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Potentiation of the Cardiac L-Type Ca(2+) Channel (α(1C)) by Dihydropyridine Agonist and Strong Depolarization Occur via Distinct Mechanisms
A defining property of L-type Ca(2+) channels is their potentiation by both 1,4-dihydropyridine agonists and strong depolarization. In contrast, non–L-type channels are potentiated by neither agonist nor depolarization, suggesting that these two processes may by linked. In this study, we have tested...
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| Autori principali: | , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The Rockefeller University Press
2001
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2233833/ https://ncbi.nlm.nih.gov/pubmed/11696608 |
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