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However, two-dimensional correlated spectroscopy (2D COSY) resolves overlapping resonances of these metabolites unambiguously by introducing a second spectral dimension and identifying cross-peak resonances because of J-coupling interactions [137]
the various methods differ in sensitivity, specificity (in particular, in distinguishing GSH from GSSG and other thiols), and susceptibility to matrix interference [119]
Every SARM initially starts in a powder state
(b) ubiquitination and subsequent degradation of IB- by the 26S proteasome
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