TFII-I
Expression of the transcription factor, TFII I, during post implantation mouse embryonic development
... 2 TFII-I expression in head region at E9 (A-D) and at E12 (E, F, ...×). TFII-I is more discretely localized at ED9 with nuclear ...power, TFII-I immunoreactivity is visible in ...
8
The adenovirus E4 ORF3 protein stimulates SUMOylation of general transcription factor TFII I to direct proteasomal degradation
... of TFII-I ...modulates TFII-I, by regulating its stability via inducing TFII-I ubiquitination and pro- teasomal degradation during ...that TFII-I is targeted by ...
11
The Human Adenovirus Type 5 L4 Promoter Is Negatively Regulated by TFII-I and L4-33K
... E4 Orf3 activates the L4P via its effect on TFII-I. A recent study by Sohn and coworkers demonstrated that in Ad5-infected HeLa cells, TFII-I is extensively posttranslationally modified by ...
11
The human adenovirus type 5 L4 promoter is negatively regulated by TFII I and by L4 33K
... factor TFII-I, which has been demon- strated to possess both transcriptional activation and repression abilities (21, ...for TFII-I were pre- dicted in the vicinity of the TSS by our in silico ...
12
TFII-I Regulates Induction of Chromosomally Integrated Human Immunodeficiency Virus Type 1 Long Terminal Repeat in Cooperation with USF
... and TFII-I, which bind cooperatively to ...and TFII-I but not by the dominant negative I- B ...and TFII-I bind to the integrated wild-type LTR in unstimulated cells and ...
11
The Adenovirus E4 ORF3 Protein Stimulates SUMOylation of General Transcription Factor TFII I to Direct Proteasomal Degradation
... of TFII-I ...modulates TFII-I, by regulating its stability via inducing TFII-I ubiquitination and pro- teasomal degradation during ...that TFII-I is targeted by ...
10
The Rous Sarcoma Virus Long Terminal Repeat Promoter Is Regulated by TFII-I
... The TFII-I protein is a 957-amino-acid phosphoprotein with an apparent molecular mass of 120 kDa (21, ...of TFII-I revealed several novel features of the protein, including six highly ...
9
Sterol Regulatory Element-Binding Protein 2 Couples HIV-1 Transcription to Cholesterol Homeostasis and T Cell Activation
... scription plays a role in HIV-1 replication. These levels of inhibition of HIV infection correlate well with the degree of suppression of TFII-I expression. To confirm that 25-OHC treatment of infected ...
11
Herpes Simplex Virus 1 ICP4 Forms Complexes with TFIID and Mediator in Virus-Infected Cells
... spectral data. Only those proteins with a Ppro score of less than 10 ⫺3 are listed. Of the 46, 14 were identified from gel slices corresponding to incorrect weights. The remaining 32 proteins were further divided into ...
12
Williams-Beuren Syndrome Hypercalcemia: Is TRPC3 a Novel Mediator in Calcium Homeostasis?
... encodes TFII-I, which suppresses cell-surface accumu- lation of transient receptor potential C3 (TRPC3) channels, involved in calcium transport in ...to TFII-I haploinsuf fi ciency and ...
7
Transcription factors COUP TFI and COUP TFII are required for the production of granule cells in the mouse olfactory bulb
... Immunohistochemistry was performed on cryostat 12 μ m or 30 μ m sections according to previous studies (Li et al., 2011; Ma et al., 2013). Sections were briefly boiled in 10 mM sodium citrate ( pH 6.0) for COUP-TFI, ...
13
BRG1 promotes COUP TFII expression and venous specification during embryonic vascular development
... Fig. 5. BRG1 binds to the COUP-TFII promoter in endothelial cells. (A) Alignment of the murine COUP-TFII promoter region with sequences from zebrafish, frog, opossum, dog, chimpanzee and human genomes from ...
10
Molecular control of two novel migratory paths for CGE derived interneurons in the developing mouse brain
... For quantification of IN subpopulations at embryonic stages, a representative area in the migratory paths was selected for each animal ( n =3) and single- or double-positive cells were counted. For quantification of IN ...
13
Molecular identification of venous progenitors in the dorsal aorta reveals an aortic origin for the cardinal vein in mammals
... Fig. 2. The dorsal aorta transiently contained both venous marker-positive and -negative endothelial cells. (A,B) Cross-sections of the DA immunostained for the venous marker Coup-TFII. (A) Coup-TFII ...
9
Endothelial cell plasticity: how to become and remain a lymphatic endothelial cell
... To accommodate the available data summarized above, two possible explanations could be considered. The first is that Sox18 is not the factor that collaborates with COUP-TFII in providing venous ECs with the ...
10
Direct transcriptional regulation of neuropilin 2 by COUP TFII modulates multiple steps in murine lymphatic vessel development
... genes. Mutations of Sp1-binding sites abolish COUP-TFII–depen- dent enhancement of NGFI-A promoter activity (31). Similarly, knockdown of Sp1, using Sp1-specific siRNA, abolishes COUP- TFII–dependent ...
15
(i,j) β I i Open Sets and (i,j) β I i Almost Continuous Functions in Ideal Bitopological Spaces
... Proof. If f is not (i, j)-β-I-i-almost continuous at x ∈ X , then there exists an ij-regular open set V containing f (x) such that for every (i, j)-β-I-i-open set U of X ...
9
C0M D I V I S I
... Placing: Lift handset + Line key + Dial number Answering: handset connected, press flashing key) Answering ringing over handset + + Dial l 0.. Placing:.[r] ...
38
I and another I
... issues of my focus on my most obvious back at my life to graduate work, I my theme, I be true to my Korean background in my want make am the image is my self-portrait.. defining the conc[r] ...
32
MPC1, a key gene in cancer metabolism, is regulated by COUP- TFII in human prostate cancer
... COUP- TFII was observed in prostate cancer patients and it is further increased in metastatic patients, which is consistent with the possibility of negative regulation of MPC1 by ...
11