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Journal Abstract Search

123 related items for PubMed ID: 8386696

  • 1. The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastoma.
    Byrne JA, Smith PJ.
    Hum Genet; 1993 Apr; 91(3):275-7. PubMed ID: 8386696
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  • 3. Maintenance of genomic imprinting at the IGF2 locus in hepatoblastoma.
    Davies SM.
    Cancer Res; 1993 Oct 15; 53(20):4781-3. PubMed ID: 8402661
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  • 4. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour.
    Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, Maw MA, Smith PJ, Reeve AE.
    Nature; 1993 Apr 22; 362(6422):749-51. PubMed ID: 8097018
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  • 7. Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.
    Satoh Y, Nakadate H, Nakagawachi T, Higashimoto K, Joh K, Masaki Z, Uozumi J, Kaneko Y, Mukai T, Soejima H.
    Br J Cancer; 2006 Aug 21; 95(4):541-7. PubMed ID: 16909133
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  • 9. Lung cancer and the human gene for ribonucleotide reductase subunit M1 (RRM1).
    Pitterle DM, Kim YC, Jolicoeur EM, Cao Y, O'Briant KC, Bepler G.
    Mamm Genome; 1999 Sep 21; 10(9):916-22. PubMed ID: 10441745
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  • 10. Aberrant imprinting of the insulin-like growth factor II receptor gene in Wilms' tumor.
    Xu YQ, Grundy P, Polychronakos C.
    Oncogene; 1997 Mar 06; 14(9):1041-6. PubMed ID: 9070652
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  • 11. Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.
    Little MH, Dunn R, Byrne JA, Seawright A, Smith PJ, Pritchard-Jones K, van Heyningen V, Hastie ND.
    Oncogene; 1992 Apr 06; 7(4):635-41. PubMed ID: 1314367
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  • 12. 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 06; 97(2):163-70. PubMed ID: 8566947
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  • 13. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
    Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK.
    Nature; 1988 Nov 24; 336(6197):374-6. PubMed ID: 2848199
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  • 14. Allelic loss but absence of mutations in the polyspecific transporter gene BWR1A on 11p15.5 in hepatoblastoma.
    Albrecht S, Hartmann W, Houshdaran F, Koch A, Gärtner B, Prawitt D, Zabel BU, Russo P, Von Schweinitz D, Pietsch T.
    Int J Cancer; 2004 Sep 10; 111(4):627-32. PubMed ID: 15239143
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  • 15. A novel imprinted gene, KCNQ1DN, within the WT2 critical region of human chromosome 11p15.5 and its reduced expression in Wilms' tumors.
    Xin Z, Soejima H, Higashimoto K, Yatsuki H, Zhu X, Satoh Y, Masaki Z, Kaneko Y, Jinno Y, Fukuzawa R, Hata Ji, Mukai T.
    J Biochem; 2000 Nov 10; 128(5):847-53. PubMed ID: 11056398
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  • 18. Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors.
    Chung WY, Yuan L, Feng L, Hensle T, Tycko B.
    Hum Mol Genet; 1996 Aug 10; 5(8):1101-8. PubMed ID: 8842727
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  • 19. The structural gene for the M1 subunit of ribonucleotide reductase maps to chromosome 11, band p15, in human and to chromosome 7 in mouse.
    Brissenden JE, Caras I, Thelander L, Francke U.
    Exp Cell Res; 1988 Jan 10; 174(1):302-8. PubMed ID: 3275546
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  • 20. Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma.
    Montagna M, Menin C, Chieco-Bianchi L, D'Andrea E.
    J Cancer Res Clin Oncol; 1994 Jan 10; 120(12):732-6. PubMed ID: 7798299
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