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The potential of ionic liquids for aromatic aliphatic separation or removal of sulfur-containing compounds such as thiophene is well established but, in spite of a number of phase diagrams reported in the literature, the values of other properties required for process design, such as viscosities and densities, are poorly characterized for these mixtures.
The present report points to several geographic regions of potential interest for pharmacogenetic applications that remain poorly characterized for NAT2 variation.
Density dependence is poorly characterized for many mosquito species, including A. aegypti (Legros et al. 2009).
Less frequent mutations in Ras are poorly characterized for their oncogenic potential.
Yet, the degree of adaptive variation within species across precipitation gradients is poorly characterized for most plants.
Ubiquitin specific proteases (USPs) contain a diverse range of ancillary domains, whose roles are poorly characterized for the majority of USPs.
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Many of them correspond to poorly characterized genes (for example, C17orf28 C1orf64, KIAA1370, KIAA1467, LOC143381, LOC400451, LOC92497 and ZNF703).
Many of the positive relationships identified were with poorly characterized species, for example, the taxa most highly correlated with high LGG abundance were three Verrucomicrobia, two of which are unclassified and the third has the representative species Prosthecobacter dejongeii [57].
However, details of the epigenetic changes and their relationship to the establishment of germ cell-specific gene expression have been poorly characterized, possibly for technical reasons.
It is a type 1 transmembrane glycoprotein that binds poorly characterized ligands (for example, bacteria, cell debris, and an astrocytoma cell-line), and, upon ligand binding, signals through DAP12 (TYROBP), an immunoreceptor tyrosine-based activation motif (ITAM -containing transmembrane adaptor proteITAM -containingkinases transmembrane with the ITadaptorin of DAprotein0- 22].
Among poplar TLPs, only the four TLPs from the poplar clade 1 belong to the eukaryote TLP subgroup I. Proteins from TLP subgroup II have been poorly characterized, except for the rosid-specific and tree-enriched clade, which contains several proteins with described antifungal or endo-β-1,3-glucanase activities (Additional file 9).
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