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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.
4 main binding protein 5 (WBP5), also known as Transcriptional Elongation Factor A like 9 (TCEAL9) has
5                                    Spt6 is a transcriptional elongation factor and histone chaperone
6 e was enriched in DNA damage repair factors, transcriptional elongation factors and E3 ubiquitin liga
7 mplexes that also contain RNA polymerase II, transcriptional elongation factors, and general pre-mRNA
8                   By recruiting the positive transcriptional elongation factor b (P-TEFb) to paused R
9                               Human positive transcriptional elongation factor b (P-TEFb), consisting
10                                 The positive transcriptional elongation factor b (P-TEFb), consisting
11 vents during initiation and P-TEFb (positive transcriptional elongation factor b) events during elong
12 tracellular signal regulated kinase/positive transcriptional elongation factor-b and NF-kappaB.
13 ne activation might include recruitment of a transcriptional elongation factor by ubiquitinated activ
14 te myeloid leukemias fuses the gene encoding transcriptional elongation factor ELL to the MLL gene wi
15  of a chimeric protein that fuses MLL to the transcriptional elongation factor ELL.
16 ains casein kinase 2 (CK2) and the chromatin transcriptional elongation factor FACT (a heterodimer of
17                             A homolog of the transcriptional elongation factor, GreA, was identified
18  of CDK9 and a cyclin T subunit, is a global transcriptional elongation factor important for most RNA
19                    Here we identify multiple transcriptional elongation factors, including ELL2, TFII
20 presses KIT mRNA expression through positive transcriptional elongation factor inhibition and decreas
21 ich has two open reading frames encoding the transcriptional elongation factor M2-1 and the putative
22                        The RNA polymerase II transcriptional elongation factor P-TEFb (cyclin-depende
23                                          The transcriptional elongation factor P-TEFb directly bound
24         Amt-87 works by activating the human transcriptional elongation factor P-TEFb, a CDK9-cyclin
25 on of GATA-1 with components of the positive transcriptional elongation factor P-TEFb, a complex cont
26 ramatically in the requirements for positive transcriptional elongation factor (P-TEF) b activity.
27 l elongation factors, including the positive transcriptional elongation factor (P-TEFb), the bromodom
28 reviously established distinct roles for the transcriptional elongation factors PAF1, negative elonga
29 ociation of RelA with the activated positive transcriptional elongation factor (PTEF-b) complex prote
30 ene containing a bromo-adjacent homology and transcriptional elongation factor S-II domain, which we
31                                    The human transcriptional elongation factor SII or Trascription El
32 nse mutation (W049) in the gene encoding the transcriptional elongation factor Spt5 (reviewed in ) wh
33         ELL is an RNA Polymerase II (Pol II) transcriptional elongation factor that interacts with th
34 ranscriptional initiation, Hog1 behaves as a transcriptional elongation factor that is selective for
35  innate response requires the recruitment of transcriptional elongation factors to rapidly induce inn