BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

202 related articles for article (PubMed ID: 17245344)

  • 1. Genome-wide analysis of allelic imbalance in prostate cancer using the Affymetrix 50K SNP mapping array.
    Tørring N; Borre M; Sørensen KD; Andersen CL; Wiuf C; Ørntoft TF
    Br J Cancer; 2007 Feb; 96(3):499-506. PubMed ID: 17245344
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
    BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrence.
    Coenen MJ; Ploeg M; Schijvenaars MM; Cornel EB; Karthaus HF; Scheffer H; Witjes JA; Franke B; Kiemeney LA
    Clin Cancer Res; 2008 Dec; 14(24):8198-204. PubMed ID: 19088036
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
    Carr J; Bown NP; Case MC; Hall AG; Lunec J; Tweddle DA
    Cancer Genet Cytogenet; 2007 Jan; 172(2):127-38. PubMed ID: 17213021
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Frequent occurrence of uniparental disomy in colorectal cancer.
    Andersen CL; Wiuf C; Kruhøffer M; Korsgaard M; Laurberg S; Ørntoft TF
    Carcinogenesis; 2007 Jan; 28(1):38-48. PubMed ID: 16774939
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Analyzing the profile of chromosomal imbalances in esophageal atypical hyperplasia and early stage esophageal squamous cell carcinoma by 250K Snp Array].
    Zhang X; Zhu ZH; Lin P; Yang H; Fu JH; Zhang LJ; Long H; Wen J; Huang XP; Fang Y; Rong TH
    Zhonghua Yi Xue Za Zhi; 2008 Oct; 88(37):2636-41. PubMed ID: 19080713
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect.
    Agnelli L; Mosca L; Fabris S; Lionetti M; Andronache A; Kwee I; Todoerti K; Verdelli D; Battaglia C; Bertoni F; Deliliers GL; Neri A
    Genes Chromosomes Cancer; 2009 Jul; 48(7):603-14. PubMed ID: 19396863
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.
    Midorikawa Y; Yamamoto S; Ishikawa S; Kamimura N; Igarashi H; Sugimura H; Makuuchi M; Aburatani H
    Oncogene; 2006 Sep; 25(40):5581-90. PubMed ID: 16785998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide loss of heterozygosity analysis from laser capture microdissected prostate cancer using single nucleotide polymorphic allele (SNP) arrays and a novel bioinformatics platform dChipSNP.
    Lieberfarb ME; Lin M; Lechpammer M; Li C; Tanenbaum DM; Febbo PG; Wright RL; Shim J; Kantoff PW; Loda M; Meyerson M; Sellers WR
    Cancer Res; 2003 Aug; 63(16):4781-5. PubMed ID: 12941794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes.
    Cheung KJ; Delaney A; Ben-Neriah S; Schein J; Lee T; Shah SP; Cheung D; Johnson NA; Mungall AJ; Telenius A; Lai B; Boyle M; Connors JM; Gascoyne RD; Marra MA; Horsman DE
    Genes Chromosomes Cancer; 2010 Aug; 49(8):669-81. PubMed ID: 20544841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microsatellite analysis of allelic imbalance in tumour and blood from patients with prostate cancer.
    Schwarzenbach H; Chun FK; Müller I; Seidel C; Urban K; Erbersdobler A; Huland H; Pantel K; Friedrich MG
    BJU Int; 2008 Jul; 102(2):253-8. PubMed ID: 18336598
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].
    Ma F; Wu FX; Li N; Liu Q; Yang W; Zhang X; Sun M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):336-9. PubMed ID: 19504452
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays.
    Calhoun ES; Hucl T; Gallmeier E; West KM; Arking DE; Maitra A; Iacobuzio-Donahue CA; Chakravarti A; Hruban RH; Kern SE
    Cancer Res; 2006 Aug; 66(16):7920-8. PubMed ID: 16912165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
    Nannya Y; Sanada M; Nakazaki K; Hosoya N; Wang L; Hangaishi A; Kurokawa M; Chiba S; Bailey DK; Kennedy GC; Ogawa S
    Cancer Res; 2005 Jul; 65(14):6071-9. PubMed ID: 16024607
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
    Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
    Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Integrated analysis of copy number alterations and loss of heterozygosity in human pancreatic cancer using a high-resolution, single nucleotide polymorphism array.
    Lin LJ; Asaoka Y; Tada M; Sanada M; Nannya Y; Tanaka Y; Tateishi K; Ohta M; Seto M; Sasahira N; Tada M; Kawabe T; Zheng CQ; Kanai F; Ogawa S; Omata M
    Oncology; 2008; 75(1-2):102-12. PubMed ID: 18787345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays.
    Lam CW; To KF; Tong SF
    Clin Biochem; 2006 Mar; 39(3):187-90. PubMed ID: 16513104
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 65(22):10188-91. PubMed ID: 16288005
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrative analysis of genomic aberrations associated with prostate cancer progression.
    Kim JH; Dhanasekaran SM; Mehra R; Tomlins SA; Gu W; Yu J; Kumar-Sinha C; Cao X; Dash A; Wang L; Ghosh D; Shedden K; Montie JE; Rubin MA; Pienta KJ; Shah RB; Chinnaiyan AM
    Cancer Res; 2007 Sep; 67(17):8229-39. PubMed ID: 17804737
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.
    Wang L; Fidler C; Nadig N; Giagounidis A; Della Porta MG; Malcovati L; Killick S; Gattermann N; Aul C; Boultwood J; Wainscoat JS
    Haematologica; 2008 Jul; 93(7):994-1000. PubMed ID: 18508791
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.