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1 nimal pole is through its degradation at the vegetal pole.
2 h toward the animal pole and back toward the vegetal pole.
3 p1 is required for their localization to the vegetal pole.
4  while DV patterning aligns along the animal-vegetal pole.
5 iated by the large micromeres located at the vegetal pole.
6 and in the distribution of germ plasm to the vegetal pole.
7 t of Dsh is blocked by UV irradiation of the vegetal pole, a treatment that inhibits development of d
8            Conversely, UV irradiation of the vegetal pole abolishes movement of Dsh-GFP.
9 ic mesoderm are co-expressed in the sea star vegetal pole, although this territory does not form a la
10 ession of endogenous Xtwn is confined to the vegetal pole and a Xtwn reporter gene is hyperinduced ve
11 thway, recruits endogenous kinesin II to the vegetal pole and colocalizes with it at the cortex.
12  blastula embryo, LvNotch is absent from the vegetal pole and concentrated in basolateral membranes o
13 nal blastomeres failed to migrate toward the vegetal pole and epiboly did not occur, a phenotype simi
14 cules are found in the blastula and gastrula vegetal pole and induce both endoderm and mesoderm in th
15 were novel mRNAs over 4-fold enriched at the vegetal pole and six were over 10-fold enriched at the a
16  are localised uniquely to the animal or the vegetal pole and, therefore, do not rely for their axial
17 tive endoderm cells, which invaginate at the vegetal pole, and in the presumptive notochord and mesen
18 rescent carboxylated beads injected into the vegetal pole are transported at least 60 degrees toward
19  ablated but does not restore the ability of vegetal pole blastomeres to induce mesoderm.
20 ong meridians running from the animal to the vegetal pole, both the formation of head structures and
21          HNF3beta is widely expressed in the vegetal pole but, as previously suggested, is excluded f
22 s lowest in animal pole tissue and higher in vegetal pole cells and the marginal zone.
23  also true of chimeras composed of animal or vegetal pole cells derived through normal cleavage to th
24  region shift 90 degrees with respect to the vegetal pole during gastrulation.
25 whereas presumptive pre-involuting mesoderm, vegetal pole endoderm, and animal cap ectoderm will not.
26 age blastomeres from which the animal or the vegetal poles have been removed can develop into normal
27 is the result of two influences: towards the vegetal pole in the movements of epiboly and towards the
28 s are selectively localized to the animal or vegetal pole, including determinants of somatic and germ
29 In Xenopus laevis, factors secreted from the vegetal pole induce mesoderm in the adjacent marginal zo
30 art of an ancestral GRN governing echinoderm vegetal pole mesoderm development.
31 subset of the GRN connections in the central vegetal pole mesoderm of the late sea star blastula and
32 pe is rescued by axin mRNA injected into the vegetal pole of axin-depleted oocytes before fertilizati
33 component of Xenopus germ plasm found in the vegetal pole of oocytes and eggs.
34            Cdx2 mRNA is localized toward the vegetal pole of oocytes, reorients after fertilization,
35  the ring of specified mesoderm cells at the vegetal pole of the blastula.
36                       Its restriction to the vegetal pole of the egg made it the ideal candidate to b
37  vegetal half of the egg cortex, move to the vegetal pole of the egg, fusing with each other as they
38 duced or arrested cell migration towards the vegetal pole of the embryo.
39 enesis a maternal factor is localized to the vegetal pole of the oocyte that is a determinant of dors
40       Primary mesenchyme cells (PMCs) at the vegetal pole of the sea urchin embryo ingress into the f
41 iption factor VegT is located throughout the vegetal pole of the Xenopus egg and is believed to play
42  Vg1 LE (VgLE) direct this transcript to the vegetal pole of Xenopus oocytes via the binding of a pro
43 e by the Na+/K+ pump was investigated in the vegetal pole of Xenopus oocytes.
44 quent to the localization of its mRNA to the vegetal pole of Xenopus oocytes.
45  in beta-catenin half-life at the animal and vegetal poles of the early embryo is sufficient to produ
46 hat factors colocalized with Vg1 mRNA at the vegetal pole relieve translational repression to allow e
47 al pole and the absence of micromeres at the vegetal pole results in the failure of macromere progeny
48 is to comprehensively interrogate animal and vegetal pole RNAs in the fully grown Xenopus laevis oocy
49 of sea urchin embryos four micromeres at the vegetal pole separate from four macromeres just above th
50 a-catenin levels, to adopt the fate of their vegetal-pole sisters, which normally have high nuclear b
51  propose potential pathways operating at the vegetal pole that highlight where future investigations
52  with a restricted VBI-forming region at the vegetal pole that is independent of the patterning activ
53 mation of a detectable parallel array at the vegetal pole, that the parallel array consists of multip
54 dian, which runs from the animal pole to the vegetal pole through the center of Spemann's organizer,
55 rminants are transported 90 degrees from the vegetal pole to the dorsal equator, even though the cort
56 eterminants, which are translocated from the vegetal pole to the future dorsal side of the embryo sho
57 ent of maternal dorsal determinants from the vegetal pole to the future dorsal side of the embryo, pr
58 s greater near the animal pole than near the vegetal pole, whereas fluorescence signals evoked by inj
59                  The Bb specifies the oocyte vegetal pole, which is key to forming the embryonic body

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