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172 related items for PubMed ID: 20009762

  • 1. New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease.
    Sánchez-Mejías A, Fernández RM, López-Alonso M, Antiñolo G, Borrego S.
    Genet Med; 2010 Jan; 12(1):39-43. PubMed ID: 20009762
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2.
    Watanabe Y, Stanchina L, Lecerf L, Gacem N, Conidi A, Baral V, Pingault V, Huylebroeck D, Bondurand N.
    Gastroenterology; 2017 Apr; 152(5):1139-1150.e4. PubMed ID: 28063956
    [Abstract] [Full Text] [Related]

  • 4. EDNRB/EDN3 and Hirschsprung disease type II.
    McCallion AS, Chakravarti A.
    Pigment Cell Res; 2001 Jun; 14(3):161-9. PubMed ID: 11434563
    [Abstract] [Full Text] [Related]

  • 5. Altered endothelin-3 and endothelin-B receptor mRNA expression in Hirschsprung's disease.
    Oue T, Puri P.
    J Pediatr Surg; 1999 Aug; 34(8):1257-60. PubMed ID: 10466607
    [Abstract] [Full Text] [Related]

  • 6. [Endothelin B receptor system and Hirschsprung disease].
    Inoue M, Kusafuka T, Okada A.
    Nihon Rinsho; 1998 Jul; 56(7):1876-80. PubMed ID: 9702069
    [Abstract] [Full Text] [Related]

  • 7. Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
    Garcia-Barceló M, Sham MH, Lee WS, Lui VC, Chen BL, Wong KK, Wong JS, Tam PK.
    Clin Chem; 2004 Jan; 50(1):93-100. PubMed ID: 14633923
    [Abstract] [Full Text] [Related]

  • 8. Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease.
    Kusafuka T, Puri P.
    Pediatr Surg Int; 1997 Jan; 12(1):19-23. PubMed ID: 9035203
    [Abstract] [Full Text] [Related]

  • 9. Genetic analysis of RET, EDNRB, and EDN3 genes and three SNPs in MCS + 9.7 in Chinese Patients with isolated Hirschsprung disease.
    Zhang XN, Zhou MN, Qiu YQ, Ding SP, Qi M, Li JC.
    Biochem Genet; 2007 Aug; 45(7-8):523-7. PubMed ID: 17554617
    [No Abstract] [Full Text] [Related]

  • 10. A De Novo novel mutation of the EDNRB gene in a Taiwanese boy with Hirschsprung disease.
    Chen WC, Chang SS, Sy ED, Tsai MC.
    J Formos Med Assoc; 2006 Apr; 105(4):349-54. PubMed ID: 16618617
    [Abstract] [Full Text] [Related]

  • 11. A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?
    Pingault V, Bondurand N, Lemort N, Sancandi M, Ceccherini I, Hugot JP, Jouk PS, Goossens M.
    J Med Genet; 2001 Mar; 38(3):205-9. PubMed ID: 11303518
    [No Abstract] [Full Text] [Related]

  • 12. Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
    Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S.
    Eur J Hum Genet; 1997 Mar; 5(4):247-51. PubMed ID: 9359047
    [Abstract] [Full Text] [Related]

  • 13. Enterocolitis causes profound lymphoid depletion in endothelin receptor B- and endothelin 3-null mouse models of Hirschsprung-associated enterocolitis.
    Frykman PK, Cheng Z, Wang X, Dhall D.
    Eur J Immunol; 2015 Mar; 45(3):807-17. PubMed ID: 25487064
    [Abstract] [Full Text] [Related]

  • 14. Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.
    Cui L, Wong EH, Cheng G, Firmato de Almeida M, So MT, Sham PC, Cherny SS, Tam PK, Garcia-Barceló MM.
    PLoS One; 2013 Mar; 8(6):e66631. PubMed ID: 23840513
    [Abstract] [Full Text] [Related]

  • 15. Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic cases of Hirschsprung's disease.
    Kusafuka T, Wang Y, Puri P.
    J Pediatr Surg; 1997 Mar; 32(3):501-4. PubMed ID: 9094028
    [Abstract] [Full Text] [Related]

  • 16. [Molecular basis of Hirschsprung disease].
    Inoue M, Okada A.
    Nihon Rinsho; 1998 Jan; 56(1):249-57. PubMed ID: 9465697
    [Abstract] [Full Text] [Related]

  • 17. [From monogenic to polygenic: model of Hirschsprung disease].
    Salomon R, Amiel J, Attié T, Pelet A, Munnich A, Lyonnet S.
    Pathol Biol (Paris); 1998 Nov; 46(9):705-7. PubMed ID: 9885824
    [Abstract] [Full Text] [Related]

  • 18. Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease.
    Cantrell VA, Owens SE, Chandler RL, Airey DC, Bradley KM, Smith JR, Southard-Smith EM.
    Hum Mol Genet; 2004 Oct 01; 13(19):2289-301. PubMed ID: 15294878
    [Abstract] [Full Text] [Related]

  • 19. Clinical relationship between EDN-3 gene, EDNRB gene and Hirschsprung's disease.
    Duan XL, Zhang XS, Li GW.
    World J Gastroenterol; 2003 Dec 01; 9(12):2839-42. PubMed ID: 14669347
    [Abstract] [Full Text] [Related]

  • 20. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.
    Amiel J, Attié T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E, Nihoul-Fékété C, Munnich A, Lyonnet S.
    Hum Mol Genet; 1996 Mar 01; 5(3):355-7. PubMed ID: 8852660
    [Abstract] [Full Text] [Related]

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