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Consequently, the current transcriptional data with n = 3 can only suggest that LT may regulate the transcriptional level of the androgen synthesis network, but cannot confirm its functional consequences

Given the potential impact of these factors on the quantification of GSH, here we examined if the type of anticoagulant used during sample collection (heparin or EDTA), deproteinization of plasma prior to storage (yes or no), storage temperature (80 o C or 4 o C), and processing time (duration of time between collection of whole blood and deproteinization of plasma) impact levels of free GSH and GSSG, in plasma

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In contrast, K d-la and K ce are produced by nonenzymatic reactions as a result of chemically reactive glycolytic by-products escaping from the cellular detoxification system

Regulation of Expression of Steroidogenic Enzymes in Leydig Cells