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 *

69 related articles for article (PubMed ID: 8814450)

  • 1. Early proliferation enhancement by monosomy 10 and intratumor heterogeneity in malignant human gliomas as revealed by smear preparations from biopsies.
    Steilen-Gimbel H; Henn W; Kolles H; Moringlane JR; Feiden W; Steudel WI; Zang KD
    Genes Chromosomes Cancer; 1996 Jul; 16(3):180-4. PubMed ID: 8814450
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intratumoral genetic heterogeneity in pilocytic astrocytomas revealed by CGH-analysis of microdissected tumor cells and FISH on tumor tissue sections.
    Wemmert S; Romeike BF; Ketter R; Steudel WI; Zang KD; Urbschat S
    Int J Oncol; 2006 Feb; 28(2):353-60. PubMed ID: 16391789
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
    Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
    Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-density genome array is superior to fluorescence in-situ hybridization analysis of monosomy 3 in choroidal melanoma fine needle aspiration biopsy.
    Young TA; Burgess BL; Rao NP; Gorin MB; Straatsma BR
    Mol Vis; 2007 Dec; 13():2328-33. PubMed ID: 18199974
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of chromosome 7, chromosome 10 and EGFR gene amplification in glioblastoma multiforme.
    Lopez-Gines C; Cerda-Nicolas M; Gil-Benso R; Pellin A; Lopez-Guerrero JA; Callaghan R; Benito R; Roldan P; Piquer J; Llacer J; Barbera J
    Clin Neuropathol; 2005; 24(5):209-18. PubMed ID: 16167544
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chromosome 3 intratumor heterogeneity in uveal melanoma.
    Mensink HW; Vaarwater J; Kiliç E; Naus NC; Mooy N; Luyten G; Brüggenwirth HT; Paridaens D; de Klein A
    Invest Ophthalmol Vis Sci; 2009 Feb; 50(2):500-4. PubMed ID: 18824727
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of chromosome aneuploidy in breast carcinoma progression by using fluorescence in situ hybridization.
    Mendelin J; Grayson M; Wallis T; Visscher DW
    Lab Invest; 1999 Apr; 79(4):387-93. PubMed ID: 10211991
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Establishment and characterization of a new human acute myelocytic leukemia cell line SH-2 with a loss of Y chromosome, a derivative chromosome 16 resulting from an unbalanced translocation between chromosomes 16 and 17, monosomy 17, trisomy 19, and p53 alteration.
    Qiu H; Xue Y; Zhang J; Pan J; Dai H; Wu Y; Wang Y; Chen S; Wu D
    Exp Hematol; 2008 Nov; 36(11):1487-95. PubMed ID: 18715689
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of chromosome 1p and loss of expression of alkaline phosphatase indicate progression of meningiomas.
    Müller P; Henn W; Niedermayer I; Ketter R; Feiden W; Steudel WI; Zang KD; Steilen-Gimbel H
    Clin Cancer Res; 1999 Nov; 5(11):3569-77. PubMed ID: 10589773
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cytogenetic analysis of gliomas by in situ hybridization of stereotactic biopsy material.
    Lippitz BE; Scheitinger C; Scholz M; Weis J; Gilsbach JM; Füzesi L
    Acta Neurochir (Wien); 1997; 139(1):22-5. PubMed ID: 9059707
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fluorescence in situ hybridization analysis of aneuploidization patterns in monoclonal gammopathy of undetermined significance versus multiple myeloma and plasma cell leukemia.
    Rasillo A; Tabernero MD; Sánchez ML; Pérez de Andrés M; Martín Ayuso M; Hernández J; Moro MJ; Fernández-Calvo J; Sayagués JM; Bortoluci A; San Miguel JF; Orfao A
    Cancer; 2003 Feb; 97(3):601-9. PubMed ID: 12548602
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene.
    Barbashina V; Salazar P; Holland EC; Rosenblum MK; Ladanyi M
    Clin Cancer Res; 2005 Feb; 11(3):1119-28. PubMed ID: 15709179
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype.
    Smith JS; Alderete B; Minn Y; Borell TJ; Perry A; Mohapatra G; Hosek SM; Kimmel D; O'Fallon J; Yates A; Feuerstein BG; Burger PC; Scheithauer BW; Jenkins RB
    Oncogene; 1999 Jul; 18(28):4144-52. PubMed ID: 10435596
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Automatized assessment of 1p36-19q13 status in gliomas by interphase FISH assay on touch imprints of frozen tumours.
    Belaud-Rotureau MA; Meunier N; Eimer S; Vital A; Loiseau H; Merlio JP
    Acta Neuropathol; 2006 Mar; 111(3):255-63. PubMed ID: 16453145
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
    Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Loss of heterozygosity on chromosomes 1 and 19 in cases of primary brain tumour].
    Born PW; Broholm H; Laursen H
    Ugeskr Laeger; 2006 Oct; 168(44):3813-6. PubMed ID: 17118240
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of structural aberrations of chromosome 17 in malignant gliomas by fluorescence in situ hybridization (FISH).
    Kwak T; Nishizaki T; Nakayama H; Kakino S; Ito H; Kimura Y
    Acta Oncol; 1995; 34(1):27-30. PubMed ID: 7865231
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fluorescence in situ hybridization study of aneuploidy of chromosomes 7, 10, X, and Y in primary and secondary glioblastomas.
    Amalfitano G; Chatel M; Paquis P; Michiels JF
    Cancer Genet Cytogenet; 2000 Jan; 116(1):6-9. PubMed ID: 10616524
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interphase cytogenetic (in situ hybridization) analysis of astrocytomas using archival, formalin-fixed, paraffin-embedded tissue and nonfluorescent light microscopy.
    Perry A; Tonk V; McIntire DD; White CL
    Am J Clin Pathol; 1997 Aug; 108(2):166-74. PubMed ID: 9260757
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fine mapping of a region of common deletion on chromosome arm 10p in human glioma.
    Voesten AM; Bijleveld EH; Westerveld A; Hulsebos TJ
    Genes Chromosomes Cancer; 1997 Oct; 20(2):167-72. PubMed ID: 9331567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.