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The aim of humanization is to make specific antibodies generated in non-human immune systems suitable for administration to humans

Emerging formulation strategies for KPV, including PEGylated and liposomal delivery vehicles, aim to extend its 15-minute half-life and improve bioavailability for both injectable and oral contexts

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Here, we discuss the increasing evidence for redox dysregulation as an important and primary contributor to ALS pathogenesis, which is associated with multiple disease mechanisms

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