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237 related items for PubMed ID: 7534105

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Cytogenetic abnormalities in mesoblastic nephroma: a link to Wilms' tumour?
    Roberts P, Lockwood LR, Lewis IJ, Bailey CC, Batcup G, Williams J.
    Med Pediatr Oncol; 1993 Feb; 21(6):416-20. PubMed ID: 8390601
    [Abstract] [Full Text] [Related]

  • 4. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
    Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, Cavenee WK.
    Am J Hum Genet; 1989 May; 44(5):711-9. PubMed ID: 2539717
    [Abstract] [Full Text] [Related]

  • 5. A third Wilms' tumor locus on chromosome 16q.
    Maw MA, Grundy PE, Millow LJ, Eccles MR, Dunn RS, Smith PJ, Feinberg AP, Law DJ, Paterson MC, Telzerow PE.
    Cancer Res; 1992 Jun 01; 52(11):3094-8. PubMed ID: 1317258
    [Abstract] [Full Text] [Related]

  • 6. Cytogenetics and molecular genetics of Wilms' tumor of childhood.
    Slater RM, Mannens MM.
    Cancer Genet Cytogenet; 1992 Jul 15; 61(2):111-21. PubMed ID: 1322233
    [Abstract] [Full Text] [Related]

  • 7. Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis.
    Grundy P, Telzerow P, Moksness J, Breslow NE.
    Med Pediatr Oncol; 1996 Nov 15; 27(5):429-33. PubMed ID: 8926924
    [Abstract] [Full Text] [Related]

  • 8. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors.
    O'Keefe D, Dao D, Zhao L, Sanderson R, Warburton D, Weiss L, Anyane-Yeboa K, Tycko B.
    Am J Hum Genet; 1997 Aug 15; 61(2):295-303. PubMed ID: 9311733
    [Abstract] [Full Text] [Related]

  • 9. 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 19; 92(26):12456-60. PubMed ID: 8618920
    [Abstract] [Full Text] [Related]

  • 10. Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development.
    Charles AK, Brown KW, Berry PJ.
    Am J Pathol; 1998 Sep 19; 153(3):991-1000. PubMed ID: 9736048
    [Abstract] [Full Text] [Related]

  • 11. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R, Squire JA.
    Med Pediatr Oncol; 1996 Nov 19; 27(5):462-9. PubMed ID: 8827075
    [Abstract] [Full Text] [Related]

  • 12. 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 19; 3(2):108-16. PubMed ID: 1676905
    [Abstract] [Full Text] [Related]

  • 13. Molecular genetics of Wilms' tumour.
    Tay JS.
    J Paediatr Child Health; 1995 Oct 19; 31(5):379-83. PubMed ID: 8554853
    [Abstract] [Full Text] [Related]

  • 14. Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.
    Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR.
    Am J Hum Genet; 2005 Nov 19; 77(5):887-91. PubMed ID: 16252245
    [Abstract] [Full Text] [Related]

  • 15. Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted.
    Weksberg R, Teshima I, Williams BR, Greenberg CR, Pueschel SM, Chernos JE, Fowlow SB, Hoyme E, Anderson IJ, Whiteman DA.
    Hum Mol Genet; 1993 May 19; 2(5):549-56. PubMed ID: 8518793
    [Abstract] [Full Text] [Related]

  • 16. Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination.
    Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR.
    Genes Chromosomes Cancer; 1992 Nov 19; 5(4):326-34. PubMed ID: 1283321
    [Abstract] [Full Text] [Related]

  • 17. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.
    Weksberg R, Nishikawa J, Caluseriu O, Fei YL, Shuman C, Wei C, Steele L, Cameron J, Smith A, Ambus I, Li M, Ray PN, Sadowski P, Squire J.
    Hum Mol Genet; 2001 Dec 15; 10(26):2989-3000. PubMed ID: 11751681
    [Abstract] [Full Text] [Related]

  • 18. p57K1P2 is expressed in Wilms' tumor with LOH of 11p15.5.
    Overall ML, Spencer J, Bakker M, Dziadek M, Smith PJ.
    Genes Chromosomes Cancer; 1996 Sep 15; 17(1):56-9. PubMed ID: 8889507
    [Abstract] [Full Text] [Related]

  • 19. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.
    Mannens M, Slater RM, Heyting C, Bliek J, de Kraker J, Coad N, de Pagter-Holthuizen P, Pearson PL.
    Hum Genet; 1988 Dec 15; 81(1):41-8. PubMed ID: 2848758
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 27(5):490-4. PubMed ID: 8827079
    [Abstract] [Full Text] [Related]

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