163 related articles for article (PubMed ID: 16818057)
1. Novel mutations of RET gene in Korean patients with sporadic Hirschsprung's disease.
Kim JH; Yoon KO; Kim JK; Kim JW; Lee SK; Kong SY; Seo JM
J Pediatr Surg; 2006 Jul; 41(7):1250-4. PubMed ID: 16818057
[TBL] [Abstract][Full Text] [Related]
2. Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
Tou J; Wang L; Liu L; Wang Y; Zhong R; Duan S; Liu W; Xiong Q; Gu Q; Yang H; Li H
BMC Med Genet; 2011 Feb; 12():32. PubMed ID: 21349203
[TBL] [Abstract][Full Text] [Related]
3. New variations of the EDNRB gene and its association with sporadic Hirschsprung's disease in Korea.
Kim JH; Yoon KO; Kim H; Kim JK; Kim JW; Lee SK; Seo JM
J Pediatr Surg; 2006 Oct; 41(10):1708-12. PubMed ID: 17011274
[TBL] [Abstract][Full Text] [Related]
4. RET 3'UTR polymorphisms and its protective role in Hirschsprung disease in southeastern Chinese.
Pan ZW; Luo CF; Liu ZJ; Li JC
J Pediatr Surg; 2012 Sep; 47(9):1699-705. PubMed ID: 22974609
[TBL] [Abstract][Full Text] [Related]
5. Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus.
de Pontual L; Pelet A; Trochet D; Jaubert F; Espinosa-Parrilla Y; Munnich A; Brunet JF; Goridis C; Feingold J; Lyonnet S; Amiel J
J Med Genet; 2006 May; 43(5):419-23. PubMed ID: 16443855
[TBL] [Abstract][Full Text] [Related]
6. RET polymorphisms and the risk of Hirschsprung's disease in a Chinese population.
Liu C; Jin L; Li H; Lou J; Luo C; Zhou X; Li JC
J Hum Genet; 2008; 53(9):825-833. PubMed ID: 18612588
[TBL] [Abstract][Full Text] [Related]
7. Incidence of RET mutations in patients with Hirschsprung's disease.
Sancandi M; Ceccherini I; Costa M; Fava M; Chen B; Wu Y; Hofstra R; Laurie T; Griffths M; Burge D; Tam PK
J Pediatr Surg; 2000 Jan; 35(1):139-42; discussion 142-3. PubMed ID: 10646792
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.
So MT; Leon TY; Cheng G; Tang CS; Miao XP; Cornes BK; Diem NN; Cui L; Ngan ES; Lui VC; Wu XZ; Wang B; Wang H; Yuan ZW; Huang LM; Li L; Xia H; Zhu D; Liu J; Nguyen TL; Chan IH; Chung PH; Liu XL; Zhang R; Wong KK; Sham PC; Cherny SS; Tam PK; Garcia-Barcelo MM
PLoS One; 2011; 6(12):e28986. PubMed ID: 22174939
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Mutation of RET proto-oncogene in Hirschsprung's disease and intestinal neuronal dysplasia.
Tou JF; Li MJ; Guan T; Li JC; Zhu XK; Feng ZG
World J Gastroenterol; 2006 Feb; 12(7):1136-9. PubMed ID: 16534860
[TBL] [Abstract][Full Text] [Related]
12. Fine mapping of the 9q31 Hirschsprung's disease locus.
Tang CS; Sribudiani Y; Miao XP; de Vries AR; Burzynski G; So MT; Leon YY; Yip BH; Osinga J; Hui KJ; Verheij JB; Cherny SS; Tam PK; Sham PC; Hofstra RM; Garcia-Barceló MM
Hum Genet; 2010 Jun; 127(6):675-83. PubMed ID: 20361209
[TBL] [Abstract][Full Text] [Related]
13. Analysis of the RET gene in subjects with sporadic Hirschsprung's disease.
Chin TW; Chiu CY; Tsai HL; Liu CS; Wei CF; Jap TS
J Chin Med Assoc; 2008 Aug; 71(8):406-10. PubMed ID: 18772120
[TBL] [Abstract][Full Text] [Related]
14. RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease.
Pasini B; Rossi R; Ambrosio MR; Zatelli MC; Gullo M; Gobbo M; Collini P; Aiello A; Pansini G; Trasforini G; degli Uberti EC
Surgery; 2002 Apr; 131(4):373-81. PubMed ID: 11935126
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Evaluation of the NK2 homeobox 1 gene (NKX2-1) as a Hirschsprung's disease locus.
Garcia-Barceló MM; Lau DK; Ngan ES; Leon TY; Liu T; So M; Miao X; Lui VC; Wong KK; Ganster RW; Cass DT; Croaker GD; Tam PK
Ann Hum Genet; 2008 Mar; 72(Pt 2):170-7. PubMed ID: 18081917
[TBL] [Abstract][Full Text] [Related]
17. Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.
Liu CP; Tang QQ; Lou JT; Luo CF; Zhou XW; Li DM; Chen F; Li X; Li JC
Biochem Genet; 2010 Jun; 48(5-6):496-503. PubMed ID: 20454948
[TBL] [Abstract][Full Text] [Related]
18. A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease.
Dvoráková S; Dvoráková K; Malíková M; Skába R; Vlcek P; Bendlová B
J Pediatr Surg; 2005 Jun; 40(6):e1-6. PubMed ID: 15991157
[TBL] [Abstract][Full Text] [Related]
19. Evaluation of the thyroid transcription factor-1 gene (TITF1) as a Hirschsprung's disease locus.
Garcia-Barceló MM; Lau DK; Ngan ES; Leon TY; Liu TT; So MT; Miao XP; Lui VC; Wong KK; Ganster RW; Cass DT; Croaker GD; Tam PK
Ann Hum Genet; 2007 Nov; 71(Pt 6):746-54. PubMed ID: 17640327
[TBL] [Abstract][Full Text] [Related]
20. Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.
Ngo DN; So MT; Gui H; Tran AQ; Bui DH; Cherny S; Tam PK; Nguyen TL; Garcia-Barcelo MM
J Pediatr Surg; 2012 Oct; 47(10):1859-64. PubMed ID: 23084198
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]