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We further related the polarizability to conductance switching by inserting single nitro-functionalized OPE switch molecules (4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol 4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol 4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol 4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol 4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol 4,4′-di ethynylphenyl -2′-nitro-1-benzenethiol
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Secondary wall NAC master switches and secondary wall MYB master switches bind to and activate the SNBE (secondary wall NAC binding element) and SMRE (secondary wall MYB-responsive element) sites, respectively, in their target gene promoters.
Amazon.com Chief Executive Jeff Bezos Jeff Bezos has created a reason to switch from bound paper books to bits a device with a wireless connection able to download digital books on the go.
Jane has a number of user-definable parameters including event costs, host switch distance bound, and the number of iterations and the set size in the genetic solver.
Finally, the processivity switch τc binds the tail of the polymerase and appears to sequester the polymerase tail away from the clamp in the DNA-free structure.
Activated Gene-Switch binds to UAS sites in the promoter of target constructs to yield transgene over-expression.
But while innovation is becoming a buzzword, and #ReShapeAid and #TalkInnovation are gaining traction on Twitter, an April report found that little is known about how to flick the innovation switch in organisations bound by red tape.
Thus, Arg168 can switch between peptide bound and unbound orientations but maintains the interdomain contact in both states.
A complimentary set of experiments revealed that wild-type (non-mutated) cohesin-dockerin complexes occupy both configurations in approximately equal amounts, and do not switch modes once bound.
Similarly to other key developmental regulators, RARs possess the capacity to function as a molecular switch; when not bound by ligand, they form a complex with co-repressors such as N-CoR (negative co-regulator) or SMRT (silencing mediator for retinoid and thyroid hormone receptors), and histone deacetylases (HDACs) to actively inhibit gene expression.
Such cis-regulatory modules (CRMs) act as genetic switches and are bound by specific TFs to drive distinct patterns of expression.
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