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Changes in the R‐region interactions depend on phosphorylation and contribute to PKA and PKC regulation of the cystic fibrosis transmembrane conductance regulator chloride channel.
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- FASEB Bioadvances, 2020, v. 2, n. 1, p. 33, doi. 10.1096/fba.2019-00053
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- Publication type:
- Article
ClC Channels and Transporters: Structure, Physiological Functions, and Implications in Human Chloride Channelopathies.
- Published in:
- Frontiers in Pharmacology, 2017, v. 8, p. 1, doi. 10.3389/fphar.2017.00151
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- Publication type:
- Article