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Journal Abstract Search

956 related items for PubMed ID: 18628790

  • 1. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
    Espinosa AB, Mackintosh C, Maíllo A, Gutierrez L, Sousa P, Merino M, Ortiz J, de Alava E, Orfao A, Tabernero MD.
    Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
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  • 6. Incidence of numerical chromosome aberrations in meningioma tumors as revealed by fluorescence in situ hybridization using 10 chromosome-specific probes.
    Sayagués JM, Tabernero MD, Maillo A, Díaz P, Rasillo A, Bortoluci A, Gomez-Moreta J, Santos-Briz A, Morales F, Orfao A.
    Cytometry; 2002 Jun 15; 50(3):153-9. PubMed ID: 12116338
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  • 7. Patient gender is associated with distinct patterns of chromosomal abnormalities and sex chromosome linked gene-expression profiles in meningiomas.
    Tabernero MD, Espinosa AB, Maillo A, Rebelo O, Vera JF, Sayagues JM, Merino M, Diaz P, Sousa P, Orfao A.
    Oncologist; 2007 Oct 15; 12(10):1225-36. PubMed ID: 17962616
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  • 12. The cytogenetic relationship between primary and recurrent meningiomas points to the need for new treatment strategies in cases at high risk of relapse.
    Espinosa AB, Tabernero MD, Maíllo A, Sayagués JM, Ciudad J, Merino M, Alguero MC, Lubombo AM, Sousa P, Santos-Briz A, Orfao A.
    Clin Cancer Res; 2006 Feb 01; 12(3 Pt 1):772-80. PubMed ID: 16467088
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  • 13. Microarray-based analysis of spinal versus intracranial meningiomas: different clinical, biological, and genetic characteristics associated with distinct patterns of gene expression.
    Sayagués JM, Tabernero MD, Maíllo A, Trelles O, Espinosa AB, Sarasquete ME, Merino M, Rasillo A, Vera JF, Santos-Briz A, de Alava E, Garcia-Macias MC, Orfao A.
    J Neuropathol Exp Neurol; 2006 May 01; 65(5):445-54. PubMed ID: 16772868
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  • 14. 1p and 3p deletions in meningiomas without detectable aberrations of chromosome 22 identified by comparative genomic hybridization.
    Carlson KM, Bruder C, Nordenskjöld M, Dumanski JP.
    Genes Chromosomes Cancer; 1997 Dec 01; 20(4):419-24. PubMed ID: 9408760
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  • 15. Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.
    Nordgren A, Corcoran M, Sääf A, Bremer A, Kluin-Nelemans HC, Schoumans J, Grandér D.
    Eur J Haematol; 2010 Jan 01; 84(1):17-25. PubMed ID: 19682064
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  • 16. Screening of genomic imbalances in glioblastoma multiforme using high-resolution comparative genomic hybridization.
    Vranová V, Necesalová E, Kuglík P, Cejpek P, Pesáková M, Budínská E, Relichová J, Veselská R.
    Oncol Rep; 2007 Feb 01; 17(2):457-64. PubMed ID: 17203188
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  • 17. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
    Pinkel D, Segraves R, Sudar D, Clark S, Poole I, Kowbel D, Collins C, Kuo WL, Chen C, Zhai Y, Dairkee SH, Ljung BM, Gray JW, Albertson DG.
    Nat Genet; 1998 Oct 01; 20(2):207-11. PubMed ID: 9771718
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  • 18. Gain at chromosomal region 5p15.33, containing TERT, is the most frequent genetic event in early stages of non-small cell lung cancer.
    Kang JU, Koo SH, Kwon KC, Park JW, Kim JM.
    Cancer Genet Cytogenet; 2008 Apr 01; 182(1):1-11. PubMed ID: 18328944
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  • 19. A copy number gain of the 6p arm is linked with advanced hepatocellular carcinoma: an array-based comparative genomic hybridization study.
    Chochi Y, Kawauchi S, Nakao M, Furuya T, Hashimoto K, Oga A, Oka M, Sasaki K.
    J Pathol; 2009 Apr 01; 217(5):677-84. PubMed ID: 19097070
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