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1 iptional networks throughout development and cellular reprogramming.
2 and describe how pioneer factors may enable cellular reprogramming.
3 NA methylation and hydroxymethylation during cellular reprogramming.
4 ific chromatin factor provides a barrier for cellular reprogramming.
5 eful tool to study the mechanisms underlying cellular reprogramming.
6 properties of stem cells and the process of cellular reprogramming.
7 properties of stem cells and the process of cellular reprogramming.
8 esponse to pathogen attack involves dramatic cellular reprogramming.
9 source of insulin(+) cells after undergoing cellular reprogramming.
10 dicates DNA methylation changes induced upon cellular reprogramming.
11 types and 134 tissues, defining an atlas of cellular reprogramming.
12 new insights into the mechanisms underlying cellular reprogramming.
13 quences of inactivating Rb in the context of cellular reprogramming.
14 that the PpCSP genes function redundantly in cellular reprogramming.
15 sive environment for cell fate change during cellular reprogramming.
16 nsect cells will be the method of choice for cellular reprogramming.
17 e therefore unavailable for purification and cellular reprogramming.
18 s provide a global view of barriers to human cellular reprogramming.
19 ons, cardiomyocytes or beta-cells, and after cellular reprogramming.
20 eash cellular plasticity and favor oncogenic cellular reprogramming.
21 t the Hippo pathway constitutes a barrier to cellular reprogramming.
22 ize their importance in ESC pluripotency and cellular reprogramming.
23 nd RBMXL1, that impede gene induction during cellular reprogramming.
24 and sequence of molecular events inherent to cellular reprogramming.
25 he absence of complex soluble chemistries or cellular reprogramming.
26 t undergoes dynamic DNA demethylation during cellular reprogramming.
27 Emerging evidence increasingly points to cellular reprogramming, a process during which fully dif
28 lethal gene interactions and oncogene-driven cellular reprogramming ('addiction'), giving rise to new
29 s shared mechanisms in stress adaptation and cellular reprogramming and address the therapeutic impli
33 lls overcomes an early epigenetic barrier in cellular reprogramming and facilitates the generation of
34 foundation for elucidating the mechanisms of cellular reprogramming and for studying the safety and e
35 including, synthetic and structural biology, cellular reprogramming and functional pharmaceutical scr
38 ction and provide an unexpected link between cellular reprogramming and host-pathogen interaction.
39 ce, which highlight innovative approaches to cellular reprogramming and how this revolutionary techni
40 emphasis on understanding the mechanisms of cellular reprogramming and its potential applications in
41 n to consider classical observations such as cellular reprogramming and multilineage locus priming.
42 , a previously unrecognized role of Jmjd3 in cellular reprogramming and provide molecular insight int
44 r supports the crucial role played by p53 in cellular reprogramming and suggests an alternative metho
45 wn that pioneer factors are also crucial for cellular reprogramming and that they are implicated in t
46 adult stem cells and pluripotent stem cells, cellular reprogramming and tissue engineering are in pro
47 tylation in other cell states such as during cellular reprogramming and to quantify non-histone prote
48 he potential oncogenicity that may arise via cellular reprogramming, and could represent a valuable i
49 linking Sox proteins with stem cell biology, cellular reprogramming, and disease with an emphasis on
50 ractions at silent genes during development, cellular reprogramming, and steroid hormone induction.
51 using a recently demonstrated microRNA-based cellular reprogramming approach, human fibroblasts from
53 ggest a fundamentally different function for cellular reprogramming as a means of 'chromosome therapy
55 transient loss of cell polarity to the total cellular reprogramming, as found by transcriptional anal
58 ng the use of transcription factors (TFs) in cellular reprogramming, based on a device commonly used
59 s process, we systematically dissected human cellular reprogramming by combining a genome-wide RNAi s
60 1.The ubiquitin-proteasome system regulates cellular reprogramming by degradation of key pluripotenc
61 ings indicate that culture conditions during cellular reprogramming can strongly influence the epigen
62 indings that establish the essential role of cellular reprogramming during neoplastic transformation
63 y which GATA3 functions as a pioneer TF in a cellular reprogramming event relevant to breast cancer,
65 trate for the first time that HMGA1 enhances cellular reprogramming from a somatic cell to a fully pl
69 iscuss how progress in stem cell biology and cellular reprogramming has enabled exciting new strategi
70 d more restricted cell fates, recent work in cellular reprogramming has proven that one cellular iden
73 d phenotypes by epigenetic remodeling during cellular reprogramming highlights the role of epigenetic
74 uncover a sequential, two-step mechanism of cellular reprogramming in which repression of pre-existi
75 during cold response, there is a proteolytic cellular reprogramming in which the proteasome acquires
76 ls to pluripotency, a "second generation" of cellular reprogramming involves lineage-restricted trans
82 ganization of the cell during the process of cellular reprogramming is valuable for stem cell researc
83 ggest that immunoediting of tumor results in cellular reprogramming may be accompanied by alterations
86 (Ambystoma mexicanum) that is indicative of cellular reprogramming of differentiated cells to a germ
87 l-based regenerative therapies hold promise, cellular reprogramming of endogenous cardiac fibroblasts
88 133, 208, and 499 capable of inducing direct cellular reprogramming of fibroblasts to cardiomyocyte-l
92 ed by PGE2 and suggest a process of adaptive cellular reprogramming of the intestinal epithelium that
95 gical problems of the new century, including cellular reprogramming, organogenesis, regeneration, gen
97 g the diverse molecular actors implicated in cellular reprogramming presents a major challenge for fu
100 actor 4 (Klf4), one of the factors directing cellular reprogramming, recognizes the CpG dinucleotide
101 a somatic cell to a pluripotent state during cellular reprogramming requires DNA methylation to silen
102 exploration include cardiac cell therapy and cellular reprogramming targeting cell death and regenera
108 al-mesenchymal transition and other modes of cellular reprogramming that influence the tumor microenv
110 ogether our findings demonstrate that during cellular reprogramming, the metabolome of fibroblasts is
111 l role for ubiquitin-specific protease 26 in cellular reprogramming through polycomb-repressive compl
112 ion is driven by advances in genome editing, cellular reprogramming, tissue engineering, and informat
114 o transcriptional and epigenetic remodeling, cellular reprogramming to pluripotency is also accompani
115 In vitro studies have demonstrated that cellular reprogramming to pluripotency reverses cellular
119 gnaling pathways and illustrates one case of cellular reprogramming where the identity of the cell of
120 une surveillance; 2) stem cell therapies and cellular reprogramming, which seek to regenerate the dep
122 sis that environmental perturbations trigger cellular reprogramming, with downstream effects on cellu
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