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10.1016/j.jhep.2019.08.005 113 MuhammadF.FanB.WangR.RenJ.JiaS.WangL.et al (2022)

Cornelia de Lange syndrome (CdLS) is a rare congenital genetic disorder Cornelia de Lange syndrome (CdLS) Associated symptoms typically include prenatal and postnatal growth delay, a characteristic shape of the craniofacial area, resulting in a distinctive facial appearance, and malformations of the upper limbs

NL-GHK-Cu increases the expression of antioxidant genes and inhibits the expression of pro-oxidant genes

These results highlight the possible therapeutic potential of cannabinoid drugs in the treatment of CICI

GSH exhibits a strong electron-donating character, owing to its sulfhydryl group on the cysteinyl position

silica group: after silica modeling, the mice were gavage - administered 1% CMC-Na for 6 days a week