BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 11106817)

  • 1. Molecular and cytogenetic analysis of glioblastoma multiforme.
    Mao X; Hamoudi RA
    Cancer Genet Cytogenet; 2000 Oct; 122(2):87-92. PubMed ID: 11106817
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of novel candidate target genes in amplicons of Glioblastoma multiforme tumors detected by expression and CGH microarray profiling.
    Ruano Y; Mollejo M; Ribalta T; Fiaño C; Camacho FI; Gómez E; de Lope AR; Hernández-Moneo JL; Martínez P; Meléndez B
    Mol Cancer; 2006 Sep; 5():39. PubMed ID: 17002787
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic analysis of glioblastoma multiforme provides evidence for subgroups within the grade.
    Mohapatra G; Bollen AW; Kim DH; Lamborn K; Moore DH; Prados MD; Feuerstein BG
    Genes Chromosomes Cancer; 1998 Mar; 21(3):195-206. PubMed ID: 9523194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The importance of genomic copy number changes in the prognosis of glioblastoma multiforme.
    Arslantas A; Artan S; Oner U; Müslümanoğlu H; Durmaz R; Cosan E; Atasoy MA; Başaran N; Tel E
    Neurosurg Rev; 2004 Jan; 27(1):58-64. PubMed ID: 12845540
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening of genomic imbalances in glioblastoma multiforme using high-resolution comparative genomic hybridization.
    Vranová V; Necesalová E; Kuglík P; Cejpek P; Pesáková M; Budínská E; Relichová J; Veselská R
    Oncol Rep; 2007 Feb; 17(2):457-64. PubMed ID: 17203188
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of chromosomal aberrations in a case of glioblastoma multiforme combining cytogenetic and molecular cytogenetic techniques.
    Zuber MA; Krupp W; Holland H; Froster UG
    Cancer Genet Cytogenet; 2002 Oct; 138(2):111-5. PubMed ID: 12505254
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Incidence of the main genetic markers in glioblastoma multiforme is independent of tumor topology.
    Necesalová E; Vranová V; Kuglík P; Cejpek P; Jarosová M; Pesáková M; Relichová J; Veselská R
    Neoplasma; 2007; 54(3):212-8. PubMed ID: 17447852
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinically distinct subgroups of glioblastoma multiforme studied by comparative genomic hybridization.
    Weber RG; Sommer C; Albert FK; Kiessling M; Cremer T
    Lab Invest; 1996 Jan; 74(1):108-19. PubMed ID: 8569172
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cytogenetic characterization of Sézary syndrome.
    Mao X; Lillington DM; Czepulkowski B; Russell-Jones R; Young BD; Whittaker S
    Genes Chromosomes Cancer; 2003 Mar; 36(3):250-60. PubMed ID: 12557225
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comprehensive analysis of genomic alterations in gliosarcoma and its two tissue components.
    Actor B; Cobbers JM; Büschges R; Wolter M; Knobbe CB; Lichter P; Reifenberger G; Weber RG
    Genes Chromosomes Cancer; 2002 Aug; 34(4):416-27. PubMed ID: 12112531
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative genetic patterns of glioblastoma multiforme: potential diagnostic tool for tumor classification.
    Wiltshire RN; Rasheed BK; Friedman HS; Friedman AH; Bigner SH
    Neuro Oncol; 2000 Jul; 2(3):164-73. PubMed ID: 11302337
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cytogenetic findings in a case of pediatric glioblastoma.
    Sawyer JR; Swanson CM; Roloson GJ; Longee DC; Chadduck WM
    Cancer Genet Cytogenet; 1992 Nov; 64(1):75-9. PubMed ID: 1333880
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of EGFR gene amplification and CDKN2 (p16/MTS1) gene deletion in glioblastoma multiforme.
    Hayashi Y; Ueki K; Waha A; Wiestler OD; Louis DN; von Deimling A
    Brain Pathol; 1997 Jul; 7(3):871-5. PubMed ID: 9217972
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Seven novel and stable translocations associated with oncogenic gene expression in malignant melanoma.
    Okamoto I; Pirker C; Bilban M; Berger W; Losert D; Marosi C; Haas OA; Wolff K; Pehamberger H
    Neoplasia; 2005 Apr; 7(4):303-11. PubMed ID: 15967107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of ZCCHC8 as fusion partner of ROS1 in a case of congenital glioblastoma multiforme with a t(6;12)(q21;q24.3).
    Coccé MC; Mardin BR; Bens S; Stütz AM; Lubieniecki F; Vater I; Korbel JO; Siebert R; Alonso CN; Gallego MS
    Genes Chromosomes Cancer; 2016 Sep; 55(9):677-87. PubMed ID: 27121553
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Distribution of epidermal growth factor receptor protein correlates with gain in chromosome 7 revealed by comparative genomic hybridization after microdissection in glioblastoma multiforme.
    Romeike BF; Jung V; Feiden W; Moringlane JR; Zang KD; Urbschat SM
    Pathol Res Pract; 2001; 197(6):427-31. PubMed ID: 11432670
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stepwise genetic changes associated with progression of nontumorigenic HPV-18 immortalized human prostate cancer-derived cell line to a malignant phenotype.
    Hukku B; Mally M; Cher ML; Peehl DM; Kung H; Rhim JS
    Cancer Genet Cytogenet; 2000 Jul; 120(2):117-26. PubMed ID: 10942801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of recurrent chromosomal rearrangements and the unique relationship between low-level amplification and translocation in glioblastoma.
    Kubota H; Nishizaki T; Harada K; Harada K; Oga A; Ito H; Suzuki M; Sasaki K
    Genes Chromosomes Cancer; 2001 Jun; 31(2):125-33. PubMed ID: 11319800
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetics of the chronic myeloid leukemia-derived cell line K562: karyotype clarification by multicolor fluorescence in situ hybridization, comparative genomic hybridization, and locus-specific fluorescence in situ hybridization.
    Gribble SM; Roberts I; Grace C; Andrews KM; Green AR; Nacheva EP
    Cancer Genet Cytogenet; 2000 Apr; 118(1):1-8. PubMed ID: 10731582
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular cytogenetic analysis of a nontumorigenic human breast epithelial cell line that eventually turns tumorigenic: validation of an analytical approach combining karyotyping, comparative genomic hybridization, chromosome painting, and single-locus fluorescence in situ hybridization.
    Nielsen KV; Niebuhr E; Ejlertsen B; Holstebroe S; Madsen MW; Briand P; Mouridsen HT; Bolund L
    Genes Chromosomes Cancer; 1997 Sep; 20(1):30-7. PubMed ID: 9290951
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.