The phrase "advantage of the engineered" is not correct and lacks clarity in written English.
It may be used in contexts discussing the benefits derived from engineered products or systems, but it requires additional context for proper understanding.
Example: "The advantage of the engineered solutions is evident in their efficiency and sustainability."
Alternatives: "benefit of the engineered" or "merit of the engineered".
Nvidia has made it possible to take advantage of the carefully engineered parallel architecture of today's graphics cards through its CUDA (Complete Unified Device Architecture).
A strategy of protein C-terminal labeling was designed and shown in Figure 1, by taking advantage of the recently engineered Ssp GyrB S11 split-intein [28].
The advantages of the highly engineered Corning glass reactor included high mixing and heat-exchange efficiency, chemical resistance under corrosive flow conditions and a small hold-up.
The most relevant advantages of the genetically engineered S-layers over less nanostructured approaches are the periodicity of functional domains in the nanometer range on the outermost surface of the S-layer lattice and the general applicability of the 'S-layer tag' to any fusion partner.
Injected galanin won't get past the blood-brain barrier into the brain, so the team took advantage of an engineered molecule called galnon that imitates the neurotransmitter.
The first systematic investigations of cortical visual responses were made by Hubel and Wiesel at the end of the 1950s and early 1960s, taking advantage of newly engineered tungsten electrodes that permitted stable extracellular recordings from nerve cells over long periods of time in awake animals.
Prior Tn-seq experiments using Mariner libraries have taken advantage of an engineered MmeI restriction site that cuts 18 20 base pairs away from the recognition site into the genomic DNA [ 27, 30].
Our work takes advantage of genetically engineered mice as well as our ability to chronically apply pharmacological disruption of transmitter systems to assay their effect on the normal development of excitatory and inhibitory pathways in the developing brain.
To distinguish between these possibilities, we take advantage of genetically engineered mice that we show have a duplicated functional retinocollicular map but only a single map in V1.
By taking advantage of genetically engineered mice deficient in IL-28R signalling, IL-28A gene transfer and recombinant IL-28A administration, we show that IL-28 cytokines are critical for driving Th1 differentiation in vivo while limiting Th2 and Th17 responses in the airways.
