ライフサイエンスコーパス: transcription factor Oct-1

1 xpression by creating a binding site for the transcription factor Oct-1.

2 nes contain binding sites for the ubiquitous transcription factor Oct-1.

3 egulator of the broadly expressed POU domain transcription factor Oct-1.

4 in did not inhibit the expression of nuclear transcription factor Oct-1.

5 amer sequence, which recruits the POU domain transcription factor Oct-1.

6 GRE in vitro along with GR is the POU domain transcription factor Oct-1.

7 ng site for the broadly expressed POU domain transcription factor Oct-1.

8 and was recruited as a coactivator with the transcription factor Oct-1.

9 The ubiquitously expressed transcription factor Oct-1, a member of the POU domain f

10 Target prediction and validation identify transcription factors Oct-1, a known co-activator of HSV

11 ith two cellular factors-the POU homeodomain transcription factor Oct-1 and the cell proliferation fa

12 f BRCA1, we demonstrated that BRCA1 binds to transcription factor OCT-1 and up-regulates the transcri

13 ctivator that functions with octamer binding transcription factors (Oct-1 and Oct-2) to mediate effic

14 The transcription factors Oct-1 and -2 inhibit and enhance,

15 o the nucleolus and shares homology with the transcription factors Oct-1 and -2, Pit-1, and POU-M1.

16 ts have presented the novel observation that transcription factors Oct-1 and NF-YA participate in the

17 Physical associations of BRCA1 protein with transcription factors Oct-1 and NF-YA, which directly bi

18 The POU domain transcription factors Oct-1 and Oct-2 interact with the

19 The POU transcription factors Oct-1 and Oct-2 regulate the activ

20 histocompatibility genes and octamer-binding transcription factors Oct-1 and Oct-2, respectively.

21 n and an activating region that recruits the transcription factors Oct-1 and Staf (ZNF143).

22 ein partially recognized by antibody against transcription factor Oct-1 binds to the LREAA element co

23 his report, we demonstrate that the cellular transcription factor Oct-1 cooperates with the EBV immed

24 However, the role for the octamer-binding transcription factor Oct-1 in the DNA damage-activated r

25 ave presented the novel observation that the transcription factor Oct-1 is induced after cells are ex

26 The POU-domain transcription factor Oct-1 is widely expressed in adult

27 ve BRAF upregulates HMGCL through an octamer transcription factor Oct-1, leading to increased intrace

28 fore, these results have implicated that the transcription factor Oct-1 might participate in cellular

29 he host cell factor HCF-1 and the POU domain transcription factor Oct-1, on TAATGARAT-containing sequ

30 y the interaction of a POU domain containing transcription factor Oct-1 or Oct-2, with the B-cell-spe

31 activation, on the DNA binding of the basal transcription factor Oct-1, or on hydrogen peroxide-indu

32 or nucleolus and has distant homology to the transcription factors Oct-1, Pit-1, and POU-M1.

33 Here, we report that the POU domain transcription factor Oct-1 represses the expression of E

34 f the ubiquitously expressed POU-homeodomain transcription factor, Oct-1, strongly represses transcri

35 FPIV) with a binding site for the ubiquitous transcription factor Oct-1 that appears crucial for horm

36 phism (SNP) that causes the helix-turn-helix transcription factor OCT-1 to bind to a novel region of

37 rs and enhancers is regulated by two related transcription factors, Oct-1 (ubiquitous) and Oct-2 (B l

38 xpression of certain genes by activating the transcription factor Oct-1, while p53 has been reported