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1  on the left side of the mouse embryo by 8.0 days post coitum.
2 e embryonic lethal, dying between 8 and 11.5 days post coitum.
3 ied during embryonic development at 9.5-14.5 days post coitum.
4  of expression in the gonad at 12.5 and 13.5 days post-coitum, after overt gonad differentiation, by
5 usly during embryonic development until 13.5 days post-coitum and in the adult heart, kidney, brain,
6 d in the developing heart at E10.5 and E11.5 days post-coitum and in the musculoskeletal system from
7  expression in the branchial arches from 9.5 days post-coitum and show that its activity in the conte
8  meiotic differentiation of germ cells (13.5 days post coitum) and from both in vivo exposed mice and
9    At the time of PGC allocation around 7.25 days post coitum, Blimp1 heterozygous embryos exhibit de
10 lethality in Cbfb(-/-) mouse embryos at 12.5 days post coitum (d.p.c.) from hemorrhages and lack of d
11   Mouse embryos deficient in Gata3 die by 11 days post coitum (d.p.c.) from pathology of undetermined
12  mouse results in embryonic lethality at 5.5 days post coitum (d.p.c.) which can be overcome by simul
13        These embryos develop normally to 7.5 days post coitum (d.p.c.), but their growth is severely
14 ulated in pancreatic endocrine cells at 18.5 days post coitum (d.p.c.), when definitive islets first
15  the epiblast at stages between 5.5 and 5.75 days post coitum (d.p.c.).
16 he AGM region and umbilical vessels on 10-11 days post coitum (d.p.c.).
17 fap2c(-/-) mice failed to survive beyond 8.5 days post coitum (d.p.c.).
18 on on mouse embryos ranging from 8.5 to 11.5 days post-coitum (d.p.c.), Pitx3 mRNA was seen only in t
19 ozygous mutation is embryonic lethal by 13.5 days post coitum, demonstrating the importance of Opa1 d
20 bition of FGF signalling between 5.5 and 7.5 days post-coitum does not block neural differentiation i
21 gs look grossly and histologically normal at days post coitum (dpc) 6.5 and 7.5 of pregnancy.
22 Lhx3/Lhx4 expression in RP epithelium at 9.0 days post coitum (dpc) and total loss of pituitary tissu
23 guishable from wild-type embryos through 6.5 days post coitum (dpc) and were able to establish all th
24        The mouse germ line originates at 6.5 days post coitum (dpc) in the proximal epiblast, apparen
25  germ cells (EGCs) derived from 11.5 or 12.5 days post coitum (dpc) primordial germ cells (PGCs).
26 rm is correctly induced and patterned at 7.5 days post coitum (dpc), but subsequently fails to develo
27 yos display profound yolk sac defects at 9.5 days post coitum (dpc), including disrupted angiogenesis
28 lls, expression of Gm114 begins at 12.5-13.5 days post coitum (dpc), the stage in mice when germ cell
29 lly comparable in size with controls at 13.5 days post coitum (dpc), their placentas were significant
30 n the XY gonad decline in numbers after 11.5 days post coitum (dpc), while germ cell numbers in XX go
31 of the developing heart starting at day 11.5 days post coitum (dpc).
32 und in the testis and ovary as early as 13.5 days post coitum (dpc).
33 eir migration to the gonads from 8.5 to 13.5 days post coitum (dpc).
34 ryos declining markedly between 9.5 and 12.5 days post coitum (dpc).
35 red into XY but not XX gonads from 11.5-16.5 days post coitum (dpc).
36 nt (GATA4-/-) mice died between 8.5 and 10.5 days post coitum (dpc).
37                                       At 3.5 days post-coitum (dpc) and 4.5 dpc, the tetraploid ESCs
38 orylated eNOS (p-eNOS) expression in 7.2-8.5 days post-coitum (dpc) mouse embryos.
39 onducted RNA-seq analysis of lungs from 18.5 days post-coitum (dpc) Src-1(-/-) /-2(-/-) (dKO) vs. WT
40 S) and 12-somite pair (-s) stages (~6.75-9.0 days post coitum, dpc) in histological sections.
41     Injection of PAF or SP-A into AF at 17.5 days post coitum enhanced uterine NF-kappaB activation a
42                                       By 9.5 days post coitum, expression in the nervous system is pr
43 CD105(+)Thy1(-)) that, when sorted from 15.5 days post-coitum fetal bones and transplanted under the
44 wing transfer, but none developed beyond 8.5 days post coitum; however, a high percentage of enucleat
45 fferent tissues was observed beginning at 16 days post coitum in developing brain neurons, primitive
46 zation on mouse embryos ranging from 9 to 16 days post-coitum localized murine Og12x mRNA in the hear
47 ntrations transiently, and declined from 6.5 days post coitum onward, as the cells underwent apoptosi
48  in the collecting duct epithelium from 13.5 days post coitum onward.
49 tochemical analysis of murine embryos at 7.8 days post coitum revealed that Csx protein is strongly e
50 eir X-linked homologues, at three ages: 13.5 days post coitum, the day of birth (P1) and adult.
51 he early anterior neural plate, but from 8.5 days post coitum they developed severe forebrain and mid
52 more, Rent1(-/-) blastocysts isolated at 3.5 days post-coitum undergo apoptosis in culture following
53 e musculoskeletal system from E13.5 to E15.5 days post-coitum, where it was co-localized with hyaluro