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Journal Abstract Search

190 related items for PubMed ID: 25487064

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  • 8. EDNRB/EDN3 and Hirschsprung disease type II.
    McCallion AS, Chakravarti A.
    Pigment Cell Res; 2001 Jun; 14(3):161-9. PubMed ID: 11434563
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  • 11. 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
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  • 15. Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.
    Chen B, Ouyang HL, Wang WH, Yin YH, Yan LN, Yang B, Xue ZF.
    Exp Anim; 2016 Jul 29; 65(3):245-51. PubMed ID: 26923755
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  • 16. 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 29; 12(1):39-43. PubMed ID: 20009762
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  • 18. Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome).
    Edery P, Attié T, Amiel J, Pelet A, Eng C, Hofstra RM, Martelli H, Bidaud C, Munnich A, Lyonnet S.
    Nat Genet; 1996 Apr 29; 12(4):442-4. PubMed ID: 8630502
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  • 19. 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 Apr 29; 5(4):247-51. PubMed ID: 9359047
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