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1 n suggested to be the homologue of the mouse anterior visceral endoderm.
2 not the topological equivalent of the murine anterior visceral endoderm.
4 o establish a primitive streak, although the anterior visceral endoderm and anterior epiblast fates a
5 omeobox gene expressed in the extraembryonic anterior visceral endoderm and in primitive streak-deriv
6 age mouse embryos, Cerr1 is expressed in the anterior visceral endoderm and in the anterior definitiv
7 es required for forebrain specification, the anterior visceral endoderm and the anterior definitive e
8 ed by two distinct organizing centres in the anterior visceral endoderm and the distal primitive stre
9 hordal plate, early definitive endoderm, and anterior visceral endoderm appear to be expanded, likely
11 The homeobox gene Hex is expressed in the anterior visceral endoderm (AVE) and rostral definitive
12 bryonic signalling centres, most notably the anterior visceral endoderm (AVE) and the node, respectiv
15 novel mechanism regulating migration of the anterior visceral endoderm (AVE) by BMP signaling throug
16 vity that drives the collective migration of anterior visceral endoderm (AVE) cells in the early mous
18 ack of proper morphogenetic movements of the anterior visceral endoderm (AVE) during pre-gastrulation
19 has been thought to take place only when the anterior visceral endoderm (AVE) emerges and starts its
27 t fail to maintain cell-cell contacts in the anterior visceral endoderm (AVE) signalling centre that
31 l polarization and migration of cells of the Anterior Visceral Endoderm (AVE), an early extraembryoni
32 equired for normal migration of cells of the Anterior Visceral Endoderm (AVE), an extraembryonic orga
33 of the mammalian embryo is laid down by the anterior visceral endoderm (AVE), an extraembryonic sign
34 of markers for visceral endoderm as well as anterior visceral endoderm (AVE), and can contribute to
36 ws us to follow the step-wise development of anterior visceral endoderm (AVE), critical for establish
37 atory elements that direct expression in the anterior visceral endoderm (AVE), primitive streak (PS)
38 ts in epiblast, extraembryonic ectoderm, and anterior visceral endoderm (AVE), resulting in phenotype
39 sterior (A-P) axis formation by inducing the anterior visceral endoderm (AVE), the extraembryonic sig
42 expression in the visceral endoderm promotes anterior visceral endoderm formation and anterior-poster
44 ks anterior-posterior neural patterning, but anterior visceral endoderm markers are expressed and cor
45 ression, Etv4/Etv5-deficient embryos exhibit anterior visceral endoderm migration defects post-implan
47 ons (e.g. amphibian dorsal morula, mammalian anterior visceral endoderm) require stabilised nuclear b
48 therefore, resembles the functioning of the anterior visceral endoderm signalling centre of the mous
49 ls begin to migrate anteriorly to create the anterior visceral endoderm, which assumes a squamous sha
50 ranscriptomes delineate the emergence of the anterior visceral endoderm, which is hallmarked by conse
51 dely expressed, at least in part because the anterior visceral endoderm, which provides signals that