‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation-Reference-Cited by-同舟云学术

‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation

Published:2017-05-11 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Fermo Elisa,Bogdanova Anna,Petkova-Kirova Polina,Zaninoni Anna,Marcello Anna Paola,Makhro Asya,Hänggi Pascal,Hertz Laura,Danielczok Jens,Vercellati Cristina,Mirra Nadia,Zanella Alberto,Cortelezzi Agostino,Barcellini Wilma,Kaestner Lars,Bianchi Paola

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-01591-w.pdf

Reference50 articles.

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2. Fanger, C. M. et al. Calmodulin mediates calcium-dependent activation of the intermediate conductance KCa channel, IKCa1. J Biol Chem 274, 5746–5754, doi: 10.1074/jbc.274.9.5746 (1999).

3. Dyrda, A. et al. Local membrane deformations activate Ca2+-dependent K+ and anionic currents in intact human red blood cells. PLoS One 5, e9447, doi: 10.1371/journal.pone.0009447 (2010).

4. Wulff, H. & Köhler, R. Endothelial small-conductance and intermediate-conductance KCa channels: an update on their pharmacology and usefulness as cardiovascular targets. J Cardiovasc Pharmacol. 61, 102–112, doi: 10.1097/FJC.0b013e318279ba20 (2013).

5. Wulff, H. & Castle, N. A. Therapeutic potential of KCa3.1 blockers: recent advances and promising trends. Expert Rev Clin Pharmacol 3, 385–396, doi: 10.1586/ecp.10.11 (2010).

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