BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

99 related articles for article (PubMed ID: 18973140)

  • 1. 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]  

  • 2. Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats.
    Mendrzyk F; Korshunov A; Toedt G; Schwarz F; Korn B; Joos S; Hochhaus A; Schoch C; Lichter P; Radlwimmer B
    Genes Chromosomes Cancer; 2006 Apr; 45(4):401-10. PubMed ID: 16419060
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Aberrant hypermethylation of the major breakpoint cluster region in 17p11.2 in medulloblastomas but not supratentorial PNETs.
    Frühwald MC; O'Dorisio MS; Dai Z; Rush LJ; Krahe R; Smiraglia DJ; Pietsch T; Elsea SH; Plass C
    Genes Chromosomes Cancer; 2001 Jan; 30(1):38-47. PubMed ID: 11107174
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
    Selzer RR; Richmond TA; Pofahl NJ; Green RD; Eis PS; Nair P; Brothman AR; Stallings RL
    Genes Chromosomes Cancer; 2005 Nov; 44(3):305-19. PubMed ID: 16075461
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Transcription mapping in a medulloblastoma breakpoint interval and Smith-Magenis syndrome candidate region: identification of 53 transcriptional units and new candidate genes.
    Seranski P; Heiss NS; Dhorne-Pollet S; Radelof U; Korn B; Hennig S; Backes E; Schmidt S; Wiemann S; Schwarz CE; Lehrach H; Poustka A
    Genomics; 1999 Feb; 56(1):1-11. PubMed ID: 10036180
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.
    Sharp AJ; Hansen S; Selzer RR; Cheng Z; Regan R; Hurst JA; Stewart H; Price SM; Blair E; Hennekam RC; Fitzpatrick CA; Segraves R; Richmond TA; Guiver C; Albertson DG; Pinkel D; Eis PS; Schwartz S; Knight SJ; Eichler EE
    Nat Genet; 2006 Sep; 38(9):1038-42. PubMed ID: 16906162
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
    Lindstrand A; Schoumans J; Gustavsson P; Hanemaaijer N; Malmgren H; Blennow E
    Clin Genet; 2010 Jun; 77(6):552-62. PubMed ID: 20236111
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.
    Sahoo T; Bacino CA; German JR; Shaw CA; Bird LM; Kimonis V; Anselm I; Waisbren S; Beaudet AL; Peters SU
    Eur J Hum Genet; 2007 Sep; 15(9):943-9. PubMed ID: 17522620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
    Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D
    Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC; de Luis O; Cruces J; Pérez Jurado LA
    Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
    McDonell N; Ramser J; Francis F; Vinet MC; Rider S; Sudbrak R; Riesselman L; Yaspo ML; Reinhardt R; Monaco AP; Ross F; Kahn A; Kearney L; Buckle V; Chelly J
    Genomics; 2000 Mar; 64(3):221-9. PubMed ID: 10756090
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
    Van Roy N; Vandesompele J; Berx G; Staes K; Van Gele M; De Smet E; De Paepe A; Laureys G; van der Drift P; Versteeg R; Van Roy F; Speleman F
    Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel gene rearrangements in transformed breast cells identified by high-resolution breakpoint analysis of chromosomal aberrations.
    Unger K; Wienberg J; Riches A; Hieber L; Walch A; Brown A; O'Brien PC; Briscoe C; Gray L; Rodriguez E; Jackl G; Knijnenburg J; Tallini G; Ferguson-Smith M; Zitzelsberger H
    Endocr Relat Cancer; 2010 Mar; 17(1):87-98. PubMed ID: 19858224
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of a region of homozygous deletion on 8p22-23.1 in medulloblastoma.
    Yin XL; Pang JC; Ng HK
    Oncogene; 2002 Feb; 21(9):1461-8. PubMed ID: 11857089
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.
    Lee JA; Inoue K; Cheung SW; Shaw CA; Stankiewicz P; Lupski JR
    Hum Mol Genet; 2006 Jul; 15(14):2250-65. PubMed ID: 16774974
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Hypermethylation as a potential prognostic factor and a clue to a better understanding of the molecular pathogenesis of medulloblastoma--results of a genomewide methylation scan].
    Frühwald MC; O'Dorisio MS; Smith L; Dai Z; Wright FA; Paulus W; Jürgens H; Plass C
    Klin Padiatr; 2001; 213(4):197-203. PubMed ID: 11528554
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.