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 uring embryonic development at 9.5-14.5 days post coitum.
2 he left side of the mouse embryo by 8.0 days post coitum.
3 ryonic lethal, dying between 8 and 11.5 days post coitum.
4 early as the endogenous gene, at day 7.5-8.0 post coitum.
5 xpression in the gonad at 12.5 and 13.5 days post-coitum, after overt gonad differentiation, by compa
6  and renal cysts if they survive to day 15.5 post coitum and die in either the fetal or the perinatal
7 during embryonic development until 13.5 days post-coitum and in the adult heart, kidney, brain, teste
8 the developing heart at E10.5 and E11.5 days post-coitum and in the musculoskeletal system from E13.5
9 ession in the branchial arches from 9.5 days post-coitum and show that its activity in the context of
10 tic differentiation of germ cells (13.5 days post coitum) and from both in vivo exposed mice and in v
11  causes embryonic lethality at day 8.5 p.c. (post coitum) before establishment of a functional cardio
12  the time of PGC allocation around 7.25 days post coitum, Blimp1 heterozygous embryos exhibit decreas
13 lity in Cbfb(-/-) mouse embryos at 12.5 days post coitum (d.p.c.) from hemorrhages and lack of defini
14 se embryos deficient in Gata3 die by 11 days post coitum (d.p.c.) from pathology of undetermined orig
15 e results in embryonic lethality at 5.5 days post coitum (d.p.c.) which can be overcome by simultaneo
16   These embryos develop normally to 7.5 days post coitum (d.p.c.), but their growth is severely retar
17 d in pancreatic endocrine cells at 18.5 days post coitum (d.p.c.), when definitive islets first begin
18 epiblast at stages between 5.5 and 5.75 days post coitum (d.p.c.).
19 M region and umbilical vessels on 10-11 days post coitum (d.p.c.).
20 (-/-) mice failed to survive beyond 8.5 days post coitum (d.p.c.).
21  mouse embryos ranging from 8.5 to 11.5 days post-coitum (d.p.c.), Pitx3 mRNA was seen only in the de
22 us mutation is embryonic lethal by 13.5 days post coitum, demonstrating the importance of Opa1 during
23 n of FGF signalling between 5.5 and 7.5 days post-coitum does not block neural differentiation in the
24 ok grossly and histologically normal at days post coitum (dpc) 6.5 and 7.5 of pregnancy.
25 Lhx4 expression in RP epithelium at 9.0 days post coitum (dpc) and total loss of pituitary tissue by
26 able from wild-type embryos through 6.5 days post coitum (dpc) and were able to establish all three g
27   The mouse germ line originates at 6.5 days post coitum (dpc) in the proximal epiblast, apparently i
28  cells (EGCs) derived from 11.5 or 12.5 days post coitum (dpc) primordial germ cells (PGCs).
29  correctly induced and patterned at 7.5 days post coitum (dpc), but subsequently fails to develop.
30 isplay profound yolk sac defects at 9.5 days post coitum (dpc), including disrupted angiogenesis in m
31 expression of Gm114 begins at 12.5-13.5 days post coitum (dpc), the stage in mice when germ cells cea
32 omparable in size with controls at 13.5 days post coitum (dpc), their placentas were significantly la
33  XY gonad decline in numbers after 11.5 days post coitum (dpc), while germ cell numbers in XX gonads
34 e developing heart starting at day 11.5 days post coitum (dpc).
35 n the testis and ovary as early as 13.5 days post coitum (dpc).
36 igration to the gonads from 8.5 to 13.5 days post coitum (dpc).
37 declining markedly between 9.5 and 12.5 days post coitum (dpc).
38 anely killed on 12.5, 14.5, 16.5, and 18.5 d post coitum (dpc).
39 nto XY but not XX gonads from 11.5-16.5 days post coitum (dpc).
40 ATA4-/-) mice died between 8.5 and 10.5 days post coitum (dpc).
41                                  At 3.5 days post-coitum (dpc) and 4.5 dpc, the tetraploid ESCs were
42 ted eNOS (p-eNOS) expression in 7.2-8.5 days post-coitum (dpc) mouse embryos.
43 ted RNA-seq analysis of lungs from 18.5 days post-coitum (dpc) Src-1(-/-) /-2(-/-) (dKO) vs. WT fetus
44 d 12-somite pair (-s) stages (~6.75-9.0 days post coitum, dpc) in histological sections.
45 sulted in embryonic lethality around day 9.5 post coitum (E9.5) in mice.
46 njection of PAF or SP-A into AF at 17.5 days post coitum enhanced uterine NF-kappaB activation and co
47                                  By 9.5 days post coitum, expression in the nervous system is predomi
48 (+)Thy1(-)) that, when sorted from 15.5 days post-coitum fetal bones and transplanted under the adult
49     The transgene was expressed from day 7.5 post coitum forward, resulting in activation of skeletal
50 transfer, but none developed beyond 8.5 days post coitum; however, a high percentage of enucleated oo
51 nt tissues was observed beginning at 16 days post coitum in developing brain neurons, primitive inner
52 n on mouse embryos ranging from 9 to 16 days post-coitum localized murine Og12x mRNA in the heart, ot
53 ression was detected more widely in 13.5 day post-coitum mouse embryos.
54 ions transiently, and declined from 6.5 days post coitum onward, as the cells underwent apoptosis dur
55 he collecting duct epithelium from 13.5 days post coitum onward.
56 tion within the cardiogenic plate of 7.5-day post coitum (p.c.) embryos, and in 8.5-day p.c. embryos
57 rominent through the looping stage (day 12.5 post coitum [pc]) but fell below the threshold of detect
58 mical analysis of murine embryos at 7.8 days post coitum revealed that Csx protein is strongly expres
59 -linked homologues, at three ages: 13.5 days post coitum, the day of birth (P1) and adult.
60 rly anterior neural plate, but from 8.5 days post coitum they developed severe forebrain and midbrain
61  Rent1(-/-) blastocysts isolated at 3.5 days post-coitum undergo apoptosis in culture following a bri
62 culoskeletal system from E13.5 to E15.5 days post-coitum, where it was co-localized with hyaluronan.