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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
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
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
25 f siamois, a wnt-inducible homeobox gene, in Spemann's organizer development was examined by fusion o
27 uggest a mechanistic basis for the action of Spemann's organizer during Xenopus development and provi
32 egion of the amniote embryo corresponding to Spemann's organizer in amphibians is Hensen's node, whic
34 oid was the first specific genetic marker of Spemann's organizer in vertebrate embryos to be discover
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
44 of neural induction occurs in the absence of Spemann's organizer signals and is thought to be caused
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
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