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1 ing of the epigenome to prime the zygote for totipotency.
2 P granules is to maintain germline fate and totipotency.
3 ce of germ cell identity and preparation for totipotency.
4 hanisms underlying plant cell plasticity and totipotency.
5 DNA demethylation to reset the epigenome for totipotency.
6 ability to reprogram somatic nuclei back to totipotency.
7 enomic basal state that is the foundation of totipotency.
8 allows the reprogramming of somatic cells to totipotency.
9 ights into reprogramming cells to a state of totipotency.
10 f the germ cell lineage is the generation of totipotency.
11 ineages whose workers have lost reproductive totipotency.
12 nd/or in maintaining germ cell and stem cell totipotency.
13 o epigenetic reorganisation and re-establish totipotency.
14 differentiation had lost their developmental totipotency.
15 actors that reprogram somatic cell nuclei to totipotency.
16 oducts and, for plant systems, expression of totipotency.
17 ajor regulators of plant embryo identity and totipotency.
18 pigenetic pathways or kinetics can establish totipotency.
23 ections, suggesting that P granules maintain totipotency and germline identity by antagonizing somati
25 ile in the cleavage-stage embryo establishes totipotency and is required for further development.
26 e of embryonic stem (ES) cells affects their totipotency and may give rise to fetal abnormalities.
27 tural as well as experimental acquisition of totipotency and pluripotency, control of transposons, an
29 e key players in the acquisition of cellular totipotency and the establishment of specific cellular s
30 ng of the epigenome in hPGCLCs and hPGCs for totipotency and the transmission of genetic and epigenet
33 eptional genomic plasticity and the state of totipotency are being unravelled, and will enhance our a
36 ion factors are key regulators of plant cell totipotency, as ectopic overexpression of either transcr
37 y, suggest that multiple mechanisms maintain totipotency at different stages of germline development,
38 ells is critical toward the establishment of totipotency, but investigations of the germline events a
39 tic reprogramming is likely to be needed for totipotency, correct initiation of embryonic gene expres
41 e chromatin structure capable of maintaining totipotency during embryogenesis and leading to differen
42 mechanisms that mediate the establishment of totipotency during the egg-to-embryo transition in mamma
43 m more advanced blastocysts no longer retain totipotency, failing to form TE and generating PE on the
44 fic functions and to retain the capacity for totipotency, germ cells repress somatic differentiation,
45 have a crucial role in establishing nuclear totipotency in normal development and in cloned animals,
48 hich these cells are specified and how their totipotency is established and maintained has important
49 s (PGCs), which reprograms the epigenome for totipotency, is linked to changes in nuclear architectur
56 plicate RNA regulation in the maintenance of totipotency, suggest that multiple mechanisms maintain t
57 c cells are generally acknowledged to retain totipotency, the potential to develop into any cell type
58 ify the early events in the establishment of totipotency, we monitored the genome-wide transcript pro
59 ryogenesis is an example of induced cellular totipotency, where embryos develop from vegetative cells
60 cell can potentially be reprogrammed back to totipotency, which in turn results in re-differentiation
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