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However, isolation of retinal cells inside the chamber arrays is likely to affect their long-term viability.
These figures show that gene gain and loss within the 44C and 65A arrays is likely greater than suggested by total gene number alone.
Similarly, assembly of non-centrosomal microtubule arrays is likely to involve targeting of microtubule nucleating, as well as minus-end protection and/or anchoring factors, to non-centrosomal sites.
Since not every gene that is interrogated by probesets on the U133A and U133B arrays is likely to be expressed in normal or diseased kidney tissue, we sought to eliminate the hybridization intensity data from probesets that detect genes that are not expressed in our samples.
The architecture of these arrays is likely key to the high sensitivity, wide dynamic range, cooperativity, and feedback control of this system (Duke and Bray, 1999; Li and Weis, 2000; Gestwicki and Kiessling, 2002; Sourjik and Berg, 2002, 2004; Li and Hazelbauer, 2005; Endres and Wingreen, 2006).
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These arrays are likely to include monophyletic groups that have arisen through tandem duplication from an ancestral gene.
Moreover, DNA arrays and RNA arrays are likely to open up completely novel areas for research (Hoheisel, 2006).
Regardless, the strong expression in testis indicates that these arrays are likely packaged into an alternate chromatin state in this organ, most likely in the germ cells, as is the case for some MAGE and GAGE CT genes [ 41].
Sequences assigned a top rank by models derived from the "GABPα and CREB1" arrays, but middle-to-low ranks by models from the "single protein" arrays are likely to be bound cooperatively by both proteins in vivo, according to our in vitro models.
Due to the effects of turbines on current speeds, optimising the area occupied by an array is likely to be an iterative procedure.
Thus, the IBC array is likely to be more representative of broader population allelic architecture.
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