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ΔF508-CFTR Modulator Screen Based on Cell Surface Targeting of a Chimeric Nucleotide Binding Domain 1 Reporter

The most common cystic fibrosis–causing mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) is deletion of phenylalanine at residue 508 (ΔF508). The ΔF508 mutation impairs folding of nucleotide binding domain 1 (NBD1) and interfacial interactions of NBD1 and the membrane spann...

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Detalhes bibliográficos
Publicado no:SLAS Discov
Main Authors: Phuan, Puay-Wah, Veit, Guido, Tan, Joseph-Anthony, Roldan, Ariel, Finkbeiner, Walter E., Haggie, Peter M., Lukacs, Gergely L., Verkman, Alan S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6133293/
https://ncbi.nlm.nih.gov/pubmed/29533733
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2472555218763310
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