ライフサイエンスコーパス: neurectoderm

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 of the notochord, together with the ventral neurectoderm above it, is thus topologically equivalent

15 to the brain segregate from the procephalic neurectoderm and form three neuromeres, called protocere

16 nding to sonic hedgehog activity both in the neurectoderm and mesoderm, suggesting that like its Dros

17 cted to the presomitic mesoderm and anterior neurectoderm and mesoderm.

18 ependent of mediolateral segmentation of the neurectoderm and of dorsal neurectoderm proliferation, b

19 n, allowing dorsally derived tissues such as neurectoderm and somitic muscle to develop.

20 r posterior development in both mesoderm and neurectoderm and that neural induction and posteriorizat

21 -localize with Cdx proteins in the posterior neurectoderm and that neural Pax3 expression is reduced

22 ified by inductive signals from the adjacent neurectoderm and underlying mesoderm.

23 ns: the head midline ectoderm, protocerebral neurectoderm and visual primordium.

24 es are expressed in the nascent mesoderm and neurectoderm, and morpholino knockdown of either causes

25 termediate, and msh in dorsal columns of fly neurectoderm, and of homologous gene families in corresp

26 progenitor-like properties upon the lateral neurectoderm, and pharyngeal mesoderm-like properties up

27 ect molecular patterning of the most rostral neurectoderm appears to depend on the presence of this a

28 We show that cells from the posterior neurectoderm are fated to give rise to mesoderm even aft

29 Thus, the FGFs that signal to the neurectoderm are the best potential candidates for redun

30 e correct anteroposterior subdivision of the neurectoderm as it begins to form the central nervous sy

31 the earliest markers of dorsal, prospective neurectoderm at early gastrulation in Xenopus laevis.

32 ricted geminin expression to the prospective neurectoderm at mid-gastrulation.

33 n of the mechanisms that pattern the rostral neurectoderm at pregastrula stages.

34 ted in an expansion of paraxial mesoderm and neurectoderm at the expense of more lateral and ventral

35 eural plate while later on expression in the neurectoderm becomes restricted to the lateral region of

36 derriere can also posteriorize neurectoderm, but appears to do so indirectly.

37 he later expression of Hesx1 in ectoderm and neurectoderm, but does not affect gene expression in mor

38 s basal repression in the prospective caudal neurectoderm by Tcf homologs that act as inhibitors of W

39 inductive interactions between mesoderm and neurectoderm can occur.

40 a role for Hedgehog signaling in generating neurectoderm capable of producing the appropriate neuron

41 ignaling cascade are deficient at generating neurectoderm-containing embryoid bodies.

42 ates transcription of geminin in prospective neurectoderm during gastrulation.

43 nt, including patterning of the mesoderm and neurectoderm during gastrulation.

44 th putative planar and vertical signals from neurectoderm failed to prevent the differentiation of ta

45 whether FGF is required specifically by the neurectoderm for anteroposterior neural patterning.

46 is expressed specifically in the prospective neurectoderm from stage 11.5 and appears to have a signi

47 ing the generation of primitive ectoderm and neurectoderm in embryoid body culture.

48 d inhibits the morphogenesis of mesoderm and neurectoderm in embryos of the frog Xenopus laevis, ther

49 r how these cells are singled out within the neurectoderm in the first place.

50 pective neural plate thereby subdividing the neurectoderm into two distinct regions.

51 l'sc expression in the procephalic neurectoderm is controlled by the head gap genes tailles

52 of beta-catenins in suppressing formation of neurectoderm is revealed when both beta-catenin genes ar

53 onsisting of presumptive dorsal mesoderm and neurectoderm (Keller explants), and (iii) in explants of

54 onsistent with homology between the anterior neurectoderm of amphioxus and the presumptive placodal e

55 or both FGF19 and FGF15, is expressed in the neurectoderm of both species, and is also expressed in t

56 similar registers in the anterior embryonic neurectoderm of Drosophila melanogaster and Saccoglossus

57 n a stereotyped pattern from the procephalic neurectoderm of each side during stages 9-11.

58 ing pathways in partitioning the dorsal head neurectoderm of the Drosophila embryo.

59 CNS), called neuroblasts, segregate from the neurectoderm of the early embryo in a stereotyped patter

60 ecordings of cultured cells dissociated from neurectoderm of Xenopus neural plate stage embryos revea

61 anterior mesendoderm and subsequent anterior neurectoderm patterning.

62 In mice, Fgf3 is expressed in the neurectoderm prior to and concomitant with placode induc

63 gmentation of the neurectoderm and of dorsal neurectoderm proliferation, both of which occur normally

64 The dorsomedial domain of the procephalic neurectoderm represents a special case.

65 essential to counteract a later, dorsal- and neurectoderm-repressing function that is shared by both

66 ain of the protocerebral and deuterocerebral neurectoderm, respectively.

67 -streak border descendants populate not only neurectoderm, somites and notochord throughout the axis,

68 Circus movements are not neurectoderm-specific because they similarly predict dif

69 Neurectoderm-specific gene expression was observed, howe

70 toderm inhibited MAPK activity and prevented neurectoderm-specific gene expression when the ectoderm

71 ons of FGF and assayed for MAPK activity and neurectoderm-specific gene expression.

72 ilies in corresponding domains of vertebrate neurectoderm, suggests that elements of dorsoventral neu

73 eased rate of proliferation in the forebrain neurectoderm that accompanies telencephalic expansion in

74 or primitive streak derivatives and anterior neurectoderm that correlates with increased Nodal expres

75 for the establishment of pattern within the neurectoderm, the paraxial mesoderm and other tissues.

76 ammalian HNF3beta in both axial mesoderm and neurectoderm; the role of Xenopus HNF3beta itself, howev

77 o the mesoderm or a paracrine fashion to the neurectoderm, whereas FGF15 signals in an autocrine fash

78 nizer of the amphibian gastrula provides the neurectoderm with both neuralizing and posteriorizing (t

79 ines a very early pattern in the presumptive neurectoderm, with opl later expressed in the telencepha