234 related articles for article (PubMed ID: 18970938)
1. Polymorphisms in the genes encoding the 4 RET ligands, GDNF, NTN, ARTN, PSPN, and susceptibility to Hirschsprung disease.
Fernandez RM; Ruiz-Ferrer M; Lopez-Alonso M; Antiñolo G; Borrego S
J Pediatr Surg; 2008 Nov; 43(11):2042-7. PubMed ID: 18970938
[TBL] [Abstract][Full Text] [Related]
2. Novel mutations at RET ligand genes preventing receptor activation are associated to Hirschsprung's disease.
Ruiz-Ferrer M; Torroglosa A; Luzón-Toro B; Fernández RM; Antiñolo G; Mulligan LM; Borrego S
J Mol Med (Berl); 2011 May; 89(5):471-80. PubMed ID: 21206993
[TBL] [Abstract][Full Text] [Related]
3. NTF-3, a gene involved in the enteric nervous system development, as a candidate gene for Hirschsprung disease.
Ruiz-Ferrer M; Fernandez RM; Antiñolo G; Lopez-Alonso M; Borrego S
J Pediatr Surg; 2008 Jul; 43(7):1308-11. PubMed ID: 18639687
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].
Amiel J; Salomon R; Attié-Bitach T; Touraine R; Steffann J; Pelet A; Nihoul-Fékété C; Vekemans M; Munnich A; Lyonnet S
J Soc Biol; 2000; 194(3-4):125-8. PubMed ID: 11324313
[TBL] [Abstract][Full Text] [Related]
6. Mutational analysis of the RET and GDNF gene in children with hypoganglionosis.
Inoue K; Shimotake T; Tomiyama H; Iwai N
Eur J Pediatr Surg; 2001 Apr; 11(2):120-3. PubMed ID: 11371032
[TBL] [Abstract][Full Text] [Related]
7. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
Fitze G; Appelt H; König IR; Görgens H; Stein U; Walther W; Gossen M; Schreiber M; Ziegler A; Roesner D; Schackert HK
Hum Mol Genet; 2003 Dec; 12(24):3207-14. PubMed ID: 14600022
[TBL] [Abstract][Full Text] [Related]
8. Ancestral RET haplotype associated with Hirschsprung's disease shows linkage disequilibrium breakpoint at -1249.
Fernandez RM; Boru G; Peciña A; Jones K; López-Alonso M; Antiñolo G; Borrego S; Eng C
J Med Genet; 2005 Apr; 42(4):322-7. PubMed ID: 15805159
[TBL] [Abstract][Full Text] [Related]
9. [Association of single nucleotide polymorphisms of Axis inhibitor-2 gene rs224030, rs8081536, rs9913621 with Hirschsprung disease].
Gao H; Zhang J; Wang W; Zhang Z; Huang Y; Zhang S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):697-700. PubMed ID: 19065536
[TBL] [Abstract][Full Text] [Related]
10. Correlation between genetic variations in Hox clusters and Hirschsprung's disease.
Garcia-Barceló MM; Miao X; Lui VC; So MT; Ngan ES; Leon TY; Lau DK; Liu TT; Lao X; Guo W; Holden WT; Moore J; Tam PK
Ann Hum Genet; 2007 Jul; 71(Pt 4):526-36. PubMed ID: 17274802
[TBL] [Abstract][Full Text] [Related]
11. Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.
Fitze G; Cramer J; Serra A; Schreiber M; Roesner D; Schackert HK
Eur J Pediatr Surg; 2003 Jun; 13(3):152-7. PubMed ID: 12939698
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in central congenital hyperventilation syndrome patients by multiplex ligation-dependent probe amplification.
Serra A; Görgens H; Alhadad K; Fitze G; Schackert HK
Ann Hum Genet; 2010 Jul; 74(4):369-74. PubMed ID: 20456320
[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. Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in 80 patients with Hirschsprung disease (using multiplex ligation-dependent probe amplification).
Serra A; Görgens H; Alhadad K; Ziegler A; Fitze G; Schackert HK
Ann Hum Genet; 2009 Mar; 73(2):147-51. PubMed ID: 19183406
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Relationship between the type of RET/GDNF/NTN or SOX10 gene mutations and long-term results after surgery for total colonic aganglionosis with small bowel involvement.
Tomiyama H; Shimotake T; Ono S; Kimura O; Tokiwa K; Iwai N
J Pediatr Surg; 2001 Nov; 36(11):1685-8. PubMed ID: 11685702
[TBL] [Abstract][Full Text] [Related]
19. Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review).
Pusch CM; Sasiadek MM; Blin N
Int J Mol Med; 2002 Oct; 10(4):367-70. PubMed ID: 12239580
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]