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Pharmacological analysis of CFTR variants of cystic fibrosis using stem cell-derived organoids

Cystic fibrosis (CF) is a life-shortening genetic disease caused by mutations of CFTR, the gene encoding cystic fibrosis transmembrane conductance regulator. Despite considerable progress in CF therapies, targeting specific CFTR genotypes based on small molecules has been hindered because of the sub...

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Bibliografske podrobnosti
izdano v:Drug Discov Today
Main Authors: Chen, Kevin G., Zhong, Pingyu, Zheng, Wei, Beekman, Jeffrey M.
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6856431/
https://ncbi.nlm.nih.gov/pubmed/31173911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.drudis.2019.05.029
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