3,974 research outputs found

    Z_3 Strings and their Interactions

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    We construct Z_3 vortex solutions in a model in which SU(3) is spontaneously broken to Z_3. The model is truncated to one in which there are only two dimensionless free parameters and the interaction of vortices within this restricted set of models is studied numerically. We find that there is a curve in the two dimensional space of parameters for which the energy of two asymptotically separated vortices equals the energy of the vortices at vanishing separation. This suggests that the inter-vortex potential for Z_3 strings might be flat for these couplings, much like the case of U(1) strings in the Bogomolnyi limit. However, we argue that the intervortex potential is attractive at short distances and repulsive at large separations leading to the possibility of unstable bound states of Z_3 vortices.Comment: 8 pages; mainly corrected typos in table

    Overweight, obesity, and colorectal cancer screening: Disparity between men and women

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    BACKGROUND: To estimate the association between body-mass index (BMI: kg/m(2)) and colorectal cancer (CRC) screening among US adults aged ≥ 50 years. METHODS: Population-based data from the 2001 Behavioral Risk Factor Surveillance Survey. Adults (N = 84,284) aged ≥ 50 years were classified by BMI as normal weight (18.5–<25), overweight (25–<30), obesity class I (30–<35), obesity class II (35–<40), and obesity class III (≥ 40). Interval since most recent screening fecal occult blood test (FOBT): (0 = >1 year since last screening vs. 1 = screened within the past year), and screening sigmoidoscopy (SIG): (0 = > 5 years since last screening vs. 1 = within the past 5 years) were the outcomes. RESULTS: Results differed between men and women. After adjusting for age, health insurance, race, and smoking, we found that, compared to normal weight men, men in the overweight (odds ratio [OR] 1.25, 95% CI = 1.05–1.51) and obesity class I (OR = 1.21, 95% CI = 1.03–1.75) categories were more likely to have obtained a screening SIG within the previous 5 years, while women in the obesity class I (OR = 0.86, 95%CI = 0.78–0.94) and II (OR = 0.88, 95%CI = 0.79–0.99) categories were less likely to have obtained a screening SIG compared to normal weight women. BMI was not associated with FOBT. CONCLUSION: Weight may be a correlate of CRC screening behavior but in a different way between men and women

    Simple Skeletal Muscle Mass Estimation Formulas: What We Can Learn From Them

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    One century ago Harris and Benedict published a short report critically examining the relations between body size, body shape, age, and basal metabolic rate. At the time, basal metabolic rate was a vital measurement in diagnosing diseases such as hypothyroidism. Their conclusions and basal metabolic rate prediction formulas still resonate today. Using the Harris-Benedict approach as a template, we systematically examined the relations between body size, body shape, age, and skeletal muscle mass (SM), the main anatomic feature of sarcopenia. The sample consisted of 12,330 non-Hispanic (NH) white and NH black participants in the US National Health and Nutrition Survey who had complete weight, height, waist circumference, age, and dual-energy X-ray (DXA) absorptiometry data. A conversion formula was used to derive SM from DXA-measured appendicular lean soft tissue mass. Weight, height, waist circumference, and age alone and in combination were significantly correlated with SM (all, p &lt; 0.001). Advancing analyses through the aforementioned sequence of predictor variables allowed us to establish how at the anatomic level these body size, body shape, and age measures relate to SM much in the same way the Harris-Benedict equations provide insights into the structural origins of basal heat production. Our composite series of SM prediction equations should prove useful in modeling efforts and in generating hypotheses aimed at understanding how SM relates to body size and shape across the adult lifespa

    Human and Animal Pentastomiasis in Malaysia : Review

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    Pentastomiasis is a zoonotic parasitic disease induced by the larval stages of pentasomes. The disease has been reported in Africa, the Middle East and Southeast Asia and caused by the nymphs of the two genera: Linguatula and Armillifer and the two species L. serrata and A. armillatus regard for more than 90% of human cases. The definitive hosts of Armillifer spp. are snakes, lizards and other reptiles. The parasites live in the upper respiratory tracts and lay eggs that are passed out through respiratory secretions, saliva or faeces. Intermediate hosts are humans, rodents and other mammals. Humans incidentally acquire the infestation by the consumption of uncooked infested snake meat or by drinking water contaminated with ova of the pentastomes. In the intestinal tract, the larvae hatch from the ova, penetrate the intestinal wall and migrate to organs in which the liver is the most common site. Human pentastomiasis was reported among aborigines in West and East Malaysia. Armillifer moniliformis was identified in wild animals and carnivores with infection rate 1.8% and 20.7% respectively. The adults of pentostomes (A. moniliformis) were recovered from two out of six snakes Python reticulates. Recently a case of human pentastomiasis was reported in Sabah, East Malaysia, caused by nymph of Armillifer moniliformis

    The RNA polymerase II C-terminal domain-interacting domain of yeast Nrd1 contributes to the choice of termination pathway and couples to RNA processing by the nuclear exosome

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    The RNA polymerase II (RNApII) C-terminal domain (CTD)- interacting domain (CID) proteins are involved in two distinct RNApII termination pathways and recognize different phosphorylated forms of CTD. To investigate the role of differential CTD-CID interactions in the choice of termination pathway, we altered the CTD-binding specificity of Nrd1 by domain swapping. Nrd1 with the CID from Rtt103 (Nrd1(CIDRtt103)) causes read-through transcription at many genes, but can also trigger termination where multiple Nrd1/Nab3-binding sites and the Ser(P)-2 CTD co-exist. Therefore, CTD-CID interactions target specific termination complexes to help choose an RNApII termination pathway. Interactions of Nrd1 with bothCTDand nascent transcripts contribute to efficient termination by the Nrd1 complex. Surprisingly, replacing the Nrd1 CID with that from Rtt103 reduces binding to Rrp6/Trf4, and RNA transcripts terminated by Nrd1(CIDRtt103) are predominantly processed by core exosome. Thus, the Nrd1 CID couples Ser(P)-5 CTD not only to termination, but also to RNA processing by the nuclear exosome

    The C-Fern (Ceratopteris richardii) Genome: Insights Into Plant Genome Evolution With the First Partial Homosporous Fern Genome Assembly

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    Ferns are notorious for possessing large genomes and numerous chromosomes. Despite decades of speculation, the processes underlying the expansive genomes of ferns are unclear, largely due to the absence of a sequenced homosporous fern genome. The lack of this crucial resource has not only hindered investigations of evolutionary processes responsible for the unusual genome characteristics of homosporous ferns, but also impeded synthesis of genome evolution across land plants. Here, we used the model fern species Ceratopteris richardii to address the processes (e.g., polyploidy, spread of repeat elements) by which the large genomes and high chromosome numbers typical of homosporous ferns may have evolved and have been maintained. We directly compared repeat compositions in species spanning the green plant tree of life and a diversity of genome sizes, as well as both short- and long-read-based assemblies of Ceratopteris. We found evidence consistent with a single ancient polyploidy event in the evolutionary history of Ceratopteris based on both genomic and cytogenetic data, and on repeat proportions similar to those found in large flowering plant genomes. This study provides a major stepping-stone in the understanding of land plant evolutionary genomics by providing the first homosporous fern reference genome, as well as insights into the processes underlying the formation of these massive genomes
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