戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 izing effects of Fgf and RA signaling in the neurectoderm.
2 FGF15 signals in an autocrine fashion to the neurectoderm.
3 n the embryo tailbud, posterior mesoderm and neurectoderm.
4 ic placode, but is expressed in the adjacent neurectoderm.
5 ng from the underlying mesoderm and adjacent neurectoderm.
6 ud mesoderm, and in the posterior end of the neurectoderm.
7 d lateral to the streak additionally produce neurectoderm.
8 rd, prechordal plate, and overlying anterior neurectoderm.
9  fkh5 in the diencephalon and more posterior neurectoderm.
10 nt role in mediating early patterning of the neurectoderm.
11 in partially overlapping domains of the head neurectoderm.
12 rect definition of the future prosencephalic neurectoderm.
13 a brain which segregate from the procephalic neurectoderm.
14 ke cells toward thoracic ventral spinal cord neurectoderm.
15 ctivation and Shh expression in the adjacent neurectoderm.
16  of the notochord, together with the ventral neurectoderm above it, is thus topologically equivalent
17 utants exhibited increased cell death in the neurectoderm and facial ectoderm, culminating in a colla
18  to the brain segregate from the procephalic neurectoderm and form three neuromeres, called protocere
19 nding to sonic hedgehog activity both in the neurectoderm and mesoderm, suggesting that like its Dros
20 cted to the presomitic mesoderm and anterior neurectoderm and mesoderm.
21 ependent of mediolateral segmentation of the neurectoderm and of dorsal neurectoderm proliferation, b
22 on the coordinated production of spinal cord neurectoderm and presomitic mesoderm cells from neuromes
23 n, allowing dorsally derived tissues such as neurectoderm and somitic muscle to develop.
24 r posterior development in both mesoderm and neurectoderm and that neural induction and posteriorizat
25 -localize with Cdx proteins in the posterior neurectoderm and that neural Pax3 expression is reduced
26 ified by inductive signals from the adjacent neurectoderm and underlying mesoderm.
27 ns: the head midline ectoderm, protocerebral neurectoderm and visual primordium.
28 es are expressed in the nascent mesoderm and neurectoderm, and morpholino knockdown of either causes
29 termediate, and msh in dorsal columns of fly neurectoderm, and of homologous gene families in corresp
30  progenitor-like properties upon the lateral neurectoderm, and pharyngeal mesoderm-like properties up
31 ect molecular patterning of the most rostral neurectoderm appears to depend on the presence of this a
32        We show that cells from the posterior neurectoderm are fated to give rise to mesoderm even aft
33            Thus, the FGFs that signal to the neurectoderm are the best potential candidates for redun
34 e correct anteroposterior subdivision of the neurectoderm as it begins to form the central nervous sy
35  the earliest markers of dorsal, prospective neurectoderm at early gastrulation in Xenopus laevis.
36 ricted geminin expression to the prospective neurectoderm at mid-gastrulation.
37 n of the mechanisms that pattern the rostral neurectoderm at pregastrula stages.
38 ted in an expansion of paraxial mesoderm and neurectoderm at the expense of more lateral and ventral
39 eural plate while later on expression in the neurectoderm becomes restricted to the lateral region of
40               derriere can also posteriorize neurectoderm, but appears to do so indirectly.
41 he later expression of Hesx1 in ectoderm and neurectoderm, but does not affect gene expression in mor
42 s basal repression in the prospective caudal neurectoderm by Tcf homologs that act as inhibitors of W
43  inductive interactions between mesoderm and neurectoderm can occur.
44  a role for Hedgehog signaling in generating neurectoderm capable of producing the appropriate neuron
45 ignaling cascade are deficient at generating neurectoderm-containing embryoid bodies.
46 ates transcription of geminin in prospective neurectoderm during gastrulation.
47 nt, including patterning of the mesoderm and neurectoderm during gastrulation.
48  lineages (cardiac, endothelial, muscle) and neurectoderm (eye, neural).
49 th putative planar and vertical signals from neurectoderm failed to prevent the differentiation of ta
50  whether FGF is required specifically by the neurectoderm for anteroposterior neural patterning.
51 is expressed specifically in the prospective neurectoderm from stage 11.5 and appears to have a signi
52 ing the generation of primitive ectoderm and neurectoderm in embryoid body culture.
53 d inhibits the morphogenesis of mesoderm and neurectoderm in embryos of the frog Xenopus laevis, ther
54 r how these cells are singled out within the neurectoderm in the first place.
55 pective neural plate thereby subdividing the neurectoderm into two distinct regions.
56           l'sc expression in the procephalic neurectoderm is controlled by the head gap genes tailles
57 of beta-catenins in suppressing formation of neurectoderm is revealed when both beta-catenin genes ar
58 onsisting of presumptive dorsal mesoderm and neurectoderm (Keller explants), and (iii) in explants of
59 onsistent with homology between the anterior neurectoderm of amphioxus and the presumptive placodal e
60 or both FGF19 and FGF15, is expressed in the neurectoderm of both species, and is also expressed in t
61  similar registers in the anterior embryonic neurectoderm of Drosophila melanogaster and Saccoglossus
62 n a stereotyped pattern from the procephalic neurectoderm of each side during stages 9-11.
63 ing pathways in partitioning the dorsal head neurectoderm of the Drosophila embryo.
64 CNS), called neuroblasts, segregate from the neurectoderm of the early embryo in a stereotyped patter
65 ecordings of cultured cells dissociated from neurectoderm of Xenopus neural plate stage embryos revea
66 anterior mesendoderm and subsequent anterior neurectoderm patterning.
67            In mice, Fgf3 is expressed in the neurectoderm prior to and concomitant with placode induc
68 gmentation of the neurectoderm and of dorsal neurectoderm proliferation, both of which occur normally
69    The dorsomedial domain of the procephalic neurectoderm represents a special case.
70 essential to counteract a later, dorsal- and neurectoderm-repressing function that is shared by both
71 ain of the protocerebral and deuterocerebral neurectoderm, respectively.
72 -streak border descendants populate not only neurectoderm, somites and notochord throughout the axis,
73                     Circus movements are not neurectoderm-specific because they similarly predict dif
74                                              Neurectoderm-specific gene expression was observed, howe
75 toderm inhibited MAPK activity and prevented neurectoderm-specific gene expression when the ectoderm
76 ons of FGF and assayed for MAPK activity and neurectoderm-specific gene expression.
77 ilies in corresponding domains of vertebrate neurectoderm, suggests that elements of dorsoventral neu
78 eased rate of proliferation in the forebrain neurectoderm that accompanies telencephalic expansion in
79 or primitive streak derivatives and anterior neurectoderm that correlates with increased Nodal expres
80  for the establishment of pattern within the neurectoderm, the paraxial mesoderm and other tissues.
81 ammalian HNF3beta in both axial mesoderm and neurectoderm; the role of Xenopus HNF3beta itself, howev
82 ication between the prechordal plate and the neurectoderm to provide cellular survival cues essential
83 o the mesoderm or a paracrine fashion to the neurectoderm, whereas FGF15 signals in an autocrine fash
84 nizer of the amphibian gastrula provides the neurectoderm with both neuralizing and posteriorizing (t
85 ines a very early pattern in the presumptive neurectoderm, with opl later expressed in the telencepha