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N6-methyladenosine (m6A) methylation is the most prevalent modification in eukaryotic mRNAs, regulating the self-renewal and differentiation of pluripotency stem cells.
Since FTIR analysis indicated that in the post-implant material alkane oxidation was the prevalent modification of the alkane groups we further characterize the interaction between the oxidized alkane polymers and TLR1/2 receptors.
Halogenation by means of chlorination is the most prevalent modification observed in GPA scaffolds.
H3K36me3 was the most prevalent modification found in the CENH3-depleted subdomains (Table 2).
A particularly prevalent modification involved in transcriptional activation is histone H3 methylation.
However, when longer chains, such as tetramers, are used as substrates, branching becomes a more prevalent modification.
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Whereas CS1 regroups ∼90% of the tiles associated with H3K4me3, H3K36me3, H3K9me3 and H2Bub as well as the majority of H3K4me2- and H3K56ac-marked sequences, H3K27me3 and H3K27me2 are the most prevalent modifications in CS2.
The most prevalent modifications found in ribosomal RNA (rRNA) molecules are the methylation of the ribose moiety at the 2'‐hydroxyl group (2'- O-methylation) and the conversion of uridine to pseudouridine.
Electrochemical anodization has become a prevalent surface modification method for biomaterials nowadays.
N6-methyladenosine (m6A) methylation, the most prevalent internal modification in mammalian mRNAs, is widely conserved in eukaryotic species that range from yeast to humans7,8,9,10.
Reversible methylation by means of N6-methyladenosine (m6A) is the most prevalent internal modification in mammalian mRNA.
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