戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 mination, or superovulation and intrauterine insemination.
2 ted to an introduced paternal template after insemination.
3 erwent IVF-ET and one underwent intrauterine insemination.
4 for embryo transfer (IVF-ET) or intrauterine insemination.
5 as accompanied the development of artificial insemination.
6 owing in vitro fertilization or intrauterine insemination.
7 3 cycles of ovarian stimulation/intrauterine insemination.
8 lexes into bovine zygotes (n = 121) 6 h post insemination.
9 ne the optimal dose, timing and location for insemination.
10 d timed condomless sex, or syringes for self-insemination.
11  taurus) pregnancies initiated by artificial insemination.
12 rough in-vitro fertilization or intrauterine insemination.
13 nagement or the women underwent intrauterine insemination.
14 nto ART and ovulation induction/intrauterine insemination.
15 ansferred with the male seminal fluid during insemination.
16 de, but not duration or frequency, following insemination.
17 nal immunization against paternal Ags during insemination.
18 determined by rectal palpation 42 days after insemination.
19  proper Ca(2+) oscillatory pattern following insemination.
20 chorionic gonadotropin test, two weeks after insemination.
21  a short time window, the first 15 min after insemination.
22 f dominant males to reduce the likelihood of insemination.
23 h semen analyses and thousands of artificial inseminations.
24 reated with superovulation and intracervical insemination (19 percent), or the 233 couples in the int
25 ng concentrations of estradiol on the day of insemination, a decreased rate of increase in progestero
26 tation of genes that are linked to traumatic insemination, a reduced chemosensory repertoire of genes
27 t may have led to the evolution of traumatic insemination across these lineages, as well as the press
28 ested whether exposure to paternal Ag during insemination activated or tolerized anti-paternal CD8+ T
29  conceptuses produced by SCNT and artificial insemination (AI) at day (d) 18 (preimplantation) and d
30 s synchronization aiming a second artificial insemination (AI) requires a reliable estimation of the
31 ure long-term sperm viability and artificial insemination (AI) success.
32 sting fertility, serial rounds of artificial insemination (AI) were conducted in 201 synchronized cro
33 collected on >7,000 bulls used in artificial insemination (AI) were used to identify 160 reliable and
34                               For artificial insemination (AI), semen was diluted 1:3 in a lactose-ba
35 sfer (ET) or frozen ET (FET), and artificial insemination (AI).
36 d intracervical insemination or intrauterine insemination alone.
37 mbers of the family Cimicidae show traumatic insemination and a suite of female adaptations to this m
38 les from 17 heifers on the day of artificial insemination and analyzed transcript abundance for 10,49
39 gate the female reproductive tract following insemination and are stored within the spermathecae, as
40 ed by in vitro fertilization or intrauterine insemination and for whom a first-trimester measurement
41 atients who underwent IVF-ET or intrauterine insemination and in the remaining eight patients, the ce
42 trospective study included both intrauterine insemination and in vitro assisted reproductive technolo
43 ssed by nonreturn to estrus after artificial insemination and in vitro embryonic development to the b
44 cally assisted reproduction via intrauterine insemination and in vitro fertilization.
45 le access to food (and therefore predictable insemination and infection cycles) up-regulated induced
46 at PA mass increased 2.7 fold by 1 min after insemination and inhibition of PA production by two meth
47                                         When insemination and ovulation are poorly synchronized, the
48 osation within eggs is evident seconds after insemination and precedes the calcium pulse of fertiliza
49 tical to achieving a successful intrauterine insemination and requires the processing of a semen samp
50  semen is widely disseminated for artificial insemination and the virus can cause significant health
51 y to result in pregnancy as is intracervical insemination and twice as likely to result in pregnancy
52 ure oocytes failed to develop normally after insemination and typically produced non-wave-like calciu
53 eased rate of increase in progesterone after insemination, and, ultimately, decreased circulating con
54  domain for ovulation induction/intrauterine insemination (aOR, 1.00; 95% CI, 0.57-1.77 for singleton
55 vulation with gonadotropins and intrauterine insemination are frequently used to treat infertility.
56 llite doctor's offices to offer intrauterine insemination as an option for patients without the clini
57 gent processes, we established cross-species insemination assays, mixing zebrafish eggs with mouse sp
58 fter infertility treatment (ie, intrauterine insemination, assisted reproductive technology, fertilit
59 sible to observe the consequences of such an insemination because the female is opaque.
60  been hypothesized, recent evidence of cross-insemination between these species in nature and the ste
61 d into queenless hives for natural mating or insemination, both of which take place when queens are o
62                                              Insemination by multiple males shifts the arena for sexu
63 nduces lifetime refractoriness to subsequent insemination by other males, enforcing the paternity of
64                         Multiple mating (and insemination) by females with different males, polyandry
65  exhibit repetitive Ca(2+) oscillations upon insemination, collectively suggesting that cell cycle-re
66             These expanded opportunities for insemination complicate the mating systems of the Ixodes
67 hat the Ca2+ wave was inhibited under normal insemination conditions but that the block of the Ca2+ w
68  Bovine fetuses were generated by artificial insemination (control) or IVP.
69 ity treatment cycles, including intrauterine insemination cycles and in vitro fertilization with or w
70 comes with ART, particularly in conventional insemination cycles.
71 h 0.77 (95% CI: 0.27, 0.97)] in conventional insemination cycles.
72 se relations were restricted to conventional insemination cycles.
73  of bovine embryos with AMBMP at day 5 after insemination decreased development to the blastocyst sta
74 tants manifest significantly female-specific insemination deficits, and although AcIr76b-/- mutant fe
75 sually in vitro fertilization (IVF) or donor insemination (DI), the practitioners have a special resp
76 of the calmodulin antagonist W-7 followed by insemination does not block cortical granule exocytosis,
77  specimens from different healthy artificial-insemination donors (n = 30) and human immunodeficiency
78  the 37 semen specimens (two from artificial-insemination donors and one from an HIV-positive patient
79 nflict theory that free female choice before insemination eliminates selective pressures for the evol
80 ity) than MOC females, showing that multiple inseminations enhance offspring and mother fitness.
81  for semen quality, bulls used in artificial insemination exhibit significant variation in fertility.
82 i) superovulation, (ii) egg retrieval, (iii) insemination/fertilization and (iv) embryo transfer.
83  four stages: Superovulation, Egg-retrieval, Insemination/Fertilization and Embryo transfer.
84                                   Artificial insemination fluid derived from epididymal flush and sem
85  DPI, intravaginal inoculation of artificial insemination fluid from these time-points failed to resu
86 nd inoculated intravaginally with artificial insemination fluid from ZIKV-infected males.
87      ZIKV RNA was detected in the artificial insemination fluid generated from epididymal flush or se
88                                              Insemination from bull A resulted in an average sperm as
89 average sperm aster diameters produced after inseminations from bull B (78.2 microm; 60.8%) or bull C
90 nt), or the 233 couples in the intracervical-insemination group (10 percent).
91 nt) than the 234 couples in the intrauterine-insemination group (18 percent), the 234 couples in the
92 times as likely as those in the intrauterine-insemination group (95 percent confidence interval, 1.2
93 ecome pregnant as those in the intracervical-insemination group (95 percent confidence interval, 2.0
94              The couples in the intrauterine-insemination group and in the group treated with superov
95 ly to conceive as those in the intracervical-insemination group.
96 treated with superovulation and intrauterine insemination had a higher rate of pregnancy (33 percent)
97 d, catalytically inactive Fyn at 45 min post-insemination had no significant effect during cleavage a
98 kinase activity during the first 2 min after insemination; however, activity had increased approximat
99 ein complex injections at various hours post insemination (hpi) (6, 8, and 18 hpi) as well as in vitr
100 in voltage-clamped sea urchin eggs following insemination in a variety of artificial seawaters.
101                             Using artificial insemination, in combination with vasectomized male mati
102 t images of embryos collected at 113 hr post-insemination, in embryo selection amongst 97 clinical pa
103 tant management, treatment with intrauterine insemination, in vitro fertilization (IVF), or intracyto
104 everal biochemical events beginning with the insemination into the female reproductive tract and, fin
105 e randomly assigned to receive intracervical insemination, intrauterine insemination, superovulation
106                                    Traumatic insemination is a bizarre form of mating practiced by so
107 the established fact that the female site of insemination is hostile to sperm, and that non-sperm com
108          In terrestrial arthropods traumatic insemination is most prevalent in the true bug infraorde
109                                    Traumatic insemination is thought to occur in the Strepsiptera and
110 induction of superovulation and intrauterine insemination is three times as likely to result in pregn
111 t physical contact with a male worm, and not insemination, is sufficient to induce female development
112 erm injection (ICSI) (733) and intra uterine insemination (IUI) (1196) treatments were included.
113 itro fertilization (IVF) and/or intrauterine insemination (IUI) cycles in a prospective study of envi
114 (3) ovulation induction (OI) or intrauterine insemination (IUI), or (4) in vitro fertilization (IVF)
115 re eligible for standard bolus intra-uterine insemination (IUI).
116                                    Traumatic insemination mechanisms and attributes are compared acro
117 tified 47,628 live-births after intrauterine insemination (n = 24,962) and in-vitro fertilization (n
118 ansgenic female fetus produced by artificial insemination of a nontransgenic adult female with semen
119                                   Artificial insemination of dairy cattle is a common practice in the
120                                              Insemination of females with fresh semen (n = 10) result
121                                              Insemination of females with semen cold-stored 24 h (n =
122 rms (0.6%) never used hormones to assist the insemination of lactating dairy cows.
123 n sequential mating trials and in artificial insemination of mixed-sperm populations.
124 y functions in sperm competition by blocking insemination of subsequent males.
125 fraction increased approximately 7 min after insemination of Xenopus laevis eggs.
126                                        Cross-inseminations of A. albopictus females by A. aegypti mal
127                    We performed instrumental inseminations of queens, each with four different males,
128 owever, ovulation induction and intrauterine insemination (OI/IUI)-2 other common forms of fertility
129 ation induction with or without intrauterine insemination [OI/IUI], and 305,898 were born after no fe
130 permless hermaphrodites was blocked by prior insemination or by genetic ablation of the ceh-18-depend
131  the start of breeding for timing artificial insemination or inducing oestrus was judged "unacceptabl
132 with either superovulation and intracervical insemination or intrauterine insemination alone.
133 these female mice were sterile after in vivo insemination or natural mating.
134  spraying were found for effects on density, insemination or parity rate.
135 cies after ovulation induction, intrauterine insemination, or IVF did not differ significantly betwee
136 ancy after ovulation induction, intrauterine insemination, or IVF.
137 semination, superovulation and intracervical insemination, or superovulation and intrauterine insemin
138                                       Of six inseminations performed with fresh semen, three resulted
139 e later classified as pregnant to artificial insemination, pregnant to natural breeding or not pregna
140 solutions that are widely used in artificial insemination programs were found to be compatible and ev
141   A fraction of sperm deposited at mating or insemination reaches the oviduct isthmus, where sperm ar
142 ating-prezygotic reproductive character, the insemination reaction mass, in two species, Drosophila m
143                      Importantly, artificial insemination reveals that sperm mediates some of the beh
144                           We used artificial insemination, RNA-sequencing and electroretinography to
145 ders, ovulation occurs weeks or months after insemination, so the pheromone-induced change in recepti
146 ate the effect of intra-uterine slow-release insemination (SRI) on pregnancy rates in women with conf
147 in our analysis significantly decreased male insemination success, further suggesting that genes rela
148 ring to determine queen mating frequency and insemination success.
149 ive intracervical insemination, intrauterine insemination, superovulation and intracervical inseminat
150 ved much higher rates of infection following insemination than did N. apis.
151                                In artificial insemination the use of sex-sorted bovine sperm results
152                                    Following insemination, the IP(3)R-1 dsRNA-injected eggs displayed
153 ulated genes between conspecific contact and insemination, the major part of the observed transcripto
154  recently fed females and do so by traumatic insemination (TI).
155               The requirements for traumatic insemination to evolve are stringent, yet surprisingly i
156 ltration of 40,000 daltons within minutes of insemination via a peroxidase-dependent mechanism, with
157 ved semen, laparoscopic oviductal artificial insemination was performed on three queens, two queens p
158 against host cells, which plays a role after insemination, we propose that polySia in semen represent
159 treated with superovulation and intrauterine insemination were 3.2 times as likely to become pregnant
160 2 vs. 31%) conception rates following single insemination were greater (P < 0.01) for CON compared wi
161 reated with superovulation and intracervical insemination were nearly twice as likely to conceive as
162                                       Twelve inseminations were performed by an intrauterine laparosc
163               Results demonstrate artificial insemination with cold-stored semen can provide a strate
164 an be transmitted horizontally by artificial insemination with fresh semen.
165 mmercial semen doses intended for artificial insemination with the 10-10-10 photo-stimulation pattern

 
Page Top