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To rule out the possibility that some of these constructs were not expressed in the germline, we monitored their expression pattern and level by GFP fluorescence (Fig. 6A).
We thus monitored their expression during ES epidermal differentiation as compared to undifferentiated ES cells.
We monitored their expression levels in human melanoma cell lines compared to normal human epidermal melanocytes (NHEM).
We selected the remaining five genes and monitored their expression in untreated and fungal-inoculated Col-0, Te-0 and Kas-1 leaves.
Here, we randomly selected four Helitrons and monitored their expression via RT PCR analysis of RNA extracted from etiolated roots and shoots.
Based on bioinformatics analysis of the apple genome, we identified three apple GAD genes and then monitored their expression in various plant organs, including apple fruit.
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We used in vitro synthesized dicistronic viral transcripts that contained two consecutive reporters Rluc and Fluc, and monitored their expressions in RRL and compared the results obtained with those from the Giardia trophozoites transfected with the same transcripts [44] (Fig. 2).
Although the significance of the upregulation of these genes in the mutant Treg cells remains to be established, it is possible that monitoring their expression (and that of other genes identified in this study) could be exploited as a means to identify cells in nonmutant populations of Treg cells that are experiencing less TCR signaling than other cells in the same populations.
Quantitative real-time PCR assay were performed using the primers (Additional files 1) designed according to these unigenes to monitor their expression profiles under 1 h and 72 h exposure to 20% PEG-6000 treatment.
Homologs that are candidates for being PM susceptibility genes were inferred by phylogenetic relationships with functionally characterized MLO genes and, in apple, by monitoring their expression following inoculation with the PM causal pathogen Podosphaera leucotricha.
Here, we describe the isolation of two major genes in these pathways, CtPAL (phenylalanine ammonia-lyase) and CtCHS (chalcone synthase) in safflower along with monitoring their expression profiles in different stress circumstances.
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controlling their expression
monitored their expressions
observing their expression
trace their expression
monitored their learning
monitored their sleep
monitored their adherence
monitored their weight
monitored their perspiration
monitored their progress
monitored their diversity
monitored their survival
monitored their performance
monitored their courtship
monitored their reproduction
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