123 related articles for article (PubMed ID: 18661771)
1. The relationship between expressions of the laminin gene and RET gene in Hirschsprung's disease.
Li AW; Zhang WT; Wang R; Feng JB; Ruan Y
World J Pediatr; 2008 May; 4(2):135-9. PubMed ID: 18661771
[TBL] [Abstract][Full Text] [Related]
2. Altered RET gene mRNA expression in Hirschsprung's disease.
Kusafuka T; Puri P
J Pediatr Surg; 1997 Apr; 32(4):600-4. PubMed ID: 9126763
[TBL] [Abstract][Full Text] [Related]
3. [Immunohistochemical study of RET protein in Hirschsprung's disease and allied Hirschsprung's disorder].
Zhang X; Wang X; Mei SP; Dong DC; Zhang Y
Zhonghua Er Ke Za Zhi; 2005 Dec; 43(12):911-5. PubMed ID: 16412353
[TBL] [Abstract][Full Text] [Related]
4. Altered expression of laminin alpha1 in aganglionic colon of endothelin receptor-B null mouse model of Hirschsprung's disease.
Fujiwara N; Nakazawa-Tanaka N; Miyahara K; Arikawa-Hirasawa E; Akazawa C; Yamataka A
Pediatr Surg Int; 2018 Feb; 34(2):137-141. PubMed ID: 28983681
[TBL] [Abstract][Full Text] [Related]
5. Expression patterns of CXCR4 in different colon tissue segments of patients with Hirschsprung's disease.
Ding X; Zhao Z; Duan W; Wang S; Jin X; Xiang L; Jin X
Exp Mol Pathol; 2013 Aug; 95(1):111-6. PubMed ID: 23769877
[TBL] [Abstract][Full Text] [Related]
6. RET gene is a major risk factor for Hirschsprung's disease: a meta-analysis.
Tomuschat C; Puri P
Pediatr Surg Int; 2015 Aug; 31(8):701-10. PubMed ID: 26164711
[TBL] [Abstract][Full Text] [Related]
7. Expression of dishevelled gene in Hirschsprung's disease.
Chen D; Mi J; Wu M; Wang W; Gao H
Int J Clin Exp Pathol; 2013; 6(9):1791-8. PubMed ID: 24040443
[TBL] [Abstract][Full Text] [Related]
8. Expression of RET proto-oncogene and GDNF deficit in Hirschsprung's disease.
Zhan J; Xiu Y; Gu J; Fang Z; Hu XL
J Pediatr Surg; 1999 Nov; 34(11):1606-9. PubMed ID: 10591552
[TBL] [Abstract][Full Text] [Related]
9. The effect of laminin-1 on enteric neural crest-derived cell migration in the Hirschsprung's disease mouse model.
Nakazawa-Tanaka N; Fujiwara N; Miyahara K; Nakada S; Arikawa-Hirasawa E; Akazawa C; Urao M; Yamataka A
Pediatr Surg Int; 2018 Feb; 34(2):143-147. PubMed ID: 29018955
[TBL] [Abstract][Full Text] [Related]
10. Studies of RET gene expression and acetylcholinesterase activity in a series of sporadic Hirschsprung's disease.
Coelho MC; Tannuri U; Benditt I; Santos MM
Pediatr Surg Int; 2008 Sep; 24(9):1017-21. PubMed ID: 18665368
[TBL] [Abstract][Full Text] [Related]
11. Altered endothelin-3 and endothelin-B receptor mRNA expression in Hirschsprung's disease.
Oue T; Puri P
J Pediatr Surg; 1999 Aug; 34(8):1257-60. PubMed ID: 10466607
[TBL] [Abstract][Full Text] [Related]
12. Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease.
Moore SW; Zaahl MG
J Pediatr Surg; 2014 Feb; 49(2):258-61; discussion 261. PubMed ID: 24528961
[TBL] [Abstract][Full Text] [Related]
13. Reduced expression of voltage-gated Kv11.1 (hERG) K(+) channels in aganglionic colon in Hirschsprung's disease.
Tomuschat C; O'Donnell AM; Coyle D; Puri P
Pediatr Surg Int; 2016 Jan; 32(1):9-16. PubMed ID: 26519040
[TBL] [Abstract][Full Text] [Related]
14. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
Edery P; Pelet A; Mulligan LM; Abel L; AttiƩ T; Dow E; Bonneau D; David A; Flintoff W; Jan D
J Med Genet; 1994 Aug; 31(8):602-6. PubMed ID: 7815416
[TBL] [Abstract][Full Text] [Related]
15. Hirschsprung's disease: a search for etiology.
Puri P; Ohshiro K; Wester T
Semin Pediatr Surg; 1998 Aug; 7(3):140-7. PubMed ID: 9718651
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Genetic bases of Hirschsprung's disease].
Passarge E; Bruder E
Pathologe; 2007 Mar; 28(2):113-8. PubMed ID: 17285323
[TBL] [Abstract][Full Text] [Related]
18. L1cam acts as a modifier gene during enteric nervous system development.
Wallace AS; Schmidt C; Schachner M; Wegner M; Anderson RB
Neurobiol Dis; 2010 Dec; 40(3):622-33. PubMed ID: 20696247
[TBL] [Abstract][Full Text] [Related]
19. SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.
Sham MH; Lui VC; Fu M; Chen B; Tam PK
Gut; 2001 Aug; 49(2):220-6. PubMed ID: 11454798
[TBL] [Abstract][Full Text] [Related]
20. Discrepancy between macroscopic and microscopic transitional zones in Hirschsprung's disease with reference to the type of RET/GDNF/SOX10 gene mutation.
Shimotake T; Tomiyama H; Aoi S; Iwai N
J Pediatr Surg; 2003 May; 38(5):698-701. PubMed ID: 12720173
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]