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  • Articles  (65)
  • Adult  (65)
  • 2010-2014  (35)
  • 1980-1984  (30)
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  • 2014  (35)
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  • Science. 211(4479): 257.  (1)
  • Science. 211(4481): 508-10.  (1)
  • Science. 211(4482): 601-3.  (1)
  • Science. 211(4485): 955-7.  (1)
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  • Articles  (65)
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  • 2010-2014  (35)
  • 1980-1984  (30)
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  • 1
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-05-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin-Frankel, Jennifer -- New York, N.Y. -- Science. 2014 May 23;344(6186):793-7. doi: 10.1126/science.344.6186.793.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24855236" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antipsychotic Agents/therapeutic use ; *Bioethical Issues ; Conflict of Interest/*economics ; Dibenzothiazepines/therapeutic use ; Drug Industry/economics/ethics ; Ethicists/*psychology ; *Ethics, Medical ; Humans ; Male ; Minnesota ; Quetiapine Fumarate ; Randomized Controlled Trials as Topic/*ethics ; Schizophrenia/drug therapy ; Suicide/*ethics ; Truth Disclosure/*ethics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2014-07-06
    Description: In 11 studies, we found that participants typically did not enjoy spending 6 to 15 minutes in a room by themselves with nothing to do but think, that they enjoyed doing mundane external activities much more, and that many preferred to administer electric shocks to themselves instead of being left alone with their thoughts. Most people seem to prefer to be doing something rather than nothing, even if that something is negative.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330241/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330241/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilson, Timothy D -- Reinhard, David A -- Westgate, Erin C -- Gilbert, Daniel T -- Ellerbeck, Nicole -- Hahn, Cheryl -- Brown, Casey L -- Shaked, Adi -- T32 MH020006/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2014 Jul 4;345(6192):75-7. doi: 10.1126/science.1250830.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Virginia, Charlottesville, VA, USA. tdw@virginia.edu. ; Department of Psychology, University of Virginia, Charlottesville, VA, USA. ; Department of Psychology, Harvard University, Cambridge, MA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24994650" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Attention ; Electroshock/psychology ; Humans ; Loneliness/*psychology ; Middle Aged ; *Pleasure ; *Thinking ; Young Adult
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-11-02
    Description: Cognitive neuroscience has revealed aging of the human brain to be rich in reorganization and change. Neuroimaging results have recast our framework around cognitive aging from one of decline to one emphasizing plasticity. Current methods use neurostimulation approaches to manipulate brain function, providing a direct test of the ways that the brain differently contributes to task performance for younger and older adults. Emerging research into emotional, social, and motivational domains provides some evidence for preservation with age, suggesting potential avenues of plasticity, alongside additional evidence for reorganization. Thus, we begin to see that aging of the brain, amidst interrelated behavioral and biological changes, is as complex and idiosyncratic as the brain itself, qualitatively changing over the life span.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gutchess, Angela -- New York, N.Y. -- Science. 2014 Oct 31;346(6209):579-82. doi: 10.1126/science.1254604.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology and Volen National Center for Complex Systems, Brandeis University, Waltham, MA, USA. Massachussetts General Hospital, Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA, USA. gutchess@brandeis.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25359965" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Aging ; Brain/*growth & development/physiology/ultrastructure ; *Cognition ; Electric Stimulation ; Humans ; Neuroimaging ; *Neuronal Plasticity ; Neurosciences/trends ; Young Adult
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-04-26
    Description: How we attend to objects and their features that cannot be separated by location is not understood. We presented two temporally and spatially overlapping streams of objects, faces versus houses, and used magnetoencephalography and functional magnetic resonance imaging to separate neuronal responses to attended and unattended objects. Attention to faces versus houses enhanced the sensory responses in the fusiform face area (FFA) and parahippocampal place area (PPA), respectively. The increases in sensory responses were accompanied by induced gamma synchrony between the inferior frontal junction, IFJ, and either FFA or PPA, depending on which object was attended. The IFJ appeared to be the driver of the synchrony, as gamma phases were advanced by 20 ms in IFJ compared to FFA or PPA. Thus, the IFJ may direct the flow of visual processing during object-based attention, at least in part through coupled oscillations with specialized areas such as FFA and PPA.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Baldauf, Daniel -- Desimone, Robert -- P30EY2621/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 2014 Apr 25;344(6182):424-7. doi: 10.1126/science.1247003. Epub 2014 Apr 10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, 02139 MA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24763592" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Attention ; Brain/*physiology ; Brain Mapping ; Diffusion Tensor Imaging ; Female ; Frontal Lobe/*physiology ; Functional Laterality ; Humans ; Magnetic Resonance Imaging ; Magnetoencephalography ; Male ; Temporal Lobe/*physiology ; Visual Cortex/physiology ; Visual Perception ; Young Adult
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2014-05-24
    Description: Novel vaccines are urgently needed to reduce the burden of severe malaria. Using a differential whole-proteome screening method, we identified Plasmodium falciparum schizont egress antigen-1 (PfSEA-1), a 244-kilodalton parasite antigen expressed in schizont-infected red blood cells (RBCs). Antibodies to PfSEA-1 decreased parasite replication by arresting schizont rupture, and conditional disruption of PfSEA-1 resulted in a profound parasite replication defect. Vaccination of mice with recombinant Plasmodium berghei PbSEA-1 significantly reduced parasitemia and delayed mortality after lethal challenge with the Plasmodium berghei strain ANKA. Tanzanian children with antibodies to recombinant PfSEA-1A (rPfSEA-1A) did not experience severe malaria, and Kenyan adolescents and adults with antibodies to rPfSEA-1A had significantly lower parasite densities than individuals without these antibodies. By blocking schizont egress, PfSEA-1 may synergize with other vaccines targeting hepatocyte and RBC invasion.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184151/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184151/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Raj, Dipak K -- Nixon, Christian P -- Nixon, Christina E -- Dvorin, Jeffrey D -- DiPetrillo, Christen G -- Pond-Tor, Sunthorn -- Wu, Hai-Wei -- Jolly, Grant -- Pischel, Lauren -- Lu, Ailin -- Michelow, Ian C -- Cheng, Ling -- Conteh, Solomon -- McDonald, Emily A -- Absalon, Sabrina -- Holte, Sarah E -- Friedman, Jennifer F -- Fried, Michal -- Duffy, Patrick E -- Kurtis, Jonathan D -- 1K08AI100997-01A1/AI/NIAID NIH HHS/ -- DP2 AI112219/AI/NIAID NIH HHS/ -- DP2-AI112219/AI/NIAID NIH HHS/ -- K08 AI100997/AI/NIAID NIH HHS/ -- P20GM103421/GM/NIGMS NIH HHS/ -- P30 AI042853/AI/NIAID NIH HHS/ -- P30AI042853/AI/NIAID NIH HHS/ -- R01 AI102907/AI/NIAID NIH HHS/ -- R01-AI076353/AI/NIAID NIH HHS/ -- R01-AI102907/AI/NIAID NIH HHS/ -- R01-AI52059/AI/NIAID NIH HHS/ -- T32-DA013911/DA/NIDA NIH HHS/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2014 May 23;344(6186):871-7. doi: 10.1126/science.1254417.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for International Health Research, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA. ; Division of Infectious Diseases, Boston Children's Hospital and Harvard Medical School, Boston, MA 02115, USA. ; Center for International Health Research, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA. Department of Pediatrics, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA. ; Department of Pathology and Laboratory Medicine, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02906, USA. ; Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20892, USA. ; Fred Hutchinson Cancer Research Center Program in Biostatistics and Biomathematics, Department of Biostatistics and Global Health, University of Washington, Seattle, WA 98109, USA. ; Center for International Health Research, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02903, USA. Department of Pathology and Laboratory Medicine, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI 02906, USA. jonathan_kurtis@brown.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24855263" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Animals ; Antibodies, Protozoan/blood/*immunology ; Antigens, Protozoan/*immunology ; Child ; Erythrocytes/*parasitology ; Hepatocytes/immunology/parasitology ; Humans ; Immunoglobulin G/blood/immunology ; Kenya ; Malaria/prevention & control ; Malaria Vaccines/*immunology ; Malaria, Falciparum/*prevention & control ; Mice ; Plasmodium berghei/immunology ; Plasmodium falciparum/*growth & development/immunology ; Protozoan Proteins/*immunology ; Recombinant Proteins/immunology ; Schizonts/*growth & development ; Young Adult
    Print ISSN: 0036-8075
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  • 6
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-11-02
    Description: Human cognitive aging differs between and is malleable within individuals. In the absence of a strong genetic program, it is open to a host of hazards, such as vascular conditions, metabolic syndrome, and chronic stress, but also open to protective and enhancing factors, such as experience-dependent cognitive plasticity. Longitudinal studies suggest that leading an intellectually challenging, physically active, and socially engaged life may mitigate losses and consolidate gains. Interventions help to identify contexts and mechanisms of successful cognitive aging and give science and society a hint about what would be possible if conditions were different.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lindenberger, Ulman -- New York, N.Y. -- Science. 2014 Oct 31;346(6209):572-8. doi: 10.1126/science.1254403.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Lifespan Psychology, Max Planck Institute for Human Development, Lentzeallee 94, 14195 Berlin, Germany. Max Planck University College London Centre for Computational Psychiatry and Ageing Research, London WC1B 5EH, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25359964" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Factors ; Aging/*physiology ; Animals ; Behavior ; Brain/*growth & development/ultrastructure ; Cognition/*physiology ; Humans ; Neuronal Plasticity/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2014-03-22
    Description: Humans can discriminate several million different colors and almost half a million different tones, but the number of discriminable olfactory stimuli remains unknown. The lay and scientific literature typically claims that humans can discriminate 10,000 odors, but this number has never been empirically validated. We determined the resolution of the human sense of smell by testing the capacity of humans to discriminate odor mixtures with varying numbers of shared components. On the basis of the results of psychophysical testing, we calculated that humans can discriminate at least 1 trillion olfactory stimuli. This is far more than previous estimates of distinguishable olfactory stimuli. It demonstrates that the human olfactory system, with its hundreds of different olfactory receptors, far outperforms the other senses in the number of physically different stimuli it can discriminate.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483192/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483192/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bushdid, C -- Magnasco, M O -- Vosshall, L B -- Keller, A -- UL1 TR000043/TR/NCATS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2014 Mar 21;343(6177):1370-2. doi: 10.1126/science.1249168.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Neurogenetics and Behavior, The Rockefeller University, 1230 York Avenue, Box 63, New York, NY 10065, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24653035" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Female ; Humans ; Male ; Middle Aged ; *Odors ; *Olfactory Perception ; Smell/*physiology ; Young Adult
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-11-29
    Description: Two studies examined how U.S. presidents are forgotten. A total of 415 undergraduates in 1974, 1991, and 2009 recalled as many presidents as possible and attempted to place them in their correct ordinal positions. All showed roughly linear forgetting of the eight or nine presidents prior to the president holding office at the time, and recall of presidents without respect to ordinal position also showed a regular pattern of forgetting. Similar outcomes occurred with 497 adults (ages 18 to 69) tested in 2014. We fit forgetting functions to the data to predict when six relatively recent presidents will recede in memory to the level of most middle presidents (e.g., we predict that Truman will be forgotten to the same extent as McKinley by about 2040). These studies show that forgetting from collective memory can be studied empirically, as with forgetting in other forms of memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Roediger, H L 3rd -- DeSoto, K A -- New York, N.Y. -- Science. 2014 Nov 28;346(6213):1106-9. doi: 10.1126/science.1259627.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Washington University, St. Louis, MO 63130, USA. roediger@wustl.edu. ; Department of Psychology, Washington University, St. Louis, MO 63130, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25430768" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; *Cognition ; Humans ; Mental Recall/*physiology ; Middle Aged ; Young Adult
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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-06-21
    Description: It is not just a manner of speaking: "Mind reading," or working out what others are thinking and feeling, is markedly similar to print reading. Both of these distinctly human skills recover meaning from signs, depend on dedicated cortical areas, are subject to genetically heritable disorders, show cultural variation around a universal core, and regulate how people behave. But when it comes to development, the evidence is conflicting. Some studies show that, like learning to read print, learning to read minds is a long, hard process that depends on tuition. Others indicate that even very young, nonliterate infants are already capable of mind reading. Here, we propose a resolution to this conflict. We suggest that infants are equipped with neurocognitive mechanisms that yield accurate expectations about behavior ("automatic" or "implicit" mind reading), whereas "explicit" mind reading, like literacy, is a culturally inherited skill; it is passed from one generation to the next by verbal instruction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Heyes, Cecilia M -- Frith, Chris D -- 091593/Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2014 Jun 20;344(6190):1243091. doi: 10.1126/science.1243091.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉All Souls College and Department of Experimental Psychology, University of Oxford, Oxford OX1 4AL, UK. cecilia.heyes@all-souls.ox.ac.uk. ; Wellcome Trust Centre for Neuroimaging, University College London, London WC1N 3BG, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24948740" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Autistic Disorder/psychology ; Brain/physiology ; Child, Preschool ; Cognition ; *Cultural Evolution ; Dyslexia/psychology ; Female ; Humans ; Learning ; Male ; *Nonverbal Communication ; *Telepathy ; *Theory of Mind
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  • 10
    Publication Date: 2014-04-26
    Description: Mutations in the mitochondrial genome are associated with multiple diseases and biological processes; however, little is known about the extent of sequence variation in the mitochondrial transcriptome. By ultra-deeply sequencing mitochondrial RNA (〉6000x) from the whole blood of ~1000 individuals from the CARTaGENE project, we identified remarkable levels of sequence variation within and across individuals, as well as sites that show consistent patterns of posttranscriptional modification. Using a genome-wide association study, we find that posttranscriptional modification of functionally important sites in mitochondrial transfer RNAs (tRNAs) is under strong genetic control, largely driven by a missense mutation in MRPP3 that explains ~22% of the variance. These results reveal a major nuclear genetic determinant of posttranscriptional modification in mitochondria and suggest that tRNA posttranscriptional modification may affect cellular energy production.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hodgkinson, Alan -- Idaghdour, Youssef -- Gbeha, Elias -- Grenier, Jean-Christophe -- Hip-Ki, Elodie -- Bruat, Vanessa -- Goulet, Jean-Philippe -- de Malliard, Thibault -- Awadalla, Philip -- New York, N.Y. -- Science. 2014 Apr 25;344(6182):413-5. doi: 10.1126/science.1251110.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CHU Sainte-Justine Research Centre, Department of Pediatrics, Faculty of Medicine, Universite de Montreal, 3175 Chemin de la Cote-Sainte-Catherine, Montreal, Quebec H3T 1C5, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24763589" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Base Sequence ; DNA, Mitochondrial/chemistry/genetics ; Female ; *Genetic Variation ; *Genome, Mitochondrial ; Genome-Wide Association Study ; High-Throughput Nucleotide Sequencing ; Humans ; Male ; Methylation ; Middle Aged ; Mutation, Missense ; Polymorphism, Single Nucleotide ; RNA/chemistry/*genetics/metabolism ; RNA Processing, Post-Transcriptional ; RNA, Transfer/chemistry/*genetics/metabolism ; Ribonuclease P/*genetics/metabolism ; Sequence Analysis, DNA ; Sequence Analysis, RNA ; Transcriptome
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  • 11
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-09-13
    Description: The science of morality has drawn heavily on well-controlled but artificial laboratory settings. To study everyday morality, we repeatedly assessed moral or immoral acts and experiences in a large (N = 1252) sample using ecological momentary assessment. Moral experiences were surprisingly frequent and manifold. Liberals and conservatives emphasized somewhat different moral dimensions. Religious and nonreligious participants did not differ in the likelihood or quality of committed moral and immoral acts. Being the target of moral or immoral deeds had the strongest impact on happiness, whereas committing moral or immoral deeds had the strongest impact on sense of purpose. Analyses of daily dynamics revealed evidence for both moral contagion and moral licensing. In sum, morality science may benefit from a closer look at the antecedents, dynamics, and consequences of everyday moral experience.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hofmann, Wilhelm -- Wisneski, Daniel C -- Brandt, Mark J -- Skitka, Linda J -- New York, N.Y. -- Science. 2014 Sep 12;345(6202):1340-3. doi: 10.1126/science.1251560. Epub 2014 Sep 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Cologne, 50931 Cologne, Germany. wilhelm.hofmann@uni-koeln.de. ; Department of Psychology, University of Illinois, Chicago, IL 60607, USA. ; Department of Social Psychology, Tilburg University, 5000, Tilburg, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25214626" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Employee Discipline ; Female ; Happiness ; Humans ; Male ; Middle Aged ; *Morals ; Personnel Loyalty ; Young Adult
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  • 12
    Publication Date: 2014-03-08
    Description: To systematically investigate the impact of immune stimulation upon regulatory variant activity, we exposed primary monocytes from 432 healthy Europeans to interferon-gamma (IFN-gamma) or differing durations of lipopolysaccharide and mapped expression quantitative trait loci (eQTLs). More than half of cis-eQTLs identified, involving hundreds of genes and associated pathways, are detected specifically in stimulated monocytes. Induced innate immune activity reveals multiple master regulatory trans-eQTLs including the major histocompatibility complex (MHC), coding variants altering enzyme and receptor function, an IFN-beta cytokine network showing temporal specificity, and an interferon regulatory factor 2 (IRF2) transcription factor-modulated network. Induced eQTL are significantly enriched for genome-wide association study loci, identifying context-specific associations to putative causal genes including CARD9, ATM, and IRF8. Thus, applying pathophysiologically relevant immune stimuli assists resolution of functional genetic variants.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064786/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4064786/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fairfax, Benjamin P -- Humburg, Peter -- Makino, Seiko -- Naranbhai, Vivek -- Wong, Daniel -- Lau, Evelyn -- Jostins, Luke -- Plant, Katharine -- Andrews, Robert -- McGee, Chris -- Knight, Julian C -- 074318/Wellcome Trust/United Kingdom -- 088891/Wellcome Trust/United Kingdom -- 090532/Wellcome Trust/United Kingdom -- 090532/Z/09/Z/Wellcome Trust/United Kingdom -- 281824/European Research Council/International -- 98082/Medical Research Council/United Kingdom -- G1001708/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2014 Mar 7;343(6175):1246949. doi: 10.1126/science.1246949.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24604202" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antigens, CD14/immunology ; Aryl Hydrocarbon Hydroxylases/genetics ; Basic-Leucine Zipper Transcription Factors/genetics ; CARD Signaling Adaptor Proteins/genetics ; Chromosome Mapping ; Crohn Disease/epidemiology/*genetics ; Cytochrome P-450 CYP1B1 ; Female ; Gene Expression Regulation/*immunology ; *Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Humans ; Immunity, Innate/*genetics ; Indoleamine-Pyrrole 2,3,-Dioxygenase/genetics ; Interferon Regulatory Factor-2/genetics ; Interferon Regulatory Factors/genetics ; Interferon-gamma/pharmacology ; Male ; Middle Aged ; Monocytes/drug effects/*immunology ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci ; Receptors, Purinergic P2/genetics ; Young Adult
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 13
    Publication Date: 2014-02-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carmona, Richard -- New York, N.Y. -- Science. 2014 Feb 7;343(6171):589. doi: 10.1126/science.343.6171.589.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24503826" target="_blank"〉PubMed〈/a〉
    Keywords: Administration, Inhalation ; Adult ; Child ; *Device Approval ; Humans ; Nicotine/*administration & dosage ; Smoking/*epidemiology/*prevention & control ; United States ; United States Food and Drug Administration
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  • 14
    Publication Date: 2014-03-08
    Description: Little is known about how human genetic variation affects the responses to environmental stimuli in the context of complex diseases. Experimental and computational approaches were applied to determine the effects of genetic variation on the induction of pathogen-responsive genes in human dendritic cells. We identified 121 common genetic variants associated in cis with variation in expression responses to Escherichia coli lipopolysaccharide, influenza, or interferon-beta (IFN-beta). We localized and validated causal variants to binding sites of pathogen-activated STAT (signal transducer and activator of transcription) and IRF (IFN-regulatory factor) transcription factors. We also identified a common variant in IRF7 that is associated in trans with type I IFN induction in response to influenza infection. Our results reveal common alleles that explain interindividual variation in pathogen sensing and provide functional annotation for genetic variants that alter susceptibility to inflammatory diseases.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124741/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124741/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lee, Mark N -- Ye, Chun -- Villani, Alexandra-Chloe -- Raj, Towfique -- Li, Weibo -- Eisenhaure, Thomas M -- Imboywa, Selina H -- Chipendo, Portia I -- Ran, F Ann -- Slowikowski, Kamil -- Ward, Lucas D -- Raddassi, Khadir -- McCabe, Cristin -- Lee, Michelle H -- Frohlich, Irene Y -- Hafler, David A -- Kellis, Manolis -- Raychaudhuri, Soumya -- Zhang, Feng -- Stranger, Barbara E -- Benoist, Christophe O -- De Jager, Philip L -- Regev, Aviv -- Hacohen, Nir -- DP1 CA174427/CA/NCI NIH HHS/ -- DP1 MH100706/DP/NCCDPHP CDC HHS/ -- DP1 MH100706/MH/NIMH NIH HHS/ -- DP2 OD002230/OD/NIH HHS/ -- F32 AG043267/AG/NIA NIH HHS/ -- P30 DK043351/DK/NIDDK NIH HHS/ -- P50 HG006193/HG/NHGRI NIH HHS/ -- R01 AI091568/AI/NIAID NIH HHS/ -- R01 AR063759/AR/NIAMS NIH HHS/ -- R01 DK097768/DK/NIDDK NIH HHS/ -- R01 HG004037/HG/NHGRI NIH HHS/ -- RC2 GM093080/GM/NIGMS NIH HHS/ -- T32 GM007753/GM/NIGMS NIH HHS/ -- T32 HG002295/HG/NHGRI NIH HHS/ -- U19 AI082630/AI/NIAID NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2014 Mar 7;343(6175):1246980. doi: 10.1126/science.1246980.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA 02142, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24604203" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Autoimmune Diseases/genetics ; Communicable Diseases/genetics ; Dendritic Cells/drug effects/*immunology ; Escherichia coli ; Female ; *Gene-Environment Interaction ; Genetic Loci ; Genome-Wide Association Study ; HEK293 Cells ; Host-Pathogen Interactions/*genetics ; Humans ; Influenza A virus ; Interferon Regulatory Factor-7/*genetics ; Interferon-beta/pharmacology ; Lipopolysaccharides/immunology ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Quantitative Trait Loci ; STAT Transcription Factors/*genetics ; Transcriptome ; Young Adult
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 15
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-03-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Underwood, Emily -- New York, N.Y. -- Science. 2014 Feb 28;343(6174):964-7. doi: 10.1126/science.343.6174.964.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24578561" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Brain/drug effects/metabolism/pathology ; Child ; Chromosomes, Human, Pair 21/genetics ; Clinical Trials as Topic ; Cognition Disorders/*drug therapy ; Down Syndrome/drug therapy/genetics/*therapy ; *Early Medical Intervention ; Female ; GABA Antagonists/therapeutic use ; Humans ; Magnetic Resonance Imaging ; Male ; Mice ; Mutagenesis, Insertional ; Picrotoxin/therapeutic use ; RNA, Long Noncoding/genetics ; gamma-Aminobutyric Acid/metabolism
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 16
    Publication Date: 2014-03-29
    Description: High-quality early childhood programs have been shown to have substantial benefits in reducing crime, raising earnings, and promoting education. Much less is known about their benefits for adult health. We report on the long-term health effects of one of the oldest and most heavily cited early childhood interventions with long-term follow-up evaluated by the method of randomization: the Carolina Abecedarian Project (ABC). Using recently collected biomedical data, we find that disadvantaged children randomly assigned to treatment have significantly lower prevalence of risk factors for cardiovascular and metabolic diseases in their mid-30s. The evidence is especially strong for males. The mean systolic blood pressure among the control males is 143 millimeters of mercury (mm Hg), whereas it is only 126 mm Hg among the treated. One in four males in the control group is affected by metabolic syndrome, whereas none in the treatment group are affected. To reach these conclusions, we address several statistical challenges. We use exact permutation tests to account for small sample sizes and conduct a parallel bootstrap confidence interval analysis to confirm the permutation analysis. We adjust inference to account for the multiple hypotheses tested and for nonrandom attrition. Our evidence shows the potential of early life interventions for preventing disease and promoting health.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028126/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4028126/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Campbell, Frances -- Conti, Gabriella -- Heckman, James J -- Moon, Seong Hyeok -- Pinto, Rodrigo -- Pungello, Elizabeth -- Pan, Yi -- 1R01HD54702/HD/NICHD NIH HHS/ -- 5R37HD065072/HD/NICHD NIH HHS/ -- 5RC1MD004344/MD/NIMHD NIH HHS/ -- R37 HD065072/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2014 Mar 28;343(6178):1478-85. doi: 10.1126/science.1248429.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Frank Porter Graham Child Development Institute, University of North Carolina, Chapel Hill, NC 27599, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24675955" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Biomarkers/blood ; Blood Preservation ; Body Mass Index ; Cardiovascular Diseases/*epidemiology/physiopathology/*prevention & control ; Child ; Cholesterol, HDL/blood ; Diet ; Early Medical Intervention/*methods ; Female ; Health ; Humans ; Male ; Metabolic Syndrome X/*epidemiology/physiopathology/*prevention & control
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 17
    Publication Date: 2014-08-16
    Description: The current view of motor learning suggests that when we revisit a task, the brain recalls the motor commands it previously learned. In this view, motor memory is a memory of motor commands, acquired through trial-and-error and reinforcement. Here we show that the brain controls how much it is willing to learn from the current error through a principled mechanism that depends on the history of past errors. This suggests that the brain stores a previously unknown form of memory, a memory of errors. A mathematical formulation of this idea provides insights into a host of puzzling experimental data, including savings and meta-learning, demonstrating that when we are better at a motor task, it is partly because the brain recognizes the errors it experienced before.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506639/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506639/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Herzfeld, David J -- Vaswani, Pavan A -- Marko, Mollie K -- Shadmehr, Reza -- 1F31NS079121/NS/NINDS NIH HHS/ -- F31 NS090860/NS/NINDS NIH HHS/ -- R01 NS078311/NS/NINDS NIH HHS/ -- R01NS078311/NS/NINDS NIH HHS/ -- T32 GM007309/GM/NIGMS NIH HHS/ -- T32EB003383/EB/NIBIB NIH HHS/ -- T32GM007057/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2014 Sep 12;345(6202):1349-53. doi: 10.1126/science.1253138. Epub 2014 Aug 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biomedical Engineering, Laboratory for Computational Motor Control, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. dherzfe1@jhmi.edu. ; Department of Neuroscience, Laboratory for Computational Motor Control, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. ; Department of Biomedical Engineering, Laboratory for Computational Motor Control, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25123484" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/*physiology ; Female ; Humans ; Learning/*physiology ; Male ; Mental Recall/*physiology ; *Psychomotor Performance ; Young Adult
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 18
    Publication Date: 2014-07-12
    Description: This paper presents a new data infrastructure for measuring economic activity. The infrastructure records transactions and account balances, yielding measurements with scope and accuracy that have little precedent in economics. The data are drawn from a diverse population that overrepresents males and younger adults but contains large numbers of underrepresented groups. The data infrastructure permits evaluation of a benchmark theory in economics that predicts that individuals should use a combination of cash management, saving, and borrowing to make the timing of income irrelevant for the timing of spending. As in previous studies and in contrast to the predictions of the theory, there is a response of spending to the arrival of anticipated income. The data also show, however, that this apparent excess sensitivity of spending results largely from the coincident timing of regular income and regular spending. The remaining excess sensitivity is concentrated among individuals with less liquidity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gelman, Michael -- Kariv, Shachar -- Shapiro, Matthew D -- Silverman, Dan -- Tadelis, Steven -- P30 AG012839/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2014 Jul 11;345(6193):212-5. doi: 10.1126/science.1247727.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Economics, University of Michigan, Ann Arbor, MI 48109, USA. ; Department of Economics, University of California, Berkeley, Berkeley, CA 94720, USA. ; Department of Economics, University of Michigan, Ann Arbor, MI 48109, USA. National Bureau of Economic Research (NBER), Cambridge, MA 02138, USA. shapiro@umich.edu. ; National Bureau of Economic Research (NBER), Cambridge, MA 02138, USA. Department of Economics, Arizona State University, Tempe, AZ 85287, USA. ; National Bureau of Economic Research (NBER), Cambridge, MA 02138, USA. Haas School of Business, University of California, Berkeley, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25013075" target="_blank"〉PubMed〈/a〉
    Keywords: Administrative Personnel ; Adolescent ; Adult ; Aged ; Female ; *Human Activities ; Humans ; *Income ; Male ; Middle Aged ; Policy Making ; Young Adult
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  • 19
    Publication Date: 2014-10-11
    Description: The United Nations (UN) recently released population projections based on data until 2012 and a Bayesian probabilistic methodology. Analysis of these data reveals that, contrary to previous literature, the world population is unlikely to stop growing this century. There is an 80% probability that world population, now 7.2 billion people, will increase to between 9.6 billion and 12.3 billion in 2100. This uncertainty is much smaller than the range from the traditional UN high and low variants. Much of the increase is expected to happen in Africa, in part due to higher fertility rates and a recent slowdown in the pace of fertility decline. Also, the ratio of working-age people to older people is likely to decline substantially in all countries, even those that currently have young populations.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230924/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4230924/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gerland, Patrick -- Raftery, Adrian E -- Sevcikova, Hana -- Li, Nan -- Gu, Danan -- Spoorenberg, Thomas -- Alkema, Leontine -- Fosdick, Bailey K -- Chunn, Jennifer -- Lalic, Nevena -- Bay, Guiomar -- Buettner, Thomas -- Heilig, Gerhard K -- Wilmoth, John -- R01 HD054511/HD/NICHD NIH HHS/ -- R01 HD070936/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2014 Oct 10;346(6206):234-7. doi: 10.1126/science.1257469. Epub 2014 Sep 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Population Division, Department of Economic and Social Affairs, United Nations, New York, NY 10017, USA. gerland@un.org raftery@u.washington.edu. ; Departments of Statistics and Sociology, University of Washington, Seattle, WA 98195-4322, USA. gerland@un.org raftery@u.washington.edu. ; Center for Statistics and the Social Sciences, University of Washington, Seattle, WA 98195-4320, USA. ; Population Division, Department of Economic and Social Affairs, United Nations, New York, NY 10017, USA. ; Department of Statistics and Applied Probability and Saw Swee Hock School of Public Health, National University of Singapore, Singapore 117546. ; Department of Statistics, Colorado State University, Fort Collins, CO 80523-1877, USA. ; James Cook University Singapore, 600 Upper Thomson Road, Singapore 574421. ; Institutional Research, University of Washington, Seattle, WA 98195-9445, USA. ; Latin American and Caribbean Demographic Center (CELADE), Population Division of the United Nations Economic Commission for Latin America and the Caribbean, Santiago, Chile. ; Population Division, United Nations, New York, NY, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25301627" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Distribution ; Aged ; Humans ; Middle Aged ; *Population Growth ; Uncertainty ; United Nations ; Work ; Young Adult
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  • 20
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-08-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Siliciano, Janet D -- Siliciano, Robert F -- New York, N.Y. -- Science. 2014 Aug 29;345(6200):1005-6. doi: 10.1126/science.1259452.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. ; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Howard Hughes Medical Institute, Baltimore, MD, USA. rsiliciano@jhmi.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25170139" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Anti-Retroviral Agents/*therapeutic use ; Bone Marrow Transplantation ; CD4-Positive T-Lymphocytes/immunology/virology ; Child ; HIV Infections/*drug therapy/*immunology/therapy ; HIV-1/isolation & purification/*physiology ; Humans ; Immunologic Memory ; Mississippi ; Treatment Failure ; Viremia/diagnosis/immunology/virology ; Virus Latency/*immunology
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  • 21
    Publication Date: 2014-04-05
    Description: When mounted on the skin, modern sensors, circuits, radios, and power supply systems have the potential to provide clinical-quality health monitoring capabilities for continuous use, beyond the confines of traditional hospital or laboratory facilities. The most well-developed component technologies are, however, broadly available only in hard, planar formats. As a result, existing options in system design are unable to effectively accommodate integration with the soft, textured, curvilinear, and time-dynamic surfaces of the skin. Here, we describe experimental and theoretical approaches for using ideas in soft microfluidics, structured adhesive surfaces, and controlled mechanical buckling to achieve ultralow modulus, highly stretchable systems that incorporate assemblies of high-modulus, rigid, state-of-the-art functional elements. The outcome is a thin, conformable device technology that can softly laminate onto the surface of the skin to enable advanced, multifunctional operation for physiological monitoring in a wireless mode.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xu, Sheng -- Zhang, Yihui -- Jia, Lin -- Mathewson, Kyle E -- Jang, Kyung-In -- Kim, Jeonghyun -- Fu, Haoran -- Huang, Xian -- Chava, Pranav -- Wang, Renhan -- Bhole, Sanat -- Wang, Lizhe -- Na, Yoon Joo -- Guan, Yue -- Flavin, Matthew -- Han, Zheshen -- Huang, Yonggang -- Rogers, John A -- New York, N.Y. -- Science. 2014 Apr 4;344(6179):70-4. doi: 10.1126/science.1250169.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Materials Science and Engineering and Frederick Seitz Materials Research Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24700852" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Elasticity ; Electrocardiography/instrumentation/methods ; Electrocardiography, Ambulatory/instrumentation/methods ; Electroencephalography/instrumentation/methods ; Electromyography/instrumentation/methods ; Electrooculography ; Equipment Design ; Humans ; Male ; Microfluidics/*instrumentation ; Monitoring, Ambulatory/*instrumentation/methods ; Monitoring, Physiologic/*instrumentation/methods ; Remote Sensing Technology ; Silicone Elastomers ; *Skin ; Wireless Technology ; Young Adult
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  • 22
    Publication Date: 2014-09-13
    Description: Cytotoxic T lymphocyte antigen-4 (CTLA-4) is an inhibitory receptor found on immune cells. The consequences of mutations in CTLA4 in humans are unknown. We identified germline heterozygous mutations in CTLA4 in subjects with severe immune dysregulation from four unrelated families. Whereas Ctla4 heterozygous mice have no obvious phenotype, human CTLA4 haploinsufficiency caused dysregulation of FoxP3(+) regulatory T (Treg) cells, hyperactivation of effector T cells, and lymphocytic infiltration of target organs. Patients also exhibited progressive loss of circulating B cells, associated with an increase of predominantly autoreactive CD21(lo) B cells and accumulation of B cells in nonlymphoid organs. Inherited human CTLA4 haploinsufficiency demonstrates a critical quantitative role for CTLA-4 in governing T and B lymphocyte homeostasis.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371526/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4371526/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kuehn, Hye Sun -- Ouyang, Weiming -- Lo, Bernice -- Deenick, Elissa K -- Niemela, Julie E -- Avery, Danielle T -- Schickel, Jean-Nicolas -- Tran, Dat Q -- Stoddard, Jennifer -- Zhang, Yu -- Frucht, David M -- Dumitriu, Bogdan -- Scheinberg, Phillip -- Folio, Les R -- Frein, Cathleen A -- Price, Susan -- Koh, Christopher -- Heller, Theo -- Seroogy, Christine M -- Huttenlocher, Anna -- Rao, V Koneti -- Su, Helen C -- Kleiner, David -- Notarangelo, Luigi D -- Rampertaap, Yajesh -- Olivier, Kenneth N -- McElwee, Joshua -- Hughes, Jason -- Pittaluga, Stefania -- Oliveira, Joao B -- Meffre, Eric -- Fleisher, Thomas A -- Holland, Steven M -- Lenardo, Michael J -- Tangye, Stuart G -- Uzel, Gulbu -- 5R01HL113304-01/HL/NHLBI NIH HHS/ -- AI061093/AI/NIAID NIH HHS/ -- AI071087/AI/NIAID NIH HHS/ -- AI095848/AI/NIAID NIH HHS/ -- HHSN261200800001E/PHS HHS/ -- P01 AI061093/AI/NIAID NIH HHS/ -- R01 AI071087/AI/NIAID NIH HHS/ -- R01 HL113304/HL/NHLBI NIH HHS/ -- R21 AI095848/AI/NIAID NIH HHS/ -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2014 Sep 26;345(6204):1623-7. doi: 10.1126/science.1255904. Epub 2014 Sep 11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA. tfleishe@cc.nih.gov lenardo@nih.gov guzel@niaid.nih.gov. ; Laboratory of Cell Biology, Division of Monoclonal Antibodies, Office of Biotechnology Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Bethesda, MD 20892, USA. tfleishe@cc.nih.gov lenardo@nih.gov guzel@niaid.nih.gov. ; Molecular Development of the Immune System Section, Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. NIAID Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. tfleishe@cc.nih.gov lenardo@nih.gov guzel@niaid.nih.gov. ; Immunology and Immunodeficiency Group, Immunology Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia. St. Vincent's Clinical School Faculty of Medicine, University of New South Wales, Sydney, NSW 2010, Australia. ; Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA. ; Immunology and Immunodeficiency Group, Immunology Division, Garvan Institute of Medical Research, Sydney, NSW 2010, Australia. ; Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06511, USA. ; Department of Pediatrics, University of Texas Medical School, Houston, TX 77030, USA. ; NIAID Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. Immunological Diseases Unit, Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. ; Laboratory of Cell Biology, Division of Monoclonal Antibodies, Office of Biotechnology Products, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Bethesda, MD 20892, USA. ; Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, MD 20892, USA. ; Radiology and Imaging and Sciences, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA. ; Clinical Research Directorate, Clinical Monitoring Research Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. ; Molecular Development of the Immune System Section, Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. NIAID Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. ; Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD 20892, USA. ; Department of Pediatrics, University of Wisconsin, Madison, WI 53706, USA. ; Department of Pediatrics, University of Wisconsin, Madison, WI 53706, USA. Department of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI 53706, USA. ; Laboratory of Pathology, National Cancer Institute, Bethesda, MD 20892, USA. ; Division of Immunology and Manton Center for Orphan Disease Research, Children's Hospital, Harvard Medical School, Boston, MA 10217, USA. ; Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. ; Merck Research Laboratories, Merck & Co., Boston, MA 02130, USA. ; Instituto de Medicina Integral Prof. Fernando Figueira-IMIP, 50070 Recife-PE, Brazil. ; NIAID Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. ; Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. tfleishe@cc.nih.gov lenardo@nih.gov guzel@niaid.nih.gov.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25213377" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; B-Lymphocytes/immunology ; CTLA-4 Antigen/*genetics ; Female ; Forkhead Transcription Factors/immunology ; *Germ-Line Mutation ; *Haploinsufficiency ; Humans ; Immune System Diseases/*genetics ; Immunity/*genetics ; Male ; Mice ; Mice, Mutant Strains ; Pedigree ; T-Lymphocytes, Regulatory/immunology ; Young Adult
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  • 23
    Publication Date: 2014-12-17
    Description: Song-learning birds and humans share independently evolved similarities in brain pathways for vocal learning that are essential for song and speech and are not found in most other species. Comparisons of brain transcriptomes of song-learning birds and humans relative to vocal nonlearners identified convergent gene expression specializations in specific song and speech brain regions of avian vocal learners and humans. The strongest shared profiles relate bird motor and striatal song-learning nuclei, respectively, with human laryngeal motor cortex and parts of the striatum that control speech production and learning. Most of the associated genes function in motor control and brain connectivity. Thus, convergent behavior and neural connectivity for a complex trait are associated with convergent specialized expression of multiple genes.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385736/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385736/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pfenning, Andreas R -- Hara, Erina -- Whitney, Osceola -- Rivas, Miriam V -- Wang, Rui -- Roulhac, Petra L -- Howard, Jason T -- Wirthlin, Morgan -- Lovell, Peter V -- Ganapathy, Ganeshkumar -- Mouncastle, Jacquelyn -- Moseley, M Arthur -- Thompson, J Will -- Soderblom, Erik J -- Iriki, Atsushi -- Kato, Masaki -- Gilbert, M Thomas P -- Zhang, Guojie -- Bakken, Trygve -- Bongaarts, Angie -- Bernard, Amy -- Lein, Ed -- Mello, Claudio V -- Hartemink, Alexander J -- Jarvis, Erich D -- DP1 OD000448/OD/NIH HHS/ -- R01 DC007218/DC/NIDCD NIH HHS/ -- R01DC007218/DC/NIDCD NIH HHS/ -- R21 DC007478/DC/NIDCD NIH HHS/ -- R24 GM092842/GM/NIGMS NIH HHS/ -- R24GM092842/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2014 Dec 12;346(6215):1256846. doi: 10.1126/science.1256846.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Neurobiology, Howard Hughes Medical Institute, and Duke University Medical Center, Durham, NC 27710, USA. apfenning@csail.mit.edu amink@cs.duke.edu jarvis@neuro.duke.edu. ; Department of Neurobiology, Howard Hughes Medical Institute, and Duke University Medical Center, Durham, NC 27710, USA. ; Department of Behavioral Neuroscience, Oregon Health & Science University, Portland, OR 97239, USA. ; Duke Proteomics and Metabolomics Core Facility, Center for Genomic and Computational Biology, Duke University Medical Center, Durham, NC 27710, USA. ; Laboratory for Symbolic Cognitive Development, Brain Science Institute, RIKEN, 2-1 Hirosawa, Wako, Saitama 351-0198, Japan. ; Centre for GeoGenetics, Natural History Museum of Denmark, University of Copenhagen, 1350 Copenhagen, Denmark. Trace and Environmental DNA Laboratory, Department of Environment and Agriculture, Curtin University, Perth, Western Australia 6102, Australia. ; China National GeneBank, BGI-Shenzhen, Shenzhen 518083, China. Centre for Social Evolution, Department of Biology, University of Copenhagen, DK-2100 Copenhagen, Denmark. ; Allen Institute for Brain Science, Seattle, WA 98103, USA. ; Department of Computer Science, Duke University, Durham, NC 27708, USA. apfenning@csail.mit.edu amink@cs.duke.edu jarvis@neuro.duke.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25504733" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Birds/genetics/physiology ; Brain/anatomy & histology/*physiology ; Brain Mapping ; Corpus Striatum/anatomy & histology/physiology ; Evolution, Molecular ; Finches/*genetics/*physiology ; *Gene Expression Regulation ; Humans ; *Learning ; Male ; Motor Cortex/anatomy & histology/physiology ; Neural Pathways ; Species Specificity ; *Speech ; Transcription, Genetic ; *Transcriptome ; *Vocalization, Animal
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  • 24
    Publication Date: 2014-01-05
    Description: In 2008, Oregon initiated a limited expansion of a Medicaid program for uninsured, low-income adults, drawing names from a waiting list by lottery. This lottery created a rare opportunity to study the effects of Medicaid coverage by using a randomized controlled design. By using the randomization provided by the lottery and emergency-department records from Portland-area hospitals, we studied the emergency department use of about 25,000 lottery participants over about 18 months after the lottery. We found that Medicaid coverage significantly increases overall emergency use by 0.41 visits per person, or 40% relative to an average of 1.02 visits per person in the control group. We found increases in emergency-department visits across a broad range of types of visits, conditions, and subgroups, including increases in visits for conditions that may be most readily treatable in primary care settings.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955206/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955206/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Taubman, Sarah L -- Allen, Heidi L -- Wright, Bill J -- Baicker, Katherine -- Finkelstein, Amy N -- P30 AG012810/AG/NIA NIH HHS/ -- P30AG012810/AG/NIA NIH HHS/ -- R01 AG034151/AG/NIA NIH HHS/ -- R01AG0345151/AG/NIA NIH HHS/ -- RC2 AG036631/AG/NIA NIH HHS/ -- RC2AGO36631/RC/CCR NIH HHS/ -- New York, N.Y. -- Science. 2014 Jan 17;343(6168):263-8. doi: 10.1126/science.1246183. Epub 2014 Jan 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉National Bureau of Economic Research (NBER), Cambridge, MA 02138, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24385603" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Ambulatory Care/statistics & numerical data ; Emergency Service, Hospital/*utilization ; Female ; Humans ; Inpatients/statistics & numerical data ; Insurance, Health ; Male ; Medicaid/*economics ; *Medically Uninsured ; Oregon ; Poverty ; United States
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  • 25
    Publication Date: 2014-02-22
    Description: The capacity to evaluate the outcomes of our actions is fundamental for adapting and optimizing behavior and depends on an action-monitoring system that assesses ongoing actions and detects errors. The neuronal network underlying this executive function, classically attributed to the rostral cingulate zone, is poorly characterized in humans, owing to the limited number of direct neurophysiological data. Using intracerebral recordings, we show that the leading role is played by the supplementary motor area (SMA), which rapidly evaluates successful and erroneous actions. The rostral part of medial prefrontal cortex, driven by the SMA, was activated later and exclusively in the case of errors. This suggests a hierarchical organization of the different frontal regions involved in implementation of action monitoring and error processing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bonini, Francesca -- Burle, Boris -- Liegeois-Chauvel, Catherine -- Regis, Jean -- Chauvel, Patrick -- Vidal, Franck -- 241077/European Research Council/International -- New York, N.Y. -- Science. 2014 Feb 21;343(6173):888-91. doi: 10.1126/science.1247412.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Aix-Marseille Universite, 13385, Marseille, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24558161" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Behavior/*physiology ; Electrodes, Implanted ; *Evoked Potentials ; Female ; Humans ; Male ; Monitoring, Physiologic ; Motor Cortex/*physiology ; Neural Pathways ; Prefrontal Cortex/*physiology ; Young Adult
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  • 26
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-11-02
    Description: The challenge of global population aging has been brought into sharper focus by the financial crisis of 2008. In particular, growing national debt has drawn government attention to two apparently conflicting priorities: the need to sustain public spending on pensions and health care versus the need to reduce budget deficits. A number of countries are consequently reconsidering their pension and health care provisions, which account for up to 40% of all government spending in advanced economies. Yet population aging is a global phenomenon that will continue to affect all regions of the world. By 2050 there will be the same number of old as young in the world, with 2 billion people aged 60 or over and another 2 billion under age 15, each group accounting for 21% of the world's population.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harper, Sarah -- New York, N.Y. -- Science. 2014 Oct 31;346(6209):587-91. doi: 10.1126/science.1254405.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Oxford Institute of Population Ageing, University of Oxford, Oxford OX2 6PR, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25359967" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Factors ; Aged ; Aged, 80 and over ; *Aging ; Birth Rate/trends ; Budgets ; Child ; Child, Preschool ; Delivery of Health Care/*economics ; Emigration and Immigration ; Female ; Humans ; Infant ; Infant, Newborn ; Life Expectancy/trends ; Male ; Middle Aged ; Mortality/trends ; *Pensions ; *Population Dynamics ; Young Adult
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  • 27
    Publication Date: 2014-05-31
    Description: The prefrontal cortex (PFC) subserves reasoning in the service of adaptive behavior. Little is known, however, about the architecture of reasoning processes in the PFC. Using computational modeling and neuroimaging, we show here that the human PFC has two concurrent inferential tracks: (i) one from ventromedial to dorsomedial PFC regions that makes probabilistic inferences about the reliability of the ongoing behavioral strategy and arbitrates between adjusting this strategy versus exploring new ones from long-term memory, and (ii) another from polar to lateral PFC regions that makes probabilistic inferences about the reliability of two or three alternative strategies and arbitrates between exploring new strategies versus exploiting these alternative ones. The two tracks interact and, along with the striatum, realize hypothesis testing for accepting versus rejecting newly created strategies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Donoso, Mael -- Collins, Anne G E -- Koechlin, Etienne -- New York, N.Y. -- Science. 2014 Jun 27;344(6191):1481-6. doi: 10.1126/science.1252254. Epub 2014 May 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉INSERM, Laboratoire de Neurosciences Cognitives (U960), 29 rue d'Ulm, 75005 Paris, France. Department d'Etudes Cognitives (DEC), Ecole Normale Superieure, 29 rue d'Ulm, 75005 Paris, France. Centre de Neuro-imagerie de Recherche (CENIR), Universite Pierre et Marie Curie, 4 place Jussieu, 75005 Paris, France. ; Department d'Etudes Cognitives (DEC), Ecole Normale Superieure, 29 rue d'Ulm, 75005 Paris, France. Brown University, Providence, RI 02912, USA. ; INSERM, Laboratoire de Neurosciences Cognitives (U960), 29 rue d'Ulm, 75005 Paris, France. Department d'Etudes Cognitives (DEC), Ecole Normale Superieure, 29 rue d'Ulm, 75005 Paris, France. Centre de Neuro-imagerie de Recherche (CENIR), Universite Pierre et Marie Curie, 4 place Jussieu, 75005 Paris, France. etienne.koechlin@upmc.fr.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24876345" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Algorithms ; Basal Ganglia/physiology ; Bayes Theorem ; Behavior ; Brain Mapping ; *Cognition ; Computer Simulation ; Female ; Gyrus Cinguli/physiology ; Humans ; Learning ; Magnetic Resonance Imaging ; Male ; Memory ; Models, Neurological ; Prefrontal Cortex/anatomy & histology/*physiology ; Probability ; *Thinking ; Young Adult
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  • 28
    Publication Date: 2014-05-09
    Description: Limited evidence exists that humans mount a mutation-specific T cell response to epithelial cancers. We used a whole-exomic-sequencing-based approach to demonstrate that tumor-infiltrating lymphocytes (TIL) from a patient with metastatic cholangiocarcinoma contained CD4+ T helper 1 (T(H)1) cells recognizing a mutation in erbb2 interacting protein (ERBB2IP) expressed by the cancer. After adoptive transfer of TIL containing about 25% mutation-specific polyfunctional T(H)1 cells, the patient achieved a decrease in target lesions with prolonged stabilization of disease. Upon disease progression, the patient was retreated with a 〉95% pure population of mutation-reactive T(H)1 cells and again experienced tumor regression. These results provide evidence that a CD4+ T cell response against a mutated antigen can be harnessed to mediate regression of a metastatic epithelial cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tran, Eric -- Turcotte, Simon -- Gros, Alena -- Robbins, Paul F -- Lu, Yong-Chen -- Dudley, Mark E -- Wunderlich, John R -- Somerville, Robert P -- Hogan, Katherine -- Hinrichs, Christian S -- Parkhurst, Maria R -- Yang, James C -- Rosenberg, Steven A -- Intramural NIH HHS/ -- New York, N.Y. -- Science. 2014 May 9;344(6184):641-5. doi: 10.1126/science.1251102.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Surgery Branch, National Cancer Institute (NCI), National Institutes of Health, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24812403" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing/*genetics ; Adoptive Transfer/*methods ; Adult ; Bile Duct Neoplasms/genetics/*therapy ; *Bile Ducts, Intrahepatic ; CD4-Positive T-Lymphocytes/*immunology ; Cholangiocarcinoma/genetics/*therapy ; Clinical Trials, Phase II as Topic ; Exome ; Female ; Humans ; Lymphocytes, Tumor-Infiltrating/*transplantation ; Mutation ; Receptor, ErbB-2/metabolism ; Th1 Cells/*transplantation
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  • 29
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉DuPont, Robert L -- Lieberman, Jeffrey A -- New York, N.Y. -- Science. 2014 May 9;344(6184):557. doi: 10.1126/science.1254989.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Robert L. DuPont was the first director of the U.S. National Institute on Drug Abuse (1973-1978) and is president of the Institute for Behavior and Health, Rockville, MD.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24812368" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Alcoholism/epidemiology ; Brain/*drug effects/pathology ; Cannabis/*adverse effects ; Humans ; Marijuana Abuse/pathology/psychology ; Marijuana Smoking/*adverse effects/epidemiology/legislation & jurisprudence ; National Institutes of Health (U.S.) ; Street Drugs/*adverse effects/legislation & jurisprudence ; United States/epidemiology ; Young Adult
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  • 30
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-05-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vogel, Gretchen -- New York, N.Y. -- Science. 2014 May 2;344(6183):462-3. doi: 10.1126/science.344.6183.462.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24786057" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Clone Cells ; Embryonic Stem Cells/*cytology ; Humans ; *Nuclear Transfer Techniques/legislation & jurisprudence ; Oocyte Donation ; Skin/*cytology ; *Stem Cell Research/legislation & jurisprudence
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  • 31
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-09-13
    Description: The global health landscape looks more promising than ever, although progress has been uneven. Here, we describe the current global burden of disease throughout the life cycle, highlighting regional differences in the unfinished agenda of communicable diseases and reproductive, maternal, and child health and the additive burden of emerging noncommunicable diseases and injuries. Understanding this changing landscape is an essential starting point for effective allocation of both domestic and international resources for health.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sepulveda, Jaime -- Murray, Christopher -- New York, N.Y. -- Science. 2014 Sep 12;345(6202):1275-8. doi: 10.1126/science.1257099.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Global Health Sciences, University of California (UC) San Francisco, San Francisco, CA, USA. sepulvedaj@globalhealth.ucsf.edu. ; Institute for Health Metrics and Evaluation (IHME), University of Washington, Seattle, WA, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25214611" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Age Factors ; Aged ; Child ; Child Welfare/trends ; Child, Preschool ; Communicable Diseases/epidemiology ; *Cost of Illness ; Diabetes Mellitus/epidemiology ; Emergencies/epidemiology ; Female ; Global Health/*trends ; Humans ; Infant ; Infant, Newborn ; Male ; Maternal Welfare/trends ; Middle Aged ; Obesity/epidemiology ; Prevalence ; Reproductive Health/trends ; Wounds and Injuries/epidemiology ; Young Adult
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  • 32
    Publication Date: 2014-08-26
    Description: Inactivated poliovirus vaccine (IPV) is efficacious against paralytic disease, but its effect on mucosal immunity is debated. We assessed the efficacy of IPV in boosting mucosal immunity. Participants received IPV, bivalent 1 and 3 oral poliovirus vaccine (bOPV), or no vaccine. A bOPV challenge was administered 4 weeks later, and excretion was assessed 3, 7, and 14 days later. Nine hundred and fifty-four participants completed the study. Any fecal shedding of poliovirus type 1 was 8.8, 9.1, and 13.5% in the IPV group and 14.4, 24.1, and 52.4% in the control group by 6- to 11-month, 5-year, and 10-year groups, respectively (IPV versus control: Fisher's exact test P 〈 0.001). IPV reduced excretion for poliovirus types 1 and 3 between 38.9 and 74.2% and 52.8 and 75.7%, respectively. Thus, IPV in OPV-vaccinated individuals boosts intestinal mucosal immunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jafari, Hamid -- Deshpande, Jagadish M -- Sutter, Roland W -- Bahl, Sunil -- Verma, Harish -- Ahmad, Mohammad -- Kunwar, Abhishek -- Vishwakarma, Rakesh -- Agarwal, Ashutosh -- Jain, Shilpi -- Estivariz, Concepcion -- Sethi, Raman -- Molodecky, Natalie A -- Grassly, Nicholas C -- Pallansch, Mark A -- Chatterjee, Arani -- Aylward, R Bruce -- MR/K010174/1/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2014 Aug 22;345(6199):922-5. doi: 10.1126/science.1255006.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉World Health Organization, India-National Polio Surveillance Project, R. K. Khanna Stadium, Africa Avenue, Safdarjung Enclave, New Delhi 110029, India. ; Enterovirus Research Center, Haffkine Institute Compound, Parel, Mumbai, India. ; World Health Organization, Ave Appia, Geneva, Switzerland. sutterr@who.int. ; World Health Organization, Ave Appia, Geneva, Switzerland. ; Panacea Biotec Ltd., New Delhi, India. ; Centers for Disease Control and Prevention, Atlanta, GA, USA. ; Department of Infectious Disease Epidemiology, Imperial College London, London, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25146288" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Antibodies, Viral/blood/immunology ; Child ; Child, Preschool ; *Disease Eradication ; Feces/virology ; Female ; Humans ; Immunity, Mucosal ; Immunization, Secondary ; India/epidemiology ; Infant ; Intestinal Mucosa/*immunology/virology ; Male ; Middle Aged ; Poliomyelitis/epidemiology/immunology/*prevention & control ; Poliovirus/*immunology/isolation & purification ; Poliovirus Vaccine, Inactivated/*administration & dosage ; Poliovirus Vaccine, Oral/*administration & dosage ; Prevalence ; Virus Shedding/immunology
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  • 33
    Publication Date: 2014-08-30
    Description: The influential notion that the hippocampus supports associative memory by interacting with functionally distinct and distributed brain regions has not been directly tested in humans. We therefore used targeted noninvasive electromagnetic stimulation to modulate human cortical-hippocampal networks and tested effects of this manipulation on memory. Multiple-session stimulation increased functional connectivity among distributed cortical-hippocampal network regions and concomitantly improved associative memory performance. These alterations involved localized long-term plasticity because increases were highly selective to the targeted brain regions, and enhancements of connectivity and associative memory persisted for ~24 hours after stimulation. Targeted cortical-hippocampal networks can thus be enhanced noninvasively, demonstrating their role in associative memory.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307924/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307924/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wang, Jane X -- Rogers, Lynn M -- Gross, Evan Z -- Ryals, Anthony J -- Dokucu, Mehmet E -- Brandstatt, Kelly L -- Hermiller, Molly S -- Voss, Joel L -- F32 NS083340/NS/NINDS NIH HHS/ -- F32-NS083340/NS/NINDS NIH HHS/ -- P50 MH094263/MH/NIMH NIH HHS/ -- P50-MH094263/MH/NIMH NIH HHS/ -- T32 NS047987/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2014 Aug 29;345(6200):1054-7. doi: 10.1126/science.1252900.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medical Social Sciences, Ken and Ruth Davee Department of Neurology, and Interdepartmental Neuroscience Program, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. ; The Sensory Motor Performance Program, Rehabilitation Institute of Chicago, Chicago, IL, USA. ; Department of Psychiatry and Behavioral Sciences, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. ; Department of Medical Social Sciences, Ken and Ruth Davee Department of Neurology, and Interdepartmental Neuroscience Program, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. joel-voss@northwestern.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25170153" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Association ; Female ; Hippocampus/*physiology ; Humans ; Magnetic Resonance Imaging ; Male ; Memory/*physiology ; Nerve Net/physiology ; Parietal Lobe/*physiology ; *Transcranial Magnetic Stimulation ; Young Adult
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  • 34
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2014-09-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Servick, Kelly -- New York, N.Y. -- Science. 2014 Sep 19;345(6203):1438-9. doi: 10.1126/science.345.6203.1438.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25237080" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/abnormalities ; Brain Diseases/*genetics ; Child ; DNA/genetics ; DNA Mutational Analysis/methods ; *Genetic Testing ; Genetic Variation ; Humans ; Mental Disorders/*genetics ; *Mosaicism ; Mutation ; Zygote
    Print ISSN: 0036-8075
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  • 35
    Publication Date: 2014-11-02
    Description: Language is a crucial and complex lifelong faculty, underpinned by dynamic interactions within and between specialized brain networks. Whereas normal aging impairs specific aspects of language production, most core language processes are robust to brain aging. We review recent behavioral and neuroimaging evidence showing that language systems remain largely stable across the life span and that both younger and older adults depend on dynamic neural responses to linguistic demands. Although some aspects of network dynamics change with age, there is no consistent evidence that core language processes are underpinned by different neural networks in younger and older adults.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shafto, Meredith A -- Tyler, Lorraine K -- 249640/European Research Council/International -- BB/H008217/1/Biotechnology and Biological Sciences Research Council/United Kingdom -- New York, N.Y. -- Science. 2014 Oct 31;346(6209):583-7. doi: 10.1126/science.1254404.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Speech, Language and the Brain, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, UK. mshafto@csl.psychol.cam.ac.uk. ; Centre for Speech, Language and the Brain, Department of Psychology, University of Cambridge, Cambridge CB2 3EB, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25359966" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Age Factors ; Aging/*physiology ; Behavior/physiology ; Brain/*growth & development/physiology/ultrastructure ; Cognition/*physiology ; Cognition Disorders/*physiopathology/psychology ; Humans ; *Language ; Linguistics ; Nerve Net/*physiology ; Neuroimaging
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  • 36
    Publication Date: 1981-08-21
    Description: A new technique has been developed for identifying, in humans, dynamic spatiotemporal electrical patterns of the brain during purposive behaviors. In this method, single-trial time-series correlations between brain macropotentials recorded from different scalp sites are analyzed by distribution-independent mathematical pattern recognition. Dynamic patterns of correlation clearly distinguished two brief visuomotor tasks differing only in type of mental judgement required (spatial or numeric). These complex patterns shifted in the anterior-posterior and left-right axes between successive 175-millisecond intervals, indicating that many areas in both cerebral hemispheres were involved even in these simple judgements. These patterns were not obtainable by conventional analysis of averaged evoked potentials or by linear analysis of correlations, suggesting that the new technique will advance the study of human brain activity related to cognition and goal-directed behaviors.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gevins, A S -- Doyle, J C -- Cutillo, B A -- Schaffer, R E -- Tannehill, R S -- Ghannam, J H -- Gilcrease, V A -- Yeager, C L -- New York, N.Y. -- Science. 1981 Aug 21;213(4510):918-22.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256287" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Brain/*physiology ; *Cognition ; Electroencephalography ; *Evoked Potentials ; Female ; Humans ; Male ; Pattern Recognition, Visual/physiology
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  • 37
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-03-20
    Description: Gender identity depends largely on postnatal environmental influences, while sex-dimorphic behavior and temperamental sex differences appear to be modified by prenatal sex hormones. A role of the prenatal endocrine milieu in the development of erotic partner preference, as in hetero-, homo-, or bisexual orientation, or of cognitive sex differences has not been conclusively demonstrated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ehrhardt, A A -- Meyer-Bahlburg, H F -- New York, N.Y. -- Science. 1981 Mar 20;211(4488):1312-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209510" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adrenal Hyperplasia, Congenital/metabolism/psychology ; Adult ; Androgens/pharmacology ; Behavior/drug effects ; Child ; Cognition/drug effects ; Embryo, Mammalian/drug effects ; Estrogens/pharmacology ; Female ; *Gender Identity ; Gonadal Steroid Hormones/*pharmacology ; Humans ; *Identification (Psychology) ; Male ; Pregnancy ; Pregnancy Complications/drug therapy ; Progestins/pharmacology/therapeutic use ; Sexual Behavior/*drug effects
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  • 38
    Publication Date: 1981-09-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Goldberg, E -- Antin, S P -- Bilder, R M Jr -- Gerstman, L J -- Hughes, J E -- Mattis, S -- New York, N.Y. -- Science. 1981 Sep 18;213(4514):1392-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268442" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amnesia/etiology/*physiopathology ; Amnesia, Retrograde/physiopathology ; Humans ; Male ; Memory/*physiology ; Mesencephalon/injuries/*physiopathology ; Skull Fractures/complications
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  • 39
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-27
    Description: Ten patients with multiple sclerosis who were treated with human fibroblast interferon (IFN-B) for 6 months showed a significant reduction in their exacerbation rates compared with their rates before treatment (P 〈 .01). The IFN-B was administered intrathecally by serial lumbar punctures. There was no significant change in the exacerbation rates of ten multiple sclerosis control patients before and during the period of observation. The IFN-B recipients have now been on the study a mean of 1.5 years, the controls, 1.2 years. The clinical condition of five of the IFN-B recipients and one of the control patients has improved, whereas the condition of five of the controls and one of the IFN-B recipients has deteriorated (P 〈 .036). These findings warrant cautious optimism about the efficacy of intrathecal IFN-B in altering the course of multiple sclerosis and support concepts of a viral or dysimmune etiology of the disease.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jacobs, L -- O'Malley, J -- Freeman, A -- Ekes, R -- CA-18533/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Nov 27;214(4524):1026-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6171035" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Clinical Trials as Topic ; Female ; Fibroblasts ; Follow-Up Studies ; Humans ; Interferons/*therapeutic use ; Male ; Multiple Sclerosis/*drug therapy
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  • 40
    Publication Date: 1981-04-17
    Description: Sensory and cognitive functions were assessed in a right-handed male before and after partial and complete callosal commissurotomy. After the initial posterior section was made, there was no evidence of interhemispheric sensory transfer, although the left hemisphere did have access to stimulus-related semantic and episodic information from the right hemisphere. After the callosum was completely sectioned, this exchange was no longer observed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sidtis, J J -- Volpe, B T -- Holtzman, J D -- Wilson, D H -- Gazzaniga, M S -- 2 R01 NS15053-02/NS/NINDS NIH HHS/ -- RR001-02/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Apr 17;212(4492):344-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6782673" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Cognition/*physiology ; Cognition Disorders/*physiopathology ; Corpus Callosum/*physiology/surgery ; Epilepsy, Tonic-Clonic/surgery ; Humans ; Language Disorders/*physiopathology ; Male ; Methods ; Perception/physiology ; Perceptual Disorders/*physiopathology ; Postoperative Complications/physiopathology ; Sensation/*physiology
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  • 41
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-04-03
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wade, N -- New York, N.Y. -- Science. 1981 Apr 3;212(4490):24-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6259731" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; *DNA, Recombinant ; *Ethics Committees, Research ; *Ethics, Medical ; Federal Government ; Female ; *Genetic Engineering/history ; Genetic Vectors ; Globins/genetics ; Government Regulation ; History, 20th Century ; Humans ; Informed Consent ; Israel ; Plasmids ; Thalassemia/*therapy ; United States
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  • 42
    Publication Date: 1981-02-06
    Description: Arginine vasopressin and a number of its synthetic analogs augment memory functions in experimental animals. One of these analogs, 1-desamino-8-D-arginine vasopressin (DDAVP), influences human learning and memory. Cognitively unimpaired, as well as cognitively impaired adults, treated with DDAVP for a period of several days, learn information more effectively, as measured by the completeness, organization, and consistency (reliability) of recall. DDAVP also appears to reverse partially the retrograde amnesia that follows electroconvulsive treatment.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weingartner, H -- Gold, P -- Ballenger, J C -- Smallberg, S A -- Summers, R -- Rubinow, D R -- Post, R M -- Goodwin, F K -- New York, N.Y. -- Science. 1981 Feb 6;211(4482):601-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7455701" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Arginine Vasopressin/*pharmacology ; Cognition/drug effects ; Deamino Arginine Vasopressin/pharmacology ; Depression/physiopathology ; Female ; Humans ; Learning/*drug effects ; Male ; Memory/*drug effects ; Middle Aged
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  • 43
    Publication Date: 1981-05-08
    Description: The cumulative effects of a repetitive stress induced by anticipation of pain (noxious foot shock) were studied on the threshold of a nociceptive flexion reflex of the lower limb. The threshold of the nociceptive reflex progressively increased with the repetition of the stress. This effect was reversed by naloxone, which even produced hyperalgesia, since a rapid and significant decrease in this threshold, below the initial values, was noted. Tha data provide evidence for involvement of endogenous opioids in the phenomenon of stress-induced analgesia in normal man.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Willer, J C -- Dehen, H -- Cambier, J -- New York, N.Y. -- Science. 1981 May 8;212(4495):689-91.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6261330" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Female ; Humans ; Male ; Naloxone/pharmacology ; Pain/*physiopathology ; Receptors, Opioid/*physiology ; Reflex/drug effects ; Stress, Psychological/*physiopathology
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  • 44
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1981 Jun 19;212(4501):1416-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233233" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Female ; Foot/*anatomy & histology ; *Functional Laterality ; Humans ; Male ; Sex Factors
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  • 45
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Antelman, S M -- Rowland, N -- New York, N.Y. -- Science. 1981 Dec 4;214(4525):1149-51.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302588" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; Endorphins/*physiology ; Feeding Behavior/drug effects/*physiology ; Humans ; Naloxone/pharmacology ; Rats ; Rats, Inbred Strains ; Stress, Psychological/*physiopathology
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-08-07
    Description: Subjects observing differently scaled environments undergo systematic shifts in the experience of time. The experience of temporal duration is compressed relative to the clock in the same proportion as scale-model environments being observed are compressed relative to the full-sized environment. This research suggests that spatial scale may be a principal mediator in the experience of time.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉DeLong, A J -- RR-07088/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Aug 7;213(4508):681-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256273" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Environment ; Humans ; Time Perception/*physiology
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  • 47
    Publication Date: 1981-05-08
    Description: The 2-[18F]fluoro-2-deoxy-D-glucose technique was used to measure regional cerebral glucose utilization by human subjects during functional activation. Normal male volunteers subjected to one or more sensory stimuli (tactile, visual, or auditory) exhibited focal increases in glucose metabolism in response to the stimulus. Unilateral visual hemifield stimulation caused the contralateral striate cortex to become more metabolically active than the striate cortex ipsilateral to the stimulated hemifield. Similarly, stroking the fingers and hand of one arm with brush produced an increase in metabolism in the contralateral postcentral gyrus, compared with the homologous ipsilateral region. The auditory stimulus, which consisted of a monaurally presented factual story caused an increase in glucose metabolism in the auditory cortex in the hemisphere contralateral to the stimulated ear. These results demonstrate that the technique is capable of providing functional maps in vivo related to both body region and submodality of sensory information in the human brain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Greenberg, J H -- Reivich, M -- Alavi, A -- Hand, P -- Rosenquist, A -- Rintelmann, W -- Stein, A -- Tusa, R -- Dann, R -- Christman, D -- Fowler, J -- MacGregor, B -- Wolf, A -- NS 10939-08/NS/NINDS NIH HHS/ -- NS 14867-02/NS/NINDS NIH HHS/ -- NS 15380-04/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1981 May 8;212(4495):678-80.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6971492" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Auditory Perception/*physiology ; Brain/*metabolism ; *Deoxy Sugars ; *Deoxyglucose/analogs & derivatives/metabolism ; Fluorodeoxyglucose F18 ; Functional Laterality ; Humans ; Male ; Sensation/*physiology ; Tomography, Emission-Computed/*methods ; Visual Perception/*physiology
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1981 Jan 16;211(4479):257.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7444464" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Aerospace Medicine ; Altitude ; *Anemia, Sickle Cell ; Humans ; Jurisprudence ; Male ; *Military Medicine ; Risk ; *Sickle Cell Trait
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  • 49
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshal, E -- New York, N.Y. -- Science. 1981 May 29;212(4498):1008.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233195" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Cultural Characteristics ; *Culture ; Female ; Humans ; Laos/ethnology ; Male ; Middle Aged ; *Mortality ; Refugees/*psychology ; Stress, Physiological ; United States
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  • 50
    Publication Date: 1981-12-04
    Description: Leucine catabolism is regulated by either of the first two degradative steps: (reversible) transamination to the keto acid or subsequent decarboxylation. A method is described to measure rates of leucine transamination, reamination, and keto acid oxidation. The method is applied directly to humans by infusing the nonradioactive tracer, L-[15N,1-13C]leucine. Leucine transamination was found to be operating several times faster than the keto acid decarboxylation and to be of equal magnitude in adult human males under two different dietary conditions, postabsorptive and fed. These results indicate that decarboxylation, not transamination, is the rate-limiting step in normal human leucine metabolism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Matthews, D E -- Bier, D M -- Rennie, M J -- Edwards, R H -- Halliday, D -- Millward, D J -- Clugston, G A -- AM-25994/AM/NIADDK NIH HHS/ -- HD-10667/HD/NICHD NIH HHS/ -- RR-00954/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Dec 4;214(4525):1129-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302583" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Carbon Isotopes ; Humans ; Kinetics ; Leucine/*metabolism ; Male ; Models, Biological ; Nitrogen Isotopes ; Oxidation-Reduction
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  • 51
    Publication Date: 1981-06-19
    Description: Twenty-five chemical workers who manufactured polybrominated biphenyls (PBB's) were given objective tests of learning and memory. Although this group had high concentrations of PBB's in adipose tissue, mean scores on all memory tests were normal. The PBB concentration was not correlated with memory performance; the most contaminated workers showed no evidence of memory dysfunction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brown, G G -- Preisman, R C -- Anderson, M D -- Nixon, R K -- Isbister, J L -- Price, H A -- New York, N.Y. -- Science. 1981 Jun 19;212(4501):1413-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6262920" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Biphenyl Compounds/*adverse effects ; Humans ; Learning/*drug effects ; Memory/*drug effects ; Polybrominated Biphenyls/*adverse effects ; Psychological Tests
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 52
    Publication Date: 1981-01-30
    Description: The densities of the brains of 11 chronic alcoholics were compared with those of 11 age-matched normal control subjects. Densities were determined from the density numbers generated by computerized tomography at three levels of the brain-the highest level of the lateral ventricles and the next two higher levels-with adjustments made to control for possible artifacts in the data. The advantage of the dominant hemisphere over the nondominant hemisphere was lessened in alcoholics.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Golden, C J -- Graber, B -- Blose, I -- Berg, R -- Coffman, J -- Bloch, S -- New York, N.Y. -- Science. 1981 Jan 30;211(4481):508-10.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7455693" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Alcoholism/*pathology ; Brain/*pathology ; Functional Laterality ; Humans ; Tomography, X-Ray Computed
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 53
    Publication Date: 1981-02-27
    Description: The concentration of norepinephrine in cerebrospinal fluid from patients with essential hypertension is higher than that from healthy normal volunteers, but the concentrations of norepinephrine in plasma from these groups are similar. This finding indicates that central nervous system noradrenergic hyperactivity occurs in essential hypertension but apparently is not reflected in abnormal function of the peripheral sympathetic nervous system in these patients.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lake, C R -- Gullner, H G -- Polinsky, R J -- Ebert, M H -- Ziegler, M G -- Bartter, F C -- New York, N.Y. -- Science. 1981 Feb 27;211(4485):955-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466370" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Blood Pressure ; Female ; Humans ; Hypertension/blood/*cerebrospinal fluid ; Middle Aged ; Norepinephrine/blood/*cerebrospinal fluid ; Posture
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  • 54
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-12-11
    Description: Sleep recordings were carried out on athletes on four successive nights after completing a 92-kilometer road race. Significant increases in total sleep time and slow-wave sleep were found after this metabolic stress. The results show a definite exercise effect on sleep and support sleep-restoration hypotheses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Shapiro, C M -- Bortz, R -- Mitchell, D -- Bartel, P -- Jooste, P -- New York, N.Y. -- Science. 1981 Dec 11;214(4526):1253-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302594" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Humans ; *Physical Exertion ; Running ; Sleep Stages/*physiology ; Sleep, REM/physiology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 55
    Publication Date: 1981-08-14
    Description: Sixteen former military personnel who were present at the "Smoky" atmospheric nuclear weapon test have been investigated for internal deposits of radioactivity. Whole-body and thorax gamma-ray measurements, thorax and skeletal actinide measurements, and urinalyses for plutonium-239 and strontium-90 indicated no evidence of radioactivity in excess of that found in the general population.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Toohey, R E -- Rundo, J -- Essling, M A -- Sha, J Y -- Oldham, R D -- Sedlet, J -- Robinson, J J -- New York, N.Y. -- Science. 1981 Aug 14;213(4509):767-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256278" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Humans ; Middle Aged ; *Military Medicine ; Plutonium/urine ; *Radiation Monitoring ; Strontium Radioisotopes/urine ; United States
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  • 56
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-03-06
    Description: Auditory brainstem potentials were recorded from abstinent chronic alcoholics and control subjects. The latencies of peaks II, III, IV, and V were significantly delayed in the alcoholic patients compared to control subjects. Brainstem transmission time was longer in alcoholics than in controls. This study provides systematic evidence that chronic alcohol abuse results in brainstem deficits suggesting possible demyelination of auditory tracts.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Begleiter, H -- Porjesz, B -- Chou, C L -- AA 02686/AA/NIAAA NIH HHS/ -- New York, N.Y. -- Science. 1981 Mar 6;211(4486):1064-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466379" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Alcoholism/*physiopathology ; Auditory Perception/*physiology ; Brain Stem/*physiopathology ; Evoked Potentials ; Humans ; Male ; Membrane Potentials
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  • 57
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-04-17
    Description: Event-related potentials following silently named object pictures were recorded directly from the exposed left hemisphere of the human cortex at sites whose relation to naming was subsequently established by electrical stimulation mapping. Two simultaneous potential changes are specific to sites where stimulation disrupts naming: slow potentials as premotor sites and focal desynchronization at posterior sites surrounding the Sylvian fissure. These anatomically specific changes are also specific to the task--present with silent naming and absent in a spatial task with the same visual input. Overt speech is also preceded by slow potentials with earliest onset at premotor sites.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Fried, I -- Ojemann, G A -- Fetz, E E -- NS 04053/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1981 Apr 17;212(4492):353-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209537" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Cerebral Cortex/*physiology ; Electric Stimulation ; Evoked Potentials ; Female ; Frontal Lobe/physiology ; Humans ; Language/*physiology ; Male ; Middle Aged
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  • 58
    Publication Date: 1981-05-08
    Description: A tritium-labeled probe that detects measles virus nucleotide sequences was hybridized in situ to cells infected with measles virus and to sections of brain tissue from patients with subacute sclerosing panencephalitis and from patients with multiple sclerosis. The measles virus genome was detected in many cells in subacute sclerosing panencephalitis where this virus would have been missed by methods such as immunofluorescence. Measles virus sequences were also found in two foci in one of four cases of multiple sclerosis. This refined method of hybridization in situ, which can be useful in the search for covert virus infections of man, provides evidence that viruses may be involved in multiple sclerosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Haase, A T -- Ventura, P -- Gibbs, C J Jr -- Tourtellotte, W W -- New York, N.Y. -- Science. 1981 May 8;212(4495):672-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7221554" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Brain/microbiology ; Child ; Child, Preschool ; Female ; Humans ; Male ; Measles virus/*genetics ; Middle Aged ; Multiple Sclerosis/*microbiology ; Nucleic Acid Hybridization ; RNA, Viral/genetics ; Subacute Sclerosing Panencephalitis/*microbiology
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  • 59
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G B -- New York, N.Y. -- Science. 1981 Nov 13;214(4522):774-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7027443" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; Clinical Trials as Topic ; Humans ; Middle Aged ; Myocardial Infarction/drug therapy/*prevention & control ; Propranolol/adverse effects/*therapeutic use
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  • 60
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-04-03
    Description: The binding of monoclonal antibody specific for colon carcinoma was inhibited by serum from patients with adenocarcinoma of the colon but not by serum from patients with other bowel diseases or from healthy volunteers. Of other malignancies studied, serum from two patients with gastric carcinoma and two patients with pancreatic carcinoma also inhibited the specific binding of monoclonal antibody. The levels of carcinoembryonic antigen in these serum samples were not correlated with their levels of binding inhibition. Such monoclonal antibodies may prove useful for the detection of colorectal carcinoma.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koprowski, H -- Herlyn, M -- Steplewski, Z -- Sears, H F -- CA-21124/CA/NCI NIH HHS/ -- RR-05540/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Apr 3;212(4490):53-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6163212" target="_blank"〉PubMed〈/a〉
    Keywords: Adenocarcinoma/*immunology ; Adult ; Aged ; Antibodies, Neoplasm/immunology ; Antibody Specificity ; Antigens, Neoplasm/*analysis ; Binding, Competitive ; Carcinoembryonic Antigen/analysis ; Cells, Cultured ; Colonic Neoplasms/*immunology ; Epitopes ; Female ; Humans ; Intestinal Diseases/immunology ; Male ; Middle Aged ; Neoplasms/immunology
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  • 61
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-08-07
    Description: Circadian rhythms of ionized calcium and phosphate concentrations have been demonstrated in human blood. A computer-derived model curve representing the 24-hour fluctuations in ionized calcium cannot be correlated consistently with curves for total calcium or phosphate. Knowledge of these circadian rhythms provides a physiological basis for further understanding the interactions between blood minerals and calcium-regulating hormones.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Markowitz, M -- Rotkin, L -- Rosen, J F -- ES-01060-06/ES/NIEHS NIH HHS/ -- RR-53/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Aug 7;213(4508):672-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256269" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Calcium/*blood ; *Circadian Rhythm ; Humans ; Male ; Phosphates/*blood
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  • 62
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-04-17
    Description: The auditory brainstem response varies in a circadian rhythm that is negatively correlated with the circadian rhythm in oral temperature. The auditory brainstem responses and oral temperature were recorded every 3 hours from three healthy male subjects during a 2-day period. The data indicate that a reduction of 1 degree C in oral temperature is associated with an increase of 200 microseconds in the latency of wave V of the auditory brainstem response, and of 160 microseconds in the interval between waves I and V.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, N K -- Donchin, E -- New York, N.Y. -- Science. 1981 Apr 17;212(4492):356-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209538" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; *Body Temperature ; Brain Stem/*physiology ; *Circadian Rhythm ; Evoked Potentials, Auditory ; Humans ; Male ; Time Factors
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  • 63
    Publication Date: 1981-03-27
    Description: These studies demonstrated increasing glucose metabolic rates in the human primary (PVC) and associative (AVC) visual cortex as the complexity of visual scenes increased. The metabolic response of the AVC increased more rapidly with scene complexity than that of the PVC, indicating the greater involvement of the higher order AVC for complex visual interpretations. Increases in local metabolic activity by as much as a factor of 2 above that of control subjects with eyes closed indicate the wide range and metabolic reserve of the visual cortex.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Phelps, M E -- Kuhl, D E -- Mazziota, J C -- P0-NS 156540-01/NS/NINDS NIH HHS/ -- R0I-GM-24839-01/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1981 Mar 27;211(4489):1445-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6970412" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Deoxy Sugars/*metabolism ; Deoxyglucose/analogs & derivatives/*metabolism ; Fluorodeoxyglucose F18 ; Humans ; Photic Stimulation ; Tomography, Emission-Computed ; Visual Cortex/*metabolism/physiology/radionuclide imaging
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  • 64
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-24
    Description: Neuropsychological variables and urine cannabinoid metabolites were evaluated in ten subjects born, raised, and educated in the United States and having histories of heavy or prolonged use of cannabis. No impairment of cognitive function was found. Cannabinoid metabolites in excess of 50 nanograms per milliliter were present in the ten urine samples. The tetrahydrocannabinol content of cannabis exceeded 8.0%.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schaeffer, J -- Andrysiak, T -- Ungerleider, J T -- New York, N.Y. -- Science. 1981 Jul 24;213(4506):465-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6972600" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Cannabinoids/*pharmacology/urine ; Cognition/*drug effects ; Female ; Humans ; Male ; Marijuana Abuse/*psychology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 65
    Publication Date: 1981-03-06
    Description: Eight chronic schizophrenia patients completed a research program consisting of ten weekly sessions of active hemodialysis and ten weekly sessions of sham dialysis in a double-blind design. Previous reports of therapeutic efficacy were not substantiated. None of the patients improved during active dialysis; four patients worsened.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schulz, S C -- van Kammen, D P -- Balow, J E -- Flye, M W -- Bunney, W E Jr -- New York, N.Y. -- Science. 1981 Mar 6;211(4486):1066-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466380" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Double-Blind Method ; Female ; Humans ; Male ; *Renal Dialysis ; Schizophrenia/*therapy ; Sex Factors
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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