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A novel transgenic rabbit model with reduced repolarization reserve: long QT syndrome caused by a dominant‐negative mutation of the KCNE1 gene
BACKGROUND AND PURPOSE: The reliable assessment of proarrhythmic risk of compounds under development remains an elusive goal. Current safety guidelines focus on the effects of blocking the KCNH2/HERG ion channel‐in tissues and animals with intact repolarization. Novel models with better predictive v...
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Publicado no: | Br J Pharmacol |
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Main Authors: | , , , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
John Wiley and Sons Inc.
2016
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4882500/ https://ncbi.nlm.nih.gov/pubmed/27076034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bph.13500 |
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