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We first characterized the expression levels of several of the PARP family members at the mRNA level, PARP-1 protein levels and PARP activity.
Therefore, to further investigate the clinical suitability of this model, we characterized the expression levels of key pathways associated with cancer progression in humans (21).
To date, only a few studies of human tumors in lung [ 22], in astrocytomas [ 30], and in meningiomas [ 15] have simultaneously characterized the expression levels of all seven 14-3-3 14-3-3 14-3-3
In addition to evaluating GATA4 as a potential prognostic factor, we characterized the expression levels of HER2-4, as well as gene copy numbers of HER2 in GCTs and correlated the expression levels to tumor recurrence and survival in a cohort of 80 GCT patients.
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Their abundances in the pheromone gland transcriptome are shown in Figures 3 and 4. We further validated and characterized the expression level and the tissue distribution of these genes by RT-PCR and qRT-PCR and summarised below.
To further establish the mechanisms responsible for different expression of c-FLIPS in a panel of NSCLC, we characterized the expression level of c-FLIPS mRNA in selected cell lines.
The aim of this study was to characterize the expression levels of microRNAs linked to development and progression of colorectal neoplasia.
Further studies are in progress to characterize the expression levels of this 59-kDa serine protease in V. cholerae strains of both El Tor and classical biotypes.
In order to characterize the expression levels of chemokine receptors CXCR4 and CCR6 on cancer cell lines, the cells were stained with human specific direct-labeled antibodies and analyzed by FACScalibur (Becton Dickinson Immunocytometry Systems), using CellQuest software.
The present work was therefore designed to build on earlier efforts to use radiolabeled toxin binding to characterize the expression levels of functionally competent VGSCs, with an eventual goal of obtaining high level expression of the most stable channels.
In order to characterize the expression levels and subcellular localization of the protein products of these mutants in X. laevis oocytes, immunocytochemistry and Western blotting were carried out using an affinity-purified antibody against DrAqp3b.
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