It was hypothesized that jamming transition in TBVM was the result of the unbalance between two time-dependent phenomena, i.e. the increase of the bulk

viscosity and the structure relaxation of nitrogen-free polymers. (C) 2011 Elsevier Ltd. All rights reserved.”
“. In infants born to hepatitis B surface antigen (HBsAg)positive mothers, failure after passiveactive immunization still occurs. The role of maternal hepatitis B DNA level and other risk factors in this setting remains unclear. This study retrospectively evaluated virologic and other risk factors associated with immunoprophylaxis failure in infants born to HBsAg-positive mothers. Between January 2007 and March 2010, we reviewed the clinical and virologic tests in 869 motherinfant pairs. All infants received the identical passiveactive AC220 price immunization schedule

after birth. The failure infants (HBsAg positive at 712 months of age) were compared to infants who were HBsAg negative when tested during this time period. Among 869 infants, 27 (3.1%) infants were immunoprophylaxis failures and the other 842 (96.9%) infants remained HBsAg negative. Mocetinostat molecular weight When mothers pre-delivery HBV DNA levels were stratified to <6, 66.99, 77.99 and =8 log10 copies/mL, the corresponding rates of immunoprophylaxis failure were 0%, 3.2% (3/95), 6.7% (19/282) and 7.6% (5/66), respectively (P < 0.001 for the trend). All failure infants were born to hepatitis B e antigen (HBeAg)positive mothers. Multivariate logistic regression analysis identified maternal HBV DNA levels [odds ratio (OR) = 1.88, 95% confidence interval (CI): 1.073.30] and detectable HBV DNA in the cord blood (OR = 39.67, 95% CI: 14.22110.64) as independent risk factors for immunoprophylaxis failure. All failure infants were born to HBeAg-positive mothers with HBV DNA levels =6 log10 copies/mL. The presence of HBV DNA in cord blood predicted failure to passiveactive immunization.”
“Cross-cultural anthropologists have

increasingly used phylogenetic methods to study cultural variation. Because cultural behaviours can be transmitted horizontally among socially defined groups, however, it is important to assess whether phylogeny-based methods-which were developed to study vertically transmitted traits MEK phosphorylation among biological taxa-are appropriate for studying group-level cultural variation. Here, we describe a spatially explicit simulation model that can be used to generate data with known degrees of horizontal donation. We review previous results from this model showing that horizontal transmission increases the type I error rate of phylogenetically independent contrasts in studies of correlated evolution. These conclusions apply to cases in which two traits are transmitted as a pair, but horizontal transmission may be less problematic when traits are unlinked.