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Haplotype analyses observed that the T-47-A46-C79 haprotectives a protective haplotype for EH, while the T-47-G46-C79 haplothee incrisked the risk.
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From those analyses, we observed that the combination of QWT magnitude and phase is effective in several image processing tools.
From these analyses, we observed that the 1Dy10, 1Dx5 and pmi transgenes were not linked, allowing us in the T3 generation to identify 1Dy10 transgenic segregants that contained no marker or silent 1Dx5 transgenes.
Using qRT-PCR analyses, we observed that the expression of suxR, suxC and suxAB is specifically induced by the presence of sucrose in the medium (Table 3).
In the stratified analyses, we observed that the CC genotype might modulate breast cancer risk (OR = 1.11, 95%CI = 1.01 1.23, Pheterogeneity = 0.210) and lung cancer risk (OR = 1.25, 95%CI = 1.06 1.46, Pheterogeneity = 0.958), comparing with the TC/TT genotype.
In immunofluorescence analyses, we observed that the signals in MTA- and α-TCP-treated cells were stronger compared to the cells of the control group.
As regards the mt gene analyses, we observed that the ND5 and CYTB genes recovered all 9 nodes of the mt genome tree.
According to above analyses, we observed that the dimerization patterns in the leucine zippers of BdbZIPs were more complex and diverse than those in other species.
From statistical analyses, we observed that the total number of CLIP-seq studies published increased dramatically after 2008 and exhibited a gradual upward trend thereafter.
Based on our preliminary analyses, we observed that the pattern for associations of DAP concentrations and birth outcomes varied by race/ethnicity.
In these analyses, we observed that the imidazole and EDTA treatments completely or thoroughly disassembled the liposome aggregates which had been induced by membrane-bound Rab5a-His12 proteins (Fig. 6B E).
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