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These findings suggest that targeting the regulatory mechanisms of MLCSs may offer new therapeutic opportunities in PD, particularly for addressing amino acid imbalances in Parkin-associated PD
Chemical properties of water-soluble porphyrins
Wang T, Marquardt C, Foker J (1976) Aerobic glycolysis during lymphocyte proliferation
demonstrated that the carbonic anhydrase 1-kininogen and selenoprotein W/1433 signaling pathways mitigated the suppression of eNOS activity and facilitated NO production in a rat model of monocrotaline-induced PAH [62]
