SLC26A9 in airways and intestine: secretion or absorption?
Author:
Affiliation:
1. Institut für Physiologie, Universität, Universitätsstraße 31, Regensburg, Germany
2. Department of Gastroenterology, Hannover Medical School, Hannover, Germany
Funder
Deutsche Forschungsgemeinschaft
UK CF Trust
Publisher
Informa UK Limited
Subject
Biochemistry,Biophysics
Link
https://www.tandfonline.com/doi/pdf/10.1080/19336950.2023.2186434
Reference85 articles.
1. Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): Physiological and pathophysiological relevance
2. Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling
3. Structural insights into the gating mechanism of human SLC26A9 mediated by its C-terminal sequence
4. Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9
5. Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
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