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Stem cell-derived organoids to model gastrointestinal facets of cystic fibrosis
Cystic fibrosis (CF) is one of the most frequently occurring inherited human diseases caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) which lead to ample defects in anion transport and epithelial fluid secretion. Existing models lack both access to early stages...
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| Udgivet i: | United European Gastroenterol J |
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| Main Authors: | , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
SAGE Publications
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5548342/ https://ncbi.nlm.nih.gov/pubmed/28815024 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050640616670565 |
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