تحميل...
Mutant MiRP1 subunits modulate HERG K(+) channel gating: a mechanism for pro-arrhythmia in long QT syndrome type 6
Mutations in KCNE2, which encodes the minK-related protein 1 (MiRP1), are associated with an increased risk of arrhythmias; however, the underlying mechanisms are unknown. MiRP1 is thought to associate with many K(+) channel α-subunits, including HERG K(+) channels, which have a major role in suppre...
محفوظ في:
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Blackwell Science Inc
2003
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| الموضوعات: | |
| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2343156/ https://ncbi.nlm.nih.gov/pubmed/12923204 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2003.046045 |
| الوسوم: |
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