A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia-Reference-Cited by-同舟云学术

A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia

Published:2017-07-04 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Hasan Sonia,Bove Cecilia^ORCID,Silvestri Gabriella,Mantuano Elide,Modoni Anna,Veneziano Liana,Macchioni Lara,Hunter Therese,Hunter Gary,Pessia Mauro,D’Adamo Maria Cristina

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-03041-z.pdf

Reference49 articles.

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2. Wykes, R. C. et al. Optogenetic and Potassium Channel Gene Therapy in a Rodent Model of Focal Neocortical Epilepsy. Sci transl med 4, 161ra152–161ra152, doi: 10.1126/scitranslmed.3004190 (2012).

3. Kole, M. H. P., Letzkus, J. J. & Stuart, G. J. Axon initial segment Kv1 channels control Axonal action potential Waveform and Synaptic efficacy. Neuron 55, 633–647, doi: 10.1016/j.neuron.2007.07.031 (2007).

4. Rasband, M. N. & Trimmer, J. S. Subunit composition and novel localization of K+ channels in spinal cord. J Comp Neurol 429, 166–176, doi: 10.1002/(ISSN)1096-9861 (2000).

5. Geiger, J. R. P. & Jonas, P. Dynamic control of Presynaptic Ca2+ inflow by Fast-Inactivating K+ channels in Hippocampal Mossy fiber Boutons. Neuron 28, 927–939, doi: 10.1016/S0896-6273(00)00164-1 (2000).

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