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The present study is concerned with the development and validation of an automated environmentally friendly pre-column derivatization combined by solid-phase enrichment (SPEn) to determine low levels of FA.
In this study, a green on-line derivatization-SPEn strategy using a packed oxidant reactor of CTH and a small ODS column has been developed for the first time to determine low levels of FA.
Most previous studies have used specific cut points to determine low levels of PG1 or PG1 : 2 ratio, but these cut points have varied across studies (Weck and Brenner, 2006; Brenner et al, 2007).
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Familiarity seems to have a role in determining low levels of these hormones.
The radioimmunoassay is reproducible, accurate and provides a means of determining low levels of ZD1694 in plasma (< 1 nM).
This, together with the unaffected accumulation of miR-135, likely determines low levels of MEF2C; vice versa, the strong downregulation of miR-133 correlates with the upregulation of MAML1.
In DMD myoblasts levels of linc-MD1 were severely reduced and this, together with the unrestricted accumulation of miR-135, likely determined low levels of its target MEF2C; conversely, the strong downregulation of miR-133 correlated with the upregulation of MAML1.
To determine whether low levels of CCR5 expression account for the block in infection of monocytes, we examined primary monocyte lineage cells during differentiation.
The nature and size of our study does not permit us to determine whether low levels of CD133+CXCR4+CD34- cells can accurately predict the progression of disease.
Modified IVC assays were performed at each time point to determine if low levels of cytolytic activity would also be detected in dLNs and spleens at day 2 or whether this trend was specific to the tumor site.
This was performed in order to determine if low levels of Cape fur seal LALBA transcript detection were due to low levels of LALBA gene transcription or low LALBA transcript stability.
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