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 *

136 related articles for article (PubMed ID: 24726125)

  • 1. A novel stop mutation in the EDNRB gene in a family with Hirschsprung's disease associated with multiple sclerosis.
    Granström AL; Markljung E; Fink K; Nordenskjöld E; Nilsson D; Wester T; Nordenskjöld A
    J Pediatr Surg; 2014 Apr; 49(4):622-5. PubMed ID: 24726125
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease.
    Kusafuka T; Wang Y; Puri P
    Hum Mol Genet; 1996 Mar; 5(3):347-9. PubMed ID: 8852658
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 87(1):69-71. PubMed ID: 10528251
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW; Zaahl MG
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from a non-inbred population.
    Auricchio A; Casari G; Staiano A; Ballabio A
    Hum Mol Genet; 1996 Mar; 5(3):351-4. PubMed ID: 8852659
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mutational analysis of the endothelin-B receptor gene in Japanese Hirschsprung's disease.
    Inoue M; Hosoda K; Imura K; Kamata S; Fukuzawa M; Nakao K; Okada A
    J Pediatr Surg; 1998 Aug; 33(8):1206-8. PubMed ID: 9721987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 7(2):115-24. PubMed ID: 11471546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Novel mutations of the endothelin B receptor gene in patients with Hirschsprung's disease and their characterization.
    Tanaka H; Moroi K; Iwai J; Takahashi H; Ohnuma N; Hori S; Takimoto M; Nishiyama M; Masaki T; Yanagisawa M; Sekiya S; Kimura S
    J Biol Chem; 1998 May; 273(18):11378-83. PubMed ID: 9556633
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Methylation analysis of EDNRB in human colon tissues of Hirschsprung's disease.
    Tang W; Li B; Tang J; Liu K; Qin J; Wu W; Geng Q; Zhang J; Chen H; Xu X; Xia Y
    Pediatr Surg Int; 2013 Jul; 29(7):683-8. PubMed ID: 23579558
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease.
    Puffenberger EG; Hosoda K; Washington SS; Nakao K; deWit D; Yanagisawa M; Chakravart A
    Cell; 1994 Dec; 79(7):1257-66. PubMed ID: 8001158
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Significance of novel endothelin-B receptor gene polymorphisms in Hirschsprung's disease: predominance of a novel variant (561C/T) in patients with co-existing Down's syndrome.
    Zaahl MG; du Plessis L; Warnich L; Kotze MJ; Moore SW
    Mol Cell Probes; 2003 Feb; 17(1):49-54. PubMed ID: 12628594
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].
    Amiel J; Salomon R; Attié-Bitach T; Touraine R; Steffann J; Pelet A; Nihoul-Fékété C; Vekemans M; Munnich A; Lyonnet S
    J Soc Biol; 2000; 194(3-4):125-8. PubMed ID: 11324313
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 575(1):144-8. PubMed ID: 26318480
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
    Moore SW; Zaahl M
    J Pediatr Surg; 2009 Oct; 44(10):1899-903. PubMed ID: 19853744
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.