(C) 2011 Elsevier

B.V. All rights reserved.”
“Three series of new aromatic polyether sulfones bearing phenyl, p-tolyl or carboxyl side groups, respectively, and polar pyridine main chain groups were developed. Most of the polymeric materials presented high molecular weights and excellent solubility in common organic solvents. More importantly, they formed stable, self-standing membranes that were thoroughly characterized in respect to their thermal, mechanical and oxidative stability, their phosphoric acid doping ability and ionic conductivity. Particularly, the copolymers bearing side p-tolyl or carboxyl groups fulfill all necessary requirements for application as proton electrolyte membranes in high temperature

fuel cells, which are glass transition temperatures higher than 220 degrees C, thermal stability this website up to 400 degrees C, oxidative LY2606368 cost stability, high doping levels (DLs) and proton conductivities of about 0.02 S/cm. Initial single fuel cell results at high temperatures, 160 degrees C or 180 degrees C, using a copolymer bearing p-tolyl side groups with a relatively low DLs around 200 wt % and dry H-2/Air feed gases, revealed efficient power generation with a current density of 0.5 A/cm(2) at 500 mV. (C) 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 4325-4334, 2011″
“Background: NPAS2 is a circadian transcription factor responsive to a wide range of intra- Selleck Gilteritinib and extracellular stimuli. Results: Deficiency of ROR caused a damped transcriptional oscillation of Npas2 and functional depletion of an RORE resulted in a complete loss of the oscillation. Conclusion: Nuclear receptors elicit cell-autonomous circadian transcription

of Npas2. Significance: Synchronous transcriptional oscillation of Npas2 with Bmal1 provides the foundation for efficient circadian input and robust oscillation. NPAS2 (MOP4) is a heme-containing sensor transcription factor responsive to a wide range of intra- and extracellular stimuli, which also functions as a circadian transcription factor. This molecule forms a heterodimer with another circadian transcription factor, BMAL1, and activates transcription via E-box elements, indicating that circadian phase synchronization between NPAS2 and BMAL1 expression is important for the efficient transcriptional activation of target genes. However, details of the mechanism of cell-autonomous circadian transcription of Npas2 remain unclear. Here, we show that one of the ROREs (retinoid-related orphan receptor response elements) in the upstream region of the transcription start site is essential for circadian transcription of the Npas2 gene.