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Furthermore, this hypothesis is supported by previous data, indicating that the viral integrated fragments might be reassembled to constitute the EsV-1 genome.
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This interpretation is supported by our previous data indicating that an increase in affinity by defucosylation was primarily ascribed to an enhanced association rate (Okazaki et al. 2004).
Upon first consideration, this would seem inconsistent with previous data indicating that TLR engagement by HZ is necessary for induction of proinflammatory genes [22].
This result reproduced previous data indicating that the substitution via knock-in of the Jβ1.2 12RSS by the Dβ1 12resultsults in direct Vβ-Jβ1.2 rearrangements [15].
Functional magnetic resonance imaging (fMRI) data indicated that the MDD group was characterized by reduced activation of striatal reward regions during reward selection, reward anticipation, and reward feedback, supporting previous data indicating hyporesponsivity of reward systems in MDD.
So far, the targets for dsRNA based pest control have been identified by small scale screens and on knowledge based approaches, i.e. by testing genes where previous data indicated an essential function.
These previous data indicate a conserved mechanism of translation modulation by organizing ribosomes into resting higher-order assemblies.
Previous data indicated that activation of procaspase-8 is regulated by cullin-3-mediated polyubiquitination (Jin et al, 2009).
Previous data indicate that AEA, through CB1, induces rapid membrane hyperpolarization by activating potassium effluxes from sperm cytoplasm [46].
While we cannot exclude this may have influenced our result, previous data indicate that flow rate does not influence plasma volume expansion by crystalloids [13].
Previous data indicate that Pol V is also present.
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