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Journal Abstract Search

108 related items for PubMed ID: 15770670

  • 21. Chromosome 22q allelic losses at microsatellite loci in human astrocytic tumors.
    Muhammad AK, Yoshimine T, Maruno M, Tokiyoshi K, Takemoto O, Hayakawa T.
    Neurol Med Chir (Tokyo); 1997 Aug; 37(8):606-10; discussion 611. PubMed ID: 9301196
    [Abstract] [Full Text] [Related]

  • 22. High-resolution array comparative genomic hybridization of chromosome arm 8q: evaluation of genetic progression markers for prostate cancer.
    van Duin M, van Marion R, Vissers K, Watson JE, van Weerden WM, Schröder FH, Hop WC, van der Kwast TH, Collins C, van Dekken H.
    Genes Chromosomes Cancer; 2005 Dec; 44(4):438-49. PubMed ID: 16130124
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  • 23. 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
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  • 24. Deletion at chromosome band 20p12.1 in colorectal cancer revealed by high resolution array comparative genomic hybridization.
    Davison EJ, Tarpey PS, Fiegler H, Tomlinson IP, Carter NP.
    Genes Chromosomes Cancer; 2005 Dec 01; 44(4):384-91. PubMed ID: 16110499
    [Abstract] [Full Text] [Related]

  • 25. Identification of oligodendroglioma specific chromosomal copy number changes in the glioblastoma MI-4 cell line by array-CGH and FISH analyses.
    Magnani I, Moroni RF, Roversi G, Beghini A, Pfundt R, Schoenmakers EF, Larizza L.
    Cancer Genet Cytogenet; 2005 Sep 01; 161(2):140-5. PubMed ID: 16102584
    [Abstract] [Full Text] [Related]

  • 26. Frequent gains at chromosome 7q34 involving BRAF in pilocytic astrocytoma.
    Bar EE, Lin A, Tihan T, Burger PC, Eberhart CG.
    J Neuropathol Exp Neurol; 2008 Sep 01; 67(9):878-87. PubMed ID: 18716556
    [Abstract] [Full Text] [Related]

  • 27. Targets of genome copy number reduction in primary breast cancers identified by integrative genomics.
    Chen W, Salto-Tellez M, Palanisamy N, Ganesan K, Hou Q, Tan LK, Sii LH, Ito K, Tan B, Wu J, Tay A, Tan KC, Ang E, Tan BK, Tan PH, Ito Y, Tan P.
    Genes Chromosomes Cancer; 2007 Mar 01; 46(3):288-301. PubMed ID: 17171680
    [Abstract] [Full Text] [Related]

  • 28. Identification of a novel homozygous deletion region at 6q23.1 in medulloblastomas using high-resolution array comparative genomic hybridization analysis.
    Hui AB, Takano H, Lo KW, Kuo WL, Lam CN, Tong CY, Chang Q, Gray JW, Ng HK.
    Clin Cancer Res; 2005 Jul 01; 11(13):4707-16. PubMed ID: 16000565
    [Abstract] [Full Text] [Related]

  • 29. Survey of genetic alterations in gastrinomas.
    Yu F, Jensen RT, Lubensky IA, Mahlamaki EH, Zheng YL, Herr AM, Ferrin LJ.
    Cancer Res; 2000 Oct 01; 60(19):5536-42. PubMed ID: 11034099
    [Abstract] [Full Text] [Related]

  • 30. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.
    Gaasenbeek M, Howarth K, Rowan AJ, Gorman PA, Jones A, Chaplin T, Liu Y, Bicknell D, Davison EJ, Fiegler H, Carter NP, Roylance RR, Tomlinson IP.
    Cancer Res; 2006 Apr 01; 66(7):3471-9. PubMed ID: 16585170
    [Abstract] [Full Text] [Related]

  • 31. Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors.
    Assämäki R, Sarlomo-Rikala M, Lopez-Guerrero JA, Lasota J, Andersson LC, Llombart-Bosch A, Miettinen M, Knuutila S.
    Genes Chromosomes Cancer; 2007 Jun 01; 46(6):564-76. PubMed ID: 17330260
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  • 32. High definition cytogenetics and oligonucleotide aCGH analyses of cisplatin-resistant ovarian cancer cells.
    Prasad M, Bernardini M, Tsalenko A, Marrano P, Paderova J, Lee CH, Ben-Dor A, Barrett MT, Squire JA.
    Genes Chromosomes Cancer; 2008 May 01; 47(5):427-36. PubMed ID: 18273836
    [Abstract] [Full Text] [Related]

  • 33. Comparative evaluation of microsatellite marker, AP-PCR and CGH studies in primary renal cell carcinoma.
    Hoefling C, Schmidt H, Meinhardt M, Lohse A, Taubert H, Fuessel S, Schmidt U, Schuster K, Baretton G, Wirth MP, Meye A.
    Int J Mol Med; 2004 Jun 01; 13(6):835-42. PubMed ID: 15138621
    [Abstract] [Full Text] [Related]

  • 34. Homozygous deletions may be markers of nearby heterozygous mutations: The complex deletion at FRA16D in the HCT116 colon cancer cell line removes exons of WWOX.
    Alsop AE, Taylor K, Zhang J, Gabra H, Paige AJ, Edwards PA.
    Genes Chromosomes Cancer; 2008 May 01; 47(5):437-47. PubMed ID: 18273838
    [Abstract] [Full Text] [Related]

  • 35. Copy number gain at 8q12.1-q22.1 is associated with a malignant tumor phenotype in salivary gland myoepitheliomas.
    Vékony H, Röser K, Löning T, Ylstra B, Meijer GA, van Wieringen WN, van de Wiel MA, Carvalho B, Kok K, Leemans CR, van der Waal I, Bloemena E.
    Genes Chromosomes Cancer; 2009 Feb 01; 48(2):202-12. PubMed ID: 19009612
    [Abstract] [Full Text] [Related]

  • 36. Frequent loss of chromosome 9, homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas.
    Weber RG, Hoischen A, Ehrler M, Zipper P, Kaulich K, Blaschke B, Becker AJ, Weber-Mangal S, Jauch A, Radlwimmer B, Schramm J, Wiestler OD, Lichter P, Reifenberger G.
    Oncogene; 2007 Feb 15; 26(7):1088-97. PubMed ID: 16909113
    [Abstract] [Full Text] [Related]

  • 37. [From identification of genomic polymorphism to diagnostic and prognostic markers of human epithelial tumors].
    Braga EA, Kiselev LL, Zabarovskiĭ ER.
    Mol Biol (Mosk); 2004 Feb 15; 38(2):179-90. PubMed ID: 15125222
    [Abstract] [Full Text] [Related]

  • 38. 1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a subset of glioblastomas.
    Ichimura K, Vogazianou AP, Liu L, Pearson DM, Bäcklund LM, Plant K, Baird K, Langford CF, Gregory SG, Collins VP.
    Oncogene; 2008 Mar 27; 27(14):2097-108. PubMed ID: 17934521
    [Abstract] [Full Text] [Related]

  • 39. Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas.
    Jones TD, Eble JN, Wang M, MacLennan GT, Delahunt B, Brunelli M, Martignoni G, Lopez-Beltran A, Bonsib SM, Ulbright TM, Zhang S, Nigro K, Cheng L.
    Clin Cancer Res; 2005 Oct 15; 11(20):7226-33. PubMed ID: 16243792
    [Abstract] [Full Text] [Related]

  • 40. High-resolution genome-wide mapping of genetic alterations in human glial brain tumors.
    Bredel M, Bredel C, Juric D, Harsh GR, Vogel H, Recht LD, Sikic BI.
    Cancer Res; 2005 May 15; 65(10):4088-96. PubMed ID: 15899798
    [Abstract] [Full Text] [Related]

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