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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 tricted by a BMP gradient established by the extraembryonic ectoderm.
5 from mouse embryonic stem cells that lack an extraembryonic ectoderm.
6  Bmp8b of the 60A class are expressed in the extraembryonic ectoderm and targeted mutation of either
7 lls) and Gata4 to reconstitute the epiblast, extraembryonic ectoderm and visceral endoderm lineages,
8 gastrulation defect in chimeras in which the extraembryonic ectoderm and visceral endoderm were deriv
9  mutants display severe defects in epiblast, extraembryonic ectoderm, and anterior visceral endoderm
10 expression in the ectoplacental cone, in the extraembryonic ectoderm, and in trophoblast giant cells
11 y trophoblast-derived ectoplacental cone and extraembryonic ectoderm, as well as in the yolk sac and
12                Conversely, dnFGFR-expressing extraembryonic ectoderm cells were detected at the abemb
13 lastocyst outgrowths increased the number of extraembryonic ectoderm cells, suggesting a continuing r
14 s TS cell sorting above ES cells, resembling extraembryonic ectoderm clustering above epiblast follow
15      Previous studies have demonstrated that extraembryonic ectoderm-derived BMP4 and BMP8B are both
16 in the mouse embryo is regulated not only by extraembryonic ectoderm-derived BMP4 and BMP8B, but also
17                                              Extraembryonic ectoderm-derived factors instruct the plu
18 imal epiblast cells that are adjacent to the extraembryonic ectoderm during gastrulation.
19 is expressed in both the trophoblast-derived extraembryonic ectoderm (ExE) and in the epiblast-derive
20 e communication between the epiblast and the extraembryonic ectoderm (ExE) of the developing mouse em
21 t stem (TS) cells in response to FGF4 in the extraembryonic ectoderm (ExE) that gives rise to tissues
22 acenta, which in mice originates through the extraembryonic ectoderm (ExE), is essential for mammalia
23 , for the establishment and proliferation of extraembryonic ectoderm from polar trophectoderm.
24                        Our results show that extraembryonic ectoderm has the capacity to form neural
25                                       In the extraembryonic ectoderm, in which cells undergo a standa
26          Upon implantation, the epiblast and extraembryonic ectoderm of the mouse embryo become envel
27 es the pluripotent epiblast distally and the extraembryonic ectoderm proximally.
28                                Moreover, the extraembryonic ectoderm relies on a broader spectrum of
29 derm was from nonneural regions, we utilized extraembryonic ectoderm (the proamnion) and transplanted
30 equirement for the gene in both epiblast and extraembryonic ectoderm, the multipotent precursors of a
31 -/- embryos showed that the epiblast and the extraembryonic ectoderm were disorganized, resulting in
32 ic day 6.5 expressed activated ERK1/2 in the extraembryonic ectoderm, whereas erk2 mutant embryos had