Institution
National Autonomous University of Mexico
Education•Mexico City, Distrito Federal, Mexico•
About: National Autonomous University of Mexico is a education organization based out in Mexico City, Distrito Federal, Mexico. It is known for research contribution in the topics: Population & Galaxy. The organization has 72868 authors who have published 127797 publications receiving 2285543 citations. The organization is also known as: UNAM & Universidad Nacional Autónoma de México.
Topics: Population, Galaxy, Catalysis, Thin film, Stars
Papers published on a yearly basis
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TL;DR: EcoCyc is an organism-specific pathway/genome database that describes the metabolic and signal-transduction pathways of Escherichia coli, its enzymes, its transport proteins and its mechanisms of transcriptional control of gene expression.
Abstract: EcoCyc is an organism-specific pathway/genome database that describes the metabolic and signal-transduction pathways of Escherichia coli, its enzymes, its transport proteins and its mechanisms of transcriptional control of gene expression. EcoCyc is queried using the Pathway Tools graphical user interface, which provides a wide variety of query operations and visualization tools. EcoCyc is available at http://ecocyc.org/.
506 citations
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TL;DR: Several AIRDs exhibit increased overt cardiovascular disease (CVD) prevalence as well as findings of advanced subclinical atherosclerosis, which may precede the appearance of a clinical disease and thus be a target of early identification and preventive therapy.
Abstract: Received October 16, 2004; revision received June 4, 2005; accepted June 7, 2005
Atherosclerosis is a multifactorial process that commences in childhood but manifests clinically later in life Atherosclerosis is increasingly considered an immune system–mediated process of the vascular system The presence of macrophages and activated lymphocytes within atherosclerotic plaques supports the concept of atherosclerosis as an immune system–mediated inflammatory disorder1,2 Inflammation can aggravate atherosclerosis via different mechanisms secondary to autoimmunity, infectious diseases, and other proatherogenic changes that occur during the inflammatory state
Autoimmune rheumatic diseases (AIRDs) are associated with higher rates of cardiovascular morbidity and mortality, primarily secondary to accelerated atherosclerosis This phenomenon can be attributed to traditional risk factors for atherosclerosis and use of specific drugs, such as corticosteroids, but also might be the result of other autoimmune and inflammatory mechanisms that are aggravated in AIRDs Several AIRDs exhibit increased overt cardiovascular disease (CVD) prevalence as well as findings of advanced subclinical atherosclerosis, which may precede the appearance of a clinical disease and thus be a target of early identification and preventive therapy
Cells of the immune system can be found within atherosclerotic plaques, which suggests that they have a role in the atherogenic process Their migration and activation within the plaques can be secondary to various stimuli, including infectious agents3 These cells probably aggravate atherosclerosis, because CD4+ and CD8+ T-cell depletion reduced fatty streak formation in C57BL/6 mice In addition, after crossing of apolipoprotein E (ApoE)-knockout mice with immunodeficient scid/scid mice, the offspring had a 73% reduction in aortic fatty streak lesions compared with the immunocompetent apoE mice Moreover, when CD4+ T cells were transferred from the immunocompetent to the immunodeficient mice, they increased lesion area in the latter by 164%4 It is therefore not surprising that as in autoimmune diseases, the cellular components …
506 citations
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University of Cambridge1, Florida Institute of Technology2, Fauna & Flora International3, Zoological Society of London4, National Autonomous University of Mexico5, Simon Fraser University6, Nelson Mandela Metropolitan University7, World Wide Fund for Nature8, Georgia State University9, State Street Corporation10, Conservation International11, University of Maine12, United Nations Environment Programme13, The Nature Conservancy14, University of Oxford15, World Bank16, Wetlands International17, International Union for Conservation of Nature and Natural Resources18, Imperial College London19, Natural Environment Research Council20, Clemson University21, George Mason University22, University of Queensland23, Bangor University24, BirdLife International25, World Resources Institute26, Wildlife Conservation Society27, Venezuelan Institute for Scientific Research28, Center for International Forestry Research29, Ocean Conservancy30, National University of Singapore31, Temple University32, Oregon State University33, University of East Anglia34
TL;DR: 100 scientific questions that, if answered, would have the greatest impact on conservation practice and policy are identified and are expected to help identify new directions for researchers and assist funders in directing funds.
Abstract: We identified 100 scientific questions that, if answered, would have the greatest impact on conservation practice and policy. Representatives from 21 international organizations, regional sections and working groups of the Society for Conservation Biology, and 12 academics, from all continents except Antarctica, compiled 2291 questions of relevance to conservation of biological diversity worldwide. The questions were gathered from 761 individuals through workshops, email requests, and discussions. Voting by email to short-list questions, followed by a 2-day workshop, was used to derive the final list of 100 questions. Most of the final questions were derived through a process of modification and combination as the workshop progressed. The questions are divided into 12 sections: ecosystem functions and services, climate change, technological change, protected areas, ecosystem management and restoration, terrestrial ecosystems, marine ecosystems, freshwater ecosystems, species management, organizational systems and processes, societal context and change, and impacts of conservation interventions. We anticipate that these questions will help identify new directions for researchers and assist funders in directing funds.
505 citations
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TL;DR: EcoCyc now supports running and modifying E. coli metabolic models directly on the EcoCyc website, and new SmartTable tools allow users to browse collections of related Eco Cyc content.
Abstract: EcoCyc (EcoCyc.org) is a freely accessible, comprehensive database that collects and summarizes experimental data for Escherichia coli K-12, the best-studied bacterial model organism. New experimental discoveries about gene products, their function and regulation, new metabolic pathways, enzymes and cofactors are regularly added to EcoCyc. New SmartTable tools allow users to browse collections of related EcoCyc content. SmartTables can also serve as repositories for user- or curator-generated lists. EcoCyc now supports running and modifying E. coli metabolic models directly on the EcoCyc website.
504 citations
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TL;DR: EcoCyc (http://Eco Cyc.org) is a comprehensive model organism database for Escherichia coli K-12 MG1655 displaying a graphical overview of all known regulatory inputs to gene expression and protein activity.
Abstract: EcoCyc (http://EcoCyc.org) is a comprehensive model organism database for Escherichia coli K-12 MG1655. From the scientific literature, EcoCyc captures the functions of individual E. coli gene products; their regulation at the transcriptional, post-transcriptional and protein level; and their organization into operons, complexes and pathways. EcoCyc users can search and browse the information in multiple ways. Recent improvements to the EcoCyc Web interface include combined gene/protein pages and a Regulation Summary Diagram displaying a graphical overview of all known regulatory inputs to gene expression and protein activity. The graphical representation of signal transduction pathways has been updated, and the cellular and regulatory overviews were enhanced with new functionality. A specialized undergraduate teaching resource using EcoCyc is being developed.
502 citations
Authors
Showing all 73617 results
Name | H-index | Papers | Citations |
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Richard Peto | 183 | 683 | 231434 |
Anton M. Koekemoer | 168 | 1127 | 106796 |
Rory Collins | 162 | 489 | 193407 |
Timothy C. Beers | 156 | 934 | 102581 |
Vivek Sharma | 150 | 3030 | 136228 |
Kjell Fuxe | 142 | 1479 | 89846 |
Prashant V. Kamat | 140 | 725 | 79259 |
Carmen García | 139 | 1503 | 96925 |
Harold A. Mooney | 135 | 450 | 100404 |
Efe Yazgan | 128 | 986 | 79041 |
Roberto Maiolino | 127 | 816 | 61724 |
Peter Nugent | 127 | 754 | 92988 |
William R. Miller | 125 | 601 | 72570 |
Nicholas A. Kotov | 123 | 574 | 55210 |
John C. Wingfield | 122 | 509 | 52291 |