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The complex and high motion in the Stefan sequence leads to a significant amount of 'estimation errors' in the SI frame which causes lower RD performance.
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However, while the design of switches and medium access control devices is possible, up to date communications have been proposed by exploiting only pairs of droplets – a header and a payload – thus leading to single droplet frames which cause an overhead of 50%; this makes current solutions scarcely applicable to real systems.
Clifton Taylor, credited with photo integration design, manipulates the images with an enticing framing technique, which causes some to grow so large they create a constellation of grainy black-and-white dots and others to recede to a sliver.
The c.1475_1476insCA insertion mutation we identified in exon 12 induced a frame shift which caused a new premature stop codon.
When a video is streamed through a bottle neck bandwidth, most of the frames are dropped and the frames partially fill the buffer, which causes choppy video.
When activated, it catalyzes the splicing of Xbp1 mRNA, which causes a frame shift during Xbp1 translation.
In addition, we found another variant lacking the region encoded by exons 5 and 6, which causes a frame shift, resulting in a stop codon in the region encoded by exon 7. hNETΔEX6 mRNA was also detected in the adrenals and fetal brain but not in the adult brain, suggesting a tissue-specific and development-dependent splicing of hNET transcripts.
In RV volumetric measurement an extremely wide field of view is necessary, which causes low frame rates.
Sequence analysis of genomic DNA from wild-type and albino cats identified a cytosine deletion in TYR at position 975 in exon 2, which causes a frame shift resulting in a premature stop codon nine residues downstream from the mutation.
Therefore, additional, as yet unidentified, mutations such as those seen in Alx4 Lst (Lst J : a 16-bp deletion within the paired-type homeodomain, which causes a frame shift potentially producing a truncated protein at amino acid position 332) may cause urogenital syndromic malformations in humans.
Since the deletion in gli2a i275 results in the loss of just four residues QLLS283-286, in a region that is not highly conserved between Gli proteins, we focused on the gli2a i276 the insertion in which causes a frame shift resulting in a premature stop codon at CDS-1167 (supplematerialmaterial Fig. S2A).
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