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Based on a database summing up 4908 African and 2178 Near Eastern/Arabian Peninsula individuals we assayed interpolation analyses of L haplogroup frequencies.
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We previously used this method to genotype 38 polymorphic AluYb8/9 loci in the four individuals that we assayed by ME-Scan in the current work [ 4] (Additional Files 6 and 7).
To proof unequivocally that GR is bound to individual IF filaments we assayed its localization at an ultrastructural level by electron microscopy.
To quantitate the amount of individual variation that is also visually apparent by microscopy (Movies 3- 5), we assayed individual animals rather than pools of animals, giving us insight into the variance of age-related genome copy number variation between individual worms.
To examine this, we assayed individual samples prepared with the three methods by qPCR, using primers for three of the miRNAs showing differences between the prep methods.
Additionally, we assayed 22 individuals from a site in Hood River, OR, which contained a mix of spotted knapweed (SK) and DK and intermediate hybrids.
To test whether exacerbation of "NF-κB-induced" pathway in CD4+ T cells from older individuals involved the PI3K pathway we assayed the effects of culturing CD4+ T cells in the presence of the PI3K inhibitor LY 294002, or rapamycin.
To determine which herb(s) contribute to life span prolongation, we assayed each individual herb for effects on C. elegans survival.
We assayed one individual in each accession by both quantitative PCR and nylon filter array hybridization, and assayed an additional individual, a sibling, in each accession using only qPCR.
We assayed that individual normal single hematopoietic stem cells had variable proliferative capabilities and, above all, ASCs were the most dormant cells.
For control, we assayed plasma from individuals with non-neurodegenerative diseases.
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