Cargando…
Potentiated L-type Ca(2+) Channels Rectify
Strong depolarization and dihydropyridine agonists potentiate inward currents through native L-type Ca(2+) channels, but the effect on outward currents is less clear due to the small size of these currents. Here, we examined potentiation of wild-type α(1C) and two constructs bearing mutations in con...
Autores principales: | Leuranguer, Valérie, Dirksen, Robert T., Beam, Kurt G. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217356/ https://www.ncbi.nlm.nih.gov/pubmed/12743165 http://dx.doi.org/10.1085/jgp.200308833 |
Ejemplares similares
-
Potentiation of the Cardiac L-Type Ca(2+) Channel (α(1C)) by Dihydropyridine Agonist and Strong Depolarization Occur via Distinct Mechanisms
por: Wilkens, Christina M., et al.
Publicado: (2001) -
Functional Impact of the Ryanodine Receptor on the Skeletal Muscle L-Type Ca(2+) Channel
por: Avila, Guillermo, et al.
Publicado: (2000) -
Role of Calcium Permeation in Dihydropyridine Receptor Function: Insights into Channel Gating and Excitation–Contraction Coupling
por: Dirksen, Robert T., et al.
Publicado: (1999) -
The Skeletal L-type Ca(2+) Current Is a Major Contributor to Excitation-coupled Ca(2+) entry
por: Bannister, Roger A., et al.
Publicado: (2009) -
Rectifying rectifier channels in Huntington disease
por: Proft, Juliane, et al.
Publicado: (2014)