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Inorganic P and N fertilizers supplied these soil resources for plants and so, in turn, fewer nutrients would be allocated to underground mycorrhizae (Johnson et al. 2013; Williams et al. 2017), leading to low AMF richness and diversity under NPK regium.
Raw microarray data has been deposited in the Plant Expression Database (www.plexdb.org), a MIAME/Plant Compliant Gene Expression Resources for Plants and Plant Pathogens (Experiments BB94 and BB95).
In tandem with our accompanying transcriptome analysis [ 19], the goal of this work was to establish equivalent resources for plants displaying distinct and unexplored BIA profiles.
The availability of genomic resources for plants aids in the development of primers for new study systems, thereby enhancing the utility of cpSSRs across plant biology.
Furthermore, the rapid growth of microarray databases and other post-genomic resources for plants besides Arabidopsis (e.g. [ 64- 66]) is providing many sources of association evidence to reinforce the approach that we have pioneered here.
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But it is also, along with water, light and nutrients, one of the four essential resources for plant growth.
Characterization of genetic diversity is a must for exploring the genetic resources for plant development and improvement.
Currently, these databases are the authoritative resources for plant protein sequences and functional information.
Therefore, they have attracted more attention as novel resources for plant diseases [ 13].
Recent advances in sequencing and genotyping technologies, along with computational tools, offer an unprecedented capability to rapidly generate genomic and transcriptomic resources for plant pathogens [ 22].
This is now feasible thanks to the tremendous development of the Next-Generation Sequencing technologies (reviewed in [ 20]) that enable establishment of transcriptomic resources for plant species without the need for associated genomic resources [ 21].
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