These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 9580670)

  • 41. 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; 87(5):580-5. PubMed ID: 10792313
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease.
    Attié T; Till M; Pelet A; Amiel J; Edery P; Boutrand L; Munnich A; Lyonnet S
    Hum Mol Genet; 1995 Dec; 4(12):2407-9. PubMed ID: 8634719
    [No Abstract]   [Full Text] [Related]  

  • 43. Pleiotropic effects of coat colour-associated mutations in humans, mice and other mammals.
    Reissmann M; Ludwig A
    Semin Cell Dev Biol; 2013; 24(6-7):576-86. PubMed ID: 23583561
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome).
    Brooks AS; Breuning MH; Osinga J; vd Smagt JJ; Catsman CE; Buys CH; Meijers C; Hofstra RM
    J Med Genet; 1999 Jun; 36(6):485-9. PubMed ID: 10874640
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model.
    Southard-Smith EM; Kos L; Pavan WJ
    Nat Genet; 1998 Jan; 18(1):60-4. PubMed ID: 9425902
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden.
    Svensson PJ; Tapper-Persson M; Anvret M; Molander ML; Eng C; Nordenskjöld A
    Clin Genet; 1999 Mar; 55(3):215-7. PubMed ID: 10334478
    [No Abstract]   [Full Text] [Related]  

  • 47. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 49. A novel mutation in the endothelin B receptor gene in a patient with Shah-Waardenburg syndrome and Down syndrome.
    Boardman JP; Syrris P; Holder SE; Robertson NJ; Carter N; Lakhoo K
    J Med Genet; 2001 Sep; 38(9):646-7. PubMed ID: 11565556
    [No Abstract]   [Full Text] [Related]  

  • 50. Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype.
    Hofstra RM; Osinga J; Buys CH
    Eur J Hum Genet; 1997; 5(4):180-5. PubMed ID: 9359036
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Clinical and genetic correlations of familial Hirschsprung's disease.
    Moore SW; Zaahl M
    J Pediatr Surg; 2015 Feb; 50(2):285-8. PubMed ID: 25638620
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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; 213(4):452-63. PubMed ID: 9853966
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Genetics of Hirschsprung disease].
    Attié T; Salomon R; Amiel J; Edery P; Pelet A; Nihoul-Fékété C; Munnich A; Lyonnet S
    C R Seances Soc Biol Fil; 1996; 190(5-6):549-56. PubMed ID: 9074720
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Nucleotide sequence of endothelin-B receptor gene reveals origin of piebald mutation in laboratory mouse.
    Kumagai T; Wada A; Tsudzuki M; Nishimura M; Kunieda T
    Exp Anim; 1998 Oct; 47(4):265-9. PubMed ID: 10067171
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons.
    Baynash AG; Hosoda K; Giaid A; Richardson JA; Emoto N; Hammer RE; Yanagisawa M
    Cell; 1994 Dec; 79(7):1277-85. PubMed ID: 8001160
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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; 5(4):247-51. PubMed ID: 9359047
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Coding-sequence mutation and polymorphism analysis of EDNRB gene in patients with Hirschsprung's disease from Zhejiang region].
    Zhou MN; Li JC; Ding SP
    Fen Zi Xi Bao Sheng Wu Xue Bao; 2006 Feb; 39(1):61-5. PubMed ID: 16944573
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Cloning and characterization of a novel endothelin receptor subtype in the avian class.
    Lecoin L; Sakurai T; Ngo MT; Abe Y; Yanagisawa M; Le Douarin NM
    Proc Natl Acad Sci U S A; 1998 Mar; 95(6):3024-9. PubMed ID: 9501209
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Reduced cell proliferation and increased apoptosis in the hippocampal formation in a rat model of Hirschsprung's disease.
    Xie D; Croaker GDH; Li J; Song ZM
    Brain Res; 2016 Jul; 1642():79-86. PubMed ID: 27017960
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.