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1 ll as the polycomb complex protein Bmi-1 and enhancer of zeste homolog 2.
2 Previous work has demonstrated that Ezh2 (enhancer of zeste homolog 2), a histone 3 lysine 27 (H3K
3 itors or depletion of the polycomb repressor enhancer of zeste homolog 2 altered relative RKIP and BA
4 stone H3 lysine 27 (H3K27) methyltransferase enhancer of zeste homolog 2 and the WD-repeat protein em
5 lso sequesters a core subunit of PRC2 (Ezh2 [enhancer of zeste homolog 2]) at the cell membrane, prev
6 sion include histone methyltransferase EZH2 (enhancer of zeste homolog 2), COX2 (cyclooxygenase-2), P
7 for multiple myeloma (MM) cell lines induce enhancer of zeste homolog 2 (ezh 2) transcript expressio
8 ) (a subunit required for PRC2 function) and enhancer of zeste homolog 2 (EZH2) (a histone methyltran
9 ating mutations in histone methyltransferase enhancer of zeste homolog 2 (EZH2) also have been observ
10 2), additional sex combs like 1 (ASXL1), PcG enhancer of zeste homolog 2 (EZH2) and DNA methyltransfe
11 ned expression of the Polycomb group protein Enhancer of Zeste Homolog 2 (EZH2) and increased tumor-i
12 ed by the polycomb histone methyltransferase enhancer of zeste homolog 2 (Ezh2) and its trimethylatio
14 DR5 expression via the epigenetic regulator enhancer of zeste homolog 2 (EZH2) and that EZH2 control
15 enewal, with the chromatin-modifying protein Enhancer of zeste homolog 2 (EZH2) emerging as a central
17 tion of the histone methyltransferase enzyme enhancer of zeste homolog 2 (EZH2) in attenuating oxidat
19 s catalyzed by the histone methyltransferase enhancer of zeste homolog 2 (EZH2) in the polycomb repre
21 with short hairpin RNA or pharmacologic PRC2/enhancer of zeste homolog 2 (EZH2) inhibitors promoted m
27 The histone H3 lysine 27 methyltransferase enhancer of zeste homolog 2 (EZH2) is highly expressed i
28 n profiling, that the polycomb group protein enhancer of zeste homolog 2 (EZH2) is overexpressed in h
30 H3 lysine 27 (H3K27) tri-methylating enzyme, enhancer of zeste homolog 2 (EZH2) mediates epigenetic s
32 , poly (ADP-ribose) polymerase 1 (PARP1), or enhancer of zeste homolog 2 (EZH2) suppressed cell growt
33 independent interaction with E2F1 to recruit enhancer of zeste homolog 2 (EZH2) to diverse repeat seq
34 m for recruiting the H3K27 methyltransferase enhancer of zeste homolog 2 (EZH2) to PR3 and MPO loci m
41 mediated repression of rap1GAP that involves Enhancer of Zeste Homolog 2 (EZH2), a histone methyltran
46 tes a physical interaction between Snail and enhancer of zeste homolog 2 (EZH2), an enzymatic subunit
51 cy of enhancer of zeste homolog 1 (Ezh1) and enhancer of zeste homolog 2 (Ezh2), which encode the enz
54 opment, and coincides with redistribution of enhancer of zeste homolog 2 (EZH2)-dependent histone H3
55 infection bypassed AR signaling by promoting enhancer of zeste homolog 2 (EZH2)-mediated epigenetic s
56 that down-regulation of miR-34a is caused by Enhancer of zeste homolog 2 (EZH2)-mediated H3 lysine 27
61 ransferase-2 (G9a), histone deacetylases and enhancer of zeste homolog-2 (EZH2), but only G9a inhibit
62 to the promoter region of NEDD4L and recruit enhancer of zeste homolog 2 histone methyltransferase to
63 tin protein 1, methyl-CpG binding protein 2, Enhancer of Zeste homolog 2, histone deacetylase 1, and
65 ablish that the polycomb group protein EZH2 (enhancer of zeste homolog 2) is down-regulated during os
67 terized by recruitment of the polycomb group enhancer of zeste homolog 2 methyltransferase and the ac
68 hylation of H3 lysine 9 and interaction with enhancer of zeste homolog 2, the catalytic subunit of po
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