suggests that most of the observed receptors were blocked from the ‘outside.’
possibly by increasing spermine permeation
exclusively homomeric GluA1flip-containing combinations. However, given that NASPM was also uniformly effective in GluA2 KO CGCs, which are thought to express both flip and flop GluA4 splice forms
varying degrees of R/G editing
it seems unlikely that these posttranscriptional modifications influence the action of intracellular NASPM.
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