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Interestingly, whilst the FFE689-91 residues appeared to be essential for SNX17 binding, the FFE689-91AAA mutant bound RABGAP1 with approximately a 3-fold increase

However, existing in vitro BBB models cannot mimic these dynamic pathological changes and spatial heterogeneity, leading to fundamental limitations in predicting drug permeability and the therapeutic window

Souhaitons que cette explication rduise en partie la confusion, plutt que den crer davantage

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