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.
196 related articles for article (PubMed ID: 9094028)
1. 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]
2. 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]
3. 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]
4. [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]
5. 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]
6. Japanese patients with sporadic Hirschsprung: mutation analysis of the receptor tyrosine kinase proto-oncogene, endothelin-B receptor, endothelin-3, glial cell line-derived neurotrophic factor and neurturin genes: a comparison with similar studies. Sakai T; Nirasawa Y; Itoh Y; Wakizaka A Eur J Pediatr; 2000 Mar; 159(3):160-7. PubMed ID: 10664228 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Congenital central hypoventilation syndrome: a novel mutation of the RET gene in an isolated case. Kanai M; Numakura C; Sasaki A; Shirahata E; Akaba K; Hashimoto M; Hasegawa H; Shirasawa S; Hayasaka K Tohoku J Exp Med; 2002 Apr; 196(4):241-6. PubMed ID: 12086152 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease. Gath R; Goessling A; Keller KM; Koletzko S; Coerdt W; Müntefering H; Wirth S; Hofstra RM; Mulligan L; Eng C; von Deimling A Gut; 2001 May; 48(5):671-5. PubMed ID: 11302967 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome. Sakai T; Wakizaka A; Nirasawa Y; Ito Y Tohoku J Exp Med; 1999 Jan; 187(1):43-7. PubMed ID: 10458491 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. Congenital central hypoventilation syndrome associated with Hirschsprung's disease: mutation analysis of the RET and endothelin-signaling pathways. Sakai T; Wakizaka A; Nirasawa Y Eur J Pediatr Surg; 2001 Oct; 11(5):335-7. PubMed ID: 11719874 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]