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At all times post-immunization, gD-2 immunized mice were incompletely protected against HSV-2 MS (Fig. 8).
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In addition, changes in lung mechanics after bleomycin delivery to mice are incompletely understood.
The consequences of adventitious infectious agents upon the interpretation of toxicology studies performed in rats and mice are incompletely understood.
The molecular mechanism underlying this paradoxical activation of TGFβ signaling in TβRIIΔk transgenic mice is incompletely characterized.
The dendritic cell system in these mice has been incompletely studied to date.
The EFI was not calculated, and complications were incompletely reported.
Outcomes were incompletely reported; there was high risk of bias.
The decrease in CD45.1+ WT donor-derived thymocytes with increased recipient ages in the CD45.2+ IL7R−/− thymus is unlikely due to immunorejection, although IL7R−/− recipient mice are considered incompletely immunodeficient.
Incompletely injured or overhemisected mice were eliminated from all the analyses.
Interestingly, the dermatitis phenotype was incompletely penetrant, and depended heavily on both the genetic background and whether the mice were housed under specific pathogen-free conditions.
Despite the central role ascribed to Stat3 in mouse pluripotency, its downstream effectors are incompletely described.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com