BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 17465989)

  • 1. Genome wide copy number abnormalities in pediatric medulloblastomas as assessed by array comparative genome hybridization.
    Lo KC; Rossi MR; Eberhart CG; Cowell JK
    Brain Pathol; 2007 Jul; 17(3):282-96. PubMed ID: 17465989
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas.
    Lo KC; Rossi MR; Burkhardt T; Pomeroy SL; Cowell JK
    Genes Chromosomes Cancer; 2007 Jan; 46(1):53-66. PubMed ID: 17044047
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Array CGH analysis of pediatric medulloblastomas.
    Rossi MR; Conroy J; McQuaid D; Nowak NJ; Rutka JT; Cowell JK
    Genes Chromosomes Cancer; 2006 Mar; 45(3):290-303. PubMed ID: 16320246
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of oncogene amplifications in medulloblastomas by comparative genomic hybridization and array-based comparative genomic hybridization.
    Tong CY; Hui AB; Yin XL; Pang JC; Zhu XL; Poon WS; Ng HK
    J Neurosurg; 2004 Feb; 100(2 Suppl Pediatrics):187-93. PubMed ID: 14758948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 11(13):4707-16. PubMed ID: 16000565
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling.
    Nord H; Pfeifer S; Nilsson P; Sandgren J; Popova S; Strömberg B; Alafuzoff I; Nistér M; Díaz de Ståhl T
    J Neurooncol; 2012 Mar; 107(1):37-49. PubMed ID: 21979893
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic alterations in childhood medulloblastoma analyzed by comparative genomic hybridization.
    Michiels EM; Weiss MM; Hoovers JM; Baak JP; Voûte PA; Baas F; Hermsen MA
    J Pediatr Hematol Oncol; 2002; 24(3):205-10. PubMed ID: 11990307
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Candidate glioblastoma development gene identification using concordance between copy number abnormalities and gene expression level changes.
    Lo KC; Rossi MR; LaDuca J; Hicks DG; Turpaz Y; Hawthorn L; Cowell JK
    Genes Chromosomes Cancer; 2007 Oct; 46(10):875-94. PubMed ID: 17620294
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isochromosome 17q is a negative prognostic factor in poor-risk childhood medulloblastoma patients.
    Pan E; Pellarin M; Holmes E; Smirnov I; Misra A; Eberhart CG; Burger PC; Biegel JA; Feuerstein BG
    Clin Cancer Res; 2005 Jul; 11(13):4733-40. PubMed ID: 16000568
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Outcome prediction in pediatric medulloblastoma based on DNA copy-number aberrations of chromosomes 6q and 17q and the MYC and MYCN loci.
    Pfister S; Remke M; Benner A; Mendrzyk F; Toedt G; Felsberg J; Wittmann A; Devens F; Gerber NU; Joos S; Kulozik A; Reifenberger G; Rutkowski S; Wiestler OD; Radlwimmer B; Scheurlen W; Lichter P; Korshunov A
    J Clin Oncol; 2009 Apr; 27(10):1627-36. PubMed ID: 19255330
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult and pediatric medulloblastomas are genetically distinct and require different algorithms for molecular risk stratification.
    Korshunov A; Remke M; Werft W; Benner A; Ryzhova M; Witt H; Sturm D; Wittmann A; Schöttler A; Felsberg J; Reifenberger G; Rutkowski S; Scheurlen W; Kulozik AE; von Deimling A; Lichter P; Pfister SM
    J Clin Oncol; 2010 Jun; 28(18):3054-60. PubMed ID: 20479417
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.
    Langdon JA; Lamont JM; Scott DK; Dyer S; Prebble E; Bown N; Grundy RG; Ellison DW; Clifford SC
    Genes Chromosomes Cancer; 2006 Jan; 45(1):47-60. PubMed ID: 16149064
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Medulloblastoma outcome is adversely associated with overexpression of EEF1D, RPL30, and RPS20 on the long arm of chromosome 8.
    De Bortoli M; Castellino RC; Lu XY; Deyo J; Sturla LM; Adesina AM; Perlaky L; Pomeroy SL; Lau CC; Man TK; Rao PH; Kim JY
    BMC Cancer; 2006 Sep; 6():223. PubMed ID: 16968546
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosome 9q and 16q loss identified by genome-wide pooled-analysis are associated with tumor aggressiveness in patients with classic medulloblastoma.
    Coco S; Valdora F; Bonassi S; Scaruffi P; Stigliani S; Oberthuer A; Berthold F; Andolfo I; Servidei T; Riccardi R; Basso E; Iolascon A; Tonini GP
    OMICS; 2011 May; 15(5):273-80. PubMed ID: 21348762
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Biological and clinical heterogeneity of MYCN-amplified medulloblastoma.
    Korshunov A; Remke M; Kool M; Hielscher T; Northcott PA; Williamson D; Pfaff E; Witt H; Jones DT; Ryzhova M; Cho YJ; Wittmann A; Benner A; Weiss WA; von Deimling A; Scheurlen W; Kulozik AE; Clifford SC; Peter Collins V; Westermann F; Taylor MD; Lichter P; Pfister SM
    Acta Neuropathol; 2012 Apr; 123(4):515-27. PubMed ID: 22160402
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic alterations in pediatric medulloblastomas detected by comparative genomic hybridization.
    Nishizaki T; Harada K; Kubota H; Ozaki S; Ito H; Sasaki K
    Pediatr Neurosurg; 1999 Jul; 31(1):27-32. PubMed ID: 10545819
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extensive genomic abnormalities in childhood medulloblastoma by comparative genomic hybridization.
    Reardon DA; Michalkiewicz E; Boyett JM; Sublett JE; Entrekin RE; Ragsdale ST; Valentine MB; Behm FG; Li H; Heideman RL; Kun LE; Shapiro DN; Look AT
    Cancer Res; 1997 Sep; 57(18):4042-7. PubMed ID: 9307291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint.
    McCabe MG; Ichimura K; Pearson DM; Liu L; Clifford SC; Ellison DW; Collins VP
    Genes Chromosomes Cancer; 2009 Feb; 48(2):121-31. PubMed ID: 18973140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Detection of chromosomal DNA imbalance in medulloblastoma by comparative genomic hybridization].
    Sun YJ; Yu SZ; Sun CY; Wang Q; Jin SM; Wu WX; An TL
    Zhonghua Bing Li Xue Za Zhi; 2010 Sep; 39(9):606-10. PubMed ID: 21092588
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Supratentorial primitive neuroectodermal tumors of the central nervous system frequently harbor deletions of the CDKN2A locus and other genomic aberrations distinct from medulloblastomas.
    Pfister S; Remke M; Toedt G; Werft W; Benner A; Mendrzyk F; Wittmann A; Devens F; von Hoff K; Rutkowski S; Kulozik A; Radlwimmer B; Scheurlen W; Lichter P; Korshunov A
    Genes Chromosomes Cancer; 2007 Sep; 46(9):839-51. PubMed ID: 17592618
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.