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1 d [Ca2+]i oscillations in eggs that had been inseminated.
2 tional resources towards oogenesis only when inseminated.
3 hronized with prostaglandin F2, artificially inseminated 2 to 3 days later, and challenged immediatel
5 In Drosophila melanogaster, the last male to inseminate a female sires approximately 80% of subsequen
6 when queens are singly rather than multiply inseminated and that increasing ovary activation is coup
10 nd use within female Drosophila melanogaster inseminated by two transgenic males with, respectively,
11 ely to attempt to mate with and successfully inseminate C. elegans hermaphrodites that do not concurr
13 nown centrosomal component, showed that snky-inseminated eggs failed to reconstitute a microtubule-or
14 ilar to the total amount of incorporation in inseminated eggs, i.e., the transcriptional capacity of
16 r most species, it is either not possible to inseminate females with sperm from a different species o
24 atids without seminal fluid are artificially inseminated into hermaphrodites, they fail to activate.
25 ilization of her eggs; the more sperm a male inseminates into a female, the more likely he is to fert
26 ulin nor nucleate microtubules when eggs are inseminated or microinjected, yet numerous maternally-nu
27 specially strong if productivity in a singly inseminated queen's colony declined because selfish work
29 ores in their semen, and queens artificially inseminated with either Nosema spores or the semen of No
30 tional eggs were divided into two groups and inseminated with two different sperm concentrations ("lo
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