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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 iated by the large micromeres located at the vegetal pole.
5 and in the distribution of germ plasm to the vegetal pole.
6 a subset of progenitors on their way to the vegetal pole.
7 lective reformation of Dvl assemblies at the vegetal pole.
8 while DV patterning aligns along the animal-vegetal pole.
9 minants (mRNAs) are first transported to the vegetal pole a few minutes after fertilization and then
10 t of Dsh is blocked by UV irradiation of the vegetal pole, a treatment that inhibits development of d
12 ic mesoderm are co-expressed in the sea star vegetal pole, although this territory does not form a la
13 ession of endogenous Xtwn is confined to the vegetal pole and a Xtwn reporter gene is hyperinduced ve
15 blastula embryo, LvNotch is absent from the vegetal pole and concentrated in basolateral membranes o
16 nal blastomeres failed to migrate toward the vegetal pole and epiboly did not occur, a phenotype simi
17 cules are found in the blastula and gastrula vegetal pole and induce both endoderm and mesoderm in th
18 were novel mRNAs over 4-fold enriched at the vegetal pole and six were over 10-fold enriched at the a
19 are localised uniquely to the animal or the vegetal pole and, therefore, do not rely for their axial
20 tive endoderm cells, which invaginate at the vegetal pole, and in the presumptive notochord and mesen
21 rescent carboxylated beads injected into the vegetal pole are transported at least 60 degrees toward
23 ong meridians running from the animal to the vegetal pole, both the formation of head structures and
26 also true of chimeras composed of animal or vegetal pole cells derived through normal cleavage to th
28 whereas presumptive pre-involuting mesoderm, vegetal pole endoderm, and animal cap ectoderm will not.
29 arrested oocytes but becomes enriched at the vegetal pole following meiotic resumption through a diss
30 age blastomeres from which the animal or the vegetal poles have been removed can develop into normal
31 is the result of two influences: towards the vegetal pole in the movements of epiboly and towards the
32 s are selectively localized to the animal or vegetal pole, including determinants of somatic and germ
33 In Xenopus laevis, factors secreted from the vegetal pole induce mesoderm in the adjacent marginal zo
35 as duet cleavage, which results in two large vegetal pole 'macromeres' and numerous small animal pole
37 subset of the GRN connections in the central vegetal pole mesoderm of the late sea star blastula and
38 is also essential for the reorganization of vegetal pole microtubules required for the segregation o
39 pe is rescued by axin mRNA injected into the vegetal pole of axin-depleted oocytes before fertilizati
44 vegetal half of the egg cortex, move to the vegetal pole of the egg, fusing with each other as they
46 enesis a maternal factor is localized to the vegetal pole of the oocyte that is a determinant of dors
48 iption factor VegT is located throughout the vegetal pole of the Xenopus egg and is believed to play
49 Vg1 LE (VgLE) direct this transcript to the vegetal pole of Xenopus oocytes via the binding of a pro
52 in beta-catenin half-life at the animal and vegetal poles of the early embryo is sufficient to produ
53 validating the approach by recovering animal-vegetal-pole proteomic asymmetry in the frog zygote, the
54 hat factors colocalized with Vg1 mRNA at the vegetal pole relieve translational repression to allow e
55 al pole and the absence of micromeres at the vegetal pole results in the failure of macromere progeny
56 is to comprehensively interrogate animal and vegetal pole RNAs in the fully grown Xenopus laevis oocy
57 of sea urchin embryos four micromeres at the vegetal pole separate from four macromeres just above th
58 a-catenin levels, to adopt the fate of their vegetal-pole sisters, which normally have high nuclear b
59 propose potential pathways operating at the vegetal pole that highlight where future investigations
60 with a restricted VBI-forming region at the vegetal pole that is independent of the patterning activ
61 mation of a detectable parallel array at the vegetal pole, that the parallel array consists of multip
62 dian, which runs from the animal pole to the vegetal pole through the center of Spemann's organizer,
63 rminants are transported 90 degrees from the vegetal pole to the dorsal equator, even though the cort
64 eterminants, which are translocated from the vegetal pole to the future dorsal side of the embryo sho
65 ent of maternal dorsal determinants from the vegetal pole to the future dorsal side of the embryo, pr
66 s greater near the animal pole than near the vegetal pole, whereas fluorescence signals evoked by inj