BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 7959730)

  • 1. An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
    Redeker E; Hoovers JM; Alders M; van Moorsel CJ; Ivens AC; Gregory S; Kalikin L; Bliek J; de Galan L; van den Bogaard R
    Genomics; 1994 Jun; 21(3):538-50. PubMed ID: 7959730
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
    Redeker E; Alders M; Hoovers JM; Richard CW; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1995; 68(3-4):222-5. PubMed ID: 7842740
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
    Mannens M; Hoovers JM; Redeker E; Verjaal M; Feinberg AP; Little P; Boavida M; Coad N; Steenman M; Bliek J
    Eur J Hum Genet; 1994; 2(1):3-23. PubMed ID: 7913866
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and "stretched" DNAs.
    Ariyama T; Inazawa J; Ezaki T; Nakamura Y; Horii A; Abe T
    Genomics; 1995 Jan; 25(1):114-23. PubMed ID: 7774908
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region.
    Reid LH; Davies C; Cooper PR; Crider-Miller SJ; Sait SN; Nowak NJ; Evans G; Stanbridge EJ; deJong P; Shows TB; Weissman BE; Higgins MJ
    Genomics; 1997 Aug; 43(3):366-75. PubMed ID: 9268640
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Isolation and mapping of 328 new cosmid markers on human chromosome 8: construction of a high-resolution cytogenetic map of chromosome 8 with 416 markers.
    Nakamura Y; Okui K; Takahashi E; Koyama K
    Cytogenet Cell Genet; 1994; 65(1-2):115-8. PubMed ID: 8404062
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.
    Hoovers JM; Kalikin LM; Johnson LA; Alders M; Redeker B; Law DJ; Bliek J; Steenman M; Benedict M; Wiegant J; Lengauer C; Taillon-Miller P; Schlessinger D; Edwards MC; Elledge SJ; Ivens A; Westerveld A; Little P; Mannens M; Feinberg AP
    Proc Natl Acad Sci U S A; 1995 Dec; 92(26):12456-60. PubMed ID: 8618920
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.
    Richard CW; Boehnke M; Berg DJ; Lichy JH; Meeker TC; Hauser E; Myers RM; Cox DR
    Am J Hum Genet; 1993 May; 52(5):915-21. PubMed ID: 8387721
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
    Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
    Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. A high-resolution cytogenetic map of 168 cosmid DNA markers for human chromosome 11.
    Hori T; Takahashi E; Tanigami A; Tokino T; Nakamura Y
    Genomics; 1992 May; 13(1):129-33. PubMed ID: 1349569
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.
    Horike S; Mitsuya K; Meguro M; Kotobuki N; Kashiwagi A; Notsu T; Schulz TC; Shirayoshi Y; Oshimura M
    Hum Mol Genet; 2000 Sep; 9(14):2075-83. PubMed ID: 10958646
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Regional localization of 64 cosmid contigs, including 18 genes and 14 markers, to intervals on human chromosome 9q34.
    Woodward K; Nahmias J; Hornigold N; West L; Pilz A; Benham F; Kwiatkowski D; Fitzgibbon J; Wolfe J; Povey S
    Genomics; 1995 Sep; 29(1):257-60. PubMed ID: 8530081
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.
    Paulsen M; Davies KR; Bowden LM; Villar AJ; Franck O; Fuermann M; Dean WL; Moore TF; Rodrigues N; Davies KE; Hu RJ; Feinberg AP; Maher ER; Reik W; Walter J
    Hum Mol Genet; 1998 Jul; 7(7):1149-59. PubMed ID: 9618174
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome.
    Gessler M; Hameister H; Henry I; Junien C; Braun T; Arnold HH
    Hum Genet; 1990 Dec; 86(2):135-8. PubMed ID: 2176177
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple genetic abnormalities of 11p15 in Wilms' tumor.
    Feinberg AP
    Med Pediatr Oncol; 1996 Nov; 27(5):484-9. PubMed ID: 8827078
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Uniparental paternal disomy in a genetic cancer-predisposing syndrome.
    Henry I; Bonaiti-Pellié C; Chehensse V; Beldjord C; Schwartz C; Utermann G; Junien C
    Nature; 1991 Jun; 351(6328):665-7. PubMed ID: 1675767
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
    Fantes JA; Oghene K; Boyle S; Danes S; Fletcher JM; Bruford EA; Williamson K; Seawright A; Schedl A; Hanson I
    Genomics; 1995 Jan; 25(2):447-61. PubMed ID: 7789978
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.