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Arachidonic acid inhibition of L-type calcium (Ca(V)1.3b) channels varies with accessory Ca(V)β subunits
Arachidonic acid (AA) inhibits the activity of several different voltage-gated Ca(2+) channels by an unknown mechanism at an unknown site. The Ca(2+) channel pore-forming subunit (Ca(V)α(1)) is a candidate for the site of AA inhibition because T-type Ca(2+) channels, which do not require accessory s...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The Rockefeller University Press
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2699108/ https://ncbi.nlm.nih.gov/pubmed/19332620 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.200810047 |
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