ライフサイエンスコーパス: extraembryonic ectoderm

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1 differentiation programs in the epiblast and extraembryonic ectoderm.

2 lantation embryo into the early epiblast and extraembryonic ectoderm.

3 mbryonic region and the absence of organized extraembryonic ectoderm.

4 Bmp8b of the 60A class are expressed in the extraembryonic ectoderm and targeted mutation of either

5 gastrulation defect in chimeras in which the extraembryonic ectoderm and visceral endoderm were deriv

6 mutants display severe defects in epiblast, extraembryonic ectoderm, and anterior visceral endoderm

7 expression in the ectoplacental cone, in the extraembryonic ectoderm, and in trophoblast giant cells

8 y trophoblast-derived ectoplacental cone and extraembryonic ectoderm, as well as in the yolk sac and

9 Conversely, dnFGFR-expressing extraembryonic ectoderm cells were detected at the abemb

10 lastocyst outgrowths increased the number of extraembryonic ectoderm cells, suggesting a continuing r

11 Previous studies have demonstrated that extraembryonic ectoderm-derived BMP4 and BMP8B are both

12 in the mouse embryo is regulated not only by extraembryonic ectoderm-derived BMP4 and BMP8B, but also

13 Extraembryonic ectoderm-derived factors instruct the plu

14 imal epiblast cells that are adjacent to the extraembryonic ectoderm during gastrulation.

15 is expressed in both the trophoblast-derived extraembryonic ectoderm (ExE) and in the epiblast-derive

16 e communication between the epiblast and the extraembryonic ectoderm (ExE) of the developing mouse em

17 t stem (TS) cells in response to FGF4 in the extraembryonic ectoderm (ExE) that gives rise to tissues

18 , for the establishment and proliferation of extraembryonic ectoderm from polar trophectoderm.

19 Our results show that extraembryonic ectoderm has the capacity to form neural

20 In the extraembryonic ectoderm, in which cells undergo a standa

21 es the pluripotent epiblast distally and the extraembryonic ectoderm proximally.

22 derm was from nonneural regions, we utilized extraembryonic ectoderm (the proamnion) and transplanted

23 equirement for the gene in both epiblast and extraembryonic ectoderm, the multipotent precursors of a

24 -/- embryos showed that the epiblast and the extraembryonic ectoderm were disorganized, resulting in

25 ic day 6.5 expressed activated ERK1/2 in the extraembryonic ectoderm, whereas erk2 mutant embryos had

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