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Using two large Swiss population-based studies, we generated and validated centile curves of 25(OH D in the general adult population.
For these studies, we generated an antibody against the idiotype on the A20 B-cell lymphoma line.
To complement our mESC studies, we generated and validated ATM−/−, LIG4−/−, and ATM−/−LIG4−/− clones of TERT-immortalized, non-transformed human RPE-1 cells (Supplementary Figure 4a g).
For expression studies, we generated a C-terminally myc-tagged SpARC1 construct.
In these studies, we generated and characterized a new TRH-Gal4 transgenic line that drives expression of effector genes in 5HT-containing neurons.
In those studies we generated transgenic mice by introducing the entire Dbl transforming genomic sequences and the onco-Dbl cDNA linked to a set of different tissue specific promoters into the germ line of FVB/N mice.
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For this study, we generated a constitutively GFP- expressing C. albicans strain.
To facilitate their study, we generated a mouse bearing enhanced green fluorescent protein (EGFP -specific CD8+ T cEGFP -specific
In this study, we generated Rag2-R229Q knock-in mice by CRISPR/Cas9-mediated gene editing in C57BL/6 zygotes.
In our study, we generated NS1 over-expressing cell lines, we found that NS1 over-expression induced pseudopodial retraction and inhibited cell migration.
In this study, we generated a monoclonal antibody (mAb2A9) targeting S. aureus GapC.
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