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Gfra1 Underexpression Causes Hirschsprung’s Disease and Associated Enterocolitis in Mice
BACKGROUND & AIMS: RET, the receptor for the glial cell line–derived neurotrophic factor (GDNF) family ligands, is the most frequently mutated gene in congenital aganglionic megacolon or Hirschsprung’s disease (HSCR). The leading cause of mortality in HSCR is HSCR-associated enterocolitis (HAEC)...
Tallennettuna:
| Julkaisussa: | Cell Mol Gastroenterol Hepatol |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6444303/ https://ncbi.nlm.nih.gov/pubmed/30594740 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcmgh.2018.12.007 |
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