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Disease: Glutathionuria

  • Characterization and physiological function of rat renal gamma-glutamyltranspeptidase
  • Glutathionuria: gamma-glutamyl transpeptidase deficiency
  • Glutathionuria: inborn error of metabolism due to tissue deficiency of gamma-glutamyl transpeptidase
  • Inborn errors in the metabolism of glutathione
  • Inhibition of gamma-glutamyl transpeptidase and induction of glutathionuria by gamma-glutamyl amino acids
  • L-2-oxothiazolidine-4-carboxylate supplementation in murine gamma-GT deficiency
  • Mice with genetic gamma-glutamyl transpeptidase deficiency exhibit glutathionuria, severe growth failure, reduced life spans, and infertility
  • New aspects of glutathione metabolism and translocation in mammals
  • Translocation of intracellular glutathione to membrane-bound gamma-glutamyl transpeptidase as a discrete step in the gamma-glutamyl cycle: glutathionuria after inhibition of transpeptidase
  • Two Japanese brothers with hereditary gamma-glutamyl transpeptidase deficiency
  • γ-glutamyl transpeptidase deficiency caused by a large homozygous intragenic deletion in GGT1
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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