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1 lucose transporter of the fertilized egg and preimplantation embryo.
2 y reprograms to a naive state resembling the preimplantation embryo.
3 in the gametes is recognized already in the preimplantation embryo.
4 acts in the ICM, which activates Oct4 in the preimplantation embryo.
5 sis is common in the blastomere stage of the preimplantation embryo.
6 us type-H (HERVH) family is expressed in the preimplantation embryo.
7 expressed by pluripotent cells in the human preimplantation embryo.
8 hromosome status resembles that of the human preimplantation embryo.
9 on of endogenous retroelements active in the preimplantation embryo.
10 derm (PrE) fate that occurs in the mammalian preimplantation embryo.
11 a mouse model of transient DNMT1 loss in the preimplantation embryo.
12 anonical WNT signaling in development of the preimplantation embryo.
13 ys essential for the continued growth of the preimplantation embryo.
14 enerated from the inner cell mass of a human preimplantation embryo.
15 econd, to resist global demethylation in the preimplantation embryo.
16 ote the in vitro development of zygotes into preimplantation embryos.
17 ntial for successful oocyte development into preimplantation embryos.
18 unction of the PI3K/Akt pathway in mammalian preimplantation embryos.
19 uring the oocyte to embryo transition and in preimplantation embryos.
20 to treat human infertility entail culture of preimplantation embryos.
21 ) facilitative glucose transporter 49-66% in preimplantation embryos.
22 accumulates in oocyte nuclei and persists in preimplantation embryos.
23 y for gene transfer into murine ES cells and preimplantation embryos.
24 r by immunocytochemical staining in wildtype preimplantation embryos.
25 f in vitro fertilization (IVF)-derived human preimplantation embryos.
26 (ES) cells and a shorter form in oocytes and preimplantation embryos.
27 iated serine protease expressed by mammalian preimplantation embryos.
28 not detected by RT-PCR in either oocytes or preimplantation embryos.
29 tors influence cellular growth in very early preimplantation embryos.
30 ounds the growing oocytes, ovulated eggs and preimplantation embryos.
31 s critical functions for spindle assembly in preimplantation embryos.
32 lls of the trophectoderm in blastocyst-stage preimplantation embryos.
33 criptomic and epigenomic approaches in mouse preimplantation embryos.
34 utcome limiting genotyping accuracy in human preimplantation embryos.
35 n is restricted to the inside cells of mouse preimplantation embryos.
36 the gene expression changes in the resulting preimplantation embryos.
37 xygen concentration in mammalian oocytes and preimplantation embryos.
38 unctions of H3K27me3 and H2AK119ub1 in mouse preimplantation embryos.
39 U5F1) CRISPR-Cas9-targeted and control human preimplantation embryos.
40 maternal Xist expression and maternal XCI in preimplantation embryos.
41 ers are accessible in GV and MII oocytes and preimplantation embryos.
42 the first time, a knockdown screen in mouse preimplantation embryos.
43 ingle-cell RNA-sequencing of human and mouse preimplantation embryos.
44 preservation of human and animal oocytes and preimplantation embryos.
45 in naive pluripotent stem cells (PSCs) with preimplantation embryos.
46 be reset in primordial germ cells (PGCs) and preimplantation embryos.
47 pplementation on the transcriptome of bovine preimplantation embryos.
48 an also serve as an imprinting mark in mouse preimplantation embryos.
49 f the H3K27me3 decrease normally observed in preimplantation embryos.
50 and H2A.Z are also accessible in oocytes and preimplantation embryos.
51 ning the role of kinesin 5 in mouse eggs and preimplantation embryos.
52 essential role for CTCF in mouse oocytes and preimplantation embryos.
53 , which are known to stimulate the growth of preimplantation embryos.
54 ne lipid rafts in mouse oocytes and cleaving preimplantation embryos.
55 at PI3K is constitutively activated in mouse preimplantation embryos.
56 th dividing and postmitotic cells, including preimplantation embryos.
57 peripheral organs including sperm, eggs, and preimplantation embryos.
58 r function of the PI3K/Akt pathway in murine preimplantation embryos.
59 mined by small RNA-sequencing using eggs and preimplantation embryos (1-cell, 2-cell, 4-cell, 8-cell,
61 his is an application of micro MRS to bovine preimplantation embryos (~8 cells) and oocytes (single c
62 allele-specific CpG methylation 5' of H19 in preimplantation embryos, although this methylation is no
63 nd motor deficiencies that produce aneuploid preimplantation embryos, among other anomalies including
65 imprinted, which occurs in all cells of the preimplantation embryo and in the extraembryonic lineage
66 f aneuploid chromosomes across 73 unselected preimplantation embryos and 365 biopsies, sampled from f
67 d with 5'-coding sequences from single human preimplantation embryos and a 10 week old whole foetus.
68 d spatial clustering are virtually absent in preimplantation embryos and are markedly reduced in fate
69 ow that AP-2gamma is present in all cells of preimplantation embryos and becomes restricted to the ex
71 mitotic origin of segmental aneuploidies in preimplantation embryos and develop a risk stratificatio
72 found that Suppressyn is expressed in human preimplantation embryos and developing placenta using it
74 slands, were coordinately expressed in mouse preimplantation embryos and embryonic stem (ES) cells bu
75 irst cleavage of zygotes, the development of preimplantation embryos and even the metabolism of indiv
77 fication phenotypes, similar to FGF4-treated preimplantation embryos and Fgf4 KO embryos, respectivel
78 to genetically ablate the OCT4 gene in human preimplantation embryos and found key differences from i
79 ngle-cell DNA methylome sequencing for human preimplantation embryos and found that tens of thousands
80 prepare amplified cDNA from human individual preimplantation embryos and isolate embryo-specific sequ
82 adotropins, and produced a reduced number of preimplantation embryos and less progeny than controls.
83 mammalian genomes can be global, as seen in preimplantation embryos and primordial germ cells (PGCs)
85 iled the mRNA translation landscape in mouse preimplantation embryos and revealed the translational d
86 enhances both the developmental potential of preimplantation embryos and the live birth rate, it migh
88 that Dnmt1 protein is also expressed in the preimplantation embryo, and may account for maintenance
89 gly, these genes are paternally expressed in preimplantation embryos, and ectopic removal of H3K27me3
91 ides a high-resolution view of aneuploidy in preimplantation embryos, and supports the conclusion tha
92 ression of repetitive parasitic sequences in preimplantation embryos, and thereby contributes to pres
96 hat are accessible to viral DNA insertion in preimplantation embryos are incompatible with expression
99 is significantly higher in in vitro-produced preimplantation embryos as compared to in vivo-conceived
100 ed methylation to maintain in the zygote and preimplantation embryo at a time when much of the remain
102 on and morphogenesis in time-lapse images of preimplantation embryos, automated 3D instance segmentat
103 pplication of CGH to single cells from human preimplantation embryos (blastomeres) and to single fibr
105 rs in mouse primordial germ cells (PGCs) and preimplantation embryos, but the precise dynamics and bi
106 provision of the methyl-donor choline to the preimplantation embryo can alter its developmental progr
107 inally, we show that chromatin compaction in preimplantation embryos can partially proceed in the abs
111 ced in ES cell lines isolated from 3-day-old preimplantation embryos, consistent with the hypothesis
113 logies (ART), where metabolic assessments of preimplantation embryos could improve treatment outcomes
115 In conclusion, TSPO was found necessary for preimplantation embryo development and ACTH-stimulated s
116 ocannabinoid signaling is critical to normal preimplantation embryo development and migration of trop
121 cate that HPAT2, HPAT3 and HPAT5 function in preimplantation embryo development to modulate the acqui
122 icO(2)) during in vitro mammalian oocyte and preimplantation embryo development using a commercially
123 epletion of maternal stores of Filia impairs preimplantation embryo development with a high incidence
124 elta9-tetrahydrocannabinol] levels constrain preimplantation embryo development with aberrant express
126 pid droplets (LDs) are stored throughout the preimplantation embryo development, but the amount of li
127 idence of an association between the rate of preimplantation embryo development, postnatal growth and
128 tent to fertilize rhesus oocytes, leading to preimplantation embryo development, pregnancy, and the b
139 ations regulate key steps in late oocyte and preimplantation embryo development; however, roles for z
144 ation and oxidative stress were increased in preimplantation embryos, fetuses, and newborns of Wester
145 ylglycine) plays key roles in mouse eggs and preimplantation embryos first in a novel mechanism of ce
148 of single cells biopsied from human eggs and preimplantation embryos following in vitro fertilization
149 f DNase I-hypersensitive site (DHS) of mouse preimplantation embryos from 1-cell to morula stage.
152 ssion of the human homologue, XIST, in human preimplantation embryos from the 5- to 10-cell stage onw
153 how that Kcnq1ot1 is paternally expressed in preimplantation embryos from the two-cell stage, and tha
154 transfer into rhesus monkey (Macaca mulatta) preimplantation embryos gives rise to transgenic placent
157 put ribosome profiling of bovine oocytes and preimplantation embryos has enabled us to define the tra
158 roRNAs (miRNAs) in the development of bovine preimplantation embryos has not been reported in detail.
159 though the transcriptional dynamics of mouse preimplantation embryos have been well characterized, th
160 nd mitochondrial DNA mutations in gametes or preimplantation embryos have now been developed and are
161 severe disturbance in the development of the preimplantation embryo in a majority of pregnancies, as
162 t (i) protocols optimized in humans generate preimplantation embryos in nonhuman primates; (ii) some,
163 o developmental periods-in germ cells and in preimplantation embryos-in which methylation patterns ar
164 that are present in oocytes, sperm and early preimplantation embryos, including atypical patterns of
165 analysed global remethylation from the mouse preimplantation embryo into the early epiblast and extra
167 Optimal development of fertilized eggs into preimplantation embryos is essential for reproduction.
170 ely linked to the Om locus that controls the preimplantation embryo-lethal phenotype known as the "DD
172 and support the notion that discarded human preimplantation embryos may be useful recipients for the
178 Thus, DNA replication stress in mammalian preimplantation embryos predisposes gene-poor regions to
181 us and the coordinate expression of CR-1a by preimplantation embryos regulates blastocyst differentia
183 nse to double-strand breaks induced in human preimplantation embryos remains uncertain due to the com
185 ablation of the geminin gene (Gmnn) in mouse preimplantation embryos resulted in apoptosis, suggestin
186 two SEs was also seen at different stages in preimplantation embryos, revealing that methylation hete
188 ments of non-DMD, but not DMD methylation in preimplantation embryos suggest that the preimplantation
189 factor in determining methylation status in preimplantation embryos, suggesting a need to reassess m
190 Transcripts encoding Dnmt1 are present in preimplantation embryos, suggesting that Dnmt1 protein i
191 e critical importance of the PI3K pathway in preimplantation embryo survival and pregnancy outcome an
192 riptionally quiescent full-grown oocytes and preimplantation embryos that display a low level of tran
193 obtained from animal model systems and human preimplantation embryos that provide the scientific basi
194 unostaining of mitotic chromosome spreads of preimplantation embryos that the 5hmC associated with th
195 ethod that facilitates chromatin analysis of preimplantation embryos, that H3K9me3 is enriched at the
196 are known to happen during X inactivation in preimplantation embryos, the accumulation of macroH2A1 a
197 does not adversely affect the development of preimplantation embryos to blastocysts and uterine prepa
198 plex in murine embryonic stem (ES) cells and preimplantation embryos to determine whether it regulate
199 ughout early embryo development from zygote, preimplantation embryos, to post-implantation embryos.
200 ovide the first global analysis of the human preimplantation embryo transcriptome, and demonstrate th
203 perm protection but also indirect effects on preimplantation embryos via oviduct expression of embryo
204 ontribute to the regulation of cavitation in preimplantation embryos via target proteins including Na
207 essential cytoplasmic complex in oocytes and preimplantation embryos with poorly understood function,
208 of the heterozygous MYBPC3 mutation in human preimplantation embryos with precise CRISPR-Cas9-based t
209 pression changes in the germ line and in the preimplantation embryo would greatly enhance the underst