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Impaired Inactivation of L-Type Ca(2+) Current as a Potential Mechanism for Variable Arrhythmogenic Liability of HERG K(+) Channel Blocking Drugs
The proarrhythmic effects of new drugs have been assessed by measuring rapidly activating delayed-rectifier K(+) current (I(Kr)) antagonist potency. However, recent data suggest that even drugs thought to be highly specific I(Kr) blockers can be arrhythmogenic via a separate, time-dependent pathway...
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Publicado no: | PLoS One |
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Main Authors: | , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Public Library of Science
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4772914/ https://ncbi.nlm.nih.gov/pubmed/26930604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0149198 |
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