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 *

110 related articles for article (PubMed ID: 23053599)

  • 1. RET promoter variations in familial African degenerative leiomyopathy (ADL): first report of a possible genetic-environmental interaction.
    Van Rensburg C; Moore SW; Zaahl M
    Pediatr Surg Int; 2012 Dec; 28(12):1235-8. PubMed ID: 23053599
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recurrent ACTG2 gene variation in African degenerative visceral leiomyopathy.
    Maluleke T; Mangray H; Arnold M; Moore HA; Moore SW
    Pediatr Surg Int; 2019 Apr; 35(4):439-442. PubMed ID: 30430282
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Clinical and genetic correlations of familial Hirschsprung's disease.
    Moore SW; Zaahl M
    J Pediatr Surg; 2015 Feb; 50(2):285-8. PubMed ID: 25638620
    [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. Chronic intestinal pseudo-obstruction in a child harboring a founder Hirschsprung RET mutation.
    Rossi V; Mosconi M; Nozza P; Murgia D; Mattioli G; Ceccherini I; Pini Prato A
    Am J Med Genet A; 2016 Sep; 170(9):2400-3. PubMed ID: 27273837
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hirschsprung's disease as a model of complex genetic etiology.
    Borrego S; Ruiz-Ferrer M; Fernández RM; Antiñolo G
    Histol Histopathol; 2013 Sep; 28(9):1117-36. PubMed ID: 23605783
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Occurrence of MEN 2a in familial Hirschsprung's disease: a new indication for genetic testing of the RET proto-oncogene.
    Decker RA; Peacock ML
    J Pediatr Surg; 1998 Feb; 33(2):207-14. PubMed ID: 9498388
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 "Janus" genetic variation.
    Moore SW; Zaahl M
    J Pediatr Surg; 2010 Feb; 45(2):393-6. PubMed ID: 20152359
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.
    Moore SW; Zaahl MG
    Pediatr Surg Int; 2008 May; 24(5):521-30. PubMed ID: 18365214
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
    Edery P; Pelet A; Mulligan LM; Abel L; Attié 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]  

  • 13. Perturbation of hoxb5 signaling in vagal neural crests down-regulates ret leading to intestinal hypoganglionosis in mice.
    Lui VC; Cheng WW; Leon TY; Lau DK; Garcia-Barcelo MM; Miao XP; Kam MK; So MT; Chen Y; Wall NA; Sham MH; Tam PK
    Gastroenterology; 2008 Apr; 134(4):1104-15. PubMed ID: 18395091
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Increased RET Activity Coupled with a Reduction in the
    Okamoto M; Uesaka T; Ito K; Enomoto H
    eNeuro; 2021; 8(3):. PubMed ID: 33958373
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Oncological implications of RET gene mutations in Hirschsprung's disease.
    Sijmons RH; Hofstra RM; Wijburg FA; Links TP; Zwierstra RP; Vermey A; Aronson DC; Tan-Sindhunata G; Brouwers-Smalbraak GJ; Maas SM; Buys CH
    Gut; 1998 Oct; 43(4):542-7. PubMed ID: 9824583
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immunohistochemical localization of RET protein in Hirschsprung's disease.
    Martucciello G; Favre A; Takahashi M; Jasonni V
    J Pediatr Surg; 1995 Mar; 30(3):433-6. PubMed ID: 7760237
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.