Calcium-activated potassium channels
Current Opinion in Neurobiology, ISSN: 0959-4388, Vol: 8, Issue: 3, Page: 321-329
1998
- 662Citations
- 374Captures
- 2Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations662
- Citation Indexes662
- 662
- CrossRef520
- Captures374
- Readers374
- 374
- Mentions2
- References2
- 2
Article Description
Calcium-activated potassium channels are fundamental regulators of neuronal excitability, participating in interspike interval and spike-frequency adaptation. For large-conductance calcium-activated potassium (BK) channels, recent experiments have illuminated the fundamental biophysical mechanisms of gating, demonstrating that BK channels are voltage gated and calcium modulated. Structurally, BK channels have been shown to possess an extracellular amino-terminal domain, different from other potassium channels. Domains and residues involved in calcium-gating, and perhaps calcium binding itself, have been identified. For small- and intermediate-conductance calcium-activated potassium channels, SK and IK channels, clones have only recently become available, and they show that SK channels are a distinct subfamily of potassium channels. The biophysical properties of SK channels demonstrate that kinetic differences between apamin-sensitive and apamin-insensitive slow afterhyperpolarizations are not attributable to intrinsic gating differences between the two subtypes. Interestingly, SK and IK channels may prove effective drug targets for diseases such as myotonic muscular dystrophy and sickle cell anemia.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0959438898800561; http://dx.doi.org/10.1016/s0959-4388(98)80056-1; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0032103066&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/9687354; https://linkinghub.elsevier.com/retrieve/pii/S0959438898800561; http://linkinghub.elsevier.com/retrieve/pii/S0959438898800561; http://api.elsevier.com/content/article/PII:S0959438898800561?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0959438898800561?httpAccept=text/plain; http://dx.doi.org/10.1016/s0959-4388%2898%2980056-1
Elsevier BV
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