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1 o be reactivated in differentiated cells via nuclear reprogramming.
2 n from oxidative to glycolytic metabolism in nuclear reprogramming.
3 ency is required to achieve a high degree of nuclear reprogramming.
4 aining healthy mtDNA, to induce somatic cell nuclear reprogramming.
5 of cellular identity during development and nuclear reprogramming.
6 fferentiation and proliferation, meiosis and nuclear reprogramming.
7 asmic components of the oocyte in supporting nuclear reprogramming.
8 odifiers to enhance chromatin remodeling and nuclear reprogramming.
9 lly, we show that enhancers are reset during nuclear reprogramming.
10 ed for pluripotency gene reactivation during nuclear reprogramming.
11 is important for the comprehensive study of nuclear reprogramming.
12 e factors affecting cell differentiation and nuclear reprogramming.
13 ities, cell cycle asynchronies, and improper nuclear reprogramming.
14 vo myomaker-mediated heterologous fusion and nuclear reprogramming.
15 mmonly considered a consequence of errors in nuclear reprogramming.
16 eactivation will help improve the success of nuclear reprogramming.
17 urrently particular interest in the field of nuclear reprogramming, a process by which the identity o
19 ipotent stem cells (iPSCs) undergo extensive nuclear reprogramming and are generally indistinguishabl
21 CD4(+) T lymphocyte donor cell, we observed nuclear reprogramming and efficient contribution of the
22 e emerging principles which appear to govern nuclear reprogramming and production of clones, and will
23 4 methylation imposes a barrier to efficient nuclear reprogramming and suggest approaches for improvi
24 s during mitosis may facilitate somatic cell nuclear reprogramming and the acquisition of new cell fa
25 s spectacular organismal transition requires nuclear reprogramming and the initiation of RNAPII at th
26 clear organization in meiosis, the events of nuclear reprogramming and the spatio-temporal regulation
28 can catalyze cellular de-differentiation and nuclear reprogramming by acting at the cell surface.
29 but attempts to recapitulate this process of nuclear reprogramming by molecular means have failed.
32 at the NT embryos have undergone significant nuclear reprogramming by the blastocyst stage; however,
35 otent stem cells (PSCs) can be generated via nuclear reprogramming by transcription factors (i.e., in
36 ether, these data demonstrate that extensive nuclear reprogramming can be achieved independently of p
38 provide invaluable models of human disease, nuclear reprogramming could limit the usefulness of iPSC
41 ms, underscoring the value of nonintegrative nuclear reprogramming for derivation of competent cardio
42 he original fibroblasts are revealed through nuclear reprogramming, generating mutant hiPSCs with a d
45 ammatory pathways are required for efficient nuclear reprogramming in the induction of pluripotency.
46 recovered in screens for genes required for nuclear reprogramming in Xenopus and mouse embryonic ste
59 ather than unfertilized eggs, as a source of nuclear reprogramming molecules and for the eventual ide
61 th distinct histone modifications as well as nuclear reprogramming of erythroid transcription factors
65 study provides definite proof for the direct nuclear reprogramming of terminally differentiated adult
66 estoration was not detected in vivo although nuclear reprogramming of the muscle-specific myosin ligh
67 as a starting point to more fully assess how nuclear reprogramming overcomes the multitude of genetic
68 ls, but also a thorough understanding of the nuclear reprogramming process taking place during nuclea
72 alogy to classical descriptions of amphibian nuclear reprogramming, the propensity of committed cells
73 they participate actively in the process of nuclear reprogramming to pluripotency by increasing epig
74 r active DNA demethylation and initiation of nuclear reprogramming towards pluripotency in human soma
75 rived from various types of somatic cells by nuclear reprogramming using defined transcription factor
76 t a signaling pathway required for efficient nuclear reprogramming was activated by the retroviral, b
79 chimera assays, indicating a high degree of nuclear reprogramming, with no evidence of passage throu
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