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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

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
    [Abstract] [Full Text] [Related]

  • 2. Characterization of chromosome 14 abnormalities by interphase in situ hybridization and comparative genomic hybridization in 124 meningiomas: correlation with clinical, histopathologic, and prognostic features.
    Tabernero MD, Espinosa AB, Maíllo A, Sayagués JM, Alguero Mdel C, Lumbreras E, Díaz P, Gonçalves JM, Onzain I, Merino M, Morales F, Orfao A.
    Am J Clin Pathol; 2005 May; 123(5):744-51. PubMed ID: 15981814
    [Abstract] [Full Text] [Related]

  • 3. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
    Weiss MM, Snijders AM, Kuipers EJ, Ylstra B, Pinkel D, Meuwissen SG, van Diest PJ, Albertson DG, Meijer GA.
    J Pathol; 2003 Jul; 200(3):320-6. PubMed ID: 12845628
    [Abstract] [Full Text] [Related]

  • 4. Intratumoral patterns of clonal evolution in meningiomas as defined by multicolor interphase fluorescence in situ hybridization (FISH): is there a relationship between histopathologically benign and atypical/anaplastic lesions?
    Sayagués JM, Tabernero MD, Maíllo A, Espinosa A, Rasillo A, Díaz P, Ciudad J, López A, Merino M, Gonçalves JM, Santos-Briz A, Morales F, Orfao A.
    J Mol Diagn; 2004 Nov; 6(4):316-25. PubMed ID: 15507670
    [Abstract] [Full Text] [Related]

  • 5. Comparative genomic hybridization analysis of genomic alterations in benign, atypical and anaplastic meningiomas.
    Arslantas A, Artan S, Oner U, Durmaz R, Müslümanoğlu H, Atasoy MA, Başaran N, Tel E.
    Acta Neurol Belg; 2002 Jun; 102(2):53-62. PubMed ID: 12161900
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 8. High-resolution analysis of DNA copy number alterations and gene expression in renal clear cell carcinoma.
    Yoshimoto T, Matsuura K, Karnan S, Tagawa H, Nakada C, Tanigawa M, Tsukamoto Y, Uchida T, Kashima K, Akizuki S, Takeuchi I, Sato F, Mimata H, Seto M, Moriyama M.
    J Pathol; 2007 Dec 15; 213(4):392-401. PubMed ID: 17922474
    [Abstract] [Full Text] [Related]

  • 9. Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci.
    Buckley PG, Jarbo C, Menzel U, Mathiesen T, Scott C, Gregory SG, Langford CF, Dumanski JP.
    Cancer Res; 2005 Apr 01; 65(7):2653-61. PubMed ID: 15805262
    [Abstract] [Full Text] [Related]

  • 10. Genomic profiling of myeloid sarcoma by array comparative genomic hybridization.
    Deeb G, Baer MR, Gaile DP, Sait SN, Barcos M, Wetzler M, Conroy JM, Nowak NJ, Cowell JK, Cheney RT.
    Genes Chromosomes Cancer; 2005 Dec 01; 44(4):373-83. PubMed ID: 16080198
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 48.