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Exact(6)
Given the dramatic effects GOF mutations has on bone development, it seems paradoxical that trpv4−/− mice develop normal skeletons at birth [39], [42].
These data coupled with the fact that TA-specific knockout mice develop normal skin add further credence to the idea that ΔNp63 might be the critical p63 isoform required for epidermal morphogenesis [22].
Note that MHC class I restricted OT-1/Itk−/− mice develop normal conventional CD8+ T cell due to efficient selection in the thymus of T cells carrying this transgenic TCR [23].
We further show that HPK1−/− mice develop normal bone marrow and splenic B-cell subset counts but exhibit an increase in B-cell reactivity, suggesting that HPK1 limits the actions emanating from the SKAP-HOM adaptor complex needed for proper B-cell activation and adhesion.
Surprisingly, whereas heterozygosity of specific CRX mutations in humans can cause severe retinal disease, Crx +/− mice develop normal photoreceptors that do not degenerate (Furukawa et al., 1999).
Although Bcl-G-deficient mice develop normal and display no obvious phenotype under steady state conditions, the function of Bcl-G under pro-inflammatory conditions and in tumor development remains to be explored in appropriate model systems.
Similar(53)
In contrast, IL-12 KO or IFN-I receptor KO mice developed normal levels of specific cytotoxicity in vivo (Fig. 6A and 6C, respectively).
Indeed, analysis of these mice 5 9 days after infection showed no detectable parasites in peripheral blood, whereas control mice developed normal blood infections with parasitemias ranging between 0.1 and 3% at day 4 post-infection.
Bik-deficient mice develop normally with a normal lifespan.
Alk7ASKA mice developed normally, and displayed normal growth and normal fasting insulinemia and glycemia (data not shown).
T cells from triple-mutant mice developed normally and showed normal cytokine secretion and proliferative responses to TCR stimulation.
Related(18)
mice develop typical
mice develop early-onset
mice develop Sjögren-like
mice develop high
mice develop early
mice develop severe
mice develop various
mice develop gastric
mice develop multifocal
mice develop renal
mice develop polyclonal
mice develop significant
mice develop hepatic
mice develop several
mice develop robust
mice develop low
mice develop complex
mice develop multiple
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