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MJP has contributed to the expression analysis of miRNAs processing machinery genes.
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At least three factors may have contributed to the expression coherence observed in our predictions.
These anthocyanins have contributed to the expression of reddish-purple color of virus-infected grapevine leaves exhibiting GLRD symptoms.
Field et al. (2009) found that the transition from nucleosome-depleted promoter to nucleosome-occupied promoter might have contributed to the expression divergence of respiration-related genes and the evolution of aerobic fermentation.
The signatures of positive selection and divergent expression suggest that neofunctionalization has contributed to the evolution of duplicated Hsf genes.
These data offer us an unprecedented opportunity to identify the genes that have experienced most significant expression change and the genetic variations that have contributed to the gene expression reprogramming underlying the evolution of aerobic fermentation.
We suspect that "leaking expression" from a few spontaneously demethylated alleles within the 14-3-3σ 14-3-3σ 14-3-3σontributed to the protein expression.
Moreover, the fact our experimental lights turned on suddenly in the morning rather than ramping smoothly could have contributed to the strong expression differences observed at ZT01.
Alternatively, increased cellular stress following harvesting and during the fixation process may have contributed to the altered expression patterns in specific miRNAs.
This, in turn, could have contributed to the imprinted expression at the host locus, involving allelic acquisition of DNA methylation at key regulatory sequences.
The concomitant influence of HN2 on Ca2+-dependent enzymes (Calm1, Calm2) may have contributed to the increased expression of AMPD (Mahnke and Sabina 2005).
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