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However, another explanation is needed to explain the persistence of cocaine sensitization in these transgenic mice because we found that the NR1 gene was eliminated in virtually all DA neurons examined.
The data that were used to calculate the genetic correlations were from the male mice because we performed detailed analysis only on males.
We did not perform an exhaustive analysis with the Confetti mice because we felt the results from our MADM analysis were compelling and statistically significant.
However, we chose to use stock C57BL/6 as controls for the experiments on M/Mt-CK−/−(129/Bl6) mice, because we wanted to emulate the conditions used in previous studies to determine whether we could recapitulate their findings.
We did not assess insulin tolerance in our mice because we have found that the measurement compromises the ability of the severely cachectic mice to successfully complete subsequent functional analyses.
We confirm in rats the previous results in mice because we also observed an increase in MMP-2 and MMP-9 that in our conditions occurs significantly in RL than in ML and LL.
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We previously detected Ehrlichia spp. DNA in I. ovatus injected mice, but did not detect A. phagocytophilum DNA in I. ovatus– or I. persulcatus injected mice (12 ) because we used only a few immunocompromised mice, i.e., most had normal immune systems.
We could not define dorsal and ventral tiers in SNc clearly, either because of the difference between rats and mice or because we lacked sufficient resolution or proper markers.
Sometimes I act like a mouse, because suddenly God thinks I'm a mouse.
We generally used ChatCre mice as homozygotes, because we found that this gave earlier and more even Cre activity at P1, when SAC dendrites are beginning to elaborate.
The primary goal of the rodent sampling scheme was to detect LCMV infection in the colony; only adult mice were sampled because we assumed that they would have the greatest likelihood of having detectable antibodies.
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