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In other tandem designs, the oxygen evolution and hydrogen evolution reactions occur at electrocatalysts (e.g., Pt) deposited on and driven by tandem semiconducting light absorbers that covert the incident light into a photovoltage [57].
No further putative events were confirmed in other tandem arrays, or between unlinked AAT loci.
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This fits in well with other tandem studies that have shown PrP is difficult to remove [1], [16], [25], [27] or even impossible [15].
In other species, tandem repeats account for <10% of the genome, with the exception of the genome of cucumber, which is composed of ∼23% of such sequences, a percentage, however, lower than that measured in the olive genome.
In other words, the tandem arrangement does not seem to be essential for 5 S methylation.
This DUF2775 domain is a specific characteristic of ST proteins and it has not been described in other type-II tandem repeat proteins [ 2].
Transcriptional regulation of duplicate F3'5'Hs in berry skin is largely dependent on genotype, consistent with the observation in other plants that tandem duplicates have highly variable expression patterns [ 29].
A recent study of human rDNA array did show rDNA units of variable length, as well as existing in configurations other than tandem repeats (e.g., single copy outside rDNA clusters, or inverted repeat) [14], [15].
The absence of S-type tandems in other L-type genomes further indicates their frequent loss and/or rapid replacement by linked units.
In other cases, such as for tandem MS spectra, reference collections could be screened to inspect the number of fragment signals.
In other cases, duplications appear as tandem copies of genes, which form clusters of evolutionarily related genes.
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