• 3-mercaptolactate cysteine disulfiduria: biochemical studies on affected and unaffected members of a family
• 3-Mercaptopyruvate sulfurtransferase activity in guinea pig and rat tissues
• A new familial malformation syndrome
• Abnormal cholesterol metabolism in the Smith-Lemli-Opitz syndrome: report of clinical and biochemical findings in four patients and treatment in one patient
• Antioxidant enzyme, 3-mercaptopyruvate sulfurtransferase-knockout mice exhibit increased anxiety-like behaviors: a model for human mercaptolactate-cysteine disulfiduria
• beta-Mercaptolactate cysteine disulfiduria in two normal sisters. Isolation and characterization of beta-mercaptolactate cysteine disulfide
• Birth defect syndromes in which orthopedic problems may be overlooked
• Evidence for a functional genetic polymorphism of the human mercaptopyruvate sulfurtransferase (MPST), a cyanide detoxification enzyme
• Increased Urinary 3-Mercaptolactate Excretion and Enhanced Passive Systemic Anaphylaxis in Mice Lacking Mercaptopyruvate Sulfurtransferase, a Model of Mercaptolactate-Cysteine Disulfiduria
• Metabolism ofL-cysteine via transamination pathway (3-mercaptopyruvate pathway)
• Redox regulation of mammalian 3-mercaptopyruvate sulfurtransferase
• Regulation of mercaptopyruvate sulfurtransferase activity via intrasubunit and intersubunit redox-sensing switches
• The mercaptopyruvate pathway in cysteine catabolism: a physiologic role and related disease of the multifunctional 3-mercaptopyruvate sulfurtransferase