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1 ntial third biological function of p53: as a transcriptional elongation factor.
2 nism that is distinct from its function as a transcriptional elongation factor.
3 ncing its interactions with coactivators and transcriptional elongation factors.
5 mplexes that also contain RNA polymerase II, transcriptional elongation factors, and general pre-mRNA
9 vents during initiation and P-TEFb (positive transcriptional elongation factor b) events during elong
11 ne activation might include recruitment of a transcriptional elongation factor by ubiquitinated activ
12 te myeloid leukemias fuses the gene encoding transcriptional elongation factor ELL to the MLL gene wi
14 ains casein kinase 2 (CK2) and the chromatin transcriptional elongation factor FACT (a heterodimer of
16 of CDK9 and a cyclin T subunit, is a global transcriptional elongation factor important for most RNA
18 presses KIT mRNA expression through positive transcriptional elongation factor inhibition and decreas
19 ich has two open reading frames encoding the transcriptional elongation factor M2-1 and the putative
22 on of GATA-1 with components of the positive transcriptional elongation factor P-TEFb, a complex cont
23 ramatically in the requirements for positive transcriptional elongation factor (P-TEF) b activity.
24 l elongation factors, including the positive transcriptional elongation factor (P-TEFb), the bromodom
25 ociation of RelA with the activated positive transcriptional elongation factor (PTEF-b) complex prote
26 ene containing a bromo-adjacent homology and transcriptional elongation factor S-II domain, which we
28 nse mutation (W049) in the gene encoding the transcriptional elongation factor Spt5 (reviewed in ) wh
30 ranscriptional initiation, Hog1 behaves as a transcriptional elongation factor that is selective for
31 innate response requires the recruitment of transcriptional elongation factors to rapidly induce inn
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