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[4] In humans, Keutel syndrome is a rare recessive genetic disorder associated with abnormalities in the gene coding for MGP and characterized by abnormal diffuse cartilage calcification

GHKCu suppresses NFB (including p65 activation) and downstream cytokines such as IL6 and TNF, and simultaneously reduces reactive oxygen species

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Cellular uptake studies revealed a 5.3-fold increase in drug internalization in Caco-2 cells when encapsulated in nanoparticles

Induction of programmed cell death Injury-induced necrosis results in the release of DAMPs from renal endothelial and epithelial cells