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Consistent with this hypothesis, plant clades, in some cases, have similar responses to soil biota (e.g. Brandt et al. 2009; Liu et al. 2012; Reinhart et al. 2012; Anacker et al. 2014).
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Contrary to our initial hypothesis, plants silenced in NaWRKY3 and NaWRKY6 expression were not limited in the ability to accumulate JA within SE* after repeated localized elicitations (data not shown).
In the plant-animal "warfare" hypothesis, plants produce toxins to kill predators and animals evolve P450s to detoxify these toxins.
The hypothesis that plant growth and development is coordinated by plant hormones or plant growth regulators first emerged in the late 19th century.
These results support the predictions of the "deficit" hypothesis, wherein plant protection is elicited by plant-mediated dietary imbalances.
In support of this hypothesis, specific plant serpins have been identified in the phloem sap of pumpkin (CmPS-1) and cucumber plants.
Nevertheless, the observation that heat-killed bacteria retain some ability to suppress SA elicitation provides some support for the hypothesis that plant responses to A. tumefaciens PAMPs contribute to the effect of A. tumefaciens on P. syringae-plant interactions.
This supports the hypothesis that plant interactions are major drivers of trait plasticity22.
These results further support the hypothesis that plant metabolism and growth are stimulated under conditions of excess Fe.
Meyer et al. (2007) and Muller et al. (2011) reported similar findings, supporting the hypothesis that plant growth under drought is essentially sink limited, because structural growth is more sensitive than C assimilation.
Moreover, this report clearly holds supporting evidence for the hypothesis that plant lectins, and in particular GNA, act on pest insects through the simultaneous interaction with multiple target glycoproteins.
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CEO of Professional Science Editing for Scientists @ prosciediting.com