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Description
Eligibility criteria included studies on healthy human subjects, treated for at least 12 weeks with LC administered orally, with no drugs or any other multi-ingredient supplements co-ingestion
Psychooncology 17 (3): 270-9, 2008
S2CID 22103245
Arch Dermatol 1985
Informed Consent The necessary informed consent was obtained in this study
In vivo LNP delivery of fLuc saRNA Given the high efficiency of our in vitro transfections, we wanted to characterize whether these formulations were capable of delivering saRNA in vivo, as it has been well established in the field that in vitro results are often non-predictive [32]
