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Yet, we cannot rule out that this arginine residue may be involved in the proton shuffling that occurs on the way to forming the chromophoric intermediate.
Yet, we cannot rule out the possibility that the mislocalization of ß-actin contributes to SMA pathogenesis by some other mechanism, perhaps by disrupting the subcellular localization of other proteins or that some compensatory mechanism occurring in Actb-MNsKO mice does not also occur in SMA mouse models.
Yet, we cannot rule out functional changes in inhibitory transmission from our data.
Yet, we cannot rule out that some of these transcripts have a biological function.
Yet, we cannot rule out the possibility that positive feedback and ultrasensitive systems may also exhibit the experimentally observed behavior.
As yet, we cannot rule out that other mechanisms also contribute to the TRAIL-potentiating effect of ATO.
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Yet, without experimental evidence, we cannot rule out a possible change in 5'-initiation rates during amino acid starvation.
Inter-rater reliability has yet to be established, and we cannot rule out the possibility that this may have influenced our results.
However, we cannot rule out that some yet untested B. stricta populations will show significant differences.
We cannot rule out that a yet to be identified roseobacter symbiont of algae would have these two genes, as putative homologs have been found in some bacteria.
We cannot rule out the presence of other, yet unrecognized, viruses in the sample, because we did not perform massive sequencing.
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