Additionally, minimal signaling modules can be tractably engineered to predictably alter cellular responses, opening up possibilities for creating biotechnologically and biomedically useful cellular devices.
Additionally, individual components and modules can also receive a "portability" score that estimate the degree to which they translate to other hosts.
Additionally, new hardware and software modules can be easily added to the existing library.
Additionally, the binding mode of individual histone tail side chains to catalytic domains or effector modules can be used as a guide to design competitive inhibitors (Culhane et al., 2010; Liu et al., 2009).
Simple motions of the modules can be combined and sequenced.
The modules can be flexibly arranged.
While structured content modules can augment progress, executive coaching capacity appears essential.
New modules can replace dead modules, reducing clone-type mortality and preserving the colony's territory.
CBM32 modules can interact with PGA and can be associated with N-acetylglucosaminidase modules [ 126].
Specifically, the black module can be considered a pluripotency/self-renewal module, while the blue, brown, and cyan modules can be considered differentiation modules in the signed network.
