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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 At the time of PGC allocation around 7.25 days post coitum, Blimp1 heterozygous embryos exhibit de
9 lethality in Cbfb(-/-) mouse embryos at 12.5 days post coitum (d.p.c.) from hemorrhages and lack of d
10 Mouse embryos deficient in Gata3 die by 11 days post coitum (d.p.c.) from pathology of undetermined
11 mouse results in embryonic lethality at 5.5 days post coitum (d.p.c.) which can be overcome by simul
13 ulated in pancreatic endocrine cells at 18.5 days post coitum (d.p.c.), when definitive islets first
17 on on mouse embryos ranging from 8.5 to 11.5 days post-coitum (d.p.c.), Pitx3 mRNA was seen only in t
18 ozygous mutation is embryonic lethal by 13.5 days post coitum, demonstrating the importance of Opa1 d
19 bition of FGF signalling between 5.5 and 7.5 days post-coitum does not block neural differentiation i
20 Lhx3/Lhx4 expression in RP epithelium at 9.0 days post coitum (dpc) and total loss of pituitary tissu
21 guishable from wild-type embryos through 6.5 days post coitum (dpc) and were able to establish all th
24 rm is correctly induced and patterned at 7.5 days post coitum (dpc), but subsequently fails to develo
25 yos display profound yolk sac defects at 9.5 days post coitum (dpc), including disrupted angiogenesis
26 lls, expression of Gm114 begins at 12.5-13.5 days post coitum (dpc), the stage in mice when germ cell
27 lly comparable in size with controls at 13.5 days post coitum (dpc), their placentas were significant
28 n the XY gonad decline in numbers after 11.5 days post coitum (dpc), while germ cell numbers in XX go
38 Injection of PAF or SP-A into AF at 17.5 days post coitum enhanced uterine NF-kappaB activation a
40 CD105(+)Thy1(-)) that, when sorted from 15.5 days post-coitum fetal bones and transplanted under the
41 wing transfer, but none developed beyond 8.5 days post coitum; however, a high percentage of enucleat
42 fferent tissues was observed beginning at 16 days post coitum in developing brain neurons, primitive
43 zation on mouse embryos ranging from 9 to 16 days post-coitum localized murine Og12x mRNA in the hear
44 ntrations transiently, and declined from 6.5 days post coitum onward, as the cells underwent apoptosi
46 tochemical analysis of murine embryos at 7.8 days post coitum revealed that Csx protein is strongly e
48 he early anterior neural plate, but from 8.5 days post coitum they developed severe forebrain and mid
49 more, Rent1(-/-) blastocysts isolated at 3.5 days post-coitum undergo apoptosis in culture following
50 e musculoskeletal system from E13.5 to E15.5 days post-coitum, where it was co-localized with hyaluro
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