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1 every cell of early cleavage embryos through gastrulae.
2 dal signals act cell-autonomously in Xenopus gastrulae.
3  tissue centered on this meridian from early gastrulae.
4 e the Sox17-governed endoderm GRN in Xenopus gastrulae.
5 erm boundary in Xenopus laevis and zebrafish gastrulae.
6 al involuting marginal zone (IMZ) of Xenopus gastrulae.
7 in the mesoderm and dorsal ectoderm of early gastrulae.
8  cannot stabilize Snai1a in PGE(2)-deficient gastrulae.
9           Regardless of how we dissect early gastrulae along meridians running from the animal to the
10 and RNA-seq approaches in Xenopus tropicalis gastrulae and find that occupancy of the corepressor, TL
11 uction occurs on the ventral side of Xenopus gastrulae and is thought to be triggered by the growth f
12 l blot and in situ hybridization analysis of gastrulae and larvae shows a progressive confinement of
13 e and later in the posterior ventral area of gastrulae and neurulae.
14 lly expressed in overlapping domains in late gastrulae, and cells expressing both genes will go on to
15  high-resolution 3D digital datasets of frog gastrulae, and morphometrics that allow simultaneous ass
16 es comparisons with mouse, cynomolgus monkey gastrulae, and post-implantation human embryos, we revea
17                                 When Xenopus gastrulae are made to misexpress Xwnt-8, or are exposed
18 ession of marker genes are affected in early gastrulae, dorsal marker gene expression is reduced at t
19 e neuroectoderm of Nodal-deficient zebrafish gastrulae exhibits reduced C and E cell behaviors, which
20                                    Zebrafish gastrulae express agtrl1b in the lateral plate mesoderm,
21 usly, axial mesoderm in floating head mutant gastrulae fails to maintain expression of notochord gene
22    We conclude that nodal signals in Xenopus gastrulae function cell autonomously at short ranges and
23                   Zebrafish spadetail mutant gastrulae have a nearly opposite phenotype; notochord ma
24           Data obtained using Xenopus laevis gastrulae have shown that integrin-fibronectin interacti
25 ifically in the ectoderm of intact zebrafish gastrulae, highlighting the in vivo relevance of our fin
26 s with a factor which accumulates in Xenopus gastrulae independent of wnt signaling.
27 roscopy to analyze cell behaviors in Xenopus gastrulae injected with monoclonal antibodies directed a
28                                Expression in gastrulae is an early response to FGF signalling.
29 is pattern of expression of the transgene in gastrulae is not dependent on the T-box sites.
30 tored by ectopic BMP inhibition in early boz gastrulae, it was not maintained during later gastrulati
31 m as well as presumptive endoderm) from late gastrulae, larval ectoderm develops properly but obvious
32 ossils recently interpreted as the preserved gastrulae of cnidarian and bilaterian metazoans can alte
33  of eFGF-loaded beads to specific regions of gastrulae reveals that anterior truncations arise from a
34 mant Artemia salina cysts contain desiccated gastrulae that are metabolically inactive, and physiolog
35                  First, in chick and Xenopus gastrulae the onset of Pax-3 expression occurs in region
36                          In Apelin-deficient gastrulae, the cardiac precursors converged inefficientl
37                           Here, we show that gastrulae with altered Galpha(12/13) signaling display d