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Variation in these responses has been selected during cereal domestication, providing an interesting comparison with the wild genome of Brachypodium.
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The latter also provide an excellent system to test if flowering time variation between wild ecotypes involves the same genes that have been selected in cereals during domestication.
Over the last century, modern cereal cultivars have been selected on land subject to conventional soil management.
Roughly equal numbers of males and female samples were selected for each cereal intake group.
The residents of the districts from which study communities were selected are predominantly agriculturalists who combine cereal production and animal husbandry, except in the Sidama Zone where instead of cereal production, enset or the false banana plant is cultivated.
Our hypothesis was that a positive correlation would exist between the consumption of cereal products and urinary DON; therefore, individuals were selected for the study following stratification into low, medium, and high cereal intake groups.
As a test case, maize (Zea mays L., cv. DEA), which is one of the most widely cultivated cereals all over the world, is selected for this study.
To generate primers that would be useful over the wide range of cereal constructs used in our research group, the boundary between rice intron 4 and 9 (obtained from the Starch Branching Enzyme 1 gene and present in all our cereal RNAi constructs) and the Nopaline Synthase (NOS) terminator (present in all our cereal silencing and over-expression constructs) were selected for primer development.
Both traits have been intensively selected during domestication or breeding, resulted in the divergence between cereal crops and their wild relatives.
The companies were earlier selected during their Summer application drive.
Both ORK10/LRK10 and POC1 are upregulated during cereal responses to pathogens and aphids and important components of the oxidative burst during the hypersensitive response.
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