Institution
University of New Mexico
Education•Albuquerque, New Mexico, United States•
About: University of New Mexico is a education organization based out in Albuquerque, New Mexico, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 28870 authors who have published 64767 publications receiving 2578371 citations. The organization is also known as: UNM & Universitatis Novus Mexico.
Topics: Population, Poison control, Laser, Health care, Large Hadron Collider
Papers published on a yearly basis
Papers
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TL;DR: C-reactive protein (CRP) is an ancient highly conserved molecule and a member of the pentraxin family of proteins that is secreted by the liver in response to a variety of inflammatory cytokines.
Abstract: C-reactive protein (CRP) is an ancient highly conserved molecule and a member of the pentraxin family of proteins. CRP is secreted by the liver in response to a variety of inflammatory cytokines. Levels of CRP increase very rapidly in response to trauma, inflammation, and infection and decrease just as rapidly with the resolution of the condition. Thus, the measurement of CRP is widely used to monitor various inflammatory states. CRP binds to damaged tissue, to nuclear antigens and to certain pathogenic organisms in a calcium-dependent manner. The function of CRP is felt to be related to its role in the innate immune system. Similar to immunoglobulin (Ig)G, it activates complement, binds to Fc receptors and acts as an opsonin for various pathogens. Interaction of CRP with Fc receptors leads to the generation of proinflammatory cytokines that enhance the inflammatory response. Unlike IgG, which specifically recognizes distinct antigenic epitopes, CRP recognizes altered self and foreign molecules based on pattern recognition. Thus, CRP is though to act as a surveillance molecule for altered self and certain pathogens. This recognition provides early defense and leads to a proinflammatory signal and activation of the humoural, adaptive immune system.
637 citations
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Massachusetts Institute of Technology1, University of Copenhagen2, University of California, Santa Cruz3, University of Tartu4, Wellcome Trust Sanger Institute5, Lawrence Berkeley National Laboratory6, Harvard University7, University of New Mexico8, Watson School of Biological Sciences9, University of California, San Francisco10, European Bioinformatics Institute11, Rutgers University12, Indiana University13, Connecticut College14, Katholieke Universiteit Leuven15, Université libre de Bruxelles16, Wesleyan University17, University of Wisconsin-Madison18, University of California, Berkeley19, Memorial Sloan Kettering Cancer Center20, Cornell University21
TL;DR: This work uses the genomes of 12 Drosophila species for the de novo discovery of functional elements in the fly, and identifies several classes of pre- and post-transcriptional regulatory motifs, and predicts individual motif instances with high confidence.
Abstract: Sequencing of multiple related species followed by comparative genomics analysis constitutes a powerful approach for the systematic understanding of any genome. Here, we use the genomes of 12 Drosophila species for the de novo discovery of functional elements in the fly. Each type of functional element shows characteristic patterns of change, or 'evolutionary signatures', dictated by its precise selective constraints. Such signatures enable recognition of new protein-coding genes and exons, spurious and incorrect gene annotations, and numerous unusual gene structures, including abundant stop-codon readthrough. Similarly, we predict non-protein-coding RNA genes and structures, and new microRNA (miRNA) genes. We provide evidence of miRNA processing and functionality from both hairpin arms and both DNA strands. We identify several classes of pre- and post-transcriptional regulatory motifs, and predict individual motif instances with high confidence. We also study how discovery power scales with the divergence and number of species compared, and we provide general guidelines for comparative studies.
636 citations
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TL;DR: Once-daily suppressive therapy with valacyclovir significantly reduces the risk of transmission of genital herpes among heterosexual, HSV-2-discordant couples.
Abstract: Background Nucleoside analogues against herpes simplex virus (HSV) have been shown to suppress shedding of HSV type 2 (HSV-2) on genital mucosal surfaces and may prevent sexual transmission of HSV. Methods We followed 1484 immunocompetent, heterosexual, monogamous couples: one with clinically symptomatic genital HSV-2 and one susceptible to HSV-2. The partners with HSV-2 infection were randomly assigned to receive either 500 mg of valacyclovir once daily or placebo for eight months. The susceptible partner was evaluated monthly for clinical signs and symptoms of genital herpes. Source partners were followed for recurrences of genital herpes; 89 were enrolled in a substudy of HSV-2 mucosal shedding. Both partners were counseled on safer sex and were offered condoms at each visit. The predefined primary end point was the reduction in transmission of symptomatic genital herpes. Results Clinically symptomatic HSV-2 infection developed in 4 of 743 susceptible partners who were given valacyclovir, as compared w...
635 citations
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TL;DR: It is shown that for sub-Saharan African birds, the apparent role of productivity diminishes with decreasing range size, whereas the significance of topographic heterogeneity increases, and the relative importance of geometric constraints from the continental edge is moderate.
Abstract: Geographic patterns in species richness are mainly based on wide-ranging species because their larger number of distribution records has a disproportionate contribution to the species richness counts. Here we demonstrate how this effect strongly influences our understanding of what determines species richness. Using both conventional and spatial regression models, we show that for sub-Saharan African birds, the apparent role of productivity diminishes with decreasing range size, whereas the significance of topographic heterogeneity increases. The relative importance of geometric constraints from the continental edge is moderate. Our findings highlight the failure of traditional species richness models to account for narrow-ranging species that frequently are also threatened.
635 citations
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TL;DR: This paper describes the synthesis method of linear array geometry with minimum sidelobe level and null control using the particle swarm optimization (PSO) algorithm, a newly discovered, high-performance evolutionary algorithm capable of solving general N-dimensional, linear and nonlinear optimization problems.
Abstract: This paper describes the synthesis method of linear array geometry with minimum sidelobe level and null control using the particle swarm optimization (PSO) algorithm. The PSO algorithm is a newly discovered, high-performance evolutionary algorithm capable of solving general N-dimensional, linear and nonlinear optimization problems. Compared to other evolutionary methods such as genetic algorithms and simulated annealing, the PSO algorithm is much easier to understand and implement and requires the least of mathematical preprocessing. The array geometry synthesis is first formulated as an optimization problem with the goal of sidelobe level (SLL) suppression and/or null placement in certain directions, and then solved by the PSO algorithm for the optimum element locations. Three design examples are presented that illustrate the use of the PSO algorithm, and the optimization goal in each example is easily achieved. The results of the PSO algorithm are validated by comparing with results obtained using the quadratic programming method (QPM).
634 citations
Authors
Showing all 29120 results
Name | H-index | Papers | Citations |
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Bruce S. McEwen | 215 | 1163 | 200638 |
David Miller | 203 | 2573 | 204840 |
Jing Wang | 184 | 4046 | 202769 |
Paul M. Thompson | 183 | 2271 | 146736 |
David A. Weitz | 178 | 1038 | 114182 |
David R. Williams | 178 | 2034 | 138789 |
John A. Rogers | 177 | 1341 | 127390 |
George F. Koob | 171 | 935 | 112521 |
John D. Minna | 169 | 951 | 106363 |
Carlos Bustamante | 161 | 770 | 106053 |
Lewis L. Lanier | 159 | 554 | 86677 |
Joseph Wang | 158 | 1282 | 98799 |
John E. Morley | 154 | 1377 | 97021 |
Fabian Walter | 146 | 999 | 83016 |
Michael F. Holick | 145 | 767 | 107937 |