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Journal Abstract Search

190 related items for PubMed ID: 25487064

  • 21. Lymphopenia in Ednrb-deficient rat was strongly modified by genetic background.
    Dang R, Sasaki N, Nishino T, Nakanishi M, Torigoe D, Agui T.
    Biomed Res; 2012; 33(4):249-53. PubMed ID: 22975636
    [Abstract] [Full Text] [Related]

  • 22. 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]

  • 23. Intestinal dysbiosis and bacterial enteroinvasion in a murine model of Hirschsprung's disease.
    Pierre JF, Barlow-Anacker AJ, Erickson CS, Heneghan AF, Leverson GE, Dowd SE, Epstein ML, Kudsk KA, Gosain A.
    J Pediatr Surg; 2014 Aug; 49(8):1242-51. PubMed ID: 25092084
    [Abstract] [Full Text] [Related]

  • 24. Bacterial Microbiome Dynamics in Post Pull-Through Hirschsprung-Associated Enterocolitis (HAEC): An Experimental Study Employing the Endothelin Receptor B-Null Mouse Model.
    Cheng Z, Zhao L, Dhall D, Ruegger PM, Borneman J, Frykman PK.
    Front Surg; 2018 Aug; 5():30. PubMed ID: 29682507
    [Abstract] [Full Text] [Related]

  • 25. Gli family zinc finger 1 is associated with endothelin receptor type B in Hirschsprung disease.
    Liu W, Pan J, Gao J, Shuai X, Tang S, Wang G, Tao K, Wu C.
    Mol Med Rep; 2018 Apr; 17(4):5844-5850. PubMed ID: 29484400
    [Abstract] [Full Text] [Related]

  • 26. Mesenchymal Stem Cells Attenuates Hirschsprung diseases - Associated Enterocolitis by Reducing M1 Macrophages Infiltration via COX-2 Dependent Mechanism.
    Meng X, Xiao J, Wang J, Sun M, Chen X, Wu L, Chen K, Li Z, Feng C, Zhuansun D, Yang J, Wu X, Yu D, Li W, Niu Y, He Y, Wei M, Chen F, Xiong B, Feng J, Zhu T.
    J Pediatr Surg; 2024 Aug; 59(8):1498-1514. PubMed ID: 38508971
    [Abstract] [Full Text] [Related]

  • 27. 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 Aug; 8(6):e66631. PubMed ID: 23840513
    [Abstract] [Full Text] [Related]

  • 28. [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]

  • 29. Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan.
    Lin YC, Lai HS, Hsu WM, Lee PI, Chen HL, Chang MH.
    J Pediatr Gastroenterol Nutr; 2008 Jan; 46(1):36-40. PubMed ID: 18162831
    [Abstract] [Full Text] [Related]

  • 30. 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]

  • 31. Hirschsprung's associated enterocolitis.
    Gosain A, Brinkman AS.
    Curr Opin Pediatr; 2015 Jun; 27(3):364-9. PubMed ID: 25944307
    [Abstract] [Full Text] [Related]

  • 32. 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
    [Abstract] [Full Text] [Related]

  • 33. Intestinal proinflammatory macrophages induce a phenotypic switch in interstitial cells of Cajal.
    Chen X, Meng X, Zhang H, Feng C, Wang B, Li N, Abdullahi KM, Wu X, Yang J, Li Z, Jiao C, Wei J, Xiong X, Fu K, Yu L, Besner GE, Feng J.
    J Clin Invest; 2020 Dec 01; 130(12):6443-6456. PubMed ID: 32809970
    [Abstract] [Full Text] [Related]

  • 34. Contribution of RET, NTRK3 and EDN3 to the expression of Hirschsprung disease in a multiplex family.
    Sánchez-Mejías A, Fernández RM, López-Alonso M, Antiñolo G, Borrego S.
    J Med Genet; 2009 Dec 01; 46(12):862-4. PubMed ID: 19556619
    [Abstract] [Full Text] [Related]

  • 35. Altered expression of laminin alpha1 in aganglionic colon of endothelin receptor-B null mouse model of Hirschsprung's disease.
    Fujiwara N, Nakazawa-Tanaka N, Miyahara K, Arikawa-Hirasawa E, Akazawa C, Yamataka A.
    Pediatr Surg Int; 2018 Feb 01; 34(2):137-141. PubMed ID: 28983681
    [Abstract] [Full Text] [Related]

  • 36. Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis.
    Huang J, Dang R, Torigoe D, Lei C, Lan X, Chen H, Sasaki N, Wang J, Agui T.
    PLoS One; 2015 Feb 01; 10(3):e0122068. PubMed ID: 25790447
    [Abstract] [Full Text] [Related]

  • 37. Impaired growth and differentiation of diploid but not immortal melanoblasts from endothelin receptor B mutant (piebald) mice.
    Sviderskaya EV, Easty DJ, Bennett DC.
    Dev Dyn; 1998 Dec 01; 213(4):452-63. PubMed ID: 9853966
    [Abstract] [Full Text] [Related]

  • 38. Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice.
    Rice J, Doggett B, Sweetser DA, Yanagisawa H, Yanagisawa M, Kapur RP.
    Dev Dyn; 2000 Jan 01; 217(1):120-32. PubMed ID: 10679935
    [Abstract] [Full Text] [Related]

  • 39. Altered neuronal density and neurotransmitter expression in the ganglionated region of Ednrb null mice: implications for Hirschsprung's disease.
    Zaitoun I, Erickson CS, Barlow AJ, Klein TR, Heneghan AF, Pierre JF, Epstein ML, Gosain A.
    Neurogastroenterol Motil; 2013 Mar 01; 25(3):e233-44. PubMed ID: 23360229
    [Abstract] [Full Text] [Related]

  • 40. 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 01; 105(4):349-54. PubMed ID: 16618617
    [Abstract] [Full Text] [Related]

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