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1 hout embryos permits immunocyte insertion in ventral ectoderm.
2 in dorsal ectoderm and ciliary band, but not ventral ectoderm.
3 cells appear to become incorporated into the ventral ectoderm.
4 ranscription factor Engrailed 1 (EN1) in the ventral ectoderm.
5 ms at the distal junction between dorsal and ventral ectoderm.
6 uggesting a role for EGF in specification of ventral ectoderm.
7 ed by Engrailed-1, which is expressed in the ventral ectoderm.
8 art through repression by Engrailed-1 in the ventral ectoderm.
9 ss much of the anterior-posterior and dorsal-ventral ectoderm.
10 I (XeIF-4AIII) expression is elevated in the ventral ectoderm, a site of active BMP signal transducti
12 expression of neural precursor genes in the ventral ectoderm also involves both the AB region and th
13 entral development in Drosophila, specifying ventral ectoderm and CNS in the absence of all endogenou
14 b bud lies at the junction of the dorsal and ventral ectoderm and directs patterning of the growing l
15 rride the initial specification of posterior-ventral ectoderm and endoderm fates, eliminating the ven
16 trulation, GFP expression is confined to the ventral ectoderm and lateral mesoderm and is lacking in
17 head mesoderm while sizzled2 is expressed in ventral ectoderm and mesoderm, tissues that modulate ant
18 induce neural markers efficiently in Xenopus ventral ectoderm, and show that suppression of both Smad
19 eural markers and inhibit epidermal genes in ventral ectoderm; and co-expression of BMP inhibitors wi
20 d here identify the non-AER border of dorsal-ventral ectoderm as a new signaling center in limb devel
21 the second quartet forms largely dorsal and ventral ectoderm as well as the circular muscles; the th
22 ng-term contribution of preAER cells to limb ventral ectoderm, as well as the ultimate fate of the ma
23 n sea urchin embryos, BMP is produced in the ventral ectoderm, but signals in the dorsal ectoderm.
24 lishes preplacodal competence throughout the ventral ectoderm by coinducing Tfap2a, Tfap2c, Foxi1 and
25 n of early ectoderm and that both dorsal and ventral ectoderm cells contribute to the apical ridge, i
26 al cell lineages, suggesting that dorsal and ventral ectoderm compartments may be important to ensure
30 ated tissue-specific markers, shows that the ventral ectoderm is expanded at expense of dorsal ectode
31 AER gene expression, a similar domain of paw ventral ectoderm is marked at E16.5, in addition to the
32 esting that normal expression of En-1 in the ventral ectoderm is required to establish and/or maintai
33 embryos was transplanted into the non-neural ventral ectoderm of host embryos at the same development
36 lead to repression of Wnt7a in the embryonic ventral ectoderm or full rescue of the embryonic dorsal/
39 hich presumptive neural plate was grafted to ventral ectoderm reiterate induction of neural crest and
40 alysis of the EGFR/Spitz/Argos module in the ventral ectoderm shows that Argos need not be long-range
41 se limb bud development, the majority of the ventral ectoderm that protrudes from the body wall later
43 nd to retain spatial information, dorsal and ventral ectoderm was subdivided along the anterior-poste
45 hermore, ectopic expression of BMP5-8 in the ventral ectoderm (which induces an O-to-P fate change in
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