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The ability to quantify the extent of glutathionylation would represent a substantial improvement in this approach, but would require double labelling using two different labels for the protein of interest and the BioGEE and as such poses significant technical challenges

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Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation

American Journal Of Physiology 1982, 242: g313-g318

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