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Pediatr Nephrol 12 : 492497 Coor C, Salmon RF, Quigley R, Marver D, Baum M 1991 Role of adenosine triphosphate (ATP) and Na-K-ATPase in the inhibition of proximal tubular transport with intracellular cystine loading

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A simple isotopic labeling method to study cysteine oxidation in alzheimer's disease: oxidized cysteine-selective dimethylation (OxcysDML)

Phenylketonuria (OMIM ID 261600) Phenylketonuria (PKU), also known as phenylalanine hydroxylase (PAH) deficiency or Flling disease, is an autosomal recessive inborn error of phenylalanine (Phe) metabolism [181]

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