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Preserving CI function with NDI1 expression maintained adipogenic and lipogenic transcription in adipocytes lacking the circadian clock

eubiosis), intestinal barrier integrity, systemic inflammation, insulin resistance, dyslipidemia, adipose tissue accumulation, and immune cell responses (TLR4, TLR2, Treg, Th1, Th2, Th17), culminating in adverse obesity rather than a healthy metabolic condition

When 14C-4-androstenedione was used as substrate (Figure 1), it was metabolised mainly to the diols, testosterone (T), DHT and androstanedione (A)