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Structures are available for NC bound to a number of different segments of the 5′ UTR, although it is not clear which of these is most biologically relevant for packaging.
Most galaxies in the Universe are gravitationally bound to a number of other galaxies.
As an example of how a QM (in this case a QM/MM refinement) can improve structure quality, I briefly describe our work on benzamidine ligands bound to a number of receptors.
ChIP-qPCR analysis showed that RUNX1 was indeed bound to a number of tested p63 binding sites with the RUNX motif (Fig 4B; Supplementary Table S8B), indicating that RUNX1 can cooperate with p63 in epidermal cells.
Under resting conditions, the glucocorticoid receptor (GR) is localised within the cytoplasm bound to a number of accessory proteins such as heat shock protein (hsp -90 and peptidyl-prolyl isomerases known as FK-binding proteins.
IMP1 bound to a number of mRNAs, post-transcriptionally promoting the expression of gene products that promote self-renewal, including Hmga2, and inhibiting the expression of gene products involved in differentiation.
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The major CfaB subunit of CFA/I binds to a number of non-acid glycosphingolipids, including glucosylceramide, lactosylceramide with phytosphingosine and/or hydroxy fatty acids, neolactotetraosylceramide, gangliotriaosylceramide, gangliotetraosylceramide, the H5 type 2 pentaglycosylceramide, the Lea-5 glycosphingolipid, the Lex-5 glycosphingolipid and the Ley-6 glycosphingolipid.
They bind to a number of extracellular matrix components including fibronectin, laminin, collagen, vitronectin, fibrinogen and thrombospondin.
E6 binds to a number of cellular proteins that mediate diverse activities in the cell, ranging from the regulation of apoptosis to the maintenance of chromosomal stability.
Compared to the background genes, a higher proportion of H2H gene pairs bind to a number of epigenetic markers, such as hypersensitive DNase, H3K4me2, H3K4me3, H3K9ac and H3K27ac (see Table 2, p < 0.01 using Chi-square test).
Hornig-Do et al 2014 provide evidence that the C-terminal mtLeuRS (Class I) binds to a number of mitochondrial tRNAs, but the rescue effect on mutations was demonstrated here only within Class I (Fig 1).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com