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2. 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]
3. [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]
4. 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]
5. Expression of RET proto-oncogene and GDNF deficit in Hirschsprung's disease. Zhan J; Xiu Y; Gu J; Fang Z; Hu XL J Pediatr Surg; 1999 Nov; 34(11):1606-9. PubMed ID: 10591552 [TBL] [Abstract][Full Text] [Related]
6. RET proto-oncogene: role in kidney development and molecular pathology. Salomon R; Attie T; Amiel J; Pelet A; Niaudet P; Lyonnet S Adv Nephrol Necker Hosp; 1998; 28():401-17. PubMed ID: 9890001 [No Abstract] [Full Text] [Related]
7. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. Angrist M; Bolk S; Halushka M; Lapchak PA; Chakravarti A Nat Genet; 1996 Nov; 14(3):341-4. PubMed ID: 8896568 [TBL] [Abstract][Full Text] [Related]
8. [Genetics of Hirschsprung disease]. Attié T; Amiel J; Jan D; Edery P; Pelet A; Salomon R; Munnich A; Lyonnet S; Nihoul-Fékété C Ann Chir; 1996; 50(7):538-41. PubMed ID: 9035423 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease. Carlomagno F; Melillo RM; Visconti R; Salvatore G; De Vita G; Lupoli G; Yu Y; Jing S; Vecchio G; Fusco A; Santoro M Endocrinology; 1998 Aug; 139(8):3613-9. PubMed ID: 9681515 [TBL] [Abstract][Full Text] [Related]
11. Update on basic research on Hirschsprung's disease. Martucciello G; Holschneider AM Eur J Pediatr Surg; 1998 Jun; 8(3):131-2. PubMed ID: 9676392 [No Abstract] [Full Text] [Related]
12. Hirschsprung's disease genes and the development of the enteric nervous system. Wartiovaara K; Salo M; Sariola H Ann Med; 1998 Feb; 30(1):66-74. PubMed ID: 9556091 [TBL] [Abstract][Full Text] [Related]
13. Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease. Salomon R; Attié T; Pelet A; Bidaud C; Eng C; Amiel J; Sarnacki S; Goulet O; Ricour C; Nihoul-Fékété C; Munnich A; Lyonnet S Nat Genet; 1996 Nov; 14(3):345-7. PubMed ID: 8896569 [TBL] [Abstract][Full Text] [Related]
14. Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function? Takahashi M; Iwashita T; Santoro M; Lyonnet S; Lenoir GM; Billaud M Hum Mutat; 1999; 13(4):331-6. PubMed ID: 10220148 [TBL] [Abstract][Full Text] [Related]
15. Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B). Svensson PJ; Anvret M; Molander ML; Nordenskjöld A Hum Genet; 1998 Aug; 103(2):145-8. PubMed ID: 9760196 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL. Woodward ER; Eng C; McMahon R; Voutilainen R; Affara NA; Ponder BA; Maher ER Hum Mol Genet; 1997 Jul; 6(7):1051-6. PubMed ID: 9215674 [TBL] [Abstract][Full Text] [Related]
18. RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems. Hofstra RM; Wu Y; Stulp RP; Elfferich P; Osinga J; Maas SM; Siderius L; Brooks AS; vd Ende JJ; Heydendael VM; Severijnen RS; Bax KM; Meijers C; Buys CH Hum Mutat; 2000; 15(5):418-29. PubMed ID: 10790203 [TBL] [Abstract][Full Text] [Related]
19. 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]