151 related articles for article (PubMed ID: 20454948)
1. 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]
2. 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]
3. 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]
4. 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]
5. RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.
Vaclavikova E; Dvorakova S; Skaba R; Pos L; Sykorova V; Halkova T; Vcelak J; Bendlova B
PLoS One; 2014; 9(6):e98957. PubMed ID: 24897126
[TBL] [Abstract][Full Text] [Related]
6. Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.
Lantieri F; Griseri P; Puppo F; Campus R; Martucciello G; Ravazzolo R; Devoto M; Ceccherini I
Ann Hum Genet; 2006 Jan; 70(Pt 1):12-26. PubMed ID: 16441254
[TBL] [Abstract][Full Text] [Related]
7. Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.
Burzynski GM; Nolte IM; Osinga J; Ceccherini I; Twigt B; Maas S; Brooks A; Verheij J; Plaza Menacho I; Buys CH; Hofstra RM
Eur J Hum Genet; 2004 Aug; 12(8):604-12. PubMed ID: 15138456
[TBL] [Abstract][Full Text] [Related]
8. Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.
Liu CP; Li XG; Lou JT; Xue Y; Luo CF; Zhou XW; Chen F; Li X; Li M; Li JC
J Pediatr Surg; 2009 Sep; 44(9):1805-11. PubMed ID: 19735829
[TBL] [Abstract][Full Text] [Related]
9. Genetic variants in
Wang Y; Jiang Q; Cai H; Xu Z; Wu W; Gu B; Li L; Cai W
Aging (Albany NY); 2020 Mar; 12(5):4379-4393. PubMed ID: 32139661
[TBL] [Abstract][Full Text] [Related]
10. Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.
Yang D; Yang J; Li S; Jiang M; Cao G; Yang L; Zhang X; Zhou Y; Li K; Tang ST
Sci Rep; 2017 Mar; 7():43222. PubMed ID: 28256518
[TBL] [Abstract][Full Text] [Related]
11. Genotyping analysis of 3 RET polymorphisms demonstrates low somatic mutation rate in Chinese Hirschsprung disease patients.
Zhang Z; Jiang Q; Li Q; Cheng W; Qiao G; Xiao P; Gan L; Su L; Miao C; Li L
Int J Clin Exp Pathol; 2015; 8(5):5528-34. PubMed ID: 26191260
[TBL] [Abstract][Full Text] [Related]
12. Association analysis of the SOX10 polymorphism with Hirschsprung disease in the Han Chinese population.
Pan ZW; Lou J; Luo C; Yu L; Li JC
J Pediatr Surg; 2011 Oct; 46(10):1930-4. PubMed ID: 22008330
[TBL] [Abstract][Full Text] [Related]
13. A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
Griseri P; Bachetti T; Puppo F; Lantieri F; Ravazzolo R; Devoto M; Ceccherini I
Hum Mutat; 2005 Feb; 25(2):189-95. PubMed ID: 15643606
[TBL] [Abstract][Full Text] [Related]
14. A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.
Borrego S; Wright FA; Fernández RM; Williams N; López-Alonso M; Davuluri R; Antiñolo G; Eng C
Am J Hum Genet; 2003 Jan; 72(1):88-100. PubMed ID: 12474140
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Association between RET proto-oncogene polymorphisms and Hirschsprung disease in Chinese Han population of Hubei district].
Du HS; Wang GB; Zhang Y; Tao KX; Tang ST; Niu YF
Zhonghua Wei Chang Wai Ke Za Zhi; 2006 Mar; 9(2):152-6. PubMed ID: 16555159
[TBL] [Abstract][Full Text] [Related]
17. A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.
Griseri P; Pesce B; Patrone G; Osinga J; Puppo F; Sancandi M; Hofstra R; Romeo G; Ravazzolo R; Devoto M; Ceccherini I
Am J Hum Genet; 2002 Oct; 71(4):969-74. PubMed ID: 12214285
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.
Sangkhathat S; Kusafuka T; Chengkriwate P; Patrapinyokul S; Sangthong B; Fukuzawa M
J Hum Genet; 2006; 51(12):1126-1132. PubMed ID: 17009072
[TBL] [Abstract][Full Text] [Related]
20. Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.
Tang CS; Gui H; Kapoor A; Kim JH; Luzón-Toro B; Pelet A; Burzynski G; Lantieri F; So MT; Berrios C; Shin HD; Fernández RM; Le TL; Verheij JB; Matera I; Cherny SS; Nandakumar P; Cheong HS; Antiñolo G; Amiel J; Seo JM; Kim DY; Oh JT; Lyonnet S; Borrego S; Ceccherini I; Hofstra RM; Chakravarti A; Kim HY; Sham PC; Tam PK; Garcia-Barceló MM
Hum Mol Genet; 2016 Dec; 25(23):5265-5275. PubMed ID: 27702942
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]