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Hydrogen peroxide and superoxide anion radicals were not detectable in the z3 mutant leaves (Additional file 6: figure S6).
Any inhibition in export of photoassimilate from leaves can induce starch excess in the leaves (Additional file 1: Table S1, and references therein).
Therefore, OsAP77::GUS may be involved in regulating vascular development and function in roots and leaves (Additional file 1 and Additional file 2).
Again, no changes were observed in the juice quality and in the N content of leaves (Additional file 3: Table S3).
In general, the concentration of P was probably in the deficient range across all treatments (below 0.1%% in stem and leaves, Additional file 1: Table S4).
Most of this Fe seems to not be translocated to shoots, since smaller Fe PQ values were detected in leaves and stems/sheaths (Figure3), even with the increased Fe content in non-flag leaves (Additional file2).
OsMKK6 showed more transcript accumulation in both roots and leaves in salt stress whereas in cold stress transcript accumulation was higher in roots but showed less accumulation of transcript in drought stressed leaves (Additional file 2: Figure S1A).
Salt, drought and cold down-regulate the expression of OsRUS6B in 14d young rice roots, but highly up-regulate the expression of OsRUS6B in 14d young rice leaves (Additional file 5: Table S3).
The patterns in the roots differed from those in the leaves (Additional file 6).
ILR3 (TDF #105b), however, was up-regulated in Mn-toxicity C. sinensis leaves (Additional file 3).
The same phenotype in the epidermal surface was also observed in rosette leaves (Additional file 2C).
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