ライフサイエンスコーパス: insemination

1 nagement or the women underwent intrauterine insemination.

2 ansferred with the male seminal fluid during insemination.

3 de, but not duration or frequency, following insemination.

4 nal immunization against paternal Ags during insemination.

5 determined by rectal palpation 42 days after insemination.

6 proper Ca(2+) oscillatory pattern following insemination.

7 nto ART and ovulation induction/intrauterine insemination.

8 a short time window, the first 15 min after insemination.

9 f dominant males to reduce the likelihood of insemination.

10 mination, or superovulation and intrauterine insemination.

11 ted to an introduced paternal template after insemination.

12 erwent IVF-ET and one underwent intrauterine insemination.

13 for embryo transfer (IVF-ET) or intrauterine insemination.

14 reated with superovulation and intracervical insemination (19 percent), or the 233 couples in the int

15 ng concentrations of estradiol on the day of insemination, a decreased rate of increase in progestero

16 tation of genes that are linked to traumatic insemination, a reduced chemosensory repertoire of genes

17 t may have led to the evolution of traumatic insemination across these lineages, as well as the press

18 ested whether exposure to paternal Ag during insemination activated or tolerized anti-paternal CD8+ T

19 conceptuses produced by SCNT and artificial insemination (AI) at day (d) 18 (preimplantation) and d

20 sting fertility, serial rounds of artificial insemination (AI) were conducted in 201 synchronized cro

21 collected on >7,000 bulls used in artificial insemination (AI) were used to identify 160 reliable and

22 d intracervical insemination or intrauterine insemination alone.

23 mbers of the family Cimicidae show traumatic insemination and a suite of female adaptations to this m

24 ed by in vitro fertilization or intrauterine insemination and for whom a first-trimester measurement

25 atients who underwent IVF-ET or intrauterine insemination and in the remaining eight patients, the ce

26 ssed by nonreturn to estrus after artificial insemination and in vitro embryonic development to the b

27 at PA mass increased 2.7 fold by 1 min after insemination and inhibition of PA production by two meth

28 osation within eggs is evident seconds after insemination and precedes the calcium pulse of fertiliza

29 semen is widely disseminated for artificial insemination and the virus can cause significant health

30 y to result in pregnancy as is intracervical insemination and twice as likely to result in pregnancy

31 ure oocytes failed to develop normally after insemination and typically produced non-wave-like calciu

32 eased rate of increase in progesterone after insemination, and, ultimately, decreased circulating con

33 domain for ovulation induction/intrauterine insemination (aOR, 1.00; 95% CI, 0.57-1.77 for singleton

34 vulation with gonadotropins and intrauterine insemination are frequently used to treat infertility.

35 sible to observe the consequences of such an insemination because the female is opaque.

36 been hypothesized, recent evidence of cross-insemination between these species in nature and the ste

37 d into queenless hives for natural mating or insemination, both of which take place when queens are o

38 Insemination by multiple males shifts the arena for sexu

39 nduces lifetime refractoriness to subsequent insemination by other males, enforcing the paternity of

40 Multiple mating (and insemination) by females with different males, polyandry

41 exhibit repetitive Ca(2+) oscillations upon insemination, collectively suggesting that cell cycle-re

42 These expanded opportunities for insemination complicate the mating systems of the Ixodes

43 hat the Ca2+ wave was inhibited under normal insemination conditions but that the block of the Ca2+ w

44 of bovine embryos with AMBMP at day 5 after insemination decreased development to the blastocyst sta

45 sually in vitro fertilization (IVF) or donor insemination (DI), the practitioners have a special resp

46 of the calmodulin antagonist W-7 followed by insemination does not block cortical granule exocytosis,

47 specimens from different healthy artificial-insemination donors (n = 30) and human immunodeficiency

48 the 37 semen specimens (two from artificial-insemination donors and one from an HIV-positive patient

49 nflict theory that free female choice before insemination eliminates selective pressures for the evol

50 ity) than MOC females, showing that multiple inseminations enhance offspring and mother fitness.

51 i) superovulation, (ii) egg retrieval, (iii) insemination/fertilization and (iv) embryo transfer.

52 four stages: Superovulation, Egg-retrieval, Insemination/Fertilization and Embryo transfer.

53 Insemination from bull A resulted in an average sperm as

54 average sperm aster diameters produced after inseminations from bull B (78.2 microm; 60.8%) or bull C

55 nt), or the 233 couples in the intracervical-insemination group (10 percent).

56 nt) than the 234 couples in the intrauterine-insemination group (18 percent), the 234 couples in the

57 times as likely as those in the intrauterine-insemination group (95 percent confidence interval, 1.2

58 ecome pregnant as those in the intracervical-insemination group (95 percent confidence interval, 2.0

59 The couples in the intrauterine-insemination group and in the group treated with superov

60 ly to conceive as those in the intracervical-insemination group.

61 treated with superovulation and intrauterine insemination had a higher rate of pregnancy (33 percent)

62 d, catalytically inactive Fyn at 45 min post-insemination had no significant effect during cleavage a

63 kinase activity during the first 2 min after insemination; however, activity had increased approximat

64 in voltage-clamped sea urchin eggs following insemination in a variety of artificial seawaters.

65 everal biochemical events beginning with the insemination into the female reproductive tract and, fin

66 e randomly assigned to receive intracervical insemination, intrauterine insemination, superovulation

67 Traumatic insemination is a bizarre form of mating practiced by so

68 the established fact that the female site of insemination is hostile to sperm, and that non-sperm com

69 In terrestrial arthropods traumatic insemination is most prevalent in the true bug infraorde

70 Traumatic insemination is thought to occur in the Strepsiptera and

71 induction of superovulation and intrauterine insemination is three times as likely to result in pregn

72 itro fertilization (IVF) and/or intrauterine insemination (IUI) cycles in a prospective study of envi

73 Traumatic insemination mechanisms and attributes are compared acro

74 ansgenic female fetus produced by artificial insemination of a nontransgenic adult female with semen

75 Artificial insemination of dairy cattle is a common practice in the

76 rms (0.6%) never used hormones to assist the insemination of lactating dairy cows.

77 n sequential mating trials and in artificial insemination of mixed-sperm populations.

78 y functions in sperm competition by blocking insemination of subsequent males.

79 fraction increased approximately 7 min after insemination of Xenopus laevis eggs.

80 Cross-inseminations of A. albopictus females by A. aegypti mal

81 permless hermaphrodites was blocked by prior insemination or by genetic ablation of the ceh-18-depend

82 the start of breeding for timing artificial insemination or inducing oestrus was judged "unacceptabl

83 with either superovulation and intracervical insemination or intrauterine insemination alone.

84 these female mice were sterile after in vivo insemination or natural mating.

85 cies after ovulation induction, intrauterine insemination, or IVF did not differ significantly betwee

86 ancy after ovulation induction, intrauterine insemination, or IVF.

87 semination, superovulation and intracervical insemination, or superovulation and intrauterine insemin

88 Of six inseminations performed with fresh semen, three resulted

89 solutions that are widely used in artificial insemination programs were found to be compatible and ev

90 ating-prezygotic reproductive character, the insemination reaction mass, in two species, Drosophila m

91 ders, ovulation occurs weeks or months after insemination, so the pheromone-induced change in recepti

92 ive intracervical insemination, intrauterine insemination, superovulation and intracervical inseminat

93 ved much higher rates of infection following insemination than did N. apis.

94 Following insemination, the IP(3)R-1 dsRNA-injected eggs displayed

95 The requirements for traumatic insemination to evolve are stringent, yet surprisingly i

96 ltration of 40,000 daltons within minutes of insemination via a peroxidase-dependent mechanism, with

97 against host cells, which plays a role after insemination, we propose that polySia in semen represent

98 treated with superovulation and intrauterine insemination were 3.2 times as likely to become pregnant

99 reated with superovulation and intracervical insemination were nearly twice as likely to conceive as

100 Twelve inseminations were performed by an intrauterine laparosc

101 an be transmitted horizontally by artificial insemination with fresh semen.

102 mmercial semen doses intended for artificial insemination with the 10-10-10 photo-stimulation pattern