However, it has to be mentioned that the role of NF-κB is more complex in regulating the answer of the intestinal epithelium to luminal agents.
In addition, E. coli genes of lateral origin exhibit more-complex regulation (tend to be regulated by more regulators) than genes which have been inherited vertically [ 14].
This result is in contrast to a previous report by Price et al. [ 14] that genes of lateral origin exhibit more-complex regulation (tend to be regulated by more regulators) than non-LGT genes.
These observations, in addition to our work, add support to the theory that FGFR1 regulation of a muscle fiber is much more complex than simply regulating embryonic myoblast differentiation.
This fundamental cellular architectural modification serves to compartmentalise transcription and translation and likely permitted the evolution of more complex mechanisms for regulating gene expression [1].
Mipp1 could therefore play a more complex role by regulating the abundance of these molecules through controlling the balance of their synthesis and degradation.
However, more complex interactions may regulate the response of oligodendrocyte lineage cells to Shh.
This discrepancy suggests that a more complex signaling pathway regulates p-4E-BP1.
These findings suggest a more complex molecular network regulating anterior segment development, as well as eye size and growth.
This suggests that the PWWP domain may play more complex roles in regulating DNMT3 enzyme association with chromatin than simply recognising H3K36me3.
