BÁO CÁO KHOA HỌC: " HIGH-THROUGHPUT SEQUENCING IDENTIFIES STAT3 AS THE DNA-ASSOCIATED FACTOR FOR P53-NF-ΚB-COMPLEX-DEPENDENT GENE EXPRESSION IN HUMAN HEART FAILURE" PPS
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formed a complex with NF-jB, and overexpression ofC/EBPb inhibited the transactivation potential of p65,Gal4-p65 (1–551) and Gal4-p65 (286–551) (data notshown). A number of reports suggest a physiological roleof C/EBPb in mediating the PKA signaling. For instance,P[r]
analyses of expression of human (Hs), D. melanogaster (Dm), A. franciscana (Af) and hybrid molecules (H/D, D/H, H/A, A/H, D/A, A/D) byWestern blot using anti-myc Ig. Ten micrograms of the cell extracts obtained in the transfection shown in (A) were analyzed.[r]
towards soluble factors and away from the cell surfacemay be generally important for the function of mem-bers of this intriguing and emerging subfamily ofserine proteases.Experimental proceduresCloning, expression and purificationCloning, expression and purification[r]
appropriate physiologic signals. Senescent cells have been identified in patients whose premalignant lesions harbor activated oncogenes, for instance, dysplastic nevi that encode an activated form of BRAF (see below), demonstrating that induction of senescence is a protective mechanism[r]
was also seen in normal human epidermal melano-cytes, and 624mel human melanoma cell lines exam-ined (Fig. 3B), and other human melanoma cell lines,G361 and SK-MEL-28 (data not shown). These resultssuggest that the potential SOX10 sites are dispensablefor me[r]
quantitation of the population of SubG1 cells 24 hafter exposure to 50 lm menadione (Fig. 4C).8-OxoG was analysed in the KD-1 clone using aflow cytometric method based on the ability of 8-oxoGto bind avidin [27]. As a control, we used a stableclone of A549 cells obt[r]
81012***Fig. 3. AGE-HSA and LPS stimulate MAP kinase phosphorylation and NF-jB nuclear translocation. HUVECs were incubated with AGE-HSA(25 lgÆmL)1), LPS (10 ngÆmL)1), or their combination, for 30 min. (A). Total (upper panel) and phosphorylated (lower panel) p38, ERK1 ⁄ 2 andJNK were[r]
murine double minute 2 (MDM2). The tumor suppressorgene p53 plays a key role in regulating the cell cycle andserves as a principal mediator of growth arrest, senes-cence, and apoptosis in response to a broad array of cellu-lar damage [3]. The p[r]
Chapter 065. Gene Therapy in Clinical Medicine (Part 3) Long-Term Expression in Genetic Disease: In Vivo Gene Transfer with Recombinant Adeno-Associated Viral (AAV) Vectors Recombinant AAV vectors have emerged as attractive gene[r]
RNeasy kit (Qiagen, Hilden,Germany), respectively.Purified total RNA was used to run a reverse transcrip-tion reaction to synthesize the complementary cDNA bythe AMV first-strand cDNA synthesis system (BBI, Tor-onto, Canada) against the reverse primers of four porcinecomplex II subunits.[r]
MKCl eluted fractions, respectively. Lanes 6, same as lane 4, except that 20 lgÆmL)1pD-TERM (R) DNA was used as atemplate. Lanes 7–9, same as in lane 4, except that pD-TERM (F) DNA carrying various nucleotide replacements (Mut1, Mut2, and Mut3 asshown in Fig[r]
production in vivo, and how glucose up-regulates theexpression of NOX2 requires further investigation.It has been reported that NF-jB, p38MAPK andp53 are the key points relating to apoptosis [12]. Aninhibitor of p38MAPK was used to confirm its rolein apoptosis. The increased leve[r]
Delta-lactoferrin enhances Skp1 gene transcription C. Mariller et al.2046 FEBS Journal 274 (2007) 2038–2053 ª 2007 The Authors Journal compilation ª 2007 FEBSdistance between these two recognition elements andthe initiation start point is crucial in order to promotethe induction[r]
due to incorrect folding although the other two syn-thesized hepcidin peptides have antimicrobial activi-tites, because we did not confirm the structure ofsynthesized peptides. These results suggest that at leastHep-JF2 acts as an antibacterial agent in Japaneseflounder.Tog[r]
E-mail: francois.boudreau@usherbrooke.ca(Received 2 June 2010, revised 11 August2010, accepted 16 August 2010)doi:10.1111/j.1742-4658.2010.07813.xThe CCAAT-Displacement-Protein (CUX1) can transcriptionally represssucrase–isomaltase gene expression, a specific product of enterocytes that[r]
specific reverse primer (XlMGPR1; Table 1). All PCR frag-ments thus obtained were digested with XhoI and HindIII,and the resulting DNA fragments were gel purified andinserted into the promoterless pGL2 vector (Promega,Madison, WI, USA) previously digested with the sameenzymes. [r]