ライフサイエンスコーパス: inseminate

1 tional resources towards oogenesis only when inseminated.

2 d [Ca2+]i oscillations in eggs that had been inseminated.

3 hronized with prostaglandin F2, artificially inseminated 2 to 3 days later, and challenged immediatel

4 In promiscuous fruit flies, the last male to inseminate a female has a fertilising advantage.

5 In Drosophila melanogaster, the last male to inseminate a female sires approximately 80% of subsequen

6 t compete against wild males to successfully inseminate a female.

7 tem from sham-inseminated cows and from cows inseminated and detected pregnant 7 days after oestrus.

8 when queens are singly rather than multiply inseminated and that increasing ovary activation is coup

9 Ten heifers were estrus synchronized, inseminated, and uterine challenged 2 weeks later.

10 k by the female and maximises the chances of inseminating both sperm storage sites.

11 Using immunofluorescence labeling of inseminated bovine oocytes and serial sectioning-ultrast

12 cles of known outcome, and cycles which were inseminated but did not result in a birth.

13 g flights for several days even when already inseminated by a number of drones.

14 nd use within female Drosophila melanogaster inseminated by two transgenic males with, respectively,

15 ely to attempt to mate with and successfully inseminate C. elegans hermaphrodites that do not concurr

16 and ULF were collected post-mortem from sham-inseminated cows and from cows inseminated and detected

17 nvasive, puncturing the female body-wall and inseminating directly into her body-cavity.

18 nown centrosomal component, showed that snky-inseminated eggs failed to reconstitute a microtubule-or

19 ilar to the total amount of incorporation in inseminated eggs, i.e., the transcriptional capacity of

20 he hypothalamo-pituitary-gonadal axis of the inseminated female.

21 r most species, it is either not possible to inseminate females with sperm from a different species o

22 them to roam across the bone to contact and inseminate females.

23 them to roam across the bone to contact and inseminate females.

24 s, the success of a male's sperm in multiply inseminated females depends on the male's genotype.

25 Paternity of offspring of multiply inseminated females is in many organisms highly skewed,

26 Sperm competition in ovaries of multiply-inseminated females may favor fertilization of immature

27 Neither exposure to previously inseminated females nor antibiotics in semen extenders i

28 Parthenogenesis rate for inseminated females was 0.71%.

29 In this study, mutant males that inseminate fertilization-defective sperm were used to re

30 If GNU eggs are inseminated, however, the male pronucleus also undergoes

31 atids without seminal fluid are artificially inseminated into hermaphrodites, they fail to activate.

32 ilization of her eggs; the more sperm a male inseminates into a female, the more likely he is to fert

33 in decreased egg viability when these males inseminate nonmated females.

34 Beef heifers were artificially inseminated on D0 and pregnancies were diagnosed on D28.

35 ulin nor nucleate microtubules when eggs are inseminated or microinjected, yet numerous maternally-nu

36 specially strong if productivity in a singly inseminated queen's colony declined because selfish work

37 Although transgenic eggs could be inseminated, the eggs did not exhibit the normal series

38 Forty-one hembras were inseminated with either fresh, papain-treated or frozen-

39 ores in their semen, and queens artificially inseminated with either Nosema spores or the semen of No

40 Females (n = 20) were inseminated with fresh or 24-48 h cold-stored raw or ext

41 Two females inseminated with fresh or cold-stored semen laid eggs th

42 uid flew two days earlier than sister queens inseminated with saline, and failed more often to return

43 tional eggs were divided into two groups and inseminated with two different sperm concentrations ("lo

44 None of the six inseminates with thawed cryopreserved semen resulted in