| Q24298668 | A novel missense mutation in the gamma-glutamylcysteine synthetase catalytic subunit gene causes both decreased enzymatic activity and glutathione production |
| Q70424031 | A tentative classification of recessively inherited ataxias |
| Q69217279 | A therapeutic trial with N-acetylcysteine in subjects with hereditary glutathione synthetase deficiency (5-oxoprolinuria) |
| Q34069114 | An ethnic-specific polymorphism in the catalytic subunit of glutamate-cysteine ligase impairs the production of glutathione intermediates in vitro. |
| Q69827470 | Blood cells as markers for metabolic disorders |
| Q40145697 | Clinical significance of the glutathione-conjugating system |
| Q39131539 | Glutathione Metabolism and Some Possible Functions of Glutathione in the Nervous System |
| Q21203014 | Inborn errors in the metabolism of glutathione |
| Q33831082 | Mitochondrial damage in muscle occurs after marked depletion of glutathione and is prevented by giving glutathione monoester |
| Q40085021 | On the Cycles of Glutathione Metabolism and Transport |
| Q38069523 | On the Function of the γ-Glutamyl Cycle in the Transport of Amino Acids and Peptides |
| Q74811878 | Patients with genetic defects in the gamma-glutamyl cycle |
| Q39105656 | Possible Role of Glutathione in Transport Processes |
| Q68890171 | Profiling of amino acids in body fluids and tissues by means of liquid chromatography |
| Q37560726 | Radioprotection by glutathione ester: transport of glutathione ester into human lymphoid cells and fibroblasts |
| Q39293102 | The Glutathione Status of Cells |
| Q41560823 | The effects of chronic isoniazid intoxication on motor end plate sprouting in rat sternocostalis muscle and on responses to partial denervation and local botulinum toxin |
| Q72580394 | The problems of neurons with long axons |
| Q35209651 | Unveiling the roles of the glutathione redox system in vivo by analyzing genetically modified mice |