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, Context (language use)
Papers published on a yearly basis
Papers
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TL;DR: A method for producing graded and reproducible focal cortical contusions in the rat is described and this lysosomal enzyme may participate in autolysis and development of focal cavitation following cortical contusion.
669 citations
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TL;DR: The third catalog of active galactic nuclei (AGNs) detected by the Fermi-LAT (3LAC) is presented in this paper, which is based on the 3FGL of sources detected between 100 MeV and 300 GeV.
Abstract: The third catalog of active galactic nuclei (AGNs) detected by the Fermi-LAT (3LAC) is presented. It is based on the third Fermi-LAT catalog (3FGL) of sources detected between 100 MeV and 300 GeV w ...
668 citations
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TL;DR: In this article, the last in a series of four review papers to appear in this journal, presents some critical applications using ionic polymer?metal composites (IPMCs).
Abstract: This paper, the last in a series of four review papers to appear in this journal, presents some critical applications using ionic polymer?metal composites?(IPMCs). Industrial and biomedical applications of IPMCs are identified and presented along with brief illustration.
666 citations
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TL;DR: How neuroinflammation has both beneficial as well as detrimental roles and recent therapeutic strategies to combat pathological responses are discussed and the time-dependent role of inflammatory factors could help in developing new diagnostic, prognostic, and therapeutic neuroprotective strategies for post-stroke inflammation.
Abstract: Stroke, the third leading cause of death and disability worldwide, is undergoing a change in perspective with the emergence of new ideas on neurodegeneration The concept that stroke is a disorder solely of blood vessels has been expanded to include the effects of a detrimental interaction between glia, neurons, vascular cells, and matrix components, which is collectively referred to as the neurovascular unit Following the acute stroke, the majority of which are ischemic, there is secondary neuroinflammation that both promotes further injury, resulting in cell death, but conversely plays a beneficial role, by promoting recovery The proinflammatory signals from immune mediators rapidly activate resident cells and influence infiltration of a wide range of inflammatory cells (neutrophils, monocytes/macrophages, different subtypes of T cells, and other inflammatory cells) into the ischemic region exacerbating brain damage In this review, we discuss how neuroinflammation has both beneficial as well as detrimental roles and recent therapeutic strategies to combat pathological responses Here, we also focus on time-dependent entry of immune cells to the ischemic area and the impact of other pathological mediators, including oxidative stress, excitotoxicity, matrix metalloproteinases (MMPs), high-mobility group box 1 (HMGB1), arachidonic acid metabolites, mitogen-activated protein kinase (MAPK), and post-translational modifications that could potentially perpetuate ischemic brain damage after the acute injury Understanding the time-dependent role of inflammatory factors could help in developing new diagnostic, prognostic, and therapeutic neuroprotective strategies for post-stroke inflammation
665 citations
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Johns Hopkins University1, University of Texas at Austin2, United States Army Medical Research Institute of Infectious Diseases3, Centers for Disease Control and Prevention4, University of New Mexico5, Food and Drug Administration6, United States Department of Health and Human Services7, National Institutes of Health8, Nuclear Threat Initiative9, New York State Department of Health10, University of Minnesota11
TL;DR: Weapons disseminating a number of HFVs could cause an outbreak of an undifferentiated febrile illness 2 to 21 days later, associated with clinical manifestations that could include rash, hemorrhagic diathesis, and shock.
Abstract: ObjectiveTo develop consensus-based recommendations for measures to be taken
by medical and public health professionals if hemorrhagic fever viruses (HFVs)
are used as biological weapons against a civilian populationParticipantsThe Working Group on Civilian Biodefense included 26 representatives
from academic medical centers, public health, military services, governmental
agencies, and other emergency management institutionsEvidenceMEDLINE was searched from January 1966 to January 2002 Retrieved references,
relevant material published prior to 1966, and additional sources identified
by participants were reviewedConsensus ProcessThree formal drafts of the statement that synthesized information obtained
in the evidence-gathering process were reviewed by the working group Each
draft incorporated comments and judgments of the members All members approved
the final draftConclusionsWeapons disseminating a number of HFVs could cause an outbreak of an
undifferentiated febrile illness 2 to 21 days later, associated with clinical
manifestations that could include rash, hemorrhagic diathesis, and shock
The mode of transmission and clinical course would vary depending on the specific
pathogen Diagnosis may be delayed given clinicians' unfamiliarity with these
diseases, heterogeneous clinical presentation within an infected cohort, and
lack of widely available diagnostic tests Initiation of ribavirin therapy
in the early phases of illness may be useful in treatment of some of these
viruses, although extensive experience is lacking There are no licensed vaccines
to treat the diseases caused by HFVs
661 citations
Authors
Showing all 29120 results
Name | H-index | Papers | Citations |
---|---|---|---|
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 |