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The role that the novel lymphatic-associated adhesion molecule CLEVER-1 plays in breast cancer metastasis has been examined by assessing its expression in human breast tumour specimens and by conducting in vitro experiments to monitor its involvement in regulating cell adhesion to human umbilical vein endothelial cells (HUVEC) and hTERT immortalised lymphatic endothelial cells (LEC).
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We investigated the in vitro transfection efficiency of the C20-18, C20-20, and C30-20 linoplexes in retinal cells using a plasmid coding for GFP and assessing its expression qualitatively by fluorescence microscopy and quantitatively by flow cytometry.
Since the anti-tumor activity of CD8+ T cells requires the expression of HLA-class I molecules by tumor cells, we assessed its expression in head and neck cancers.
This model was validated by assessing its ability to predict gene expression under novel conditions.
Since miRNA miR-483-5p is located within intron 2 of IGF2, the expression of this gene was assessed by qPCR to assess its co-expression with miR-483-5p miR-483-5p miR-483-5p
One effective and generally accepted alternative is to evaluate activity of a miRNA by assessing the expression of its targets.
Having determined the transfer of miR-29b from the astrocyte released exosomes to the neurons, the next step was to examine the functionality of the transferred miR-29b in the neurons by assessing the expression of its target gene, PDGF-B.
Statistical analyses are performed for each GS by assessing the expression pattern formed by its members within the entire data set (21,673 genes).
We investigated autophagy in colon cancer cells by assessing the expression of the autophagic marker LC3B and its effects on cell death and proliferation.
It would be important to verify the activity of HPV by assessing viral oncogene expression and level of expression.
Mock T cells were demonstrated by assessing the expression of eGFP.
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CEO of Professional Science Editing for Scientists @ prosciediting.com