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Choosing a form that does not absolutely minimize the number of cells affects the prediction of the portion of inhibitory cells in the neocortex.
Phosphatase recruitment occurs via immunoreceptor tyrosine-based inhibitory motifs (ITIMs) located in the cytoplasmic portion of inhibitory receptors expressed on the surface of leukocytes [ 5].
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These results show that at least a portion of the inhibitory effects of gluconate replacement requires the presence of β subunits.
Increased apparent RNA binding in the UV crosslinking assay for ΔNΔRS and ΔRS: Δ5-10 proteins may be a consequence of removal of a portion of the inhibitory N-terminus, whereas the R8E mutation may not increase RNA binding to the same extent in this assay because it preserves the length of the inhibitory N-terminal extension to RRM1.
A significant portion of the inhibitory effect of cytokinins on the root and hypocotyl elongation growth of young seedlings is mediated through an increase in ethylene action caused by a cytokinin-induced increase in ethylene biosynthesis [ 75].
Although the pretreatment liquor was separated from the WIS using a mechanical press, the solids were not washed prior to addition to the growth medium, which implied that a portion of the inhibitory by-products from the pretreatment liquor were carried into the SSF medium.
Both proteins can inhibit or delay the precipitation of calcium phosphate in vitro [2], [3], [62] [64], [66], [110], [111] and both bovine fetuin-A and human albumin have been shown to account for a significant portion of the calcification-inhibitory effect associated with each serum [62], [66].
The amylin-induced inhibition of histamine released from rat fundic mucosal segments in vitro was mediated via increased somatostatin release [ 19] but using a selective somatostatin receptor antagonist Rossowski et al showed in vivo in rats that a portion of the acid-inhibitory actions of both amylin and the related peptide adrenomedullin were somatostatin-independent [ 49].
Non-inhibitory antibody HF only recognized N-terminal portion of erbB2 ECD, but inhibitory antibody Herceptin bound to C-terminal portion of it exclusively.
Circular dichroism studies suggested that the limits of the minimum inhibitory domain are dictated by requirements for appropriate folding and maintenance of a secondary structure for the inhibitory portion of the prodomain.
However, a complex between kinesin-1 motor dimer and an auto-inhibitory portion of the kinesin-1 tail domain has been structurally characterised, providing insight into the molecular basis of kinesin transport efficiency [17].
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