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Several glyco-engineering modifications have been reported in the past two decades.
Adaptive immunity modifications have been reported, this appeared less documented, particularly in comparison with healthy volunteers which have been rarely reported.
Since then, a range of modifications have been reported, with the fibres applied to a wide variety of analytical applications, in liquid and gas phase analyses or detection.
In this context, epigenetic modifications have been reported in animal models of psychiatric disorders [48].
Because tRNA modifications have been reported to occur in nucleoli [18], [19], we sought to identify the sub-nuclear structures associated with Dnmt2.
Even though new findings with regard to the impact of several histone modifications have been reported, inconsistency of precise information with regard to histone modification for a particular event is a major challenge.
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Altered expression of these - and other - histone modifications has been reported in cancer [ 3].
Another comprehensive survey of two types of histone modifications has been reported for pluripotent and lineage-committed mouse cells, revealing how these modifications change during development [ 35].
As both marks co-occur in active genes, H3K4me3 in promoter regions close to the TSS, and H3K36me3 in transcribed regions, it has been intriguing why correlation between these two histone modifications has been reported as approximately 0 so far.
A suppressed electroosmotic flow is required, and different strategies for surface modification have been reported [ 32– 32].
No DNases specific to the S-modification have been reported so far.
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