A Question of Strategic Nuclear Weapons Policy

Both books are about America’s strategic nuclear weapons policy. Jan Lodal, author of The Price of Dominance, knows a lot about the subject from having helped make nuclear weapons policy in both the Richard Nixon and Gerald Ford administrations, and at the Pentagon during the Jimmy Carter administration. George Quester, author of Nuclear Monopoly, is also an expert, having written important books about nuclear strategy and nuclear proliferation for more than three decades

(1R,2R,3R,4R,5S)-2,3-Bis[(2S′)-2-acet­oxy-2-phenyl­acet­oxy]-4-azido-1-[(2,4-dinitro­phen­yl)hydrazono­meth­yl]bicyclo­[3.1.0]hexa­ne

In the title compound, C38H29N7O12, the five-membered ring adopts an envelope conformation in which the ‘flap’ is cis to the cyclo­propane group. This conformation is similar to those of other bicyclo­[3.1.0]hexane analogues for which crystal structures have been reported. The absolute configuration of the stereogenic centers on the cyclo­pentane ring, as determined by comparison with the known configurations of the stereogenic centers in the (2S)-2-acet­oxy-2-phenyl­acet­oxy groups, is 1(R), 2(R), 3(R), 4(R) and 5(S). An intramolecular N—H⋯O hydrogen bond is present

Effect of mixing on the early hydration of alite and OPC systems

The kinetics of hydration of cementitious materials is sensitive to the mixing procedure. High shear mixing conditions lead to an increase in the kinetics of hydration at early age compared to low shearing conditions such as hand mixing. In this study the effect of mixing speed and procedure was studied on alite and Portland cement in the presence or not of aggregates. The kinetics of hydration was monitored using isothermal calorimetry at 20 degrees C. The early reactivity was enhanced both with an increase in the speed of mixing and the shearing conditions. The principal features are a shortening of the induction period; a higher rate of hydrate precipitation during the acceleration period as well as an increase in the height of the main heat evolution peak. Analysis of the results in terms of dissolution theory, coupled with quantitative simulation with the plc modelling platform indicate different effects of mixing prior to and after the end of the induction period. Before the end of the induction period mixing has an impact on the rate of dissolution in the fast dissolution regime and high undersaturation, which appears to be (at least partially) controlled by the rate of transport of ions away from the alite surface. After the end of the induction period the main effect of mixing appears to be the production of more C-S-H nuclei, due to the possible detachment of the primary C-S-H (metastable) by mechanical action. This higher nucleation density leads to a denser microstructure for systems mixed at high intensities. (C) 2012 Elsevier Ltd. All rights reserved

Succession Planning in US Pharmacy Schools

The deans, associate and assistant deans, and department chairs of a college or school of pharmacy retain historic memories of the institution and share the responsibility for day-to-day operation, sustainability, and future planning. Between the anticipated retirement of baby boomers who are senior administrative faculty members and the steady increase in number of colleges and schools of pharmacy, the academy is facing a shortage of qualified successors. Succession planning involves planning for the effective transition of personnel in leadership positions within an organization. This paper describes the subject of succession planning at a sample population of AACP institutions by obtaining perspectives on the subject from the deans of these institutions via standardized interview instruments. The instruments were utilized with 15 deans; all interview data were blinded and analyzed using analyst triangulation. The majority of deans responded that some level of succession planning was desirable and even necessary; however, none claimed to have a formal succession planning structure in place at his or her home institution. Although widely accepted and well-recognized in the corporate and military sectors, succession planning within pharmacy schools and colleges is neither universally documented nor implemented. Differences exist within the administrative structure of these non-academic and academic institutions that may preclude a uniform succession planning format. While the evidence presented suggests that succession planning is needed within the academy, a concerted effort must be made towards implementing its practice

IL-4 Suppresses the Responses to TLR7 and TLR9 Stimulation and Increases the Permissiveness to Retroviral Infection of Murine Conventional Dendritic Cells

<div><p>Th2-inducing pathological conditions such as parasitic diseases increase susceptibility to viral infections through yet unclear mechanisms. We have previously reported that IL-4, a pivotal Th2 cytokine, suppresses the response of murine bone-marrow-derived conventional dendritic cells (cDCs) and splenic DCs to Type I interferons (IFNs). Here, we analyzed cDC responses to TLR7 and TLR9 ligands, R848 and CpGs, respectively. We found that IL-4 suppressed the gene expression of IFNβ and IFN-responsive genes (IRGs) upon TLR7 and TLR9 stimulation. IL-4 also inhibited IFN-dependent MHC Class I expression and amplification of IFN signaling pathways triggered upon TLR stimulation, as indicated by the suppression of IRF7 and STAT2. Moreover, IL-4 suppressed TLR7- and TLR9-induced cDC production of pro-inflammatory cytokines such as TNFα, IL-12p70 and IL-6 by inhibiting IFN-dependent and NFκB-dependent responses. IL-4 similarly suppressed TLR responses in splenic DCs. IL-4 inhibition of IRGs and pro-inflammatory cytokine production upon TLR7 and TLR9 stimulation was STAT6-dependent, since DCs from STAT6-KO mice were resistant to the IL-4 suppression. Analysis of SOCS molecules (SOCS1, −2 and −3) showed that IL-4 induces SOCS1 and SOCS2 in a STAT6 dependent manner and suggest that IL-4 suppression could be mediated by SOCS molecules, in particular SOCS2. IL-4 also decreased the IFN response and increased permissiveness to viral infection of cDCs exposed to a HIV-based lentivirus. Our results indicate that IL-4 modulates and counteracts pro-inflammatory stimulation induced by TLR7 and TLR9 and it may negatively affect responses against viruses and intracellular parasites.</p></div