glutathione synthetase deficiency testing and anemia Hemolytic Anemia, Recurrent Metabolic Acidosis, and Incomplete Albinism Associated With Glutathione Glutathione synthetase deficiency | MedLink
Description
A cellular model for Friedreich ataxia reveals small-molecule glutathione peroxidase mimetics as novel treatment strategy
Targeting the periplasmic component of efflux pumps has been shown to sensitize the pathogen to various antimicrobials
On the other hand, Cu 2+ phenantroline complexes can lead to DNA damage ( DFO is a strong (but not entirely specific) chelator of Fe 3+
Idiopathic Parkinson's disease, progressive supranuclear palsy and glutathione metabolism in the substantia nigra of patients
Crit Care Med 2007, 35: S545-S552
This dimer is considered as the classical dimerization mode in GSTs
