BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 12(1):19-23. PubMed ID: 9035203
    [TBL] [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
    [TBL] [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; 5(4):247-51. PubMed ID: 9359047
    [TBL] [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
    [TBL] [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; 8(6):e66631. PubMed ID: 23840513
    [TBL] [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
    [TBL] [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
    [TBL] [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
    [TBL] [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; 13(19):2289-301. PubMed ID: 15294878
    [TBL] [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; 9(12):2839-42. PubMed ID: 14669347
    [TBL] [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; 5(3):355-7. PubMed ID: 8852660
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.