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In addition, despite the evidence that the transcriptional activity of CaRF can be acutely enhanced by the activation of L-type voltage gated calcium channels in neurons [14], we did not find extensive overlap between the list of putative CaRF target genes (Table S4) and several large published sets of neuronal activity-dependent genes [19], [41], [42].
The pyrosequencing-based transcriptomic study by Lowe et al. detected a number of redundant genes, including tandem arrangements [ 21], but we did not find extensive overlap in multicopy genes between both studies: only three genes (hsp70, hsp90 and S-adenosyl-methionine synthetase) in our list from Table 2 were also found to be redundant in the Lowe et al. analysis.
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We found extensive overlap in Aβ levels between AD and PA brains.
We found extensive overlap with only subtle quantitative differences between Aβ levels, peptide profiles, solubility, and SDS-stable oligomeric assemblies in the PA and AD brains.
Meyer and Paulay [ 13] tested different threshold methods in COI barcodes of cowries and found extensive overlap of overall intraspecific distances with interspecific distances, resulting in minimum error rates of ~17% to screen for putative new species.
Finally, we found extensive overlap between the proteins that we define as our "Normal Pap test Core Proteome" and lists of cervical-vaginal fluid proteins identified by others using different sampling methods [ 10, 11, 13- 15, 17- 22].
We found extensive overlap between Dichaete core binding intervals and the high stringency (1% FDR) Kr and Hb binding intervals determined by BDTNP at all of the core temporal transcription factors.
Although the levels of the different forms of Aβ in prefrontal cortex from patients with AD tended to be higher than those from patients with PA, the authors found extensive overlap between the two groups and suggest that PA is likely to represent a prodromal stage of AD.
Similarly to the PDZbase data, we found extensive binding overlap between the PDZs in terms of raw numbers although with a distribution that was mildly shifted towards even more binding overlap between PDZs (Fig. S5).
We again found extensive binding overlap, with 902 of 1478 Prospero intervals also Dichaete core intervals.
We found extensive and significant overlap using these contrasting clustering methods in both PAG and cortex.
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