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Since the amplitude and time profile of input signals depends on biological context, such as distance to an infection site or pathogen loading, we use microfluidics to manipulate dose (A ) and duration (B ) of LPS and TNF input signals, which induces digital activation of NF-κB.
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Each column gives the FLNe profile of inputs observed for a given area and each row its outputs.
After excluding BRAIN as a main factor, the connectivity profile of inputs to each of the areas V1, V2, and V4 was determined (Fig. 12 A with V1 in green, V2 in blue, and V4 in red).
A theoretical analysis is performed to predict the linear and turning motions of each segment, and the optimal profiles of input signals are obtained for fast locomotion.
A comprehensive comparison of various CIs, i.e., RMS, kurtosis, crest factor, FM0, FM4, M6A, NB4, energy ratio, NA4, energy operator and two new proposed condition indicators (PS-I and PS-II), have been performed for no crack, initial crack and advanced crack for different fluctuating profiles of input speed.
*Although no independent microarray profiles of input DNA were available, we extracted input DNA profiles from the input channel (of the two-channel microarray) for each ChIP-chip profile.
Importantly, we found that there is a significant variation among multiple sequencing profiles of input DNA libraries and that this variation most likely arises from both differences in experimental condition and sequencing depth.
In addition, our compiled dataset comprises another 62 ChIP-chip profiles (biological replicates) in the same set of biological conditions (i.e., three ChIP-chip biological replicates at each developmental stage/IP combination), nine sequencing profiles of input DNA, and four pairs of ChIP-seq/ChIP-seq replicates (Table 2).
To understand the differential functions of histone modifications distribution, we generated the composite profiles of input control, representative histone modifications H3K4me3, H3K9ac, H4ac, H3K9me3, H3K36me2 and H3K36me3 in the entire gene body and extending 1.5 kb upstream and 1.5 kb downstream of 3750 genes expressed at the trophozoite stage.
The different profiles of inputs to the anterior medial and anterior ventral thalamic nuclei reinforce other anatomical and electrophysiological findings suggesting that these adjacent thalamic nuclei serve different, but complementary, functions supporting memory.
Under these premises, it is claimed that any acceleration and velocity profile of the input shaft can be tracked accurately.
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