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This targeted mechanism minimizes the risk of off-target effects and supports the compounds favorable safety profile

Melanoma cell surface-expressed phosphatidylserine as a therapeutic target for cationic anticancer peptide, temporin-1CEa

Jamet et al., 2015), and, as previously indicated, it is thought to be involved in competition between meningococcal strains that possess different toxins and IORFs for niche colonization

Neither compound has a clear superiority in clinical outcomes the choice is typically guided by physician preference, patient convenience, and regulatory context at the time of prescribing