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However, the native habitat of the clones and differential expression of photosynthesis-related genes may also be some of the reasons for the observed differences in gas exchange characteristics of the clones we studied.
We have found the clones in the naked cuticle behave somewhat differently from the ones we studied before, that is, like them they do not change in cell number but the clones we studied changed very little in shape.
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Applying the method on a large set of DNA and RNA psbA clones from the Mediterranean Sea, we studied the distribution of cyanobacterial psbA genes and transcripts in their natural environment.
To assess the specificity of the new clones we performed AE-studies with laminarin, lichenan and different concentrations of xylan.
All the clones we generated in this study produced both type 1 and type 2 cytokines: IFN-γ, TNF-α, IL-13 and in some cases IL-10.
Because we could not differentiate between the ortets and their vegetatively propagated ramets in our study clones, we call all of them "stems" in this paper.
Considering the modest number of small RNA clones we sequenced during this study and the specific developmental stage of our total RNA source, we suspect that a number of novel miRNAs still await to be discovered in mosquitoes.
The ancestor produces an average cell size of 0.37-0.39 fl, depending on the experiment, whereas the clones we chose for further study had average cell sizes of at least 0.44 fl.
Among the seven clones studied, the clone Cachaco (ABB) expressed the lowest sensitivity to gamma irradiation.
In order to verify the pseudoautosomal location of the BAC clone studied here, we performed segregation analyses using nucleotide polymorphisms in the genes ESP1, PAR2, ACBP1 and ScOPA09.
(Here, to amplify the tail of the clone size distribution, we have studied the behaviour of a 'derivative' of the cumulative distribution known as the first incomplete moment.
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