BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 10828613)

  • 1. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.
    Steenman MJ; Zijlstra N; Kruitbosch DL; Wiesmeijer C; Larizza L; Voûte PA; Westerveld A; Mannens MM
    Cytogenet Cell Genet; 2000; 88(3-4):289-95. PubMed ID: 10828613
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.
    Steenman M; Tomlinson G; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1999; 86(2):157-61. PubMed ID: 10545709
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium.
    Kutsche K; Glauner E; Knauf S; Pomarino A; Schmidt M; Schröder B; Nothwang H; Schüler H; Goecke T; Kersten A; Althaus C; Gal A
    Cytogenet Cell Genet; 2000; 91(1-4):141-7. PubMed ID: 11173847
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.
    Negrini M; Sabbioni S; Ohta M; Veronese ML; Rattan S; Junien C; Croce CM
    Cancer Res; 1995 Jul; 55(13):2904-9. PubMed ID: 7796419
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.
    Van Roy N; Laureys G; Van Gele M; Opdenakker G; Miura R; van der Drift P; Chan A; Versteeg R; Speleman F
    Eur J Cancer; 1997 Oct; 33(12):1974-8. PubMed ID: 9516836
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.
    Mannens M; Alders M; Redeker B; Bliek J; Steenman M; Wiesmeyer C; de Meulemeester M; Ryan A; Kalikin L; Voûte T; De Kraker J; Hoovers J; Slater R; Feinberg A; Little P; Westerveld A
    Med Pediatr Oncol; 1996 Nov; 27(5):490-4. PubMed ID: 8827079
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor.
    Newsham I; Daub D; Besnard-Guerin C; Cavenee W
    Genomics; 1994 Feb; 19(3):433-40. PubMed ID: 8188285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome.
    Matsumoto N; David DE; Johnson EW; Konecki D; Burmester JK; Ledbetter DH; Weber JL
    Eur J Hum Genet; 2000 Nov; 8(11):875-83. PubMed ID: 11093278
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome.
    Trembath DG; Semina EV; Jones DH; Patil SR; Qian Q; Amendt BA; Russo AF; Murray JC
    Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):82-91. PubMed ID: 14991915
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells.
    Chernova O; Cowell JK
    Cancer Genet Cytogenet; 1998 Aug; 105(1):60-8. PubMed ID: 9689932
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour.
    Vernon EG; Malik K; Reynolds P; Powlesland R; Dallosso AR; Jackson S; Henthorn K; Green ED; Brown KW
    Oncogene; 2003 Mar; 22(9):1371-80. PubMed ID: 12618763
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
    Lynch RA; Piper M; Bankier A; Bhugra B; Surti U; Liu J; Buckler A; Dear PH; Menon AG
    Genomics; 1998 Aug; 52(1):17-26. PubMed ID: 9740667
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.
    Prawitt D; Enklaar T; Klemm G; Gärtner B; Spangenberg C; Winterpacht A; Higgins M; Pelletier J; Zabel B
    Hum Mol Genet; 2000 Jan; 9(2):203-16. PubMed ID: 10607831
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5.
    Sait SN; Nowak NJ; Singh-Kahlon P; Weksberg R; Squire J; Shows TB; Higgins MJ
    Genes Chromosomes Cancer; 1994 Oct; 11(2):97-105. PubMed ID: 7529555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene.
    Popovici C; Basset C; Bertucci F; Orsetti B; Adélaide J; Mozziconacci MJ; Conte N; Murati A; Ginestier C; Charafe-Jauffret E; Ethier SP; Lafage-Pochitaloff M; Theillet C; Birnbaum D; Chaffanet M
    Genes Chromosomes Cancer; 2002 Nov; 35(3):204-18. PubMed ID: 12353263
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel formation and amplification of the PAX7-FKHR fusion gene in a case of alveolar rhabdomyosarcoma.
    Weber-Hall S; McManus A; Anderson J; Nojima T; Abe S; Pritchard-Jones K; Shipley J
    Genes Chromosomes Cancer; 1996 Sep; 17(1):7-13. PubMed ID: 8889501
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
    Lai CS; Fisher SE; Hurst JA; Levy ER; Hodgson S; Fox M; Jeremiah S; Povey S; Jamison DC; Green ED; Vargha-Khadem F; Monaco AP
    Am J Hum Genet; 2000 Aug; 67(2):357-68. PubMed ID: 10880297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.
    Grundy RG; Aledo R; Cowell JK
    Int J Mol Med; 1998 May; 1(5):801-8. PubMed ID: 9852299
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcription factor GATA-2 gene is located near 3q21 breakpoints in myeloid leukemia.
    Wieser R; Volz A; Vinatzer U; Gardiner K; Jäger U; Mitterbauer M; Ziegler A; Fonatsch C
    Biochem Biophys Res Commun; 2000 Jun; 273(1):239-45. PubMed ID: 10873593
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.