The anti-protozoal drug pentamidine blocks KIR2.x-mediated inward rectifier 
current by entering the cytoplasmic pore region of the channel.

de Boer, T. P.; Nalos, L.; Stary, A.; Kok, B.; Houtman, M. J. C.; Antoons, G.; van Feen, T. A. B.; Beekman, J. D. M.; de Groot, B. L.; Opthof, T.; Rook, M. B.; Vos, M. A.; van der Heyden, M. A. G.

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The anti-protozoal drug pentamidine blocks K_IR2.x-mediated inward rectifier current by entering the cytoplasmic pore region of the channel.

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Stary, A.
Research Group of Computational Biomolecular Dynamics, MPI for biophysical chemistry, Max Planck Society;

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de Groot, B. L.
Research Group of Computational Biomolecular Dynamics, MPI for biophysical chemistry, Max Planck Society;

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de Boer, T. P., Nalos, L., Stary, A., Kok, B., Houtman, M. J. C., Antoons, G., et al. (2010). The anti-protozoal drug pentamidine blocks K_IR2.x-mediated inward rectifier current by entering the cytoplasmic pore region of the channel. British Journal of Pharmacology, 159(7), 1532-1541. Retrieved from http://www3.interscience.wiley.com/cgi-bin/fulltext/123301886/PDFSTART.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-D617-6

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