171 related articles for article (PubMed ID: 17640327)
1. 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]
2. 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]
3. TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease.
Garcia-Barcelo M; Ganster RW; Lui VC; Leon TY; So MT; Lau AM; Fu M; Sham MH; Knight J; Zannini MS; Sham PC; Tam PK
Hum Mol Genet; 2005 Jan; 14(2):191-204. PubMed ID: 15548547
[TBL] [Abstract][Full Text] [Related]
4. HOXB5 cooperates with NKX2-1 in the transcription of human RET.
Zhu J; Garcia-Barcelo MM; Tam PK; Lui VC
PLoS One; 2011; 6(6):e20815. PubMed ID: 21677782
[TBL] [Abstract][Full Text] [Related]
5. GT-repeat extension in the IL11 promoter is associated with Hirschsprung's disease (HSCR).
Haase MG; Schulze A; Grover S; Kemnitz I; König IR; Fitze G
Gene; 2018 Nov; 677():163-168. PubMed ID: 30056070
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. 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]
10. SRY interference of normal regulation of the RET gene suggests a potential role of the Y-chromosome gene in sexual dimorphism in Hirschsprung disease.
Li Y; Kido T; Garcia-Barcelo MM; Tam PK; Tabatabai ZL; Lau YF
Hum Mol Genet; 2015 Feb; 24(3):685-97. PubMed ID: 25267720
[TBL] [Abstract][Full Text] [Related]
11. Correlation between multiple RET mutations and severity of Hirschsprung's disease.
Ishii K; Doi T; Inoue K; Okawada M; Lane GJ; Yamataka A; Akazawa C
Pediatr Surg Int; 2013 Feb; 29(2):157-63. PubMed ID: 23114404
[TBL] [Abstract][Full Text] [Related]
12. Variants in RET associated with Hirschsprung's disease affect binding of transcription factors and gene expression.
Sribudiani Y; Metzger M; Osinga J; Rey A; Burns AJ; Thapar N; Hofstra RM
Gastroenterology; 2011 Feb; 140(2):572-582.e2. PubMed ID: 20977903
[TBL] [Abstract][Full Text] [Related]
13. Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease.
Miao X; Leon TY; Ngan ES; So MT; Yuan ZW; Lui VC; Chen Y; Wong KK; Tam PK; Garcia-Barceló M
Hum Mol Genet; 2010 Apr; 19(8):1461-7. PubMed ID: 20089534
[TBL] [Abstract][Full Text] [Related]
14. Two distinct mutations of the RET receptor causing Hirschsprung's disease impair the binding of signalling effectors to a multifunctional docking site.
Geneste O; Bidaud C; De Vita G; Hofstra RM; Tartare-Deckert S; Buys CH; Lenoir GM; Santoro M; Billaud M
Hum Mol Genet; 1999 Oct; 8(11):1989-99. PubMed ID: 10484767
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.
Cornes BK; Tang CS; Leon TY; Hui KJ; So MT; Miao X; Cherny SS; Sham PC; Tam PK; Garcia-Barcelo MM
PLoS One; 2010 Jun; 5(6):e10918. PubMed ID: 20532249
[TBL] [Abstract][Full Text] [Related]
19. A study on genetic polymorphism of RET proto-oncogene in Hirschsprung's disease in children.
Kumari M; Das C; Mukhopadhyay M; Patra RD; Mitra PK; Mukhopadhyay B
Afr J Paediatr Surg; 2020; 17(3 & 4):104-107. PubMed ID: 33342844
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
