The crosslinked fibrous membranes had improved thermally stability and retained physical integrity upon exposure (2 hr at 40 degrees C) to carbon disulfide, the solvent for Friedel-Craft reactions of the

styrene moiety. Hydrolysis (0.01N NaOH) of the auto-crosslinked fibrous membrane significantly improved its hydrophilicity by reducing the water contact angles from 90.6 degrees to 62.5 degrees in a matter of seconds. These ultra-high specific surface PSMA fibrous membranes have shown superior organic and aqueous solvent compatibility to be used as highly reactive and easily retrievable supports for solid-phase Protease Inhibitor Library cell assay synthesis. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 114: 784-793, 2009″
“We present our investigation on the critical behavior of the spinel compound CdCr2S4 via the ac susceptibility and dc magnetization measurements. The analysis of ac susceptibility in terms of scaling behavior yields exponent values of delta=5.38 +/- 0.01, gamma+beta=1.77 +/- 0.03 and gamma=1.44 +/- 0.02. Both delta and gamma are slightly larger than that predicted by Heisenberg model. Detailed analyses of the inverse of the susceptibility and the electron spin resonance

experiment reveal that the existence of correlated magnetic polarons has a key impact on the ferromagnetism of the spinel CdCr2S4. see more The abnormal critical exponent value of delta of CdCr2S4 may be attributed to the formation of the correlated magnetic polarons and abnormal spin-phonon coupling.”
“Background-Ethnic differences in cardiac arrhythmia incidence have been reported, with

a particularly high incidence of sudden cardiac death and low incidence Vorinostat chemical structure of atrial fibrillation in individuals of African ancestry. We tested the hypotheses that African ancestry and common genetic variants are associated with prolonged duration of cardiac repolarization, a central pathophysiological determinant of arrhythmia, as measured by the electrocardiographic QT interval.

Methods and Results-First, individual estimates of African and European ancestry were inferred from genome-wide single-nucleotide polymorphism (SNP) data in 7 population-based cohorts of African Americans (n=12 097) and regressed on measured QT interval from ECGs. Second, imputation was performed for 2.8 million SNPs, and a genome-wide association study of QT interval was performed in 10 cohorts (n=13 105). There was no evidence of association between genetic ancestry and QT interval (P=0.94). Genome-wide significant associations (P<2.5×10(-8)) were identified with SNPs at 2 loci, upstream of the genes NOS1AP (rs12143842, P=2×10(-15)) and ATP1B1 (rs1320976, P=2×10(-10)). The most significant SNP in NOS1AP was the same as the strongest SNP previously associated with QT interval in individuals of European ancestry.