ライフサイエンスコーパス: transcription factor TFIIH

1 dent kinase 7 (CDK7), a subunit of the basal transcription factor TFIIH.

2 s of recruitment and activity of the general transcription factor TFIIH.

3 in transcription, as a module of the general transcription factor TFIIH.

4 CTD is phosphorylated at Ser 5 by the basal transcription factor TFIIH.

5 L interacts with p44, a subunit of the basal transcription factor TFIIH.

6 , also functions as a subunit of the general transcription factor TFIIH.

7 a DNA helicase and a subunit of the general transcription factor TFIIH.

8 e repairosome and the RNA polymerase H basal transcription factor TFIIH.

9 h include the multisubunit RNA polymerase II transcription factor TFIIH.

10 nt of the CTD kinase activity of the general transcription factor TFIIH.

11 odification of XPB, a subunit of the general transcription factor TFIIH.

12 th a CDK-activating kinase (CAK) and part of transcription factor TFIIH.

13 nstructural protein NSs and the host general transcription factor TFIIH.

14 E. coli, and is not a component of the basal transcription factor, TFIIH.

15 versible inhibitor of the XPB subunit of the transcription factor TFIIH and initiation of RNA polymer

16 itute the TFIIK kinase subcomplex of general transcription factor TFIIH and to mutations in Cak1, whi

17 In contrast, general transcription factors TFIIH and TFIIA play a significant

18 We now report that TAF7 interacts with the transcription factors, TFIIH and P-TEFb, resulting in th

19 major CTD kinase is a subunit of the general transcription factor TFIIH, and is encoded by an essenti

20 timulates the CTD kinase activity of general transcription factor TFIIH, and subsequent CTD phosphory

21 allelic mutations in components of the basal transcription factor TFIIH, and these mutations lead to

22 bind to XPB, the largest subunit of general transcription factor TFIIH, and to cause degradation of

23 (HSSB)], and the multisubunit (7-10) general transcription factor TFIIH are required for the dual inc

24 K, a subcomplex of RNA polymerase II general transcription factor TFIIH, are encoded by the yeast cyc

25 minary studies, we have identified the basal transcription factor TFIIH as the potential target for u

26 erase II (Pol II) C-terminal domain (CTD) as transcription factor TFIIH-bound CAK.

27 extracts, which was complemented by the NER/transcription factor TFIIH, but not by purified Mms19 pr

28 ith transcription sites and with the general transcription factor TFIIH, but not with the splicing fa

29 Tat can also interact with the multisubunit transcription factor TFIIH complex and increase the phos

30 Here, we show that the general transcription factor TFIIH complex is continuously requi

31 orchestrated by the core form of the general transcription factor TFIIH, containing the helicases XPB

32 The general transcription factor TFIIH contains three ATP-dependent

33 nt Srb4, but not on the Kin28 subunit of the transcription factor TFIIH, even though both proteins ar

34 The DNA helicases XPB and XPD, components of transcription factor TFIIH, have been implicated in a p5

35 (OC) requires DNA unwinding mediated by the transcription factor TFIIH helicase-related subunit XPB/

36 cates that the AR interacts with the general transcription factor TFIIH in a physiological condition.

37 ementing protein (XPB), a component of human transcription factor TFIIH, in both B lymphocytes and ep

38 arge subunit of RNA polymerase II by general transcription factor TFIIH is believed to be an importan

39 Further, we show that the basal transcription factor TFIIH is constitutively recruited b

40 The transcription factor TFIIH is involved in both basal tra

41 XPB, the largest subunit of the eukaryotic transcription factor TFIIH, is essential for both initia

42 The multisubunit DNA repair and transcription factor TFIIH maintains an intricate cross-

43 During transcription initiation, the general transcription factor TFIIH marks RNA polymerase II by ph

44 Basal transcription factor TFIIH phosphorylates the RNA polyme

45 The human basal transcription factor TFIIH plays a central role in two d

46 General transcription factor TFIIH, previously described as a 10

47 pendent kinase 7 (CDK7), part of the general transcription factor TFIIH, promotes gene transcription

48 tations in the XPD subunit of the DNA repair/transcription factor TFIIH result in distinct clinical e

49 ction between SCL and a subunit of the basal transcription factor TFIIH, suggesting a potential means

50 CDK7 is the kinase subunit of the general transcription factor TFIIH that phosphorylates the C-ter

51 tion by disrupting the assembly of the basal transcription factor TFIIH through sequestration of its

52 rboxy-terminal domain (CTD) of Pol II by the transcription factor TFIIH through the associated CAK ki

53 General transcription factor TFIIH, which contains CDK7, phospho

54 ukaryotes, XPB is an integral subunit of the transcription factor TFIIH, which plays a dual role in D

55 ntosum group D (XPD) protein is a subunit of transcription factor TFIIH with DNA helicase activity.