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The expression of IL-28RA on human DCs has been mostly seen on plasmacytoid DCs, while conflicting reports exist for expression of IL28RA on human monocyte derived DCs, possibly due to whether one looks at protein or mRNA.
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However, experimental evidence does exist for the expression of viral psbA and hli genes in culture and viral psbA genes in the environment, suggesting that host-derived viral genes actively contribute to host cellular processes in some capacity [32], [59].
While several advanced methods exist for differential expression analysis of RNA-seq data, proper tools to anal.yze RNA-seq time-course have not been proposed.
Our observations also suggest that a strong homeostatic mechanism may exist for Mer expression on the surface of monocytes and dendritic cells in peripheral blood.
Commercial platforms exist for measuring 3′ expression or exon expression; however, there is not a single cost-effective platform for measuring expression at multiple levels.
Similar issues exist for analyzing gene expression regulation logic at the protein level.
Presently, multiple options exist for conducting gene expression profiling studies in swine.
Today, numerous methods and tools exist for analyzing gene expression data.
However, few systems exist for mesenchymal transgene expression, which is required to modulate paracrine signals originating in the mesenchyme.
Multiple solutions now exist for whole-genome expression profiling of FFPE tissues, including both microarray- and sequencing-based platforms.
Given that evidences exist for the affected expression and activity of some selenoproteins depending on sexual dimorphism in mouse [ 22] and human [ 23], we decided to check for a gender specific association of -105G/A SEpolymorphismhism with the autoimmune disorders under study; however, we did not detect a gender-bias in our results.
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