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(2016) 37:e140

Cystinosis stands as a prototypic disorder for a subgroup of lysosomal storage diseases caused by defective lysosomal transporters [2]

An increased F2-isoprostane result may reflect smoking, metabolic dysfunction, inflammation, or another source of oxidative activity

The cellular models in this recent study also demonstrated the profound regenerative capabilities of liposomal delivery

Research parameters include absorption kinetics, systemic distribution, first-pass metabolic avoidance, and potential olfactory or trigeminal transport pathways to the central nervous system