BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 8387721)

  • 1. 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]  

  • 2. 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]  

  • 3. An ordered NotI fragment map of human chromosome band 11p15.
    Higgins MJ; Smilinich NJ; Sait S; Koenig A; Pongratz J; Gessler M; Richard CW; James MR; Sanford JP; Kim BW
    Genomics; 1994 Sep; 23(1):211-22. PubMed ID: 7829073
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
    Newsham I; Claussen U; Lüdecke HJ; Mason M; Senger G; Horsthemke B; Cavenee W
    Genes Chromosomes Cancer; 1991 Mar; 3(2):108-16. PubMed ID: 1676905
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
    Puech A; Ahnine L; Lüdecke HJ; Senger G; Ivens A; Jeanpierre C; Little P; Horsthemke B; Claussen U; Jones C
    Genomics; 1992 Aug; 13(4):1274-80. PubMed ID: 1380484
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. A radiation hybrid map of human chromosome 18.
    Francke U; Chang E; Comeau K; Geigl EM; Giacalone J; Li X; Luna J; Moon A; Welch S; Wilgenbus P
    Cytogenet Cell Genet; 1994; 66(3):196-213. PubMed ID: 8125019
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
    Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK
    Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma.
    Henry I; Jeanpierre M; Couillin P; Barichard F; Serre JL; Journel H; Lamouroux A; Turleau C; de Grouchy J; Junien C
    Hum Genet; 1989 Feb; 81(3):273-7. PubMed ID: 2921038
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region.
    Weksberg R; Glaves M; Teshima I; Waziri M; Patil S; Williams BR
    Genomics; 1990 Dec; 8(4):693-8. PubMed ID: 2276740
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors.
    Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W
    Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Reassessment of breakpoints in chromosome 11p15.
    Henry I; van Heyningen V; Puech A; Scrable H; Augereau P; Boehm T; Rabbitts T; Mannens M; Rochefort H; Jones C
    Cytogenet Cell Genet; 1993; 62(1):52-3. PubMed ID: 8422757
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
    Slatter RE; Elliott M; Welham K; Carrera M; Schofield PN; Barton DE; Maher ER
    J Med Genet; 1994 Oct; 31(10):749-53. PubMed ID: 7837249
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.
    Schwienbacher C; Sabbioni S; Campi M; Veronese A; Bernardi G; Menegatti A; Hatada I; Mukai T; Ohashi H; Barbanti-Brodano G; Croce CM; Negrini M
    Proc Natl Acad Sci U S A; 1998 Mar; 95(7):3873-8. PubMed ID: 9520460
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.