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1 erm boundary in Xenopus laevis and zebrafish gastrulae.
2 dal signals act cell-autonomously in Xenopus gastrulae.
3 tissue centered on this meridian from early gastrulae.
4 in the mesoderm and dorsal ectoderm of early gastrulae.
5 cannot stabilize Snai1a in PGE(2)-deficient gastrulae.
6 every cell of early cleavage embryos through gastrulae.
8 and RNA-seq approaches in Xenopus tropicalis gastrulae and find that occupancy of the corepressor, TL
9 uction occurs on the ventral side of Xenopus gastrulae and is thought to be triggered by the growth f
10 l blot and in situ hybridization analysis of gastrulae and larvae shows a progressive confinement of
12 lly expressed in overlapping domains in late gastrulae, and cells expressing both genes will go on to
13 high-resolution 3D digital datasets of frog gastrulae, and morphometrics that allow simultaneous ass
15 ession of marker genes are affected in early gastrulae, dorsal marker gene expression is reduced at t
17 usly, axial mesoderm in floating head mutant gastrulae fails to maintain expression of notochord gene
18 We conclude that nodal signals in Xenopus gastrulae function cell autonomously at short ranges and
22 roscopy to analyze cell behaviors in Xenopus gastrulae injected with monoclonal antibodies directed a
25 tored by ectopic BMP inhibition in early boz gastrulae, it was not maintained during later gastrulati
26 m as well as presumptive endoderm) from late gastrulae, larval ectoderm develops properly but obvious
27 ossils recently interpreted as the preserved gastrulae of cnidarian and bilaterian metazoans can alte
28 of eFGF-loaded beads to specific regions of gastrulae reveals that anterior truncations arise from a
29 mant Artemia salina cysts contain desiccated gastrulae that are metabolically inactive, and physiolog
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