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The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress

Parallel increases in markers of oxidative stress during sleep deprivation demonstrate that the capacity to undergo redox reactions is biochemically constrained during time spent awake by the availability of NAD+ as an oxidizing substrate [7,8]

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Oocyte-derived E-cadherin acts as a multiple functional factor maintaining the primordial follicle pool in mice

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