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The difference between 2HA and WT is not as pronounced in standard growth conditions except for the increased main root elongation of seven day old seedlings.
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Using a multi-cellular model, we also analyse the roles of cytokinin and auxin in specifying the three main regions of the primary root (elongation, transition and division zones), our simulation results being in good agreement with independent experimental observations.
Folic acid supplementation inhibits primary root elongation and induces lateral root formation in a concentration-dependent manner.
Low phosphate increases lateral root development and reduces primary root elongation through altered auxin distribution [ 111- 116], suggesting an alteration in root architecture in osmotic-stressed roots.
In contrast, severe water deficit decelerated primary root elongation implying that the root had adapted by metabolic alterations.
In A. thaliana, one of the hallmarked cytokinin actions is inhibition of primary root elongation.
The deployment of these traits is often accompanied by an arrest in primary root elongation.
Similarly, primary root elongation was estimated by screening 10 DAS Arabidopsis SlIPT3 and SlIPT4 complemented plants.
During plant growth, the acropetal auxin flow from the aboveground plant part to the root increases during development and plays a key role in regulating elongation of the main root and development of lateral roots [ 39, 40].
We found that, the coleoptiles elongated abnormally and root elongation was inhibited (Figure 6).
Reduction of ARD is considered as an indication of increment of lateral root elongation and/or lateral root production from main roots (Postma et al. 2014).
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