Sentence examples for using the same transgenic from inspiring English sources

Using the same transgenic plasmid construct (Figure 1) and bitransgenic system as described above, we also generated mice expressing tetracycline-regulatable alleles carrying a mutant EGFRT790M cDNA alone.

This method permits detection of the bicistronic and any putative monocistronic transcripts, as shown in previous reports using the same transgenic mouse line as well as in other animal and cellular models [7], [19], [22] [24].

Using the same transgenic line, it was shown that during renal injury no interstitial stem cells could contribute to tubular repair as there is no apparent dilution of the nephron epithelium with cells that did not originally express Six2 [20].

This was despite the fact that the percentage of CD69 positive cells among CFSE+ T cells and their early proliferative capacity were not significantly altered by the presence of regulatory T cells (Fig. S2), in agreement with previous data obtained using the same transgenic model [24].

Using the same transgenic approach, we expand the unplugged/MuSK expression domain to the entire muscle surface, but find that AChR prepattern and synapses remain restricted to the central muscle region, consistent with the idea that in vivo additional, extrinsic and/or muscle intrinsic mechanisms restrict unplugged/MuSK signaling to the mid-muscle region.

The effects of DHA intake on classical markers of AD neuropathology in 3xTg-AD mice were limited to a decrease of phosphorylated tau, in accordance with a previous report using the same transgenic animals fed during a similar amount of time, but with almost twice the daily dose of DHA [22].

Recently, it was shown, using the same Aβ42 transgenic fly model as we used in this study, that Aβ deposition and toxicity could be reduced by co-expression of an engineered high-affinity Aβ-binding affibody (ZAβ3).

In addition, another recent report using the same K14-FoxN1 transgenic mice showed that FoxN1 expressed in the bone marrow (BM) of K14+ stroma, which is not a prominent site of FoxN1 expression, promoted T-lineage production, but inhibited B-lineage production.

MAB breeding plants were validated by PCR using the same primers as transgenic plants.

Using the same gene construct, we generated transgenic sensor mice DRESSA that can produce SEAP under the control of AhR.

When GFP expression was compared between the different transgenic lines using the same settings on the confocal microscope, we found that the GFP signals were always lower in the transgenic U lines bearing the pGFP-ZAM sensor transgene than they were with the flipped-out transgenes.