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In hepatocytes, oxalate overload caused mitochondrial dysfunction and lipid accumulation by inhibiting the transcription of peroxisome proliferator-activated receptor and blocking mitochondrial FAO

We demonstrate the power and potential of this strategy for the preparation of various challenging targets in the efficient chemical syntheses of -conotoxin SI peptide, RANTES protein from the chemokine family, EETI-II trypsin inhibitor knotted mini protein, plectasin antimicrobial peptide and the linaclotide peptide drug

consequently, astrocyte dysfunction can impair synaptic transmission, induce excitotoxicity, and cognitive and motor impairments (Dodge et al., 2013)

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