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Comparative sequence analysis indicated that many of these newly identified sites are highly conserved across five sequenced sensu stricto yeast species and, therefore, are probably functional in vivo binding sites that may be used in a condition-specific manner.
They show "that standard deviations of speeds at not clearly identified sites are considerably higher than at clear built-up or clearly non built-up sites".
These identified sites are often known by various terms in literature, such as hazardous locations, hotspots, black spots, priority investment locations, collision-prone locations, or dangerous sites.
Other results of this survey show that both the standard deviations and the relative standard deviation of speeds at not clearly identified sites are considerably higher than at clearly built-up or clearly non-built-up sites.
Our validation studies prove that the identified sites are bona fide binding sites and that they are transcriptionally capable of driving PPARγ specific transcription.
Our validation studies prove that the identified sites are bona fide binding sites for both PPARγ and RXR and that they are functionally capable of driving PPARγ specific transcription.
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Risk assessment of the identified sites is also being performed through independent studies.
The identified sites were.
The editing level of ndhB-1977 was medium (~57%) in both leaf and floral tissues but the editing efficiency of other four newly identified sites was poor (5 17%).
The identified sites were excluded from all methylation analysis.
These experimentally identified sites were taken from SpliceAid2 [ 38].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com