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In human, many regulatory sequences, including promoters, tend to have high G+C content [24], and, as predicted by the relationship between nucleosome preferences and base composition, nucleosome occupancy at human promoters and other regulatory sites in vivo correlates with G+C content (green traces in Figure 2).
In human, many CNVs are in linkage disequilibrium with nearby genetic markers and thus appear to be ancient [ 6].
This yields a total of 369 proteins (29 in worm, 66 in fly, 135 in mouse and 139 in human), many of them of unknown function.
In human, many studies support vitrification as the method of choice for ovarian tissue cryopreservation, providing similar results to conventional freezing, with the additional advantage of preserving the ultrastructure of stromal tissue that is usually affected by freezing [ 1, 2, 13, 17– 17].
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In humans, many of the important enzymes have been thoroughly characterized including the elucidation of their three-dimensional structures.
The identification of these pathways was not a simple matter, and indeed, in humans, many remain incompletely known or are simply conjectural.
Even though 3D PHH cultures are able to recapitulate many of the host responses described in humans, many interactions of HBV and its surrounding host involves other liver-resident cells.
In humans, many of the genes shared with coral are involved in complex functions such as early neural development.
Of the thousands of miRNAs described to date in humans, many exhibit tissue-specific patterns of expression can be detected in circulating blood.
Of the genes whose promoter regions were most affected by selection in humans, many are involved in neural development, including such things as how the axons of nerve cells are directed to form connections with other nerve cells.
In humans, many emerging viruses have come from other animals.
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