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If a secondary shift in lifestyle resulted in X. peckii's ancestors becoming diurnal again (which indeed they are), then the abundance of receptor cells within each unit could have led to a secondary increase of visual resolution within each eyelet.
Our reconstruction supports colony fission as a secondary shift among ants (Cronin et al., 2013).
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In hylobatids, which engage primarily in suspensory orthograde locomotion and posture, there apparently is a secondary ventral shift of the septum so that the transposition is lost.
Local deviation of Cα chemical shifts from random coil values (termed secondary shift) gives information about the secondary structure propensity of the backbone.
Under this hypothesis, the genetic similarity between eastern and central-western African populations from the Sahel would then be explained by two non-mutually exclusive processes, namely significant gene flow across the Sahel, or secondary shift from pastoralism to agriculturalism in those Sahelian and East African populations that practice agriculture nowadays.
Use of FITC-E2 dL5 FITC-E2 dL5asy reagent secondarye fluoreagente to the far red and conshiftsthe enhances the signal-to-background ratio ofluorescencells relatove thefaroredcein-landled antibodies alone.
Thus, considering all results the initial effect of adaptation in V1 consists in short-term repulsive shifts; at a secondary stage attractive shifts build up progressively over time.
The secondary structure of TGF-β313 was assessed by analyzing the secondary shifts using the program PECAN, which provide a sensitive and accurate indicator of secondary structure propensities.
The NMR data were consistent with this interpretation and analysis of the secondary shifts, shown in Figure 7B, indicated that residues 10 29 form a helix in solution.
The correlation of 13Cα secondary shifts with both 3D structure and heteronuclear 15N NOE values indicates that natural abundance carbon chemical shifts are useful probes for backbone structure and dynamics of membrane peptides.
If these ΔδCα secondary shifts are entirely attributed to the 2% bound state, secondary shifts in the CR-bound state are ∼50-fold larger and therefore indicative of a high population of α-helical backbone ϕ and ψ angles, even while not rigidly anchored to the CR micelle.
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