ライフサイエンスコーパス: transcription factor E2F1

1 e NAD(+)-dependent deacetylase SIRT1 and the transcription factor E2F1.

2 ating myoblasts by the cell cycle-associated transcription factor E2F1.

3 n of AMP kinase and the proapoptotic nuclear transcription factor E2F1.

4 53, but also on its ability to signal to the transcription factor E2F1.

5 B1 and upstream of the cell cycle regulatory transcription factor E2F1.

6 r suppressors p53 and retinoblastoma and the transcription factor E2F1.

7 inhibits the EC cycle and downregulates the transcription factor E2F1.

8 ed the activity of the cell cycle regulatory transcription factor E2F1.

9 icantly with those bound by the S-phase gene transcription factor E2F1.

10 actor PCNA and of the proliferation-specific transcription factor E2F1.

11 he SETD6 promoter has a binding site for the transcription factor E2F1.

12 chromatin accessibility and activity of the transcription factor E2F1.

13 t of rapamycin complex 1-S6K pathway and the transcription factor E2F1.

14 p19ARF was found to complex with transcription factors E2F1, -2, and -3.

15 The activating E2F transcription factors, E2F1-3, contribute to these embry

16 s directly and specifically activated by the transcription factor E2F1--a factor perturbed in the maj

17 es indicated that DDB can associate with the transcription factor E2F1 and can function as a transcri

18 restored RB1 function and downstream targets transcription factor E2F1 and cycling-dependent kinase 2

19 The transcription factor E2F1 and pathways linked to tumor s

20 The A-, E-, and D-type cyclins as well as transcription factor E2F1 and the E1A viral oncoprotein

21 Mice deficient for the transcription factors E2F1 and E2F2 suffer from a chroni

22 Here, we investigated the contribution of transcription factors E2F1 and E2F2 to NAFLD-related HCC

23 s JG cell renin production via repression of transcription factors E2f1 and Pde3b.

24 d protein levels of cyclins A, B, and E, the transcription factor E2F1, and the cyclin-dependent kina

25 mice are not dependent on either p53 or the transcription factor E2F1, as mice null for these genes

26 A typical transcription factor E2F1 associated with its DNA-bindin

27 ained induction of NF-kappaB signaling and a transcription factor E2F1-dependent metabolic pathway by

28 ivation of AMP kinase (AMPK) and the nuclear transcription factor E2F1, detailed auditory pathology w

29 The cell cycle-regulating transcription factors E2F1/DP1 activate genes whose prod

30 of ChIP-seq data from a panel of cell cycle transcription factors (E2F1, E2F4, E2F6, and GABPA) from

31 Loss of the transcription factor E2F1 elicits a complex metabolic ph

32 astoma susceptibility gene product (pRb) and transcription factor E2F1, exhibit altered immunostainin

33 The transcription factor E2F1 functions as a key regulator f

34 tional regulators in the nucleus, leading to transcription factor E2F1 hyperactivation.

35 n catastrophe depends on accumulation of the transcription factor E2F1 in cyclin F-depleted cells.

36 onomous role of the cell-cycle regulator and transcription factor E2F1 in the maintenance of beta-cel

37 Moreover, the transcription factor E2F1 induces EZH2 during the GC rea

38 The transcription factor E2F1 is a key regulator of prolifer

39 cular, we found that the cell cycle effector transcription factor E2F1 is a required input for the la

40 The transcription factor E2F1 is an additional target of c-M

41 The transcription factor E2F1 is an important regulator of c

42 The transcription factor E2F1 is believed to be involved in

43 The transcription factor E2F1 is known to regulate cell prol

44 The level of the p105Rb-regulated transcription factor, E2F1, is reduced, as is transcript

45 is mechanistically linked to suppression of transcription factor E2F1-mediated cell cycle regulation

46 Deregulation of the transcription factor E2F1, normally repressed by CCAAT e

47 n p130 and increased the Rb family-regulated transcription factor E2F1, overexpression of which inhib

48 We show that Cdk4 and its downstream transcription factor E2f1 regulate mouse pancreas develo

49 We have selected such mutations in the transcription factor E2F1 that affect its ability to het

50 The transcription factor E2F1 that is expressed in granule n

51 ecifically determines the recruitment of the transcription factor E2F1 to selected target genes that

52 The nuclear-localized TyrRS activates transcription factor E2F1 to upregulate the expression o

53 hanistic studies showed that PELP1 modulates transcription factor E2F1 transactivation functions, tha

54 s have also shown that downregulation of the transcription factor E2F1 was a key mechanism of TNF's e

55 rubicin-induced upregulation mediated by the transcription factor E2F1, was enhanced by Cry1/Cry2 dou

56 D cells leads to increased expression of the transcription factor E2F1, which in turn stimulates expr