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118 related items for PubMed ID: 11453919

  • 1. A case of adult T-cell leukaemia/lymphoma characterized by multiplex-fluorescence in situ hybridization, comparative genomic hybridization, fluorescence in situ hybridization and cytogenetics.
    Mao X, Lillington DM, Czepulkowski B, Young BD, Russell-Jones R, Whittaker S.
    Br J Dermatol; 2001 Jul; 145(1):117-22. PubMed ID: 11453919
    [Abstract] [Full Text] [Related]

  • 2. [Identification of complex chromosomal aberrations in acute leukemia by using conventional cytogenetics combined with multiplex fluorescence in situ hybridization].
    Yu F, Li CW, Wei H, Liu XP, Lin D, Gong JY, Qin S, Xu FY, Mi YC, Wang JX.
    Zhonghua Xue Ye Xue Za Zhi; 2010 May; 31(5):289-93. PubMed ID: 21122305
    [Abstract] [Full Text] [Related]

  • 3. Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sézary syndrome and mycosis fungoides.
    Mao X, Lillington D, Scarisbrick JJ, Mitchell T, Czepulkowski B, Russell-Jones R, Young B, Whittaker SJ.
    Br J Dermatol; 2002 Sep; 147(3):464-75. PubMed ID: 12207585
    [Abstract] [Full Text] [Related]

  • 4. Molecular cytogenetic characterization of Sézary syndrome.
    Mao X, Lillington DM, Czepulkowski B, Russell-Jones R, Young BD, Whittaker S.
    Genes Chromosomes Cancer; 2003 Mar; 36(3):250-60. PubMed ID: 12557225
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  • 5. [Detection of the complex chromosomal aberrations in acute lymphoblastic leukemia by means of multiplex fluorescence in situ hybridization].
    Li JY, Ma L, Xiao B, Pan JL, Qiu HR, Wu YF, Wen BZ, Xue YQ.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2006 Feb; 14(1):42-5. PubMed ID: 16584589
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  • 6. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
    Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, Sterba J, Kuglik P.
    Neoplasma; 2008 Feb; 55(1):23-30. PubMed ID: 18190236
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  • 7. Discrepant cytogenetic and fluorescence in situ hybridization results in a 26-year-old male with early T-cell acute lymphocytic leukemia.
    Chinnappan D, Cowan J, Rastogi A, Miller KB, Blanchard R, Wyandt HE.
    Cancer Genet Cytogenet; 1998 Oct 15; 106(2):116-21. PubMed ID: 9797775
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 30(3):267-73. PubMed ID: 11170284
    [Abstract] [Full Text] [Related]

  • 9. Chromosomal imbalances: a hallmark of tumour relapse in primary cutaneous CD30+ T-cell lymphoma.
    Prochazkova M, Chevret E, Beylot-Barry M, Sobotka J, Vergier B, Delaunay M, Turmo M, Ferrer J, Kuglik P, Merlio JP.
    J Pathol; 2003 Nov 15; 201(3):421-9. PubMed ID: 14595754
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  • 11. Application of molecular cytogenetic techniques in a case study of human cutaneous metastatic melanoma.
    Wiltshire RN, Dennis TR, Sondak VK, Meltzer PS, Trent JM.
    Cancer Genet Cytogenet; 2001 Dec 15; 131(2):97-103. PubMed ID: 11750048
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  • 12. Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.
    Weise A, Liehr T, Efferth T, Kuechler A, Gebhart E.
    Cytogenet Genome Res; 2002 Dec 15; 98(2-3):118-25. PubMed ID: 12697993
    [Abstract] [Full Text] [Related]

  • 13. Characterization of three hairy cell leukemia- derived cell lines (ESKOL, JOK-1, and hair-M) by multiplex-FISH, comparative genomic hybridization, FISH, PRINS, and dideoxyPRINS.
    Lindbjerg Andersen C, Ostergaard M, Nielsen B, Pedersen B, Koch J.
    Cytogenet Cell Genet; 2000 Dec 15; 90(1-2):30-9. PubMed ID: 11060441
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  • 16. Discovery of over-expressed genes and genetic alterations in breast cancer cells using a combination of suppression subtractive hybridization, multiplex FISH and comparative genomic hybridization.
    Xie D, Jauch A, Miller CW, Bartram CR, Koeffler HP.
    Int J Oncol; 2002 Sep 15; 21(3):499-507. PubMed ID: 12168092
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  • 17. Chromosome analysis and molecular cytogenetic investigations of an epithelioid hemangioendothelioma.
    Tsarouha H, Kyriazoglou AI, Ribeiro FR, Teixeira MR, Agnantis N, Pandis N.
    Cancer Genet Cytogenet; 2006 Sep 15; 169(2):164-8. PubMed ID: 16938576
    [Abstract] [Full Text] [Related]

  • 18. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
    Xu W, Li JY, Liu Q, Zhu Y, Pan JL, Qiu HR, Xue YQ.
    Int J Lab Hematol; 2010 Feb 15; 32(1 Pt 1):e86-95. PubMed ID: 20089000
    [Abstract] [Full Text] [Related]

  • 19. Cytogenetic study of malignant triton tumor: a case report.
    Haddadin MH, Hawkins AL, Long P, Morsberger LA, Depew D, Epstein JI, Griffin CA.
    Cancer Genet Cytogenet; 2003 Jul 15; 144(2):100-5. PubMed ID: 12850371
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