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Class of small non-coding RNAs that bind to complementary mRNAs, leading to mRNA degradation and inhibition of protein translation.
Merging silver with DNA, for example, has allowed scientists to make nanowires, which, thanks to DNA's ability to specifically bind to complementary sequences, can then form circuitlike patterns.
Specificity is provided by the RNA fragments generated by NMD, which bind to complementary nucleotide sequences in the gene paralogues (Fig. 1).
Instead, they bind to complementary sequences in target mRNAs, preventing those mRNAs from being turned into proteins, and blocking gene expression.
When one or more input strands bind to complementary sequences on the loop, the loop breaks, activating the DNAzyme and switching the gate on.
In many systems, it is mediated by lectins present on the surface of the infectious organism that bind to complementary carbohydrates on the surface of the host tissues.
Here's how it works: Double-stranded RNA molecules called siRNA (short interfering RNA) bind to complementary messenger RNA, then enlist the help of proteins, the RNA-induced silencing complex.
A lot of tumour cells express proteins on their surfaces so-called "checkpoint" proteinsurfaces so-calledplementary molecheckpoint-cells in a way that proteins that immune system to leave the tumour alone.
However, they can themselves (epi-miRNAs) repress key enzymes that drive epigenetic remodeling and also bind to complementary sequences in gene promoters, recruiting specific protein complexes that modulate chromatin structure and gene expression.
They bind to complementary target sites in mRNA that are often located in 3′ untranslated region (UTR) but can also be found in 5′UTR or even coding region (Forman and Coller, 2010; Li et al., 2011).
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MicroRNAs (miRs) are small noncoding RNAs that bind to complementary/partially complementary sites in the 3' untranslated regions of target genes to regulate protein production of the target transcript and to induce mRNA degradation or mRNA cleavage.
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