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Exact(47)
b PLs from saline and S. pneumoniae infected WT and PAI-1−/− mice were assayed for plasmin activity.
For HFD experiments, mice were assayed after 20 to 26 weeks on HFD.
Intraperitoneal macrophages from WT and CD36−/− mice were assayed for capacity to efflux CE to HDL.
BKS db/+ and db/db mice were assayed at 6 weeks and at 10- and 14-weeks of age.
Quantitative differences in CXCL13 expression in the thymus between Hexb+/−FcRγ+/+, Hexb−/−FcRγ+/+ and Hexb−/−FcRγ−/− mice were assayed by real-time RT-PCR (Fig. 6A).
Neurons isolated from L1+/y and L1−/y mice were assayed for neurite outgrowth using different concentrations of L1 antibody 557 (Fig. 3Aa).
Similar(13)
In order to discard the possible effect of mouse blood present in the trypomastigote suspension, blood from T. cruzi uninfected mice was assayed in parallel in all co-infection experiments.
The expression of eGFP in tissues of F1 transgenic mice was assayed by confocal microscopy (LSM 510, Zeiss, Oberkochen, Germany).
Spontaneous locomotor activity of wild-type and Id2−/− mice was assayed using the open-field test (Walsh and Cummins, 1976).
The antioxidant status of the plasma from AH and AC exposed mice was assayed with an antioxidant reductive capacity assay (NWK-ARC01; Northwest Life Science Specialties, Vancouver, WA).
The gene expression profile of the gastric fundus of wild type and W/W V mice was assayed by murine microarray analysis displaying a total of 8734 elements.
Related(20)
mice were estimated
mice were analysed
birds were assayed
specimens were assayed
studies were assayed
mice were experimented
mice were sampled
individuals were assayed
mice were evaluated
mice were ascertained
mice were corroborated
mice were quantified
mice were measured
mice were investigated
ones were assayed
mice were split
mice were administered
mice were sacrificed
mice were chosen
mice were hunted
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