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

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1ch) that confer different biophysical properties including sensitivity to Mg 2+ block, sensitivity to allosteric modulators, deactivation time course, single channel conductance, channel open probability for an agonist-bound receptor, and agonist potency (Fig

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Every couple of days, a small amount of oil should be added to the pack to keep it fully saturated
