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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...
Kaydedildi:
| Yayımlandı: | United European Gastroenterol J |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
SAGE Publications
2016
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| Konular: | |
| Online Erişim: | 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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