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Thus, both the fully paired and two-unpaired nucleotide slipped-junction variants can form and interconvert in J1/2 and J4/5.
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In the detwinned, single-variant domain, a new twin variant can form, gradually replacing the existing variant via the twinning process.
Three different PcG complex variants can be formed depending on the different combinations of these subunits.
Furthermore, our studies demonstrate that multiple splice variants can be formed due to inclusion of extra (supplementary) exons from what is classically thought of as hPLP1 intron 1.
Acid and basic variants can be formed by chemical and enzymatic modifications [ 11], with the acidic fraction typically containing a variety of protein species such as deamidated, sialylated and glycated forms, while the basic fraction contains, e.g., oxidated and C-terminal lysine variants.
Variants can adopt different forms but they can also occur in different locations throughout the genome.
One is that, because of the error-prone replication of RNA viruses, attenuated virus variants can revert to virulent forms, as extensively documented for live poliovirus vaccines [41], [42], [43].
Herein, we show that the fibrils formed by peptide variants can be coated with a layer of silica to produce silica nanowires using tetraethyl-orthosilicate.
Other possible explanation is that miRNA size variants can result from paralogue genes [ 26], or different allelic forms.
Three variants can be seen enroute.
All variants can be found in blood.
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