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Journal Abstract Search

345 related items for PubMed ID: 8841187

  • 1. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
    Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T.
    Nat Genet; 1996 Oct; 14(2):171-3. PubMed ID: 8841187
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  • 3. 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; 17(1):56-9. PubMed ID: 8889507
    [Abstract] [Full Text] [Related]

  • 4. Functional analysis of the p57KIP2 gene mutation in Beckwith-Wiedemann syndrome.
    Bhuiyan ZA, Yatsuki H, Sasaguri T, Joh K, Soejima H, Zhu X, Hatada I, Morisaki H, Morisaki T, Mukai T.
    Hum Genet; 1999 Mar; 104(3):205-10. PubMed ID: 10323243
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  • 6. Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5.
    Kondo M, Matsuoka S, Uchida K, Osada H, Nagatake M, Takagi K, Harper JW, Takahashi T, Elledge SJ, Takahashi T.
    Oncogene; 1996 Mar 21; 12(6):1365-8. PubMed ID: 8649840
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  • 7. Imprinting status of 11p15 genes in Beckwith-Wiedemann syndrome patients with CDKN1C mutations.
    Li M, Squire J, Shuman C, Fei YL, Atkin J, Pauli R, Smith A, Nishikawa J, Chitayat D, Weksberg R.
    Genomics; 2001 Jun 15; 74(3):370-6. PubMed ID: 11414765
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  • 8. Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome.
    Lee MP, DeBaun M, Randhawa G, Reichard BA, Elledge SJ, Feinberg AP.
    Am J Hum Genet; 1997 Aug 15; 61(2):304-9. PubMed ID: 9311734
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  • 9. Beckwith-Wiedemann syndrome: multiple molecular mechanisms.
    Enklaar T, Zabel BU, Prawitt D.
    Expert Rev Mol Med; 2006 Jul 17; 8(17):1-19. PubMed ID: 16842655
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  • 10. Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour.
    Taniguchi T, Okamoto K, Reeve AE.
    Oncogene; 1997 Mar 13; 14(10):1201-6. PubMed ID: 9121769
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  • 11. CDKN1C expression in Beckwith-Wiedemann syndrome patients with allele imbalance.
    Algar EM, Deeble GJ, Smith PJ.
    J Med Genet; 1999 Jul 13; 36(7):524-31. PubMed ID: 10424812
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  • 13. Overgrowth syndromes and genomic imprinting: from mouse to man.
    Li M, Squire JA, Weksberg R.
    Clin Genet; 1998 Mar 13; 53(3):165-70. PubMed ID: 9630066
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  • 15. New p57KIP2 mutations in Beckwith-Wiedemann syndrome.
    Hatada I, Nabetani A, Morisaki H, Xin Z, Ohishi S, Tonoki H, Niikawa N, Inoue M, Komoto Y, Okada A, Steichen E, Ohashi H, Fukushima Y, Nakayama M, Mukai T.
    Hum Genet; 1997 Oct 13; 100(5-6):681-3. PubMed ID: 9341892
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  • 16. Molecular biology of Beckwith-Wiedemann syndrome.
    Weksberg R, Squire JA.
    Med Pediatr Oncol; 1996 Nov 13; 27(5):462-9. PubMed ID: 8827075
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  • 17. Analysis of CDKN1C in Beckwith Wiedemann syndrome.
    Algar E, Brickell S, Deeble G, Amor D, Smith P.
    Hum Mutat; 2000 Nov 13; 15(6):497-508. PubMed ID: 10862080
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  • 18. Acute lymphocytic leukaemia in a child with Beckwith-Wiedemann syndrome harbouring a CDKN1C mutation.
    Abadie C, Bernard F, Netchine I, Sanlaville D, Roque A, Rossignol S, Coupier I.
    Eur J Med Genet; 2010 Nov 13; 53(6):400-3. PubMed ID: 20826236
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  • 19. p57KIP2 targeted disruption and Beckwith-Wiedemann syndrome: is the inhibitor just a contributor?
    Swanger WJ, Roberts JM.
    Bioessays; 1997 Oct 13; 19(10):839-42. PubMed ID: 9363677
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  • 20. Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.
    Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER.
    Eur J Hum Genet; 2005 Sep 13; 13(9):1025-32. PubMed ID: 15999116
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