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Neuronal-microglial interactions in the medial temporal lobes (MTL) are believed to regulate memory related processes such as LTP and neurogenesis.
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In rodents, clock genes drive circadian rhythms in white blood cell function, and glucocorticoids are believed to regulate these rhythms.
Tyrosine phosphorylation of flagellar proteins, occurring during sperm capacitation, is believed to regulate sperm motility [24].
Each miR is believed to regulate multiple genes.
p38 is believed to regulate both apoptosis and autophagy.
Cxs have long been believed to regulate chemoresistance by exerting GJIC.
Now, Sirt1 is believed to regulate apoptotic thresholds by deacetylating p53 [ 6, 12].
Cxs have long been believed to regulate tumor development during carcinogenesis by exerting GJIC.
Myc is believed to regulate expression of 15% of all genes [ 77].
There, it is believed to regulate the ER machinery responsible for Ca2+ release.
Discrete and independent circadian and homeostatic processes are believed to regulate sleep.
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