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Journal Abstract Search

195 related items for PubMed ID: 16258161

  • 1. Mass spectrometry-based loss of heterozygosity analysis of single-nucleotide polymorphism loci in paraffin embedded tumors using the MassEXTEND assay: single-nucleotide polymorphism loss of heterozygosity analysis of the protein tyrosine phosphatase receptor type J in familial colorectal cancer.
    van Puijenbroek M, Dierssen JW, Stanssens P, van Eijk R, Cleton-Jansen AM, van Wezel T, Morreau H.
    J Mol Diagn; 2005 Nov; 7(5):623-30. PubMed ID: 16258161
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  • 2. LOH of PTPRJ occurs early in colorectal cancer and is associated with chromosomal loss of 18q12-21.
    Ruivenkamp C, Hermsen M, Postma C, Klous A, Baak J, Meijer G, Demant P.
    Oncogene; 2003 May 29; 22(22):3472-4. PubMed ID: 12776199
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  • 3. Allele-specific loss of heterozygosity in multiple colorectal adenomas: toward an integrated molecular cytogenetic map II.
    Mao X, Hamoudi RA, Talbot IC, Baudis M.
    Cancer Genet Cytogenet; 2006 May 29; 167(1):1-14. PubMed ID: 16682279
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  • 4. Single nucleotide polymorphism analysis in the human phosphatase PTPrj gene using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry.
    Powell N, Dudley E, Morishita M, Bogdanova T, Tronko M, Thomas G.
    Rapid Commun Mass Spectrom; 2004 May 29; 18(19):2249-54. PubMed ID: 15384144
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  • 5. Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays.
    Lips EH, Dierssen JW, van Eijk R, Oosting J, Eilers PH, Tollenaar RA, de Graaf EJ, van't Slot R, Wijmenga C, Morreau H, van Wezel T.
    Cancer Res; 2005 Nov 15; 65(22):10188-91. PubMed ID: 16288005
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  • 6. Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer.
    Lesueur F, Pharoah PD, Laing S, Ahmed S, Jordan C, Smith PL, Luben R, Wareham NJ, Easton DF, Dunning AM, Ponder BA.
    Hum Mol Genet; 2005 Aug 15; 14(16):2349-56. PubMed ID: 16000320
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  • 13. Frequent occurrence of uniparental disomy in colorectal cancer.
    Andersen CL, Wiuf C, Kruhøffer M, Korsgaard M, Laurberg S, Ørntoft TF.
    Carcinogenesis; 2007 Jan 15; 28(1):38-48. PubMed ID: 16774939
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  • 14. Allele-specific loss of heterozygosity at the DAL-1/4.1B (EPB41L3) tumor-suppressor gene locus in the absence of mutation.
    Kittiniyom K, Mastronardi M, Roemer M, Wells WA, Greenberg ER, Titus-Ernstoff L, Newsham IF.
    Genes Chromosomes Cancer; 2004 Jul 15; 40(3):190-203. PubMed ID: 15138999
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  • 15. Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
    Küry S, Buecher B, Robiou-du-Pont S, Scoul C, Colman H, Le Neel T, Le Houérou C, Faroux R, Ollivry J, Lafraise B, Chupin LD, Sébille V, Bézieau S.
    BMC Cancer; 2008 Nov 07; 8():326. PubMed ID: 18992148
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  • 16. 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
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  • 17. The relationship between global methylation level, loss of heterozygosity, and microsatellite instability in sporadic colorectal cancer.
    Matsuzaki K, Deng G, Tanaka H, Kakar S, Miura S, Kim YS.
    Clin Cancer Res; 2005 Dec 15; 11(24 Pt 1):8564-9. PubMed ID: 16361538
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  • 18. Recent advances in molecular diagnostics of colorectal cancer by genomic arrays: proposal for a procedural shift in biological sampling and pathological report.
    Castorina S, Barresi V, Luca T, Privitera G, Musso N, Capizzi C, Condorelli DF.
    Ital J Anat Embryol; 2010 Dec 15; 115(1-2):39-45. PubMed ID: 21072988
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  • 19. [Loss of heterozygosity on chromosome 3 in sporadic colorectal carcinoma].
    Peng Z, Ling Y, Bai S.
    Zhonghua Yi Xue Za Zhi; 2001 Mar 25; 81(6):336-9. PubMed ID: 11798895
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