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"Every time we use a tool to interact with our environment, such as a computer mouse, car or glasses, our brain assimilates properties of the tool into neuronal space.
Additional studies described here show that the postulated key event of hepatocellular proliferation was observed in CD-1 mice for both PPZ and PB, and that PPZ is also a potent activator of the mouse CAR nuclear receptor.
To elucidate the underlying toxicity mechanisms and test potentially safer CAR T cells, we developed a mouse model in which human CD19 (hCD19 -specific mouse CAR T cells were adoptively transferred into mice whCD19 -specificells express a hCD19 transgene at hemouseous levels.
Mouse CAR was originally cloned as an 8 exon protein.
In contrast with other species, mouse CAR (mCAR) was initially cloned as a protein composed of 8 exons [18] and was named mCAR1.
We therefore performed western blot analysis using an antibody that recognizes both human and mouse CAR (Santa Cruz, sc-15405), and observed substantial regional variation in the abundance of endogenous mCAR protein in adult wild type mice.
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At launch, there are 15 different themes available, including various Disney princesses, Frozen, Mickey Mouse, Cars, Planes, and Muppets, to name a few, and there are dozens more themes in the pipeline, we're told.
While most Mack spinning coasters feature outward facing seats, the Cobra's Curse cars have forward-facing seats that look similar to Mack's Wild Mouse cars, according to Screamscape.
This is definitely a mouse for car lovers and there's apparently quite a market for car mice, as RoadMice.com offers about a skillion different models of wired and wireless mice that look just like real-life cars.
These contributions are demonstrated for freeform surface design, with examples of computer mouse and car seat exterior surfaces.
Subsequent studies uncovered TCPOBOP, the most potent known member of the phenobarbital-like class of CYP2B inducers, as the first agonist of mouse (m) CAR, in that TCPOBOP dose-dependently restores mCAR activity following inhibition by the inverse agonists (Tzameli et al., 2000).
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