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Focusing on tomato, a plant often used as a model to study Fe deficiency (Strategy I) and a crop of economic importance, no information is available at genome-wide transcriptional level.
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The two-step culture method applied here dramatically increased neutral lipid accumulation, up to 2.4-fold, more than previous N limitation or continuous deficiency strategies.
The aforementioned results imply that CNL nitrogen-deficiency strategy for lipid production on large-scale deserves further exploration.
In this study, three nutrient-deficiency strategies, viz nitrogen-, phosphorus- and iron-deficiency were applied to trigger the lipid hyperaccumulation in an oleaginous Chlorella pyrenoidosa.
To identify the gene disrupted by the RE-A complementation group, we employed a deficiency mapping strategy.
Very few information is available about the changes of nitrogen metabolism occurring under Fe deficiency in Strategy I plants.
Monitoring population salt and iodine intakes can help to ensure that salt-reduction and iodine deficiency elimination strategies can be implemented synergistically [ 10].
Key recommendations are as follows: Studies of zinc deficiency and strategies for its reversal should occur in the target population, namely children with or likely to have EE, given the disturbances seen in zinc homeostasis in this setting.
Given the genetic heterogeneity of CoQ10 deficiency the optimal strategy for genetic testing is debated.
Iron deficiency induces in Strategy I plants physiological, biochemical and molecular modifications capable to increase iron uptake from the rhizosphere.
By using the genetic deficiency and overexpression strategy, we demonstrated that SKAP55 unexpectedly inhibits CD8+ CTL cytotoxicity with enhanced PD-1 expression.
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