These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

62 related articles for article (PubMed ID: 9094028)

  • 1. Mutation analysis of the RET, the endothelin-B receptor, and the endothelin-3 genes in sporadic cases of Hirschsprung's disease.
    Kusafuka T; Wang Y; Puri P
    J Pediatr Surg; 1997 Mar; 32(3):501-4. PubMed ID: 9094028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comprehensive characterization of the genetic landscape of familial Hirschsprung's disease.
    Xiao J; Hao LW; Wang J; Yu XS; You JY; Li ZJ; Mao HD; Meng XY; Feng JX
    World J Pediatr; 2023 Jul; 19(7):644-651. PubMed ID: 36857021
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Abnormalities of the enteric nervous system in heterozygous endothelin B receptor deficient (spotting lethal) rats resembling intestinal neuronal dysplasia.
    von Boyen GB; Krammer HJ; Süss A; Dembowski C; Ehrenreich H; Wedel T
    Gut; 2002 Sep; 51(3):414-9. PubMed ID: 12171966
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A gene regulatory network explains RET-EDNRB epistasis in Hirschsprung disease.
    Chatterjee S; Chakravarti A
    Hum Mol Genet; 2019 Sep; 28(18):3137-3147. PubMed ID: 31313802
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new experimental approach is required in the molecular analysis of intestinal neuronal dysplasia type B patients.
    Sánchez-Mejías A; Fernández RM; Antiñolo G; Borrego S
    Exp Ther Med; 2010 Nov; 1(6):999-1003. PubMed ID: 22993632
    [TBL] [Abstract][Full Text] [Related]  

  • 6. High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease.
    Ding HY; Lei W; Xiao SJ; Deng H; Yuan LK; Xu L; Zhou JL; Huang R; Fang YL; Wang QY; Zhang Y; Zhang L; Zhu XC
    Pediatr Surg Int; 2024 Jan; 40(1):38. PubMed ID: 38253735
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High intestinal vascular permeability in a murine model for Hirschsprung's disease: implications for postoperative Hirschsprung-associated enterocolitis.
    Suda K; Yamada S; Miyahara K; Fujiwara N; Kosaka S; Abe K; Seo S; Nakamura S; Lane GJ; Yamataka A
    Pediatr Surg Int; 2022 Nov; 39(1):15. PubMed ID: 36449111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A potential regulatory region near the EDN3 gene may control both harness racing performance and coat color variation in horses.
    Jäderkvist Fegraeus K; Velie BD; Axelsson J; Ang R; Hamilton NA; Andersson L; Meadows JRS; Lindgren G
    Physiol Rep; 2018 May; 6(10):e13700. PubMed ID: 29845762
    [TBL] [Abstract][Full Text] [Related]  

  • 9. RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling.
    Widowati T; Melhem S; Patria SY; de Graaf BM; Sinke RJ; Viel M; Dijkhuis J; Sadewa AH; Purwohardjono R; Soenarto Y; Hofstra RM; Sribudiani Y
    Eur J Hum Genet; 2016 Jun; 24(6):823-9. PubMed ID: 26395553
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Knockout mouse models of Hirschsprung's disease.
    Zimmer J; Puri P
    Pediatr Surg Int; 2015 Sep; 31(9):787-94. PubMed ID: 26137873
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Impaired Cellular Immunity in the Murine Neural Crest Conditional Deletion of Endothelin Receptor-B Model of Hirschsprung's Disease.
    Gosain A; Barlow-Anacker AJ; Erickson CS; Pierre JF; Heneghan AF; Epstein ML; Kudsk KA
    PLoS One; 2015; 10(6):e0128822. PubMed ID: 26061883
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Enterocolitis causes profound lymphoid depletion in endothelin receptor B- and endothelin 3-null mouse models of Hirschsprung-associated enterocolitis.
    Frykman PK; Cheng Z; Wang X; Dhall D
    Eur J Immunol; 2015 Mar; 45(3):807-17. PubMed ID: 25487064
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic basis of Hirschsprung's disease.
    Tam PK; Garcia-Barceló M
    Pediatr Surg Int; 2009 Jul; 25(7):543-58. PubMed ID: 19521704
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 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. Exon 5 of the RET proto-oncogene: a newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg.
    Dvorakova S; Vaclavikova E; Duskova J; Vlcek P; Ryska A; Bendlova B
    J Endocrinol Invest; 2005 Nov; 28(10):905-9. PubMed ID: 16419493
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Animal models in pediatric surgery.
    Mortell A; Montedonico S; Puri P
    Pediatr Surg Int; 2006 Feb; 22(2):111-28. PubMed ID: 16331525
    [No Abstract]   [Full Text] [Related]  

  • 19. Novel mutation of Endothelin-B receptor gene in Waardenburg-Hirschsprung disease.
    Sangkhathat S; Chiengkriwate P; Kusafuka T; Patrapinyokul S; Fukuzawa M
    Pediatr Surg Int; 2005 Dec; 21(12):960-3. PubMed ID: 16237557
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.
    Gath R; Goessling A; Keller KM; Koletzko S; Coerdt W; Müntefering H; Wirth S; Hofstra RM; Mulligan L; Eng C; von Deimling A
    Gut; 2001 May; 48(5):671-5. PubMed ID: 11302967
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.