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Furthermore, using surface biotinylation and live-cell labeling methods, we detect a subpopulation of STIM1 on the surface of hippocampal neurons.
Combining predicted DNA-duplex destabilized regions (potential promoter motifs) and using a promoter score threshold inferred from shuffled sequence (see Materials and Methods), we detect four and seven promoter candidates in Andalucia and Reclinomonas-94 mtDNA, respectively (supplementary table S5, Supplementary Material online; arrows in fig. 1).
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Based on these two methods, we detected multicollineraity problem for nine variables and those variables were excluded from the analysis.
However, during the implementation of the methods, we detected certain parts of the methods that had to be manually encoded, usually in the form of (nested) loops.
Using the miRWalk database (see Methods), we detected 966 validated and 1,075 predicted genes associated with the highly co-expressed miRNAs in both cells and MVs.
Using molecular methods, we detected three different spotted fever group rickettsiae, including Rickettsia helvetica.
Using these multivariate projection methods we detected differences between tumours and normal tissue, radiation treatment-induced changes and temporal effects.
In mitochondrial fractions prepared by both methods, we detected the band of HMGB1 by Western blot (Fig 2C).
Through the CRS-PCR and DNA sequencing methods, we detected two VDR genetic variants (p.Gly14Ala and p.His305Gln) in this study.
Using a threshold similar to the one used for Ndt80 (see Methods), we detected 479 Sum1 targets (Additional file 1).
Using these methods, we detected the pneumococcus in samples from 56% more patients compared to those found based on conventional methods.
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