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The embryonic expression pattern described here is consistent with a role for Ce HCF-1 in early embryogenesis and the embryonic lethality observed upon loss of Ce HCF-1.
Thus, the pattern described here provides new insights into the relationship between environmental variability and the corresponding population dynamics.
The temporal release pattern described here is only investigated for ST-elevation AMI and not for non-ST-elevation AMI.
Based on its spatial expression pattern described here, one could speculate that MT1-MMP might be involved in maintaining axonal integrity and/or in glial reactivity.
Interestingly, the response pattern is considerably different in that case, providing further evidence that the pattern described here is not due to pitch.
Based on its spatial expression pattern described here, one can hypothesize that MMP-2 might be involved in glial reactivity upon retinal damage.
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We used this DoG edge map at multiple scales on Tile Illusion patterns described here for prediction and measurement of both tilt magnitude and its direction, by further analysis on their DoG edge maps by our model.
The intracellular patterns described here for Hfq-MT are unique when compared with the intracellular distribution of other MT-tagged E. coli proteins [17].
However, based on targeted gene sequencing in Lingulodinium polyedrum [15] and Symbiodinium [16], as well as two genes from Karlodinium veneficum, the patterns described here probably apply to many dinoflagellates.
This will provide more insight into the generality of the patterns described here, and the extent to which journal impact factors provide biased estimates of impact, either up- or downward.
All together, it is likely that the investigations of the above questions will lead to better understanding of how the hippocampal ensemble patterns described here contribute to the global representation of various episodic memories in the brain [65].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com