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1 (EVL) integrity and cell protrusions at the blastula stage.
2 ed in the endoderm/mesoderm beginning at mid-blastula stage.
3 increased beta-catenin levels before the mid-blastula stage.
4 A in the egg and are not detected beyond the blastula stage.
5 s major control of CyIIIa function after the blastula stage.
6 when administered to Xenopus embryos at the blastula stage.
7 vates early steps for both fates during late blastula stage.
8 en is lost from micromeres at the mesenchyme blastula stage.
9 gment cells and their precursors starting at blastula stage.
10 nd localized to prospective oral ectoderm at blastula stage.
11 nisms which determine this process up to mid-blastula stage.
12 ipts are present throughout all cells at the blastula stage.
13 agments necessary for development beyond the blastula stage.
14 dy competent to receive a BMP4 signal at the blastula stage.
15 S-null (NS(-/-)) mice was aborted before the blastula stage.
16 o pattern mesendoderm differentiation at the blastula stage.
17 t the mesoderm/endoderm boundary at the late blastula stage.
18 n immobilized in rosettes until the hatching blastula stage.
19 ion of beta catenin in ventral nuclei at the blastula stage.
20 -related signals released by endoderm at the blastula stage.
21 nset of zygotic transcription, after the mid-blastula stage.
22 F2 is essential for development past the mid-blastula stage.
23 ntrotus purpuratus embryos at the mesenchyme blastula stage.
24 nes occurs sequentially, spanning the entire blastula stage.
25 levels of retinoic acid detection during the blastula stage.
26 ation in the vegetal plate at the mesenchyme-blastula stage.
27 earing in embryonic nuclei shortly after the blastula stage.
28 nd translation during the early cleavage and blastula stages.
29 tween the late blastula and early mesenchyme blastula stages.
30 nhancer activation during cleavage and early blastula stages.
31 ential for repression of target genes during blastula stages.
32 sea urchin embryos during cleavage and early blastula stages.
33 sms to repress BMP transcription during late blastula stages.
34 y present in the enveloping layer during the blastula stages.
35 nerates superficial ectoderm lesions at late blastula stages.
36 oteins at the hoxb1a promoter already during blastula stages.
37 ion of the embryo during late cleavage/early blastula stages.
38 ting to veg(1) derivatives by the mesenchyme blastula stage; (2) Spgcm, an orthologue of the fruit fl
39 xpressed by micromere descendants during the blastula stage, a time when signaling has been shown to
40 ges, and also symmetrically during the early blastula stages, a period when heretofore largely unknow
41 lates in embryos beginning at the mesenchyme blastula stage; a RNA gel blot and in situ hybridization
42 s broadly in the oral ectoderm at mesenchyme blastula stage and at later embryonic stages is refined
43 inning in the micromere lineage of the early blastula stage and continuing after gastrulation during
44 ol of gcm expression by the early mesenchyme blastula stage and maintains it through pigment cell dif
45 d Sp-SERCA mRNA begin at the 18 hour hatched blastula stage and peak 4-5-fold higher by 25 h at the m
46 tion of LvTbx2/3 initiated at the mesenchyme blastula stage and protein was present into the pluteus
47 creases dramatically in embryos at the early blastula stage and remains at a constant level throughou
48 iched in the vegetal plate of the mesenchyme blastula stage and Sp-vasa, Sp-nanos2, Sp-seawi, and Sp-
49 me1 and H3K27ac, are established as early as blastula stage and that Smad2/3 only strongly associates
50 2/3 mRNA begins in micromeres at the hatched blastula stage and then is lost from micromeres at the m
51 ET activity leads to loss of pluripotency at blastula stages and a loss of neural crest at neurula st
52 n the generation of endodermal cells at late blastula stages and in the maintenance of endodermal sox
53 cally in presumptive mesendoderm during late blastula stages and in the prechordal plate during late
54 ta5, which is expressed in the endoderm from blastula stages and show that its transcription is induc
55 luding the cells of the animal hemisphere at blastula stages and the neural plate border and neural c
56 ty between the end of oogenesis and the late blastula stage, and at least a further 20-fold reduction
57 al mesendodermal gene expression at the late blastula stage, and fate mapping and gene expression stu
58 such as noggin, follistatin, and Xnr3-at the blastula stage, and requires beta-Catenin signaling.
59 Strong zygotic expression begins during the blastula stage, and the transcript is present at moderat
61 enchyme (mesodermal) domain at late-cleavage blastula stage; and (3) Spfoxc, which is first expressed
63 The arrest in interphase caused by treating blastula stage animals caps with aphidicolin can be reve
64 disrupted synchronous cell divisions during blastula stages, apparently as a result of delayed progr
66 nt on FoxN2/3, but only until the mesenchyme blastula stage as foxN2/3 mRNA disappears from PMCs at t
67 y genes expressed in this lineage up to late blastula stage, as identified in a genomewide survey.
68 probably skeletogenic territories during the blastula stage, as shown by in situ hybridization analys
69 hat BMP4 mRNAs accumulate transiently during blastula stages, beginning around the 200-cell stage, 14
73 is also expressed in a gradient as early as blastula stages, but do not find any evidence of diffusi
74 axis formation is marked earlier at the late-blastula stage by the appearance of a cluster of cells w
75 wo cell populations are generated during the blastula stages by perpendicularly oriented divisions.
76 Tfap2a in embryos blocked for Bmp from late blastula stage can restore development of both PPE and N
78 a dramatic inhibition of ciliogenesis at the blastula stage characterized by the assembly of short, p
80 alization of activated MAPK occurs in morula/blastula stage embryo animal and marginal zones coincidi
81 ocalized to the prospective oral side of the blastula stage embryo, a process that requires lefty.
82 of 3.0 kilobase pairs was undetected in the blastula stage embryo, induced in gastrula embryo, expre
83 NE is restricted to the anterior of the late blastula stage embryo, where it forms a simple neural te
85 red for opl regulation, we removed from late blastula stage embryos either the presumptive prechordal
86 phosphorylation of membrane proteins of the blastula stage embryos, but EGF4 stimulates phosphorylat
89 roximately 36, 000 founder fish by injecting blastula-stage embryos with one of two pseudotyped retro
92 t levels throughout early development and at blastula stages enriched in the ventral side of the anim
93 Apoptosis remains infrequent during the late blastula stage followed by a gradual increase in frequen
94 xI1e (also known as Xema) is required at the blastula stage for normal formation of both the central
95 afish bozozok (boz) locus is required at the blastula stages for formation of the embryonic shield, t
97 issociated from whole embryos after the late blastula stage have the ability to differentiate in vitr
100 he up-regulation of CyIIIa that occurs after blastula stage is a function of zygotically transcribed
101 nopus, mesoderm induction by endoderm at the blastula stage is well documented, but the molecular nat
102 velopment, but, for a short interval at late blastula stage, is asymmetrically inactivated in future
103 hat single cells in the vegetal plate of the blastula stage Lytechinus variegatus embryo could be lab
104 ations, other results show that in explanted blastula-stage marginal zones a distinct pattern develop
106 rget site purifies a 21-kDa polypeptide from blastula-stage nuclear extracts, and the amino acid sequ
107 binding experiments reveal that a protein in blastula-stage nuclei interacts specifically with the my
108 ease in concentration dramatically after the blastula stage of development, suggesting that the up-re
110 gylocentrotus purpuratus is expressed at the blastula stage of embryogenesis throughout the vegetal p
114 The Xlim-1 gene is activated in the late blastula stage of Xenopus embryogenesis in the mesoderm,
115 ear SpSoxB1 gradually expands so that, after blastula stage, only cells in differentiating ectoderm a
117 ranscripts began to accumulate at mesenchyme blastula stage primarily in ectoderm and then later were
118 n when the fish had been light deprived from blastula stage, ruling out a "trial and error" period of
119 he initial veg(2) endomesodermal domain; the blastula-stage separation of the central veg(2) mesoderm
120 ls removed from the embryo prior to the late blastula stage show no ability to differentiate when cul
121 es the loss of intercellular adhesion at the blastula stage, similar to that reported previously for
124 act embryos, it can only do so prior to late blastula stage (stage 9), well before the onset of gastr
125 ssed in the endodermal progenitors from late blastula stages, suggesting that it functions early duri
126 the presumptive SMCs and endoderm during the blastula stage, the time at which these two cell types a
128 tant of the FGF receptor (XFD) after the mid-blastula stage uncouples mesoderm induction, which is no
129 n SMC types are segregated in the mesenchyme blastula stage vegetal plate and that prospective germ l
130 ase during zebrafish development through the blastula stage was investigated through the use of domin
133 sh, fgf8 and ntl expression commences during blastula stages, whereas myogenesis, as indicated by myo