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In addition to regulating the transcription of several differentiation markers, we also show that PHDGH differentially modulates the stability of the major factors that play pivotal role in differentiation and stemness through post-translational modifications.
In present studies, along with the previously reported RAPD markers, we also detected some new RAPD marker for this plant species and both the cases only monomorphic bands are produced.
In addition to examining CIMP markers, we also examined the potential for methylation based dysregulation of the DNMT genes themselves.
To investigate whether such an increase can be observed in some myopathy models which do not have any effective diagnosis markers, we also measured these muscle-specific miRNAs in serum of steroid treated dogs.
Using the newly developed markers, we also observed substantial evolutionary rate variation among different primate lineages.
In addition to these markers, we also amplified the loci C2M34 (chromosome 2) and C3M69 (chromosome 3) (21 ).
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Because of the query of CD133 as a glioma stem cell marker, we also detected the proportion of CD15- and NESTIN-positive GL261 cells after hypoxia exposure.
For each marker, we also calculated the distance between EOC patients and Healthy Controls (women enrolled in prospective screening trials who remained free of ovarian cancer for at least two years after serum collection).
As a positive marker, we also used nuclear protein of mice treated with 3MC.
Consistent with our observations on the CD80 marker, we also found a similar trend with the expression of CD86 marker; that is, treatment of H37Rv-infected DCs with 10 mM NAC and 20 μM L-GSH resulted in 2.5-fold increase in the expression of CD86 compared to H37Rv-infected DCs and 5-fold increase in comparison to uninfected control.
In addition to genetic and protein markers, we now also have microRNAs, epigenetic markers, lipids, metabolites, and imaging markers.
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