Sentence examples for rat germ cells from inspiring English sources

We have investigated expression of GPER in mouse and rat germ cells at differential maturative stages.

The re-establishment of 5mC in male rat germ cells appears to begin at e19.5.

In accord, long-term apoptotic cell death process has been reported in adult rat germ cells exposed in utero to flutamide and vinclozolin [ 37, 38].

Thus, the stable presence of 5hmC, 5fC and 5caC in rat germ cells between e14.5 and e16.5, and in testicular somatic cells throughout late gestation, may indicate potential functionality of these modifications during germ cell development.

Our study, showing the stable persistence of 5hmC in fetal rat germ cells until e16.5, suggests that the removal of 5mC through conversion to 5hmC might also occur in the rat.

There was no/little detectable 5mC in germ cells between e14.5 and e18.5, suggesting that, as in mice, rat germ cells are hypomethylated relative to surrounding somatic cells by e14.5.

DBP-induced rat germ cell aggregation was evident at E21.5 but largely resolved by PND4, findings we confirmed quantitatively.

Here, we have investigated the spatiotemporal relationship between 5mC, 5hmC, 5fC and 5caC specifically during late (e14.5 e21.5) male fetal rat germ cell development by immunofluorescence using previously validated antibodies [ 13, 14, 41- 44].

Highly enriched populations of rat testicular germ cells were prepared by sequential enzymatic dissociation of rat testis.

The qRT-PCR of total RNA from rat testicular germ cells and from sorted germ cells, namely pachytene spermatocytes and spermatids, showed that the rat X-chromosomal G6pd gene was silenced in pachytene spermatocytes and reactivated postmeiotically in spermatids (Figure 8).

The present study was designed to determine the effects of ghrelin treatment on in vivo quality and quantity expression of apoptosis and proliferation specific indices in rat testicular germ cells.