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1 inding-sites of insulator-complexes upon the midblastula transition.
2 d at the nuclear periphery shortly after the midblastula transition.
3 ately 150 genes are transcribed prior to the midblastula transition.
4 widespread pausing occurs de novo during the midblastula transition.
5 d RNA polymerase II C-terminal domain at the midblastula transition.
6 d myosin cages continued to divide until the midblastula transition.
7 arly embryogenesis, and then falls after the midblastula transition.
8 ic ribonucleoprotein (RNP) bodies during the midblastula transition.
9 L dynamically regulate RNA metabolism at the midblastula transition.
10 endent G(2) cell cycle arrest just after the midblastula transition.
11 to zygotic genetic control occurs called the midblastula transition.
12 mbryo, Xcdc6A becomes undetectable following midblastula transition.
13 but arrest in G2 phase immediately after the midblastula transition.
14 it is anchored in the cytoplasm prior to the midblastula transition.
15 nt in embryos exposed to gamma-IR before the midblastula transition.
16 h cycloheximide (100 microg/ml) prior to the midblastula transition.
17      This developmental change is termed the midblastula transition.
18 branes at different time points prior to the midblastula transition.
19 edly, in the rapid cell cycles preceding the midblastula transition, a defined timing program was pre
20  affects the onset of cellularization at the midblastula transition and found that nuclear cell-cycle
21 hancers are de-methylated shortly before the midblastula transition and reside in a unique epigenetic
22 ryo, concentrating on the period between the midblastula transition and the early tailbud stage.
23 on starts 6 hours after fertilization at the midblastula transition and therefore the first steps in
24  interacts through cleavage stages until the midblastula transition, and a second protein binds from
25 hout the animal hemisphere shortly after the midblastula transition, and becomes restricted to prospe
26 tely after fertilization, shortly before the midblastula transition, and during gastrulation.
27 tivate Smad2 phosphorylation until after the midblastula transition, and the onset of responsiveness
28  microg/ml) delayed development prior to the midblastula transition but resumed DNA synthesis, initia
29 absent during cycles 2-12, reappeared at the midblastula transition coincident with the disappearance
30 nt, zygotic gene expression initiated at the midblastula transition converts maternal information on
31 tions that cause developmental arrest at the midblastula transition, defects in cell viability, embry
32 ted with the same dose of gamma-IR after the midblastula transition developed normally and exhibited
33                                       At the midblastula transition during Xenopus development, the c
34 e cortical regions of blastomeres; after the midblastula transition exogenous plakoglobin accumulates
35                                 Prior to the midblastula transition exogenous plakoglobin is cytoplas
36 n of a homeobox gene, vega1, is activated at midblastula transition in all blastomeres, but is down-r
37 odeling of the cell cycle that occurs at the midblastula transition in early Xenopus laevis embryos.
38 echanism that may influence the onset of the midblastula transition in vivo.
39 upport a model for cell-cycle control at the midblastula transition in which titration of a maternal
40  change in the response to DNA damage at the midblastula transition in Xenopus embryos.
41 t of transcriptional quiescence prior to the midblastula transition in Xenopus, dorsal specification
42  in genes controlling processes prior to the midblastula transition, including egg development, blast
43   Additionally, cyclin E1 is degraded at the midblastula transition independently of protein synthesi
44 s of gamma-irradiation (gamma-IR) before the midblastula transition induced apoptotic cell death and
45 xes accumulate in the nucleus only after the midblastula transition, irrespective of the stage at whi
46 h to zygotic control of embryogenesis at the midblastula transition is accompanied by significant inc
47                            The timing of the midblastula transition is controlled by the ratio of nuc
48 ggest that a developmental checkpoint at the midblastula transition is maternally regulated and can t
49 l and biochemical changes that accompany the midblastula transition, lead to a continuation of the ma
50               In Xenopus laevis embryos, the midblastula transition (MBT) at the 12th cell division m
51                   In Drosophila embryos, the midblastula transition (MBT) dramatically remodels the c
52                                       At the midblastula transition (MBT) during Xenopus laevis devel
53  to zygotic regulation of development at the midblastula transition (MBT) follows mitosis 13, when th
54                                   During the midblastula transition (MBT) in Drosophila embryos, Rif1
55                   A conserved feature of the midblastula transition (MBT) is a requirement for a func
56                                          The midblastula transition (MBT) is the first morphological
57 a division cycles and fail to undergo timely midblastula transition (MBT) or arrest following ionizin
58  was accelerated when the embryo entered the midblastula transition (MBT) phase.
59  many genes whose onset of expression at the midblastula transition (MBT) requires Smicl and is corre
60  in eggs, and after fertilization, until the midblastula transition (MBT) when levels of cyclin E1 pr
61 nslation start site die at approximately the midblastula transition (MBT) without apoptosis.
62                               The Drosophila midblastula transition (MBT), a major event in embryogen
63 phase and accumulates continuously until the midblastula transition (MBT), after which it is degraded
64 avage phase of development terminates at the midblastula transition (MBT), at which point the cell cy
65 anscription of beta-catenin starts after the midblastula transition (MBT), but does not rescue dorsal
66                               At the Xenopus midblastula transition (MBT), cell cycles lengthen, and
67           These rapid divisions pause at the midblastula transition (MBT), coinciding with a dramatic
68 of many metazoan embryos are followed by the midblastula transition (MBT), during which the cell cycl
69 ion of ten DNA replication factors after the midblastula transition (MBT), including a marked decline
70 ome in many organisms is quiescent until the midblastula transition (MBT), when large-scale transcrip
71         Completion of 12 divisions marks the midblastula transition (MBT), when the cell cycle length
72  first major developmental transition is the midblastula transition (MBT), when zygotic transcription
73      Overexpression of cyclin E prior to the midblastula transition (MBT), with or without cdk2, resu
74 rapid embryonic cell cycles slow down at the midblastula transition (MBT).
75 (N/C) volume ratio reaching a maximum at the midblastula transition (MBT).
76 through multiple mitotic divisions until the midblastula transition (MBT).
77 ed for Dicer processing of pre-miRNAs at the midblastula transition (MBT).
78 y to longer, asynchronous cell cycles at the midblastula transition (MBT).
79 tially established and maintained during the midblastula transition (MBT).
80 ing, and cell cycle checkpoints comprise the midblastula transition (MBT).
81 s when irradiated before, but not after, the midblastula transition (MBT).
82 s laevis zygotic transcription begins at the midblastula transition (MBT).
83  that retains it in the cytoplasm before the midblastula transition (MBT).
84 le develops in Xenopus laevis embryos at the midblastula transition (MBT).
85 e cytoplasm from oocyte maturation until the midblastula transition (MBT).
86 hases are established, a period known as the midblastula transition (MBT).
87 cycles that pause before gastrulation at the midblastula transition (MBT).(1) These cleavage division
88 indle assembly do not appear until after the midblastula transition (MBT; 4000 cells).
89                        Strikingly, following midblastula transition, nuclear-localized Eomesodermin i
90 moothing of the enveloping cell layer at the midblastula transition occurred normally and expression
91 eus to activate the transcription, after the midblastula transition, of target genes such as Xbra and
92                                Following the midblastula transition, PIAS2b and XCtBP are present on
93 se that VegT activation of Sox17alpha at the midblastula transition prevents mesodermal gene expressi
94 aster embryos approach cell cycle 14 and the midblastula transition, rapid embryonic cell cycles slow
95 alize Xenopus embryos if expressed after the midblastula transition, strengthening the idea that zygo
96                                       At the midblastula transition, the Xenopus laevis embryonic cel
97 signaling is thought to function first after midblastula transition to regulate axial patterning via
98 r, the onset of Sox17alpha expression at the midblastula transition was dependent on VegT, but not on
99 c accumulation of zygotic transcripts at the midblastula transition, we observe the formation of gian
100 ncrease in cell-cycle length observed at the midblastula transition when cells become smaller and the
101 cription begins in many organisms during the midblastula transition when the cell cycle of the dividi
102 n the blastocoel, suggesting that before the midblastula transition Xenopus embryos use apoptosis to
103                                           At midblastula transition, zygotic transcription begins and

 
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