BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 2570677)

  • 1. Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.
    Lavedan C; Barichard F; Azoulay M; Couillin P; Molina Gomez D; Nicolas H; Quack B; Rethoré MO; Noel B; Junien C
    Cytogenet Cell Genet; 1989; 50(2-3):70-4. PubMed ID: 2570677
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
    Gessler M; Bruns GA
    Genomics; 1988 Aug; 3(2):117-23. PubMed ID: 2852160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
    Glaser T; Lewis WH; Bruns GA; Watkins PC; Rogler CE; Shows TB; Powers VE; Willard HF; Goguen JM; Simola KO
    Nature; 1986 Jun 26-Jul 2; 321(6073):882-7. PubMed ID: 3014343
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regional mapping of catalase and Wilms tumor--aniridia, genitourinary abnormalities, and mental retardation triad loci to the chromosome segment 11p1305----p1306.
    Narahara K; Kikkawa K; Kimira S; Kimoto H; Ogata M; Kasai R; Hamawaki M; Matsuoka K
    Hum Genet; 1984; 66(2-3):181-5. PubMed ID: 6325323
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A deletion map of the WAGR region on chromosome 11.
    Gessler M; Thomas GH; Couillin P; Junien C; McGillivray BC; Hayden M; Jaschek G; Bruns GA
    Am J Hum Genet; 1989 Apr; 44(4):486-95. PubMed ID: 2539014
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
    Davis LM; Stallard R; Thomas GH; Couillin P; Junien C; Nowak NJ; Shows TB
    Science; 1988 Aug; 241(4867):840-2. PubMed ID: 2841760
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The gene for catalase is assigned between the antigen loci MIC4 and MIC11.
    Couillin P; Azoulay M; Metezeau P; Grisard MC; Junien C
    Genomics; 1989 Jan; 4(1):7-11. PubMed ID: 2536636
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.
    Glaser T; Rose E; Morse H; Housman D; Jones C
    Genomics; 1990 Jan; 6(1):48-64. PubMed ID: 2154397
    [TBL] [Abstract][Full Text] [Related]  

  • 9. HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
    Porteous DJ; Bickmore W; Christie S; Boyd PA; Cranston G; Fletcher JM; Gosden JR; Rout D; Seawright A; Simola KO
    Proc Natl Acad Sci U S A; 1987 Aug; 84(15):5355-9. PubMed ID: 3037545
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
    Boyd PA; Christie S; Hastie ND; Porteous DJ
    Hum Genet; 1989 Mar; 81(4):349-52. PubMed ID: 2564837
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Aniridia, Wilms' tumor and human chromosome 11.
    Bickmore WA; Hastie ND
    Ophthalmic Paediatr Genet; 1989 Dec; 10(4):229-48. PubMed ID: 2560823
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
    Seawright A; Fletcher JM; Fantes JA; Morrison H; Porteous DJ; Li SS; Hastie ND; Van Heyningen V
    Somat Cell Mol Genet; 1988 Jan; 14(1):21-30. PubMed ID: 2829363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
    Glaser T; Driscoll DJ; Antonarakis S; Valle D; Housman D
    Genomics; 1989 Nov; 5(4):880-93. PubMed ID: 2574149
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a family.
    Henry I; Hoovers J; Barichard F; Berthéas MF; Puech A; Prieur F; Gessler M; Bruns G; Mannens M; Junien C
    Genes Chromosomes Cancer; 1993 May; 7(1):57-62. PubMed ID: 7688557
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of a reciprocal translocation t(5;11) (q11;p13) in a WAGR patient.
    Puissant H; Azoulay M; Serre JL; Piet LL; Junien C
    Hum Genet; 1988 Jul; 79(3):280-2. PubMed ID: 2841227
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial occurrence of the aniridia-Wilms tumor syndrome with deletion 11p13-14.1.
    Yunis JJ; Ramsay NK
    J Pediatr; 1980 Jun; 96(6):1027-30. PubMed ID: 6246230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The distal region of 11p13 and associated genetic diseases.
    Mannens M; Hoovers JM; Bleeker-Wagemakers EM; Redeker E; Bliek J; Overbeeke-Melkert M; Saunders G; Williams B; van Heyningen V; Junien C
    Genomics; 1991 Oct; 11(2):284-93. PubMed ID: 1769647
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Wilms tumour: a developmental anomaly.
    Hastie ND; Bickmore W; Pritchard-Jones K; Porteous DJ; van Heyningen V
    Princess Takamatsu Symp; 1989; 20():145-50. PubMed ID: 2562179
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cloning of breakpoints of a chromosome translocation identifies the AN2 locus.
    Gessler M; Simola KO; Bruns GA
    Science; 1989 Jun; 244(4912):1575-8. PubMed ID: 2544995
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.
    Turleau C; de Grouchy J; Tournade MF; Gagnadoux MF; Junien C
    Clin Genet; 1984 Oct; 26(4):356-62. PubMed ID: 6094051
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.