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1 ation depends on the node, the equivalent of Spemann's organizer.
2 ignalling cascade that leads to induction of Spemann's organizer.
3 gate with the prime meridian passing through Spemann's organizer.
4 is involved in the Wnt-mediated induction of Spemann's organizer.
5 enetic protein (BMP) antagonist expressed in Spemann's organizer.
6 he inductive and morphogenetic activities of Spemann's organizer.
7 mois function is required for development of Spemann's organizer.
8 d group of cells in the superficial layer of Spemann's organizer.
9       Xnot-2 is a homeobox gene expressed in Spemann's organizer.
10  (BMPs) and dorsalizing signals generated by Spemann's organizer.
11 xistence of an unknown zygotic Wnt ligand in Spemann's organizer.
12  is controlled by the inducing activities of Spemann's organizer.
13 equired for the trunk-inducing activities of Spemann's organizer.
14 forms critical functions within the cells of Spemann's organizer.
15 ulation in amphibians, secreted factors from Spemann's organizer act on dorsal ectoderm to induce the
16                                        After Spemann's organizer and its derivatives have endowed the
17 role of the FGFR pathway in the functions of Spemann's organizer and other vertebrate-signaling cente
18 y provide a link between regulatory genes in Spemann's organizer and the execution of cell behaviors
19 transmembrane protein expressed initially in Spemann's organizer and then in paraxial mesoderm.
20 er activity by direct repression of Xwnt8 in Spemann's organizer and this activity is essential for a
21  alignment zone, a subpopulation of cells in Spemann's organizer, and spreads through much of the mar
22 ith BMP-4 RNA cannot be rescued by grafts of Spemann's organizer at gastrula stages.
23                 An abundant cDNA enriched in Spemann's organizer, cerberus, was isolated by different
24        In addition, our results suggest that Spemann's organizer contains multiple organizers, which
25 f siamois, a wnt-inducible homeobox gene, in Spemann's organizer development was examined by fusion o
26                                              Spemann's organizer develops in response to dorsal deter
27 uggest a mechanistic basis for the action of Spemann's organizer during Xenopus development and provi
28 unction of Xolloid is to limit the extent of Spemann's organizer field.
29                                              Spemann's organizer has potent neural inducing and mesod
30     A number of secreted factors produced by Spemann's organizer have recently been identified.
31                      The avian equivalent of Spemann's organizer, Hensen's node, begins to lose its a
32 egion of the amniote embryo corresponding to Spemann's organizer in amphibians is Hensen's node, whic
33 at these determinants may directly establish Spemann's organizer in this region.
34 oid was the first specific genetic marker of Spemann's organizer in vertebrate embryos to be discover
35 s and has been implicated in the activity of Spemann's organizer in Xenopus.
36                                 Transplanted Spemann's organizer induces dorsal embryonic cell fates
37 ses, in part, that a factor(s) secreted from Spemann's organizer is responsible for converting latera
38 the hypothesis that the midline that bisects Spemann's organizer is the embryo's anterior midline.
39 le to the vegetal pole through the center of Spemann's organizer, is the embryo's anterior midline, n
40 ction of the central nervous system (CNS) by Spemann's Organizer led to the isolation of noggin and c
41 opose that the noncell-autonomous effects of Spemann's organizer on dorsoventral patterning are execu
42 her BMP inhibitors expressed dorsally in the Spemann's organizer play roles in establishment and/or m
43                                              Spemann's organizer plays an essential role in patternin
44 of neural induction occurs in the absence of Spemann's organizer signals and is thought to be caused
45 the entire marginal zone mesoderm, including Spemann's Organizer (the Organizer).
46 s from the mesodermal and endodermal tissue (Spemann's organizer) to the prospective neural tissue.
47 hat underlying the formation and function of Spemann's organizer, we describe the current status of o
48                               In amphibians, Spemann's organizer, which is homologous to the node, pa

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