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The results from the atomistic simulations as well as the experiments show that there is a larger probability of the PVDF torsions to be near ±180° at temperatures above the melting point, which is associated more with the β-conformation than the α-conformation.
As the experiments show all activation steps in the Smad pathway even in the cells overexpressing COX-2, a Smad-independent pathway seems to be responsible for the escape of the cells from TGF- β-induced growth inhibition.
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One possible explanation for inconsistency might be the potency of the context memory conditioning procedure, as the experiments showing spared remote memory used a greater number of context-shock pairings, likely creating a stronger context fear memory.
However, as the experiments shown in [5],[11],[15], applying the MC simulation to estimate the EIS is computational expensive, and the standard greedy algorithm with MC simulation (run 10,000 times to get the average) requires days to select 50 seeds in some real-world social networks with tens of thousands of nodes.
The MHCII is unavailable to third party peptides, as the experiments shown in Figures 1a b, as well as Figure 3c are performed adding a large excess of exchange peptide and clearly no mass action effect can be detected for peptides with intrinsic low affinity for MHCII.
As the experiments shown so far were performed near room temperature, we verified the occurrence of rod cone coupling also near body temperature.
As expected, the experiments showed that no ISM could compete with the performance of MI for large non-linear intensity distortions.
As expected, the experiments showed that cocaine didn't strengthen brain signals in cells without working NMDA receptors.
Thus, the infiltration of bacteria with a syringe, as in the experiments shown in Figure 1a, might bypass the first steps of the natural infection process, notably the steps reported to be regulated by ABA [ 55].
As suggested by the experiments showing that Cdc42V12 interacts with APC222 653, Cdc42V12 interacted with GFP-APC in the cytoplasm and also at the leading edges of cells.
Temporal synchronisation of the flow, photolysis and mirror movement of the interferometer was achieved as demonstrated by the experiments shown here.
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