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1 yos occurred between 14.5 and 16.5 days post-coitus.
2 pathogens and foreign male Ags introduced at coitus.
3 , vaginal coitus with use of a condom, or no coitus.
4  response at the female genital mucosa after coitus.
5 d epithelium and deeper stromal tissue after coitus.
6 radrenergic areas at 1 h, but not 2 h, after coitus.
7 ioallantoic fusion and die by 10.5 days post coitus.
8 ccur without coitus or with condom-protected coitus.
9 cells were also abundant and increased after coitus.
10 s are now adults, 17 of who have experienced coitus and 7 have not.
11 t gestational time points between 8.5 d post coitus and birth.
12 ent, allowing for silent transmission during coitus and contributing to high seroprevalence of HSV-2
13 ary entries to document sex partner-specific coitus and event-specific condom use.
14               The neural connections between coitus and GnRH release involves norepinephrine (NE) and
15 ryo expresses RDH1 as early as 7.0 days post-coitus, and expression is especially intense within the
16     Fbw7-null mice die around 10.5 days post coitus because of a combination of deficiencies in hemat
17                                              Coitus, biting, and scratching are transfer mechanisms f
18 gina in response to the prospect of imminent coitus, but this has been difficult to assess experiment
19     In situ hybridization shows that in post coitus day 12.5 and 14.5 mouse embryos, distribution of
20 orta, umbilical, vitelline) of 9.5 days post coitus (dpc) to 11.5 dpc mouse embryos by single-cell RN
21 rimary endothelial cells from 9.5-days after coitus (dpc) yolk sac and P-Sp.
22 ylinder stage at approximately 6.5 days post coitus (dpc), but development was arrested before 7.5 dp
23 and embryonic tissues 7.5 to 11.5 days after coitus (dpc), resolved an SP in each, and demonstrated t
24 rom chamber differentiation at 9.5 days post coitus (dpc).
25 nses in the proximal region at 0.5 days post-coitus (dpc).
26  needed, vaginally or rectally, pre- or post-coitus, for flexible HIV prophylaxis.
27 jects reporting deep kissing with or without coitus had the same higher risk of infection than those
28 application (i.e., with or without simulated coitus) had a much more significant effect.
29 erated within 4 hr of sexual stimulation and coitus in female mice; prolactin-triggered oviductal flu
30 may influence cervical immune function after coitus in women, and potentially be a determinant of fer
31 indow of protection by TFV gel that supports coitus-independent use.
32 t the participation of ACh in the control of coitus-induced ovulation may include activation of alpha
33                                              Coitus induces fluid flow to guide sperm in the oviduct.
34 ctic acid content and acidity for CVM during coitus may contribute to both vaginal and penile protect
35                Depending on the frequency of coitus, men with average semen HIV-1 loads and without s
36 show severe defects at 3.5 d.p.c. (days post-coitus) morula/blastocyst stage and lethality before 8.5
37  Leukocyte recruitment did not occur without coitus or with condom-protected coitus.
38 ng mouse embryos (days 7, 11, 15 and 17 post coitus, p.c.).
39 plied vaginally or rectally, before or after coitus, providing the basis for a new method of flexible
40 th available data, condom use at most recent coitus rose from a median of 19.3% to 28.4%.
41  stages of embryonic development, day 7 post coitus the embryo expresses little or no lumican.
42 n 48 h later, 12 h after unprotected vaginal coitus, vaginal coitus with use of a condom, or no coitu
43 otinic ACh receptor (nAChR) before and after coitus was determined by immunocytochemistry.
44 pendent growth restriction at 15.5 days post-coitus while Egfr(Wa5) heterozygous placentas are only s
45  h after unprotected vaginal coitus, vaginal coitus with use of a condom, or no coitus.