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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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Detaylı Bibliyografya
Yayımlandı:United European Gastroenterol J
Asıl Yazarlar: Hohwieler, Meike, Perkhofer, Lukas, Liebau, Stefan, Seufferlein, Thomas, Müller, Martin, Illing, Anett, Kleger, Alexander
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: SAGE Publications 2016
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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