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As previously commented, in order to reduce the error accumulation effect and to increase the method robustness against noise, clutter, and target scintillation, it is interesting to define a reference profile [18].
It is interesting to define the sorting motif recognized by the Syp1 μHD and to learn whether other yeast adaptors similarly use peptide sorting motifs.
To better understand the physiological role of CMR, it is interesting to define the supply of building blocks for growth that comes from each of its two processes: glycolysis and glutamine utilization by reductive carboxylation.
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Owing to the similarities between CTR-NT and TSA-NT array results, it was interesting to define the probe sets exclusively expressed in the blastocysts of either group.
Another possible generalization could relate to fractional analysis: it would be interesting to define the fractional analog of γ and apply it to chaos discrimination in fractional dynamical systems (such systems are studied, e.g., in [10 12]).
With respect to the latter, it will be interesting to define whether trastuzumab resistance is accompanied by increased levels of Erk5 or pErk5.
With the 3D structure of TRPV4 available [33], it will be interesting to define the changes within the homotetrameric structure itself that lead to alterations in channel gating, potentiation, and desensitization.
It will be interesting to define whether the effects described here are produced by a direct action of SKF 81297 on the granule cells of the DG, or by an indirect mechanism involving a polysynaptic circuit.
It will be interesting to define the role played by each MMP during different neurological disorders.
It would be interesting to define whether a non-sumoylated H2A.Z mutant affects GAL1 gene anchoring and activation kinetics.
Further, it will be interesting to define a set of indicators that enables the monitoring of community pharmacists' role evolution.
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