Hope for the Best, Prepare for the Worst: Response of Tall Steel Buildings to the ShakeOut Scenario Earthquake

This work represents an effort to develop one plausible realization of the effects of the scenario event on tall steel moment-frame buildings. We have used the simulated ground motions with three-dimensional nonlinear finite element models of three buildings in the 20-story class to simulate structural responses at 784 analysis sites spaced at approximately 4 km throughout the San Fernando Valley, the San Gabriel Valley, and the Los Angeles Basin. Based on the simulation results and available information on the number and distribution of steel buildings, the recommended damage scenario for the ShakeOut drill was 5% of the estimated 150 steel moment-frame structures in the 10–30 story range collapsing, 10% red-tagged, 15% with damage serious enough to cause loss of life, and 20% with visible damage requiring building closure

Agriculture, food security, nutrition and the Millennium Development Goals

"...Today, 1.1 billion people live on less than one US dollar per day (the internationally recognized poverty threshold)—430 million in South Asia, 325 million in Sub-Saharan Africa, 260 million in East Asia and the Pacific, and 55 million in Latin America. Too many children live lives characterized by hunger and illness, and all too often succumb to early death. Moreover, another 1.6 billion people live on between one and two dollars per day, often sliding temporarily below the one dollar per day threshold. To enable all these people to live in dignity, the eight goals to achieve by 2015 are: 1. Eradicate extreme poverty and hunger 2. Achieve universal primary education 3. Promote gender equality and empower women 4. Reduce child mortality 5. Improve maternal health 6. Combat HIV/AIDS, malaria, and other diseases 7. Ensure environmental sustainability 8. Develop a global partnership for development." from TextMillenium Development Goals ,HIV/AIDS ,Gender issues ,Equality ,Nutrition ,Impact ,

Stochastic Gene Expression in Single Gene Oscillator Variants

It is infeasible to understand all dynamics in cell, but we can aim to understand the impact of design choices under our control. Here we consider a single gene oscillator as a case study to understand the influence of DNA copy number and repressor choice on the resulting dynamics. We first switch the repressor in the oscillator from the originally published lacI to treRL, a chimeric repressor with a lacI DNA binding domain that is inducible by trehalose. This slightly modified system produces faster and more regular oscillations than the original lacI oscillator. We then compare the treRL oscillator at three different DNA copy numbers. The period and amplitude of oscillations increases as the copy number is decreased. We cannot explain the change in period with differential equation models without changing delays or degradation rates. The correlation and phase coherence between daughter cells after cell division also tend to fall off faster for the lower copy oscillator variants. These results suggest that lower copy number variants of our single gene oscillator produce more synchronized oscillations

Primary Complex

A primary complex (PC) is a localised lesion formed due to the reaction of the body tissues to the first exposure to tubercle bacilli. The lung is the most frequent site of primary infection. Inhaled bacilli get implanted in the periphery of the lung where a "tubercle" is formed. Initially the response consists of an accumulation of polymorphs, followed by macrophages and 4-6 weeks later lymphocytes appear in large numbers. The bacilli also spread to the draining hilar lymph nodes where the same changes occur. The lesion at the point of entry and that in the node together form the primary complex

Transiently Transfected Purine Biosynthetic Enzymes Form Stress Bodies

It has been hypothesized that components of enzymatic pathways might organize into intracellular assemblies to improve their catalytic efficiency or lead to coordinate regulation. Accordingly, de novo purine biosynthesis enzymes may form a purinosome in the absence of purines, and a punctate intracellular body has been identified as the purinosome. We investigated the mechanism by which human de novo purine biosynthetic enzymes might be organized into purinosomes, especially under differing cellular conditions. Irregardless of the activity of bodies formed by endogenous enzymes, we demonstrate that intracellular bodies formed by transiently transfected, fluorescently tagged human purine biosynthesis proteins are best explained as protein aggregation.This work was supported by grants from the United States National Institutes of Health, National Science Foundation, and Welch (F1515) and Packard Foundations to EMM. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.Cellular and Molecular Biolog