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1 temporarily suppressed Sox2 broadly over the anterior endoderm.
2 rom naive endoderm precursors into committed anterior endoderm.
3 eart mesoderm is induced by signals from the anterior endoderm.
4 s, is proposed to be equivalent to the mouse anterior endoderm.
5 ite side of the embryo, in a small domain of anterior endoderm.
6 rimitive streak and correct specification of anterior endoderm.
7 on, we observe ectopic insulin expression in anterior endoderm.
8 odes a secreted protein that is expressed in anterior endoderm and has the unique property of inducin
9 erturbation of GATA-6 expression in the deep anterior endoderm and in the overlying heart mesoderm sh
10  occur without any stable differentiation of anterior endoderm and is in fact enhanced under conditio
11  region that separates the ectoderm from the anterior endoderm and mesoderm.
12 px are important for early expression in the anterior endoderm and neural plate and regulatory elemen
13 nt-mediated, Nieuwkoop-like signal to induce anterior endoderm, and later in this tissue to block fur
14    Extrinsic influences such as the adjacent anterior endoderm are known to be required for cardiac f
15 ted that one or more additional factors from anterior endoderm are required.
16 growth factors beta (TGFbeta) 2, 3, and 4 in anterior endoderm at Hamburger and Hamilton (H-H) stage
17           Although BMP-2 is expressed in the anterior endoderm, BMP activity is necessary but not suf
18 ologous to the node, partially overlaps with anterior endoderm cells expressing homologues of the AVE
19 ss this, we used vital dyes to label exposed anterior endoderm cells of early somite stage mouse embr
20            Together our results suggest that anterior endoderm-derived TGFbetas may specify prechorda
21 ein that inhibits Wnt-8c and is expressed in anterior endoderm during gastrulation.
22                                              Anterior endoderm elicits aspects of prechordal mesoderm
23 while ectopic HNF3beta inhibits mesoderm and anterior endoderm formation in explant assays and in viv
24 the A6.3 blastomeres, which form part of the anterior endoderm, hematopoietic mesoderm and muscle der
25 ggest a role for a molecule expressed in the anterior endoderm in the induction of head structures in
26 oss-regulatory network that specifies future anterior endoderm in veg2 descendants and institutes a d
27 id or transplantation of normal chick embryo anterior endoderm is sufficient to rescue apoptosis as w
28 , we now provide direct evidence that Sox17+ anterior endoderm is the only source of differentiated C
29    Basal contact with either neural plate or anterior endoderm/lateral mesenchyme or posterior mesode
30 riments suggest that, in vivo, signalling by anterior endoderm may determine the extent of prechordal
31 n, all of which are transiently expressed in anterior endoderm mimic distinct aspects of its patterni
32                                   The dorsal/anterior endoderm of the Xenopus gastrula, which express
33 rms blood, but coculture of this tissue with anterior endoderm or infection with RCAS-crescent induce
34 roper spatial and temporal expression in the anterior endoderm prechordal plate and anterior neural p
35 esxl is expressed during gastrulation in the anterior endoderm, prechordal plate, and the prospective
36 at meis3 and pbx4 regulate shh expression in anterior endoderm, thereby influencing patterning and gr
37 cification, RA has the capacity to transfate anterior endoderm to a pancreatic fate.
38 ta-catenin activity must be repressed in the anterior endoderm to maintain foregut identity and to al
39 s study reveals a complex network regulating anterior endoderm transcription in the early embryo.
40                                      Xenopus anterior endoderm was found to derive in part from cells
41 /- headless embryos, Cerr1 expression in the anterior endoderm was weak or absent.
42 region were always in close association with anterior endoderm, we sought to determine if the endoder
43 ar to the effect of explants cocultured with anterior endoderm, when cultured with TGFbetas 1-3 (3 ng
44         sonic hedgehog (shh) is expressed in anterior endoderm, where it is required to repress pancr
45 e hhex is one of the earliest markers of the anterior endoderm, which gives rise to foregut organs su