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Cross-pollination from GM to non-GM maize was determined phenotypically across 16 directional transects.
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Grain yields of soybean and maize were determined at physiological maturity by harvesting a central area of each plot (Table 2).
In our previous study, partial sequences of the wx gene in Chinese waxy maize were determined and several deletions at the wx genes were identified [9].
Previous studies show that flowering time in maize is determined by two components: base maturity and photoperiod sensitivity, and the two components are governed by separate genetic mechanisms [8], [11] [12].
Seedlings of maize were irrigated with 100 ml of 0.6 mM NaHS alone or in combination with 0.6 mM sodium citrate for 6 h, and then transferred to heat stress, during the treatment and heat stress, endogenous trehalose content in coleoptiles and roots of maize seeds was determined.
The starch content in maize kernels was determined using a fermentable carbohydrate assay as described by Zhou and Bao [ 77].
The exon-intron structure of the maize CDPK genes was determined based on the predicted sequences.
With attention to allocated scores by prioritization models, crops cultivation priority was determined as maize, rape and soybean in land units, respectively and maize crop was preferred to other plants.
The expression profile of the maize IBM2 Syn10 double haploid population [ 19] was determined by microarray hybridization to 60-mer probes.
Crop yield was determined by grain weight for Maize, wheat and broad bean, dry leaf weight for tobacco, and fresh stem and tuber weight for sugarcane and potato.
The distribution of distances between covered predicted sites with sequencing coverage was determined for all enzymes in maize and rice.
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