It has been previously described that S. cerevisiae strains present different patterns of gene expression according to environmental stress factors (James et al. 2003; Kvitek et al. 2008).
In the present study, we report 12 CpGs, 2 of which had not been previously described, that are differentially methylated in smokers compared with nonsmokers.
It has been previously described that gene expression values for the inactive state often follow an exponential distribution, while the values corresponding to the activated state tend to follow a normal distribution [ 26].
Moreover, it has been previously described that acetic acid enters glucose-repressed yeast cells primarily by facilitated diffusion through Fps1.
It has been previously described that expression of the membrane-bound death receptor ligand FasL is mediated by NFAT [37].
It has been previously described that considerable natural variation in gene expression levels exists within and among human populations [49].
It has been previously described that AAP overdose is the most common cause of acute liver failure (ALF) in western countries [51], [52].
It has been previously described that cofilin-actin rods are not detected by rhodamine-phalloidin, even though rhodamine-phalloidin normally binds filamentous actin.
It has been previously described that overexpression of the ARF6 exchange factor, EFA6, increases the amount of ARF6 bound to GST-GGA3 beads.
It has been previously described that Securin−/−/Separase+/S1121A double mutant ES cells [30], Hela cells over-expressing human S1126A mutant Separase [31], and male Separase S1121A mutant PGCs undergo aberrant mitosis and mitotic arrest, resulting in aneuploidy [28].
Interestingly, it has been previously described that some promoters are only accessible for transcription factors during S-phase thanks to the loose chromatine organization during the DNA replication [39].
