?Skinny? and ?Fat? DNA: Two New Double Helices
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In slow roll inflation, the running of the spectral tilt is generically proportional to the square of the deviation from scale invariance, α{sub s}∝(n{sub s}−1){sup 2}, and is therefore currently undetectable. We present a mechanism able to generate a much larger running within slow roll. The mechanism is based on a curvaton field with a large mass term, and a time evolving normalization. This may happen for instance to the angular direction of a complex field in presence of an evolving radial direction. At the price of a single tuning between the mass term and the rate of change of the normalization, the curvaton can be made effectively light at the CMB scales, giving a spectral tilt in agreement with observations. The lightness is not preserved at later times, resulting in a detectable running of the spectral tilt. This mechanism shows that fields with a large mass term do not necessarily decouple from the inflationary physics, and provides a new tool for model building in inflation.
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This study demonstrated that a single intramuscular dose of testosterone undecanoate (750 mg) administered to physically active males before a 20-day simulated, multi-stressor military operation increased circulating total and free testosterone concentrations within normal physiological ranges and spared FFM. However, testosterone administration did not attenuate decrements in physical performance across multiple measures of power, strength, anaerobic or aerobic capacity.
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Understanding CRISPR-Cas systems—the adaptive defence mechanism that about half of bacterial species and most of archaea use to neutralise viral attacks—is important for explaining the biodiversity observed in the microbial world as well as for editing animal and plant genomes effectively. The CRISPR-Cas system learns from previous viral infections and integrates small pieces from phage genomes called spacers into the microbial genome. The resulting library of spacers collected in CRISPR arrays is then compared with the DNA of potential invaders. One of the most intriguing and least well understood questions about CRISPR-Cas systems is the distribution of spacers across the microbial population. Here, using empirical data, we show that the global distribution of spacer numbers in CRISPR arrays across multiple biomes worldwide typically exhibits scale-invariant power law behaviour, and the standard deviation is greater than the sample mean. We develop a mathematical model of spacer loss and acquisition dynamics which fits observed data from almost four thousand metagenomes well. In analogy to the classical ‘rich-get-richer’ mechanism of power law emergence, the rate of spacer acquisition is proportional to the CRISPR array size, which allows a small proportion of CRISPRs within the population to possess a significant number of spacers. Our study provides an alternative explanation for the rarity of all-resistant super microbes in nature and why proliferation of phages can be highly successful despite the effectiveness of CRISPR-Cas systems.
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The Purpose of this report is to examine in some detail the the consequences of these conventions on the interpretation of the morph assays. In particular we are interested in explaining the large number of observed negative and "inconclusive" findings among the RMR-1029 replicates, and exploring the basis for estimating the probability that a repository sample could contain a morph at concentrations well above the nominal detection limit but nonetheless give a negative or inconclusive test result. In the next section we briefly describe the assay characterization process and interpretation criteria used by the various assay developers.