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These findings well corresponded to the cellular association of the Arg-PEG-BDB/DNA complex determined by flow cytometry.
The crystal structures of the Brx1 and Ebp2 complex determined here and the Nsa1 structure (Lo et al., 2017) were fitted as rigid body.
Previous structures of Arp2/3 complex, determined in the absence of a nucleation-promoting factor and actin, reveal its inactive conformation.
Successive reduction of the associated Lw− units leads to partial dissociation of the complex, determined by the identification of free radical dianion structures in solution.
The stoichiometric composition of the PVP PEG hydrogen-bonded complex, determined from the Tg composition relationship, corresponds to the data obtained with independent methods.
During complexation, the relaxation of polyelectrolyte inside the complex and the exchange of polyelectrolyte between complex determined the aggregation and precipitation rate.
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We also characterized how pH regulates H2 production and consumption via each hydrogenase complex, determining the significance of each at low and high pH.
Each of these contrasting social indicators operated independently of the other, indicating complex determining mechanisms.
Also the negative cooperativity between GDP and agonist binding at the receptor/G-protein complex determines agonist efficacy.
This CLOCK-SIRT complex determines the degree of histone acetylation and amplitude of transcription for circadian and metabolic genes.
While defining ethical norms in HIV prevention research is complex, determining the process by which ethical standards are to be established can be an equal challenge.
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