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An imidazoline I1 receptor antagonist (Ki = 42 nM), selective for the imidazoline I1 receptor over alpha1-, alpha2A-, alpha2B-, and alpha2C-adrenergic receptors (Kis = >100, >20, >20, and >20 µM, respectively), binds to TMED9 in a thermal shift assay and releases MUC1-fs from TMED9-containing vesicles in kidney cells isolated from patients with MUC1 kidney disease, reduces kidney MUC1-fs accumulation in transgenic mice heterozygous for human MUC1-fs at 1, 10, and 50 mg/kg
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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