Population
In vitro translation system and Xenopus oocytes expressing Kir3.1 and Kir3.2 subunits
Design
Preclinical
Authors
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Hypothesis-generating for GIRK channel assembly; leaves open roles in native cardiac physiology or therapy.
Multiple elements distributed throughout the Kir3.1 polypeptide, including the C-terminal domains, contribute to intersubunit binding interactions in G-protein-activated inwardly rectifying K+ channels.
Woodward et al. (1997) studied this question.
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