr virus status.
    Vaghefi P, Martin A, Prévot S, Charlotte F, Camilleri-Broët S, Barli E, Davi F, Gabarre J, Raphael M, Poirel HA.
    AIDS; 2006 Nov 28; 20(18):2285-91. PubMed ID: 17117014
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  • 15. 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 28; 20(1):30-7. PubMed ID: 9290951
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  • 16. Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping.
    Macville M, Schröck E, Padilla-Nash H, Keck C, Ghadimi BM, Zimonjic D, Popescu N, Ried T.
    Cancer Res; 1999 Jan 01; 59(1):141-50. PubMed ID: 9892199
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  • 17. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
    Tan YQ, Di YF, Song YZ, Cheng DH, Li LY, Lu GX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 01; 24(4):392-6. PubMed ID: 17680527
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  • 18. Genomic alterations in lung adenocarcinomas detected by multicolor fluorescence in situ hybridization and comparative genomic hybridization.
    Shen H, Zhu Y, Wu YJ, Qiu HR, Shu YQ.
    Cancer Genet Cytogenet; 2008 Mar 01; 181(2):100-7. PubMed ID: 18295661
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  • 19. Frequent aberrations of chromosome 8 in aggressive B-cell non-Hodgkin lymphoma.
    Pienkowska-Grela B, Witkowska A, Grygalewicz B, Rymkiewicz G, Rygier J, Woroniecka R, Walewski J.
    Cancer Genet Cytogenet; 2005 Jan 15; 156(2):114-21. PubMed ID: 15642390
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  • 20. Spectral karyotyping analysis of head and neck squamous cell carcinoma.
    Singh B, Gogineni S, Goberdhan A, Sacks P, Shaha A, Shah J, Rao P.
    Laryngoscope; 2001 Sep 15; 111(9):1545-50. PubMed ID: 11568603
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