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Speck RM, DeMichele A, Farrar JT, Hennessy S, Mao JJ, Stineman MG, Barg FK

PAH deficiency leads to phenylketonuria (PKU), a metabolic disorder characterized by elevated phenylalanine levels and decreased tyrosine levels

Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family

In studies at the University of California at San Francisco, young (age 2025), male medical students were found to have about 200 nanograms/mL of GHK in their blood plasma, while the healthy, male medical school faculty (average age of 60) had only 80 nanograms/mL [9] In our studies, the LD50 (median lethal dose in 50% of mice) for GHK-Cu was 8 mgs per 25 g mice for GHK-Cu