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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 20885788)

  • 21. High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays.
    Squire JA; Pei J; Marrano P; Beheshti B; Bayani J; Lim G; Moldovan L; Zielenska M
    Genes Chromosomes Cancer; 2003 Nov; 38(3):215-25. PubMed ID: 14506695
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Convergence of congenic mapping and allele-specific alterations in tumors for the resolution of the Skts1 skin tumor susceptibility locus.
    de Koning JP; Wakabayashi Y; Nagase H; Mao JH; Balmain A
    Oncogene; 2007 Jun; 26(28):4171-8. PubMed ID: 17311004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Germline Variants Impact Somatic Events during Tumorigenesis.
    Ramroop JR; Gerber MM; Toland AE
    Trends Genet; 2019 Jul; 35(7):515-526. PubMed ID: 31128889
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
    Selvarajah S; Yoshimoto M; Ludkovski O; Park PC; Bayani J; Thorner P; Maire G; Squire JA; Zielenska M
    Cytogenet Genome Res; 2008; 122(1):5-15. PubMed ID: 18931480
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Identification of four distinct regions of allelic imbalances on chromosome 1 by the combined comparative genomic hybridization and microsatellite analysis on hepatocellular carcinoma.
    Leung TH; Wong N; Lai PB; Chan A; To KF; Liew CT; Lau WY; Johnson PJ
    Mod Pathol; 2002 Nov; 15(11):1213-20. PubMed ID: 12429801
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chromosomal aberrations in UVB-induced tumors of immunosuppressed mice.
    Dworkin AM; Tober KL; Duncan FJ; Yu L; VanBuskirk AM; Oberyszyn TM; Toland AE
    Genes Chromosomes Cancer; 2009 Jun; 48(6):490-501. PubMed ID: 19296524
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genome-wide genetic characterization of bladder cancer: a comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis.
    Hoque MO; Lee CC; Cairns P; Schoenberg M; Sidransky D
    Cancer Res; 2003 May; 63(9):2216-22. PubMed ID: 12727842
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomic imbalances in CML blast crisis: 8q24.12-q24.13 segment identified as a common region of over-representation.
    Gribble SM; Reid AG; Roberts I; Grace C; Green AR; Nacheva EP
    Genes Chromosomes Cancer; 2003 Aug; 37(4):346-58. PubMed ID: 12800146
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Multiple epithelial and nonepithelial tumors in hereditary nonpolyposis colorectal cancer: characterization of germline and somatic mutations of the MSH2 gene and heterogeneity of replication error phenotypes.
    Huang RL; Chao CF; Ding DC; Yu CP; Chang CC; Lai HC; Yu MH; Liu HS; Chu TY
    Cancer Genet Cytogenet; 2004 Sep; 153(2):108-14. PubMed ID: 15350299
    [TBL] [Abstract][Full Text] [Related]  

  • 30. UV-B-type mutations and chromosomal imbalances indicate common pathways for the development of Merkel and skin squamous cell carcinomas.
    Popp S; Waltering S; Herbst C; Moll I; Boukamp P
    Int J Cancer; 2002 May; 99(3):352-60. PubMed ID: 11992403
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
    Hallor KH; Staaf J; Bovée JV; Hogendoorn PC; Cleton-Jansen AM; Knuutila S; Savola S; Niini T; Brosjö O; Bauer HC; Vult von Steyern F; Jonsson K; Skorpil M; Mandahl N; Mertens F
    Clin Cancer Res; 2009 Apr; 15(8):2685-94. PubMed ID: 19336518
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.
    Sun JX; He Y; Sanford E; Montesion M; Frampton GM; Vignot S; Soria JC; Ross JS; Miller VA; Stephens PJ; Lipson D; Yelensky R
    PLoS Comput Biol; 2018 Feb; 14(2):e1005965. PubMed ID: 29415044
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Arsenic-related DNA copy-number alterations in lung squamous cell carcinomas.
    Martinez VD; Buys TP; Adonis M; Benítez H; Gallegos I; Lam S; Lam WL; Gil L
    Br J Cancer; 2010 Oct; 103(8):1277-83. PubMed ID: 20842114
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pronounced allelic imbalance at D9S162 in skin squamous cell carcinoma of organ transplant recipients.
    Mühleisen B; Petrov I; Frigerio S; Dziunycz P; French LE; Hofbauer GF
    Arch Dermatol; 2012 Jun; 148(6):697-703. PubMed ID: 22508773
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.
    Marescalco MS; Capizzi C; Condorelli DF; Barresi V
    J Oral Pathol Med; 2014 Jan; 43(1):20-7. PubMed ID: 23750501
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Allelic imbalance studies of chromosome 9 suggest major differences in chromosomal instability among nonmelanoma skin carcinomas.
    Gomes GP; Moraes AM; Stoff HO; Ward LS
    Sao Paulo Med J; 2004 Jan; 122(1):18-21. PubMed ID: 15160522
    [TBL] [Abstract][Full Text] [Related]  

  • 37. De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one.
    Goel A; Nguyen TP; Leung HC; Nagasaka T; Rhees J; Hotchkiss E; Arnold M; Banerji P; Koi M; Kwok CT; Packham D; Lipton L; Boland CR; Ward RL; Hitchins MP
    Int J Cancer; 2011 Feb; 128(4):869-78. PubMed ID: 20473912
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 48(2):202-12. PubMed ID: 19009612
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Thymidylate synthetase allelic imbalance in clear cell renal carcinoma.
    Colavito D; Cartei G; Dal Bianco M; Stecca A; Zustovich F; Dalle Carbonare M; Ragazzi E; Farina M; Colombrino E; Leon A
    Cancer Chemother Pharmacol; 2009 Nov; 64(6):1195-200. PubMed ID: 19306093
    [TBL] [Abstract][Full Text] [Related]  

  • 40. High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer.
    Tan IB; Malik S; Ramnarayanan K; McPherson JR; Ho DL; Suzuki Y; Ng SB; Yan S; Lim KH; Koh D; Hoe CM; Chan CY; Ten R; Goh BK; Chung AY; Tan J; Chan CX; Tay ST; Alexander L; Nagarajan N; Hillmer AM; Tang CL; Chua C; Teh BT; Rozen S; Tan P
    Genome Biol; 2015 Feb; 16(1):32. PubMed ID: 25808843
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.