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Considering the correspondences between the HREM image and the atomic positions, analysis of the boundaries indicates that they are next-nearest neighbor antiphase boundaries (APB), with two possible shift vectors.
Depth resolution of their surveys is unable to detect deeper fracture systems, but the precision of these lateral surveys to locate sharp boundaries indicates that dense surveys such as line H-1 with 5-m electrode spacing, and longer AB spreads, would be useful in further exploration.
Analysis of human-chimpanzee divergence across intron-exon boundaries indicates that although genes in relatively open chromatin generally display little selection at their synonymous sites, those in closed regions show markedly lower divergence at their fourfold degenerate sites than in neighbouring introns and intergenic regions.
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Bending of the NW occurs right at the grains boundaries, indicating that they are held together by weak forces.
The NE is very close to the Pareto boundaries, indicating that it is indeed very close to being a Pareto-efficient operating point for various CCCs.
It turns out that there exist sharp temperature drops across these grain boundaries, indicating that the LTCs near grain boundaries are much smaller than those inside the bulk tungsten.
The primary phase (about 79%0 is fcc Cu-base solution with AsCuNi (21%) in the grain boundaries, indicating that it formed from the mixture of liquid and fcc on cooling.
Much of the blue amphibole growth is truncated on the detrital grain boundaries indicating that these were blueschist-overprinted amphibolite clasts (equivalent of the high-grade blocks) at the time of deposition.
Recently, Abou-Ras et al. identified Se-Se-terminated Σ3{112} twin boundaries, indicating that Cu is depleted and In is enriched in the two atomic planes next to the twin boundary by high-resolution scanning transmission electron microscopy and electron energy-loss spectroscopy[18].
This is by far the highest degree of correlation observed at such boundaries, indicating that this may be a prominent function of NFI proteins.
A total of 161 of 313 genes bear at least one binding site for Klf5 within 100 kb from the gene boundaries, indicating that they can be considered Klf5 primary targets.
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