ライフサイエンスコーパス: blastula stage

1 increased beta-catenin levels before the mid-blastula stage.

2 A in the egg and are not detected beyond the blastula stage.

3 s major control of CyIIIa function after the blastula stage.

4 when administered to Xenopus embryos at the blastula stage.

5 vates early steps for both fates during late blastula stage.

6 en is lost from micromeres at the mesenchyme blastula stage.

7 gment cells and their precursors starting at blastula stage.

8 o pattern mesendoderm differentiation at the blastula stage.

9 nd localized to prospective oral ectoderm at blastula stage.

10 nisms which determine this process up to mid-blastula stage.

11 ipts are present throughout all cells at the blastula stage.

12 agments necessary for development beyond the blastula stage.

13 dy competent to receive a BMP4 signal at the blastula stage.

14 S-null (NS(-/-)) mice was aborted before the blastula stage.

15 t the mesoderm/endoderm boundary at the late blastula stage.

16 n immobilized in rosettes until the hatching blastula stage.

17 ion of beta catenin in ventral nuclei at the blastula stage.

18 -related signals released by endoderm at the blastula stage.

19 nes occurs sequentially, spanning the entire blastula stage.

20 nset of zygotic transcription, after the mid-blastula stage.

21 F2 is essential for development past the mid-blastula stage.

22 ntrotus purpuratus embryos at the mesenchyme blastula stage.

23 levels of retinoic acid detection during the blastula stage.

24 ation in the vegetal plate at the mesenchyme-blastula stage.

25 earing in embryonic nuclei shortly after the blastula stage.

26 nd translation during the early cleavage and blastula stages.

27 tween the late blastula and early mesenchyme blastula stages.

28 ential for repression of target genes during blastula stages.

29 sea urchin embryos during cleavage and early blastula stages.

30 sms to repress BMP transcription during late blastula stages.

31 y present in the enveloping layer during the blastula stages.

32 oteins at the hoxb1a promoter already during blastula stages.

33 nerates superficial ectoderm lesions at late blastula stages.

34 ion of the embryo during late cleavage/early blastula stages.

35 ting to veg(1) derivatives by the mesenchyme blastula stage; (2) Spgcm, an orthologue of the fruit fl

36 xpressed by micromere descendants during the blastula stage, a time when signaling has been shown to

37 ges, and also symmetrically during the early blastula stages, a period when heretofore largely unknow

38 lates in embryos beginning at the mesenchyme blastula stage; a RNA gel blot and in situ hybridization

39 s broadly in the oral ectoderm at mesenchyme blastula stage and at later embryonic stages is refined

40 inning in the micromere lineage of the early blastula stage and continuing after gastrulation during

41 ol of gcm expression by the early mesenchyme blastula stage and maintains it through pigment cell dif

42 d Sp-SERCA mRNA begin at the 18 hour hatched blastula stage and peak 4-5-fold higher by 25 h at the m

43 tion of LvTbx2/3 initiated at the mesenchyme blastula stage and protein was present into the pluteus

44 creases dramatically in embryos at the early blastula stage and remains at a constant level throughou

45 iched in the vegetal plate of the mesenchyme blastula stage and Sp-vasa, Sp-nanos2, Sp-seawi, and Sp-

46 me1 and H3K27ac, are established as early as blastula stage and that Smad2/3 only strongly associates

47 2/3 mRNA begins in micromeres at the hatched blastula stage and then is lost from micromeres at the m

48 n the generation of endodermal cells at late blastula stages and in the maintenance of endodermal sox

49 cally in presumptive mesendoderm during late blastula stages and in the prechordal plate during late

50 ta5, which is expressed in the endoderm from blastula stages and show that its transcription is induc

51 luding the cells of the animal hemisphere at blastula stages and the neural plate border and neural c

52 ty between the end of oogenesis and the late blastula stage, and at least a further 20-fold reduction

53 al mesendodermal gene expression at the late blastula stage, and fate mapping and gene expression stu

54 such as noggin, follistatin, and Xnr3-at the blastula stage, and requires beta-Catenin signaling.

55 Strong zygotic expression begins during the blastula stage, and the transcript is present at moderat

56 is expressed only during cleavage and early blastula stages, and exclusively in micromeres.

57 enchyme (mesodermal) domain at late-cleavage blastula stage; and (3) Spfoxc, which is first expressed

58 ce the otic marker Pax8 when recombined with blastula stage animal caps.

59 The arrest in interphase caused by treating blastula stage animals caps with aphidicolin can be reve

60 disrupted synchronous cell divisions during blastula stages, apparently as a result of delayed progr

61 ng domain of SpAN mRNA accumulation at early blastula stage ( approximately 150 cells).

62 nt on FoxN2/3, but only until the mesenchyme blastula stage as foxN2/3 mRNA disappears from PMCs at t

63 y genes expressed in this lineage up to late blastula stage, as identified in a genomewide survey.

64 probably skeletogenic territories during the blastula stage, as shown by in situ hybridization analys

65 hat BMP4 mRNAs accumulate transiently during blastula stages, beginning around the 200-cell stage, 14

66 cts using the tbr driver, which is active in blastula stage, block ingression.

67 Soon after the hatching blastula stage, BMP2/4 transcripts can be detected in pr

68 Second, sqt mRNA is expressed in blastula stage boz mutants, indicating that boz is not e

69 is also expressed in a gradient as early as blastula stages, but do not find any evidence of diffusi

70 axis formation is marked earlier at the late-blastula stage by the appearance of a cluster of cells w

71 wo cell populations are generated during the blastula stages by perpendicularly oriented divisions.

72 Tfap2a in embryos blocked for Bmp from late blastula stage can restore development of both PPE and N

73 a dramatic inhibition of ciliogenesis at the blastula stage characterized by the assembly of short, p

74 After the blastula stage, cyclin E mRNA and protein levels are ver

75 alization of activated MAPK occurs in morula/blastula stage embryo animal and marginal zones coincidi

76 ocalized to the prospective oral side of the blastula stage embryo, a process that requires lefty.

77 of 3.0 kilobase pairs was undetected in the blastula stage embryo, induced in gastrula embryo, expre

78 NE is restricted to the anterior of the late blastula stage embryo, where it forms a simple neural te

79 NA is localized to the vegetal region of the blastula-stage embryo.

80 red for opl regulation, we removed from late blastula stage embryos either the presumptive prechordal

81 phosphorylation of membrane proteins of the blastula stage embryos, but EGF4 stimulates phosphorylat

82 genes that are repressed by maternal rest in blastula stage embryos.

83 s in animal cap explants from Xenopus laevis blastula stage embryos.

84 roximately 36, 000 founder fish by injecting blastula-stage embryos with one of two pseudotyped retro

85 e mRNA evenly distributed among the cells of blastula-stage embryos.

86 During the blastula stages Endo16 expression expands radially until

87 t levels throughout early development and at blastula stages enriched in the ventral side of the anim

88 Apoptosis remains infrequent during the late blastula stage followed by a gradual increase in frequen

89 xI1e (also known as Xema) is required at the blastula stage for normal formation of both the central

90 afish bozozok (boz) locus is required at the blastula stages for formation of the embryonic shield, t

91 In zebrafish, the endoderm originates at the blastula stage from the most marginal blastomeres.

92 issociated from whole embryos after the late blastula stage have the ability to differentiate in vitr

93 ally, and ndr1 and ndr2 are expressed during blastula stage in the blastoderm margin.

94 LvBrac initially appears at mesenchyme blastula stage in two distinct regions with embryonic ex

95 he up-regulation of CyIIIa that occurs after blastula stage is a function of zygotically transcribed

96 nopus, mesoderm induction by endoderm at the blastula stage is well documented, but the molecular nat

97 velopment, but, for a short interval at late blastula stage, is asymmetrically inactivated in future

98 hat single cells in the vegetal plate of the blastula stage Lytechinus variegatus embryo could be lab

99 ations, other results show that in explanted blastula-stage marginal zones a distinct pattern develop

100 arget sites for specific proteins present in blastula-stage nuclear extract.

101 rget site purifies a 21-kDa polypeptide from blastula-stage nuclear extracts, and the amino acid sequ

102 binding experiments reveal that a protein in blastula-stage nuclei interacts specifically with the my

103 ease in concentration dramatically after the blastula stage of development, suggesting that the up-re

104 transcription of the late H1 gene at the mid-blastula stage of development.

105 gylocentrotus purpuratus is expressed at the blastula stage of embryogenesis throughout the vegetal p

106 At the mid-blastula stage of embryogenesis, temporally correlated w

107 on of the sea urchin late H1 gene at the mid-blastula stage of embryogenesis.

108 e in a temporally specific manner at the mid-blastula stage of embryogenesis.

109 The Xlim-1 gene is activated in the late blastula stage of Xenopus embryogenesis in the mesoderm,

110 ear SpSoxB1 gradually expands so that, after blastula stage, only cells in differentiating ectoderm a

111 A localizes to gcm+cells from the mesenchyme blastula stage onwards.

112 ranscripts began to accumulate at mesenchyme blastula stage primarily in ectoderm and then later were

113 n when the fish had been light deprived from blastula stage, ruling out a "trial and error" period of

114 he initial veg(2) endomesodermal domain; the blastula-stage separation of the central veg(2) mesoderm

115 ls removed from the embryo prior to the late blastula stage show no ability to differentiate when cul

116 es the loss of intercellular adhesion at the blastula stage, similar to that reported previously for

117 Furthermore, SSAP can undergo blastula-stage-specific homodimerization through its GQ-

118 on, and conversely, boz mRNA is expressed in blastula stage sqt mutants.

119 act embryos, it can only do so prior to late blastula stage (stage 9), well before the onset of gastr

120 ssed in the endodermal progenitors from late blastula stages, suggesting that it functions early duri

121 the presumptive SMCs and endoderm during the blastula stage, the time at which these two cell types a

122 We then used blastula stage transplantation experiments to demonstrat

123 tant of the FGF receptor (XFD) after the mid-blastula stage uncouples mesoderm induction, which is no

124 n SMC types are segregated in the mesenchyme blastula stage vegetal plate and that prospective germ l

125 ase during zebrafish development through the blastula stage was investigated through the use of domin

126 This transition occurs well after the blastula stage when the basal transcription machinery ca

127 ples of total RNA from embryos up to the mid-blastula stage, when zygotic transcription begins.

128 sh, fgf8 and ntl expression commences during blastula stages, whereas myogenesis, as indicated by myo

129 This gene is activated in blastula stage Xenopus embryos, its expression peaks dur

130 During blastula stages Xnr1, Xnr2 and Xnr4 are expressed in a d

131 This virus was injected into blastula-stage zebrafish, and 16% of the injected embryo