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Journal Abstract Search

378 related items for PubMed ID: 9584186

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  • 3. Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
    Sperandeo MP, Ungaro P, Vernucci M, Pedone PV, Cerrato F, Perone L, Casola S, Cubellis MV, Bruni CB, Andria G, Sebastio G, Riccio A.
    Am J Hum Genet; 2000 Mar; 66(3):841-7. PubMed ID: 10712200
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  • 4. Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.
    Dao D, Walsh CP, Yuan L, Gorelov D, Feng L, Hensle T, Nisen P, Yamashiro DJ, Bestor TH, Tycko B.
    Hum Mol Genet; 1999 Jul; 8(7):1337-52. PubMed ID: 10369881
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  • 5. Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.
    Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP.
    Proc Natl Acad Sci U S A; 1999 Apr 27; 96(9):5203-8. PubMed ID: 10220444
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  • 6. Disruption of imprinted genes at chromosome region 11p15.5 in paediatric rhabdomyosarcoma.
    Anderson J, Gordon A, McManus A, Shipley J, Pritchard-Jones K.
    Neoplasia; 1999 Oct 27; 1(4):340-8. PubMed ID: 10935489
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  • 7. Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.
    Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER.
    J Med Genet; 2000 Dec 27; 37(12):921-6. PubMed ID: 11106355
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  • 8. Loss of Igf2 imprinting in monoclonal mouse hepatic tumor cells is not associated with abnormal methylation patterns for the H19, Igf2, and Kvlqt1 differentially methylated regions.
    Ishizaki T, Yoshie M, Yaginuma Y, Tanaka T, Ogawa K.
    J Biol Chem; 2003 Feb 21; 278(8):6222-8. PubMed ID: 12475990
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  • 11. 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 21; 5(8):1101-8. PubMed ID: 8842727
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  • 12. Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome.
    Grandjean V, Smith J, Schofield PN, Ferguson-Smith AC.
    Proc Natl Acad Sci U S A; 2000 May 09; 97(10):5279-84. PubMed ID: 10779549
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  • 13. Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting.
    Engemann S, Strödicke M, Paulsen M, Franck O, Reinhardt R, Lane N, Reik W, Walter J.
    Hum Mol Genet; 2000 Nov 01; 9(18):2691-706. PubMed ID: 11063728
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  • 14. Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.
    Yatsuki H, Joh K, Higashimoto K, Soejima H, Arai Y, Wang Y, Hatada I, Obata Y, Morisaki H, Zhang Z, Nakagawachi T, Satoh Y, Mukai T.
    Genome Res; 2002 Dec 01; 12(12):1860-70. PubMed ID: 12466290
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  • 15. An enhancer deletion affects both H19 and Igf2 expression.
    Leighton PA, Saam JR, Ingram RS, Stewart CL, Tilghman SM.
    Genes Dev; 1995 Sep 01; 9(17):2079-89. PubMed ID: 7544754
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  • 16. Expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 and the methylation patterns at the KvDMR1 and H19/IGF2 imprinting control regions is conserved between human and bovine.
    Robbins KM, Chen Z, Wells KD, Rivera RM.
    J Biomed Sci; 2012 Nov 15; 19(1):95. PubMed ID: 23153226
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  • 17. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
    Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W.
    Hum Mol Genet; 1996 Dec 15; 5(12):2027-32. PubMed ID: 8968759
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  • 18. The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.
    Cerrato F, Sparago A, Di Matteo I, Zou X, Dean W, Sasaki H, Smith P, Genesio R, Bruggemann M, Reik W, Riccio A.
    Hum Mol Genet; 2005 Feb 15; 14(4):503-11. PubMed ID: 15640248
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  • 19. ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.
    Arima T, Kamikihara T, Hayashida T, Kato K, Inoue T, Shirayoshi Y, Oshimura M, Soejima H, Mukai T, Wake N.
    Nucleic Acids Res; 2005 Feb 15; 33(8):2650-60. PubMed ID: 15888726
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