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The incomplete loss of culturability when compared to the autoclaved microcosm is likely due to the larger initial inoculum size (approximately 2×107 cfu/mL, almost 10-fold higher).
Many small punctate carriers were still visible, which we attribute to the incomplete loss of DHC1 expression in these experiments.
As mentioned above, the incomplete loss of trnT-GGU (halfway between trnE-UUC and psbD in the C. japonica cp genome, Figure 9) from the C. japonica cp genome may have been the result of genome rearrangement.
Infections using a WNVKUN harboring a C10519→G point mutation in WNVKUNxrRNA1 results in a significant and reproducible decrease in sfRNA1 formation, corresponding with the incomplete loss of Xrn1 resistance we observe in vitro.
An interesting facet of the RPE phenotype in yap −/− embryos is the incomplete loss of RPE and the ability to rescue the phenotype through low-temperature rearing, implying that another protein, or proteins, can supplement for the loss of Yap.
Therefore, although the genetic background can modify the phenotype of Cdo;Boc double mutants, it is not sufficient to explain the incomplete loss of Shh activity in the absence of all Cdo family function.
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The further improvement of brake specific fuel consumption is mainly limited by four factors, i.e., the back flow loss, the exergy loss, the incomplete expansion loss, and the combustion loss.
Although the IR of P. thunbergii, which is 495-bp in length, contains a duplicated trnI-CAU gene and a partial psbA gene (red boxes in Figure 7F), presumably due to incomplete loss of the large IR [ 29], the IRs of Pinus cp genomes are thought to be structurally different from those of other plants, being composed of two or more genes including the trnI-CAU gene.
We also detected the dimer in C172S mutant and incomplete loss of activity of DTT-treated Del-N35TCTP, suggesting that the dimeric form still remained after the disruption of disulfide bond by Cys172.
Close examination of the earlier data reveals hallmarks of egg chamber damage, including incomplete loss of GFP from the alleged clone and loss of GFP from adjacent nurse cells.
Since null alleles were available for only two of the 41 mutants tested, the lack of strong phenotypes for many of the tested genotypes could be due to incomplete loss of function (Table S1, column 9).
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