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Analysis of Xenopus embryos suggests a mechanism for the homophilic cell sorting observed in the female conditional Efnb1 mutant mouse embryos studied here [Lee et al., 2008].
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For mouse embryo studies, noon on the day that a vaginal plug was observed was designated as e0.5, and for postnatal studies, the day of birth was designated as P0.
The inability of study-level meta-analysis to overcome partial consistency on a limited number of studies was also observed in the meta-analysis of mouse embryo studies [ 3].
Table 2 summarizes the assignment of observations within conditions (mouse embryo studies or series and treatments) to each of the two components (Mix1 and Mix2) of a mixture model describing the gene Actin sub-network.
Surprisingly, these specificities of the mouse dentition appear to be a benefit for experimental studies on odontogenesis: it is very advantageous that the jaw of a mouse embryo allows studying and comparing the formation of a tooth with continuous/unlimited growth (incisor), the origin of a toothless diastema, and successive development of molars with limited growth (Fig. 6c).
If LC3 and p62 are degraded by the proteasome, the macroautophagy pathway would no longer be available and could explain the shift from the usage of macroautophagy to other forms of autophagy and proteasome-mediated protein degradation observed after TNFα stimulation in this study and the mouse embryo fibroblast study [ 29].
After receiving a B.Sc. (1951), he studied mouse embryos, artificial insemination, and infertility at the University of Edinburgh (Ph.D., 1955).
The developmentally restricted differentiation potential of the stem cells of the early mouse embryo has been studied for understanding transcriptional and epigenetic regulation in lineage specification.
LH helped with the mouse embryo fibroblast studies.
Despite considerable progress in defining the role of the interactions between signalling pathways and regionalised genetic activity in the induction of PS precursors, the inaccessibility of mouse embryos renders the study of the transition from pluripotency to lineage restriction difficult.
To date, mouse embryos have not been extensively studied by microarray analysis (Carter et al. 2003; Smith and Greenfield 2003), partly because of their small size and limited RNA content.
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