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1 translation is carried out in the absence of elongation factor P.
2 cus encodes a protein similar in sequence to elongation factor P, a protein thought to be involved in
12 Post-translational modification of bacterial elongation factor P (EF-P) with (R)-beta-lysine at a con
15 d ribosomes are rescued by the translational elongation factor P (EF-P), which by stimulating peptide
16 nship, we examined the bacterial translation elongation factor P (EF-P), which plays a critical role
20 y than the wild-type strain, indicating that elongation factor P is important but not essential for t
22 the importance of the positive transcription elongation factor (P-TEF)b in control of global RNA synt
23 ated AhR recruits the positive transcription elongation factor (P-TEFb) and RNA polymerase II (RNA PI
24 artner of CDK9 in the positive transcription elongation factor (P-TEFb) complex, and binds cooperativ
25 linT1) subunit of the positive transcription elongation factor (P-TEFb) complex, which then cooperati
27 evealed roles for the positive transcription elongation factor (P-TEFb) component Cyclin T1 (Ccnt1).
29 evating levels of the positive transcription elongation factor (P-TEFb), instating a large proliferat
30 tors, including the positive transcriptional elongation factor (P-TEFb), the bromodomain-containing p
32 only recruited after positive transcription elongation factor (P-TEFb)-mediated phosphorylation and
35 of the Tat-associated kinase TAK and of the elongation factor P-TEFb (positive transcription elongat
36 layed by the biogenesis of the transcription elongation factor P-TEFb (Positive Transcription Elongat
37 nd MePCE captures the positive transcription elongation factor P-TEFb and prevents phosphorylation of
41 BRCA1 but also associates with the positive elongation factor P-TEFb through interaction with the re
42 se CDK9, is a component of the transcription elongation factor P-TEFb which binds the human immunodef
43 H and Tat-associated kinase (a transcription elongation factor P-TEFb) and requires the carboxyl-term
44 elongation by inactivating the transcription elongation factor P-TEFb, a CDK9-cyclin T1 (CycT1) heter
45 orks by activating the human transcriptional elongation factor P-TEFb, a CDK9-cyclin T1 heterodimer t
46 h components of the positive transcriptional elongation factor P-TEFb, a complex containing cyclin T1
47 e mediated through the binding of TAT-SF1 to elongation factor P-TEFb, a proposed component of the tr
48 sed to respond to the positive transcription elongation factor P-TEFb, and then enter productive elon
50 on by recruitment of the human transcription elongation factor P-TEFb, consisting of CDK9 and cyclin
51 on by recruitment of the human transcription elongation factor P-TEFb, consisting of Cdk9 and cyclin
53 1 (hCycT1), a major subunit of the essential elongation factor P-TEFb, has been proposed to act as a
54 h AFF4, ELLs, and the positive transcription elongation factor P-TEFb, providing evidence that the dy
55 polymerase II or cyclin T, a subunit of the elongation factor P-TEFb, reveals that all three factors
56 block is associated with recruitment of the elongation factor P-TEFb, the co-activator GRIP1, the ch
57 scription is mediated by human transcription elongation factor P-TEFb, which interacts with Tat and p
65 interaction with the positive transcription elongation factor, P-TEFb, and directs the factor to pro
68 es Tat to recruit the positive transcription elongation factor, P-TEFb, which functions to promote th