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The characteristics, cultivation conditions, and a basic in vivo growth pattern were previously described for the canine prostate cell line CT1258 [ 13, 14].
These changes in the dispersion pattern were previously suggested in genes involved in cancer pathogenesis [ 4, 37] and other diseases [ 38], although within-gene residual heterogeneity is not commonly considered in gene expression analyses [ 8, 9].
A similar two-peak pattern were previously reported by [ 78, 84] with regard to TGA/DTG analysis of straw, waste wood and duckweed, respectively, although in these cases the high temperature peak was observed at a somewhat lower range of temperatures of 460°C, 440°C, and 560°C, respectively (at the same heating rate of 20°C/min).
Similar(56)
A very similar XRD pattern was previously observed for the amorphous iron oxide/hydroxide materials (Kwon et al. 2005).
A similar pattern was previously observed using more limited data sets [14].
A similar pattern was previously reported elsewhere [4], and these results are consistent with our observations of infectious activity in both cell types.
Yet another distribution pattern was previously observed during division of yeast cells, where clustering of peroxisomes tends to be restricted mainly to the bud [35].
A similar activation pattern was previously shown for the flanking FRG2 gene that belongs to the same chromatin loop as DUX4c [39].
This pattern was previously observed in cells expressing the inactive Gap1-92 mutant containing a single glutamate-to-lysine substitution at position 300 and shown by membrane fractionation to be stacked in the ER [4].
Indeed, a similar pattern was previously observed in Panamá along the Chagres River basin.
This staining pattern was previously observed in Papss2bm/bm-mutant cartilage [ 40].
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