Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Targeted Therapeutics for Cystic Fibrosis-Reference-Cited by-同舟云学术

Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Targeted Therapeutics for Cystic Fibrosis

Published:2024 Issue: Volume: Page:239-284
ISSN:
Container-title:Ion Channels as Targets in Drug Discovery
language:en
Short-container-title:

Author:

Veselu Diana-Florentina^ORCID,Yeh Han-I^ORCID,Rodrat Mayuree^ORCID,Bradbury Jacob D.^ORCID,Manzanares Fornies Yanira^ORCID,Li Hongyu^ORCID,Shoemark Deborah K.^ORCID,Oliveira A. Sofia F.^ORCID,Hwang Tzyh-Chang^ORCID,Sheppard David N.^ORCID

Publisher

Springer International Publishing

Link

https://link.springer.com/content/pdf/10.1007/978-3-031-52197-3_8

Reference299 articles.

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3. Al Salmani MK, Sondo E, Balut C, et al. Molecular physiology and pharmacology of the cystic fibrosis transmembrane conductance regulator. In: Hamilton KL, Devor DC, editors. Studies of epithelial transporters and ion channels, physiology in health and disease. 2nd ed. Rockville/Berlin: The American Physiological Society/Springer-Verlag; 2020. p. p605–70.

4. Aleksandrov L, Aleksandrov AA, Chang X-B, et al. The first nucleotide binding domain of cystic fibrosis transmembrane conductance regulator is a site of stable nucleotide interaction, whereas the second is a site of rapid turnover. J Biol Chem. 2002;277:15419–25.

5. Alton EWFW, Boyd AC, Davies JC, et al. Genetic medicines for CF: hype versus reality. Pediatr Pulmonol. 2016;51:S5–S17.

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