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Non-pathogenic strains carried only 1 to 4 of these genes, indicating that these five genes might be the main virulence genes of ERIC-1 strains.
The presence of H2AZ and H3.3 in the genome potentially correlated with actively transcribed genes, indicating that H2AZ and H3.3 were necessary for creating relaxed and transcriptionally active chromatin structures31,32,33.
Also, EPA and 5-HEPE decreased the expression of these genes, indicating that IDO, RALDH and TGFβ are not involved in the enchancement of ATM mediated Treg induction by EPA (Supplementary Fig. 3C).
Similar results were obtained with E. coli strains lacking yeaH or both yeaG and yeaH genes, indicating that yeaG and yeaH are functionally linked (Fig. 1D and Table S1).
Bacterial symbionts and fungal and bacterial pathogens induce the expression of different SWEET genes, indicating that the sugar efflux function of SWEET transporters is probably targeted by pathogens and symbionts for nutritional gain.
The ganglion cell-specific genes included both Brn3b-dependent and Brn3b-independent genes, indicating that Math5 regulates distinct branches of the gene network responsible for retinal ganglion cell differentiation.
Evaluation of the duplex PCR on six samples isolated from Palm Oil Mill Effluent (POME) showed that only four isolates contained both the nifH and nifD genes, indicating that these isolates were potential hydrogen-producing bacteria.
Strikingly, Fir1 was included in these 13 genes, indicating that Fir1 RNAi) does not affect neoblast maintenance before amputation.
Interestingly, the t(14 18 -negative 14 18 -negativeated by overexpresubsetof cell cycle-associstedominatedindicating that these tumors are significantly more proliferative, suggesting distinctive pathogenetic mechanisms.
Those genes produced twice as much RNA as did clean genes, indicating that integration spurs genes to action.
The major physiological effects of rice mutants lead to sterility (6 genes), indicating that the genes in this category are important for fertilization and embryo development.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com