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Journal Abstract Search

129 related items for PubMed ID: 1676905

  • 1. 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
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  • 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
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  • 3. 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
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  • 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
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  • 7. The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15.
    Byrne JA, Little MH, Smith PJ.
    Cancer Genet Cytogenet; 1992 Apr; 59(2):206-9. PubMed ID: 1316226
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  • 9. 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; 81(1):41-8. PubMed ID: 2848758
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  • 10. 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 Dec; 2(1):3-23. PubMed ID: 7913866
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  • 11. Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.
    Mannens M, Slater RM, Heyting C, Geurts van Kessel A, Goedde-Salz E, Frants RR, Van Ommen GJ, Pearson PL.
    Hum Genet; 1987 Feb; 75(2):180-7. PubMed ID: 3028933
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  • 12. 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
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  • 13. Beck-Wiedemann syndrome and Wilms' tumour.
    Ward A.
    Mol Hum Reprod; 1997 Feb 15; 3(2):157-68. PubMed ID: 9239720
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  • 14. 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 Feb 15; 68(3-4):222-5. PubMed ID: 7842740
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  • 16. Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse.
    Hatada I, Mukai T.
    Nat Genet; 1995 Oct 15; 11(2):204-6. PubMed ID: 7550351
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  • 17. 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 15; 19(3):433-40. PubMed ID: 8188285
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  • 18. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
    Crider-Miller SJ, Reid LH, Higgins MJ, Nowak NJ, Shows TB, Futreal PA, Weissman BE.
    Genomics; 1997 Dec 15; 46(3):355-63. PubMed ID: 9441738
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  • 19. A developmental context for multiple genetic alterations in Wilms' tumor.
    Feinberg AP.
    J Cell Sci Suppl; 1994 Dec 15; 18():7-12. PubMed ID: 7883796
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  • 20. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
    Lee MP, Hu RJ, Johnson LA, Feinberg AP.
    Nat Genet; 1997 Feb 15; 15(2):181-5. PubMed ID: 9020845
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