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Journal Abstract Search


263 related items for PubMed ID: 22974609

  • 1. RET 3'UTR polymorphisms and its protective role in Hirschsprung disease in southeastern Chinese.
    Pan ZW, Luo CF, Liu ZJ, Li JC.
    J Pediatr Surg; 2012 Sep; 47(9):1699-705. PubMed ID: 22974609
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  • 2. Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.
    Liu CP, Li XG, Lou JT, Xue Y, Luo CF, Zhou XW, Chen F, Li X, Li M, Li JC.
    J Pediatr Surg; 2009 Sep; 44(9):1805-11. PubMed ID: 19735829
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  • 3. A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
    Griseri P, Bachetti T, Puppo F, Lantieri F, Ravazzolo R, Devoto M, Ceccherini I.
    Hum Mutat; 2005 Feb; 25(2):189-95. PubMed ID: 15643606
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  • 4. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
    Fitze G, Appelt H, König IR, Görgens H, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK.
    Hum Mol Genet; 2003 Dec 15; 12(24):3207-14. PubMed ID: 14600022
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  • 6. RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
    Vaclavikova E, Dvorakova S, Skaba R, Pos L, Sykorova V, Halkova T, Vcelak J, Bendlova B.
    PLoS One; 2014 Dec 15; 9(6):e98957. PubMed ID: 24897126
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  • 7. TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease.
    Garcia-Barcelo M, Ganster RW, Lui VC, Leon TY, So MT, Lau AM, Fu M, Sham MH, Knight J, Zannini MS, Sham PC, Tam PK.
    Hum Mol Genet; 2005 Jan 15; 14(2):191-204. PubMed ID: 15548547
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  • 9. Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
    Burzynski GM, Nolte IM, Osinga J, Ceccherini I, Twigt B, Maas S, Brooks A, Verheij J, Plaza Menacho I, Buys CH, Hofstra RM.
    Eur J Hum Genet; 2004 Aug 15; 12(8):604-12. PubMed ID: 15138456
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  • 10. Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
    Tou J, Wang L, Liu L, Wang Y, Zhong R, Duan S, Liu W, Xiong Q, Gu Q, Yang H, Li H.
    BMC Med Genet; 2011 Feb 25; 12():32. PubMed ID: 21349203
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  • 19. Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung disease.
    Basel-Vanagaite L, Pelet A, Steiner Z, Munnich A, Rozenbach Y, Shohat M, Lyonnet S.
    Eur J Hum Genet; 2007 Feb 25; 15(2):242-5. PubMed ID: 17091122
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