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1 ocysts, but this was unable to improve their preimplantation development.
2 As representing genes expressed during human preimplantation development.
3 s to follow the fate of their progeny during preimplantation development.
4 has been investigated at different stages of preimplantation development.
5 yos were arrested at the morula stage during preimplantation development.
6  proliferation linked to blastocyst size and preimplantation development.
7 sure proper embryo sheltering during in vivo preimplantation development.
8 aled the translational dynamics during mouse preimplantation development.
9 tion of most genes and many ERVs involved in preimplantation development.
10 ehensively mapped at the blastocyst stage of preimplantation development.
11 ormations is poorly defined during mammalian preimplantation development.
12 s during mouse MZT are essential for ZGA and preimplantation development.
13 slational regulation that accompanies bovine preimplantation development.
14  species correlates with the duration of its preimplantation development.
15 es to overcome chromosome instability during preimplantation development.
16 e karyotypic complexity afflicting mammalian preimplantation development.
17 g its critical roles in ESC pluripotency and preimplantation development.
18 ating H3K27ac dynamics and are essential for preimplantation development.
19 neage restriction and cell commitment during preimplantation development.
20 rol is a critical developmental milestone in preimplantation development.
21  contents are required for fertilization and preimplantation development.
22 failed fertilization or embryo arrest during preimplantation development.
23 eres comprising a single embryo during human preimplantation development.
24 , and differentiation are coordinated during preimplantation development.
25 uct function in supporting fertilization and preimplantation development.
26 s, DNA methylation is globally erased during preimplantation development.
27 ole in maintaining energy homeostasis during preimplantation development.
28 ly disrupts oocyte chromatin methylation and preimplantation development.
29 nd the inner cell mass (ICM) lineages during preimplantation development.
30 Ctr9 and Rtf1, are required during mammalian preimplantation development.
31 tic reprogramming is required for successful preimplantation development.
32 l roles during oogenesis, fertilization, and preimplantation development.
33 l genome in zygotes is gradually lost during preimplantation development.
34  developing intestinal epithelium and during preimplantation development.
35 ed proteins and multi-component complexes in preimplantation development.
36 e function and chromosome segregation during preimplantation development.
37 ividual HDACs have distinct functions during preimplantation development.
38 the acetylation state of histone H4K5 during preimplantation development.
39 ylases (HDAC) HDAC1, HDAC2, and HDAC3 during preimplantation development.
40 l roles during oogenesis, fertilization, and preimplantation development.
41        Zscan4 thus seems to be essential for preimplantation development.
42 ether PI3K is intrinsically activated during preimplantation development.
43  the question whether they play any roles in preimplantation development.
44 TP production to survive and proceed through preimplantation development.
45 file changes in open chromatin during bovine preimplantation development.
46 h notable differences between species during preimplantation development.
47 ing oocyte growth and is required for normal preimplantation development.
48 re present in oocytes and persist throughout preimplantation development.
49 tion, which has been shown to persist during preimplantation development.
50  microarrays to explore gene activity during preimplantation development.
51 blastomas arising in Ptc1+/- mice can direct preimplantation development.
52 are required for maintaining imprints during preimplantation development.
53                                 During mouse preimplantation development, a subset of retrotransposon
54 ns of oocyte-derived Dnmt1o and Dnmt1 during preimplantation development add further support to the n
55 tected in human oocytes and at all stages of preimplantation development analyzed.
56  are present in the nucleus at all stages of preimplantation development and associate with mitotic c
57 t genome-scale DNA methylation maps of human preimplantation development and embryonic stem cell deri
58 and transition processes during human embryo preimplantation development and gastric cancer processio
59  model indicates that Mcl-1 is essential for preimplantation development and implantation, and sugges
60 s directly involved in genome defense during preimplantation development and in PGCs at the time of g
61 e temporal landscape of H3K9me3 during human preimplantation development and its regulation for diver
62 GA), begins during the 2-cell stage in mouse preimplantation development and marks a vital transition
63 or the study of gene expression during human preimplantation development and obviate the need for res
64 at embryos without Stella are compromised in preimplantation development and rarely reach the blastoc
65 nic genome activation, as well as subsequent preimplantation development and term viability.
66 ally suppressed during oocyte maturation and preimplantation development and that endo-siRNAs, rather
67 horylated Akt was detected throughout murine preimplantation development, and its presence at the pla
68 evelopment to blastocyst, the final stage of preimplantation development, and promoted mitochondrial
69 of aneuploidy, digyny, progressive delays in preimplantation development, and severe degeneration bef
70 tage-specific expression in ICM cells during preimplantation development, and show that Mbd3 is requi
71                                    Moreover, preimplantation development appears to be normal followi
72 es exhibiting differential expression during preimplantation development are of unknown identity and/
73 at Myh9 (NMHC II-A) is the major NMHC during preimplantation development as its maternal-zygotic loss
74  is a prolonged process that extends through preimplantation development, as characterized by slow co
75 anding of retrotransposon roles during early preimplantation development, as well as their rich funct
76 on translational regulation during mammalian preimplantation development but also revealed insights i
77 are not only expressed in oocytes and during preimplantation development, but also display distinct s
78 e methylation acquired in the oocyte through preimplantation development, but become fully methylated
79  fertilized and their embryos undergo normal preimplantation development, but the embryos fail to imp
80                             During mammalian preimplantation development, cells reduce in size and th
81  highlights significant differences in human preimplantation development compared with mouse and prov
82                                       During preimplantation development, contractile forces generate
83                                              Preimplantation development culminates with the emergenc
84 al low protein diet exclusively during mouse preimplantation development (Emb-LPD) is sufficient to c
85           Polarisation of cells during mouse preimplantation development first occurs within blastome
86 king from the eight-cell stage to the end of preimplantation development (>100 nuclei).
87               However, the roles of PADI1 in preimplantation development have not been addressed.
88 iling the expression of microRNAs throughout preimplantation development identified several candidate
89 ion using methyl-beta-cyclodextrin inhibited preimplantation development in culture.
90 ed during oocyte growth and persists through preimplantation development in mice.
91 hat seven isotypes of PKC are present during preimplantation development in mouse, some are of matern
92 amined at the mRNA and protein levels during preimplantation development in the mouse.
93  We focus on how imprinted XCI occurs during preimplantation development, including a brief discussio
94 nal and zygotic Dgcr8 alleles did not impair preimplantation development, including the determination
95                                        Human preimplantation development involves extensive remodelin
96 of DNA methylation patterns during mammalian preimplantation development involves the concurrent main
97 me-wide DNA methylation reprogramming during preimplantation development is a dynamic balance between
98                                              Preimplantation development is a period of dynamic epige
99 are present in the blastocyst, each stage of preimplantation development is characterized by a differ
100                                       Proper preimplantation development is essential to assemble a b
101                                Understanding preimplantation development is important both for basic
102               The role of miRNAs, if any, in preimplantation development is not known.
103             A major feature occurring during preimplantation development is the dramatic remodelling
104                    While Oct-4's role during preimplantation development is to maintain embryonic cel
105                                     Although preimplantation development is unaffected, conditional a
106 tially packaged sperm and egg genomes during preimplantation development is unknown.
107       Although it is essential for mammalian preimplantation development, its role remains unclear.
108 tween the two alleles are established during preimplantation development, likely due to loss of KRAB
109                         During germ cell and preimplantation development, mammalian cells undergo nea
110        Recent studies suggest that mammalian preimplantation development may also be regulated by the
111 n of oocyte maturation and the initiation of preimplantation development occur during transcriptional
112                                 However, the preimplantation development of contractility mutants has
113 e transient retrotransposon induction during preimplantation development of eight mammals.
114   Our findings show that the dynamics during preimplantation development of gene inactivation and acq
115                                          The preimplantation development of the mammalian embryo enco
116 tivation of the FGF signaling pathway during preimplantation development of the mouse embryo is known
117 ttranslational modification is essential for preimplantation development of the mouse embryo.
118 ic primitive endoderm (PrE) formation during preimplantation development of the rabbit.
119 he single-cell transcriptional data of mouse preimplantation development, our algorithm outperforms c
120                                       During preimplantation development, outside and inside cells re
121 protein, is correlated with a faster rate of preimplantation development (Ped fast phenotype) in mice
122               Melatonin was added during the preimplantation development period.
123 ing is vital for immunoregulation and normal preimplantation development, potentially providing insig
124 ucture of chromatin and its reprogramming in preimplantation development remain poorly understood.
125 mb domains are reprogrammed during mammalian preimplantation development remains largely unclear.
126 vation, the full range of their functions in preimplantation development remains largely unknown.
127 -species comparison of open chromatin during preimplantation development reveals strong similarity in
128 nge in promoter utilization may occur during preimplantation development such that TATA-less promoter
129 duction of HDAC2 has no noticeable effect on preimplantation development, suggesting that individual
130 le may be a more informative model for human preimplantation development than mice.
131                                 During mouse preimplantation development, the generation of the inner
132 omplex and hybrid N-glycans in oogenesis and preimplantation development, the Mgat1 gene in oocytes w
133                                       During preimplantation development, the number of cellular MTOC
134      It has been suggested that during mouse preimplantation development, the zygotically expressed t
135                                       During preimplantation development, there is passive DNA demeth
136 nt, maternal HDAC3 protein was stable during preimplantation development, thereby preventing an exami
137 ingle-cell gene-expression analysis in human preimplantation development to instruct human stem cell
138 and breast cancer cells could support normal preimplantation development to the blastocyst stage but
139 os segregate three different lineages during preimplantation development: trophoblast, epiblast and h
140 ted that H19 imprinting could be lost during preimplantation development under certain culture condit
141 powerful tool for the study of fertilization/preimplantation development, vertical viral gene transmi
142 attern of expression of miRNAs during bovine preimplantation development was determined by small RNA-
143                                              Preimplantation development was normal until the blastoc
144 tional regulation during human oogenesis and preimplantation development, we defined stage-specific t
145 aling dynamics and fate specification during preimplantation development, we generated a transgenic m
146 d trafficks to the eight-cell nucleus during preimplantation development, where it maintains DNA meth
147 rnal LPD treatment during post-fertilization preimplantation development which may reflect the relati

 
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