ライフサイエンスコーパス: embryonic ectoderm

1 the trophoblast, which is derived from extra-embryonic ectoderm.

2 shA is co-expressed with neural genes in the embryonic ectoderm.

3 e diversification of cell fates in the early embryonic ectoderm.

4 ch originate as clusters of cells within the embryonic ectoderm.

5 equently in the VE associated with the extra-embryonic ectoderm.

6 Rac or Rho, blocked the effect of IQGAP1 on embryonic ectoderm.

7 ially in the region of the distal tip of the embryonic ectoderm.

8 tain molecular pattern in the adjacent extra-embryonic ectoderm.

9 NFPC could mediate cell adhesion within the embryonic ectoderm.

10 endently mutable functions in patterning the embryonic ectoderm.

11 ains similar to the normal wg pattern in the embryonic ectoderm.

12 RHA for the survival and differentiation of embryonic ectoderm.

13 for restricting the mesodermal competence of embryonic ectoderm.

14 ng to create positional information over the embryonic ectoderm.

15 inner ear develops from a thickening of the embryonic ectoderm, adjacent to the hindbrain, known as

16 s LEF1, TCF4, and TCF3 are phosphorylated in embryonic ectoderm after Wnt8 stimulation and HIPK2 over

17 hat imaginal disc cells are derived from the embryonic ectoderm and belong to either an anterior or p

18 non-metameric patterns - transiently in the embryonic ectoderm and dorsal nerve cord.

19 tant embryos at E8.5 show an increase in the embryonic ectoderm and endoderm, morphological and molec

20 in promotes polarization and survival of the embryonic ectoderm and formation of Reichert's membrane.

21 ested overexpression of Fz in the developing embryonic ectoderm and found that it phenocopied overexp

22 sion within the deep, sensorial layer of the embryonic ectoderm and in a restricted group of cells in

23 the polar trophectoderm - early-streak extra-embryonic ectoderm and late-streak chorionic ectoderm -

24 y in the determination of neuroblasts in the embryonic ectoderm and many other cell types.

25 endoderm to become associated with the extra-embryonic ectoderm and subsequently contributes to the y

26 hyury is first expressed in the distal extra-embryonic ectoderm and subsequently on one side of the e

27 the patterning of the visceral mesoderm, the embryonic ectoderm and the imaginal discs.

28 that grows in close apposition to the extra-embryonic ectoderm and the visceral endoderm.

29 uced in proximal epiblast cells by the extra-embryonic ectoderm, and is not acquired through the inhe

30 s the adoption of an appendageal fate within embryonic ectoderm, and its expression persists in speci

31 to induce cardiac differentiation in Xenopus embryonic ectoderm (animal pole) explants, frequently re

32 role for TAF1 in the differentiation of the embryonic ectoderm, as a cytosolic cofactor of NFPC.

33 significant contribution of 4n cells to the embryonic ectoderm at gastrulation in every chimera anal

34 lls are derived from a stratification of the embryonic ectoderm at the onset of the formation of a tr

35 body temperature, sweat glands develop from embryonic ectoderm by a poorly defined mechanism.

36 brate head originate from thickenings in the embryonic ectoderm called cranial sensory placodes.

37 ablating or stabilizing beta-catenin in the embryonic ectoderm causes dramatic changes in facial mor

38 tive form of NFPC disrupted the integrity of embryonic ectoderm, causing cells in the deep layer to d

39 , the embryonic basement membrane forms, the embryonic ectoderm cavitates and the parietal endoderm d

40 nt growth patterns exhibited by single extra-embryonic ectoderm cells at the onset of gastrulation.

41 nitive endoderm) contain CXCR4 message while embryonic ectoderm cells express SDF-1.

42 f the mouse blastocyst consists of a core of embryonic ectoderm cells surrounded by an outer layer of

43 stine-specific deletion of the PRC2 proteins embryonic ectoderm development (EED) (a subunit required

44 coordinated via combinatorial regulation of embryonic ectoderm development (EED) and lysine-specific

45 The WD-repeat protein embryonic ectoderm development (EED) is a non-catalytic

46 ne of Drosophila and its mammalian homologue embryonic ectoderm development (eed) play pivotal roles

47 C2 components enhancer of zeste 2 (Ezh2) and embryonic ectoderm development (Eed) to characterize the

48 C2)--[Su-(var)3-9; E(z); Trithorax] (SET)-7, embryonic ectoderm development (EED), and SU(Z)12 (suppr

49 The mouse Polycomb-group gene, embryonic ectoderm development (eed), appears to regulat

50 ssion of Polycomb group (PcG) proteins CBX7, embryonic ectoderm development (EED), enhancer of zeste

51 lines, in which the essential PRC2 subunits embryonic ectoderm development (EED), suppressor of zest

52 n ES cells as premature expression occurs in embryonic ectoderm development (Eed)-deficient ES cells.

53 of zeste homolog 2 and the WD-repeat protein embryonic ectoderm development (EED).

54 contrast with a recent study suggesting that Embryonic Ectoderm Development EED isoforms may affect s

55 NA of the recently positionally cloned mouse embryonic ectoderm development gene, eed.

56 ve characterized an induced mutation, called embryonic ectoderm development or eed, that disrupts A-P

57 icient strains are suppressed by mutation of embryonic ectoderm development or Su-(var)3-9; E(z); Tri

58 Here, we report the identification of the embryonic ectoderm development polycomb histone-methylat

59 implicating the Polycomb group protein, Eed (embryonic ectoderm development protein) in imprinted X i

60 hat the mouse Polycomb group (PcG) gene Eed (embryonic ectoderm development) acts to maintain repress

61 The murine PcG gene eed (embryonic ectoderm development) encodes a 441-amino-acid

62 their function, we used the full-length Eed (embryonic ectoderm development) protein, a mammalian hom

63 Here we show that the gene eed (embryonic ectoderm development), a member of the mouse P

64 ning of a classical mouse mutation, eed (for embryonic ectoderm development), which is the highly con

65 rations overlap those following knockdown of embryonic ectoderm development, a common cofactor of EZH

66 NANOG represses embryonic ectoderm differentiation but has little effect

67 Low levels of OCT4 induce embryonic ectoderm differentiation in the absence of BMP

68 nce of two active X chromosomes in the extra-embryonic ectoderm (ExE) of X/X(Xist-) female embryos.

69 or another extra-embryonic tissue, the extra-embryonic ectoderm (ExE), in patterning the AVE and epib

70 tion before later random inactivation in the embryonic ectoderm from which the fetus is derived.

71 equired for normal placode patterning within embryonic ectoderm, hair follicle downgrowth, and adopti

72 in cells of the trophectoderm-derived extra-embryonic ectoderm in Eed(-/-) embryos remain transcript

73 lecule essential for the histogenesis of the embryonic ectoderm in Xenopus, and demonstrate that the

74 toskeleton that is co-expressed with Inca in embryonic ectoderm, including in the NC.

75 o function like Drosophila Ubx (DUbx) in the embryonic ectoderm indicates that the Ubx protein may ha

76 before gastrulation and progressively divide embryonic ectoderm into neural and non-neural regions, f

77 nd BMP-4 genes is to subdivide the primitive embryonic ectoderm into neural versus non-neural domains

78 We propose that patterning of the embryonic ectoderm is a multistep process that sequentia

79 We also demonstrate that much of the embryonic ectoderm is competent to generate an otic plac

80 Patterning of the embryonic ectoderm is dependent upon the action of negat

81 expression in the trophoblast-derived extra-embryonic ectoderm is essential for the normal formation

82 During vertebrate neurulation, the embryonic ectoderm is patterned into lineage progenitors

83 We showed that the embryonic ectoderm lineage was lost in the Mp(-/-) EBs,

84 hogenetic movement in which the edges of the embryonic ectoderm move together over the amnioserosa.

85 Dorsal-ventral patterning within the embryonic ectoderm of Drosophila requires two TGFbeta li

86 rogrammed cell death was observed within the embryonic ectoderm of GATA6-deficient embryos, a finding

87 nds are expressed in distinct domains in the embryonic ectoderm of Lytechinus variegatus.

88 hological abnormalities were observed in the embryonic ectoderm of mutant embryos at 7.5 dpc.

89 e to a hypothetical network operating in the embryonic ectoderm of the cephalochordate amphioxus.

90 as an extracellular morphogen to pattern the embryonic ectoderm of the Drosophila embryo.

91 ions between primitive endoderm and adjacent embryonic ectoderm or nascent mesoderm are required earl

92 not transform the segmental identity of the embryonic ectoderm or repress the Distal-less target gen

93 antois appear to develop normally, the small embryonic ectoderm remains undifferentiated and generate

94 data indicate that the activity of IQGAP1 in embryonic ectoderm requires Cdc42 function.

95 enic placodes are specialized regions of the embryonic ectoderm that are central to the development o

96 urogenic placodes are specialized regions of embryonic ectoderm that generate the majority of the neu

97 lso upregulated when neurulization occurs in embryonic ectoderm that has been disaggregated and reagg

98 sensory placodes arise from a region of the embryonic ectoderm that lies between the neural plate an

99 d plays important roles in patterning of the embryonic ectoderm through differential sensitivity to b

100 - ranging from its early induction from the embryonic ectoderm to the establishment of the three car

101 eIF4AII and activation of PKC sensitizes the embryonic ectoderm to the neuralising effect of noggin.

102 Cells of the embryonic ectoderm were less polarized as assessed by hi

103 e scattered throughout a large region of the embryonic ectoderm, where they intermingle with future n

104 tera there is a dramatic modification of the embryonic ectoderm, whereby mosquitoes contain separate

105 ly at the junction of the epiblast and extra-embryonic ectoderm, whereupon they move laterally.

106 not differentiate into primitive endoderm or embryonic ectoderm, which are prominent features of earl

107 however, because the smad2 mutants contained embryonic ectoderm within their interiors.