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Intratumoral Glycine levels were quantified using cross-platform global metabolomic profiling
The human dopamine transporter (hDAT) contains a high-affinity, extracellular, and allosteric Zn 2+ (zinc ion) binding site which, upon zinc binding, inhibits dopamine reuptake, inhibits amphetamine-induced hDAT internalization, and amplifies amphetamine-induced dopamine efflux
doi: 10.3389/fnut.2022.861664 9 XuDLiuLZhaoYYangLChengJHuaRet al
LisabethLDSNCHEZBNLimDChervinRDCaseEMorgensternLBet al
Trn thc t, Glutathione phn ng vi mt lng ln cc cht chuyn ha hu c b oxy ha, to ra cc hp cht lin hp t c hi hn, c th d dng chuyn ha v loi b di dng acid Mercapturic
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