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11. Functional analyses of RET mutations in Chinese Hirschsprung disease patients. Leon TY; So MT; Lui VC; Hofstra RM; Tam PK; Ngan ES; Garcia-Barceló MM Birth Defects Res A Clin Mol Teratol; 2012 Jan; 94(1):47-51. PubMed ID: 22131258 [TBL] [Abstract][Full Text] [Related]
12. Diminished Ret expression compromises neuronal survival in the colon and causes intestinal aganglionosis in mice. Uesaka T; Nagashimada M; Yonemura S; Enomoto H J Clin Invest; 2008 May; 118(5):1890-8. PubMed ID: 18414682 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Establishment of an induced pluripotent stem cell model of Hirschsrpung disease, a congenital condition of the enteric nervous system, from a patient carrying a novel RET mutation. Wang Y; Lai X; Huang L; Liu G; Zai Z; Zhu D; Zhang Y; Liang Z; Yao Z; Chen Y; Wen Z; Xia H Neuroreport; 2018 Aug; 29(12):975-980. PubMed ID: 29965875 [TBL] [Abstract][Full Text] [Related]
17. Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3. Leon TY; Ngan ES; Poon HC; So MT; Lui VC; Tam PK; Garcia-Barcelo MM J Pediatr Surg; 2009 Oct; 44(10):1904-12. PubMed ID: 19853745 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease. Sribudiani Y; Chauhan RK; Alves MM; Petrova L; Brosens E; Harrison C; Wabbersen T; de Graaf BM; Rügenbrink T; Burzynski G; Brouwer RWW; van IJcken WFJ; Maas SM; de Klein A; Osinga J; Eggen BJL; Burns AJ; Brooks AS; Shepherd IT; Hofstra RMW Gastroenterology; 2018 Jul; 155(1):118-129.e6. PubMed ID: 29601828 [TBL] [Abstract][Full Text] [Related]
20. Neural precursor death is central to the pathogenesis of intestinal aganglionosis in Ret hypomorphic mice. Uesaka T; Enomoto H J Neurosci; 2010 Apr; 30(15):5211-8. PubMed ID: 20392943 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]