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With these modifications, we obtained accelerations pulses that reached amplitudes of 10 kG and durations of 0.5 ms.
Based on suggested modifications we obtained analytical expressions for bit error rate probability analysis of quantization-based watermarking methods in AWGN and uniform noise channels.
After de novo and reference-guided assembly as in [ 19] with minor modifications, we obtained eight complete cp genomes and five draft cp genomes (Table 2).
Using all 24 modifications, we obtained a maximal classification accuracy of ∼70% and AUC of 0.75 for group I exon intron boundaries in IMR90.
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end{aligned} Similarly to analysis of Theorem 4.1 with only technical modifications, we obtain begin{aligned} biglvert u^{ k+1)}-u^ bigrvert leqhat{Z} biglvert u^{ k)}-u^ bigrvert, end{aligned} where (hat{Z}=psi_{1}^{j+1}(I+ vert Omega^{-1}A vert +N +psi_{3} N) and (psi _{3}=2sum _{i=0}^{j}psi_{1}^{i}psi_{2}+I).
Through surface modification, we obtained two types of MNPs with controlled difference on their surface charges, MNP-PEI having a higher positive charge than MNP-PEI-PEG, and used them as models to analyse the ability of various assays in discriminating the subtle difference in the level of effect those nanoparticles could impose to cells.
For all three stages and each histone modification, we obtained average transcribed genome coverage of ~50× (Additional file 1: Figure S2).
By forcing dimerization of scFv-scTRAIL based on scFv linker modification, we obtained a targeted scTRAIL composed predominantly of dimers (Db-scTRAIL), exceeding the activity of nontargeted scTRAIL ∼100-fold on Huh-7 hepatocellular and Colo205 colon carcinoma cells.
As a result of several modifications noted above, we obtained acceptable reproducibility of V0.
With some suitable modifications, we can obtain similar properties for higher-order contingent-type derivatives of perturbation maps in [31].
In a way similar to the proof of Theorem 4.2, with suitable modifications, we can obtain that the conclusion of Theorem 4.4 holds.
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