Sentence examples for mouse embryo where from inspiring English sources

One dmrt2 gene is also expressed in the mouse embryo, where it is necessary for somite differentiation but with an impact on axial skeleton development.

This observation is consistent with high Nanog expression levels in the area of primitive streak formation in the mouse embryo, where Nanog expression co-localized with the primitive streak marker Mixl1 [43], [43].

This is very similar to the findings made in the mouse embryo, where wounding or scraping stimulates an accumulation of phospho-MAPK in the nucleus [5], and suggest that an event(s) or factor(s) separate from or in addition to growth factor stimulation is required to force nuclear translocation of phospho-MAPK in the primary cells.

The normal expression of dll4 and ephB4a suggests that arterial-venous differentiation is correct while expression of gata1 and scl1 in blood precursors at 20 hpf is consistent with the observation made in the mouse embryo where hematopoiesis was not affected [9], [10].

In the mouse embryo, where sFRP-3 affects axis elongation similarly to its effect in Xenopus [20], the concomitant transplacental delivery of both sFRP-3 and EGF (but not of FGF8) restored a normal embryo morphology in the majority of the embryos and also restored sFRP-3-dependent inhibition of myogenesis as it does in vitro.

Here, we discuss the present understanding of epigenetic regulation in the early mouse embryo where a large number of studies have characterized the establishment of different cell lineages.

Similar observations have been found in mouse embryos, where endogenous homologous templates were found to compete with ssDNA oligos for HDR repair (Wu et al., 2013).

We found that both HF2-BE2 and BE2 could convert target C to T efficiently in mouse embryos, where the editing efficiency of HF2-BE2 appeared higher than that of BE2.

To cover a later phase of olfactory neurogenesis, we investigated E13.5 mouse embryos, where the vomeronasal organ has separated from the olfactory epithelium.

In the present study, we analyzed 2 lines in detail: Tg(Pde1C-EGFP) mouse embryos, in which the EGFP transgene labeled all preplate neurons, and Tg(Girk4-EGFP) mouse embryos, where EGFP expression was restricted to Cajal Retzius neurons.

In fact, the increased dosage of Brachyury has been shown to exert strong effects on development, as seen in transgenic mouse embryos where three copies of this gene resulted in an extension of the anterior-posterior axis [ 161].