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A promoted formation of NHSK was observed even using polymer with helical conformation, and the formation mechanism of NHSK was attributed to the unique "groove structure" formed by the stacked SWNTs in parallel arrays, which could facilitate the orientation of helical polymer chains along the SWNTs axis and the lateral formation of stable nucleus.
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Cytokinin has an antagonistic role to auxin by promoting cell differentiation, inhibition of lateral root formation and preventing their formation in close proximity to each other [ 21- 23].
These TFs have been shown to modulate/control root development and phosphate acquisition [ 34], shoot regeneration and photoperiodicity [ 35], lateral root formation [ 36], root cap formation [ 37].
Furthermore, interfering with ABERRANT LATERAL ROOT FORMATION 4 (ALfunctiontion, which controls lateral root development, impairs callus formation (Sugimoto et al., 2010).
These conversions have dramatic consequences; for example, red light inhibits stem elongation and lateral root formation but stimulates leaf expansion, chloroplast development, red flower coloration, and spore germination.
In A. thaliana, LBD16 seems to be involved in lateral root formation [61].
Several ARFs regulate the expression of LOB genes involved in lateral root formation [72].
Both adhesive systems showed RDIZ and resin tag and adhesive lateral branch formation.
Lateral root formation is a major determinant of root systems architecture.
HS are relatively recalcitrant to bacteria degradation and affect rooting including induction of lateral root formation and root hair initiation.
Interestingly, in A. thaliana, several studies have shown that adventitious and lateral root formation is under auxin control [3].
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