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Journal Abstract Search

120 related items for PubMed ID: 8804863

  • 21. SOX10 mutations in patients with Waardenburg-Hirschsprung disease.
    Pingault V, Bondurand N, Kuhlbrodt K, Goerich DE, Préhu MO, Puliti A, Herbarth B, Hermans-Borgmeyer I, Legius E, Matthijs G, Amiel J, Lyonnet S, Ceccherini I, Romeo G, Smith JC, Read AP, Wegner M, Goossens M.
    Nat Genet; 1998 Feb; 18(2):171-3. PubMed ID: 9462749
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  • 22. Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung disease.
    Syrris P, Carter ND, Patton MA.
    Am J Med Genet; 1999 Nov 05; 87(1):69-71. PubMed ID: 10528251
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  • 25. Functional characterization of three mutations of the endothelin B receptor gene in patients with Hirschsprung's disease: evidence for selective loss of Gi coupling.
    Fuchs S, Amiel J, Claudel S, Lyonnet S, Corvol P, Pinet F.
    Mol Med; 2001 Feb 05; 7(2):115-24. PubMed ID: 11471546
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  • 27. Exclusion of EDNRB and KIT as the basis for white spotting in Border Collies.
    Metallinos D, Rine J.
    Genome Biol; 2000 Feb 05; 1(2):RESEARCH0004. PubMed ID: 11178229
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  • 28. Genetic variation in the GDNF promoter affects its expression and modifies the severity of Hirschsprung's disease (HSCR) in rats carrying Ednrb(sl) mutations.
    Huang J, Dang R, Torigoe D, Li A, Lei C, Sasaki N, Wang J, Agui T.
    Gene; 2016 Jan 01; 575(1):144-8. PubMed ID: 26318480
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  • 32. 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
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  • 33. Localization of endothelin-A and -B receptors during the postnatal development of rat cerebellum.
    Furuya S, Hiroe T, Ogiso N, Ozaki T, Hori S.
    Cell Tissue Res; 2001 Sep 01; 305(3):307-24. PubMed ID: 11572084
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  • 36. Endothelin B receptor deficient transgenic rescue rats: a rescue phenomenon in the brain.
    Riechers CC, Knabe W, Sirén AL, Gariepy CE, Yanagisawa M, Ehrenreich H.
    Neuroscience; 2004 Sep 01; 124(4):719-23. PubMed ID: 15026112
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  • 37. Functional analysis of five endothelin-B receptor mutations found in human Hirschsprung disease patients.
    Abe Y, Sakurai T, Yamada T, Nakamura T, Yanagisawa M, Goto K.
    Biochem Biophys Res Commun; 2000 Aug 28; 275(2):524-31. PubMed ID: 10964697
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  • 39. Reduced endothelin-3 expression in sporadic Hirschsprung disease.
    Kenny SE, Hofstra RM, Buys CH, Vaillant CR, Lloyd DA, Edgar DH.
    Br J Surg; 2000 May 28; 87(5):580-5. PubMed ID: 10792313
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