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  • 1
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    Syntactic analysis of seismic wave forms using augmental transition network grammars waveforms grammars (1982)
    In:  Geoexploration, Luxembourg, EGS-Gauthier-Villars, vol. 20, no. 6b, pp. 161-182, pp. 1310
    Details
    Publication Date: 1982
    Keywords: Waves ; Filter- ; Detectors
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    BIBLIOGRAPHY SEISMOLOGY
  • 2
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    Automatic analysis of microearthquake network data (1978)
    In:  Geoexploration, Luxembourg, EGS-Gauthier-Villars, vol. 16, no. 6b, pp. 159-175, pp. 1310
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    Publication Date: 1978
    Keywords: Detectors
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    BIBLIOGRAPHY SEISMOLOGY
  • 3
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    Glitch noise recognition using augmented transition network grammars (1981)
    MIT Lincoln Lab.
    In:  Semiannual Technical Summary Report, Lexington, Mass., MIT Lincoln Lab., vol. 11, no. 7-75, pp. 19-21
    Details
    Publication Date: 1981
    Keywords: Artificial intelligence (AI) ; Pattern recognition ; Detectors ; AUD
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    BIBLIOGRAPHY SEISMOLOGY
  • 4
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    Automatic processing of local earthquake data (1978)
    MIT
    In:  Ph.D. Thesis, Cambridge MA, MIT, vol. 11, no. 7-75, pp. 45, 46
    Details
    Publication Date: 1978
    Keywords: Seismic networks ; Detectors
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    BIBLIOGRAPHY SEISMOLOGY
  • 5
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    Dynamic waveform matching (1983)
    In:  Third International Symposium on Computer-aided Seismic Analysis and Discrimination, Lexington, Mass., MIT Lincoln Lab., vol. 11, no. 7-75, pp. 27-30
    Details
    Publication Date: 1983
    Keywords: Detectors ; Synthetic seismograms
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    BIBLIOGRAPHY SEISMOLOGY
  • 6
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    AIDS in a new millennium (2000)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 2000-08-06
    Description: As we enter the new millennium the world is still facing the challenge of responding to the AIDS pandemic. A new report from the Joint United Nations Programme on HIV/AIDS presents the latest statistics on prevalence, spread, and impact of the disease. In their Perspective, Schwartlander and his colleagues discuss the newly released statistics and the strategies needed to combat the further spread of HIV/AIDS and to reduce prevalence in the most severely affected countries.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schwartlander, B -- Garnett, G -- Walker, N -- Anderson, R -- New York, N.Y. -- Science. 2000 Jul 7;289(5476):64-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉UNAIDS, 20 Avenue Appia, Geneva 27 CH-1211, Switzerland. schwartlanderb@unaids.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10928930" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/drug therapy/*epidemiology/prevention & ; control/transmission ; Anti-HIV Agents/therapeutic use ; *Disease Outbreaks ; Female ; *Global Health ; HIV Infections/drug therapy/*epidemiology/prevention & control/transmission ; Health Policy ; Humans ; Infectious Disease Transmission, Vertical ; Male ; Population Dynamics ; Prevalence ; Risk-Taking ; Sexual Behavior ; United Nations
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 7
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    Chaos, persistence, and evolution of strain structure in antigenically diverse infectious agents (1998)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1998-05-23
    Description: The effects of selection by host immune responses on transmission dynamics was analyzed in a broad class of antigenically diverse pathogens. Strong selection can cause pathogen populations to stably segregate into discrete strains with nonoverlapping antigenic repertoires. However, over a wide range of intermediate levels of selection, strain structure is unstable, varying in a manner that is either cyclical or chaotic. These results have implications for the interpretation of longitudinal epidemiological data on strain or serotype abundance, design of surveillance strategies, and the assessment of multivalent vaccine trials.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gupta, S -- Ferguson, N -- Anderson, R -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 1998 May 8;280(5365):912-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Trust Centre for the Epidemiology of Infectious Disease, Zoology Department, University of Oxford, South Parks Road, Oxford OX1 3PS, UK. sunetra.gupta@zoology.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/9572737" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Antibody Formation ; *Antigenic Variation ; Antigens, Bacterial/immunology ; Antigens, Protozoan/immunology ; Antigens, Viral/immunology ; Bacteria/classification/genetics/*immunology/pathogenicity ; Cross Reactions ; Eukaryota/classification/genetics/*immunology/pathogenicity ; Humans ; Immunity ; Infection/epidemiology/*immunology/microbiology/parasitology/transmission ; Mathematics ; Models, Biological ; Nonlinear Dynamics ; Serotyping ; Viruses/classification/genetics/*immunology/pathogenicity
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 8
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    A DOC2 protein identified by mutational profiling is essential for apicomplexan parasite exocytosis (2012)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 2012-01-17
    Description: Exocytosis is essential to the lytic cycle of apicomplexan parasites and required for the pathogenesis of toxoplasmosis and malaria. DOC2 proteins recruit the membrane fusion machinery required for exocytosis in a Ca(2+)-dependent fashion. Here, the phenotype of a Toxoplasma gondii conditional mutant impaired in host cell invasion and egress was pinpointed to a defect in secretion of the micronemes, an apicomplexan-specific organelle that contains adhesion proteins. Whole-genome sequencing identified the etiological point mutation in TgDOC2.1. A conditional allele of the orthologous gene engineered into Plasmodium falciparum was also defective in microneme secretion. However, the major effect was on invasion, suggesting that microneme secretion is dispensable for Plasmodium egress.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354045/" 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/PMC3354045/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Farrell, Andrew -- Thirugnanam, Sivasakthivel -- Lorestani, Alexander -- Dvorin, Jeffrey D -- Eidell, Keith P -- Ferguson, David J P -- Anderson-White, Brooke R -- Duraisingh, Manoj T -- Marth, Gabor T -- Gubbels, Marc-Jan -- AI057919/AI/NIAID NIH HHS/ -- AI081220/AI/NIAID NIH HHS/ -- AI087874/AI/NIAID NIH HHS/ -- AI088314/AI/NIAID NIH HHS/ -- HG004719/HG/NHGRI NIH HHS/ -- K08 AI087874/AI/NIAID NIH HHS/ -- K08 AI087874-02/AI/NIAID NIH HHS/ -- R01 AI057919/AI/NIAID NIH HHS/ -- R01 HG004719/HG/NHGRI NIH HHS/ -- R21 AI081220/AI/NIAID NIH HHS/ -- R21 AI088314/AI/NIAID NIH HHS/ -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2012 Jan 13;335(6065):218-21. doi: 10.1126/science.1210829.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Boston College, Chestnut Hill, MA 02467, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22246776" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Calcium/*metabolism ; Calcium-Binding Proteins/chemistry/genetics/*metabolism ; Cell Line ; *Exocytosis ; Genes, Protozoan ; Genetic Complementation Test ; Genome, Protozoan ; Humans ; Models, Molecular ; Molecular Sequence Data ; Movement ; Mutagenesis ; Organelles/*metabolism ; Plasmodium falciparum/genetics/growth & development/physiology ; Point Mutation ; Protein Structure, Tertiary ; Protozoan Proteins/chemistry/genetics/*metabolism ; Recombinant Fusion Proteins/metabolism ; Toxoplasma/genetics/growth & development/*physiology/ultrastructure
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 9
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    Microcephalin, a gene regulating brain size, continues to evolve adaptively in humans (2005)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 2005-09-10
    Description: The gene Microcephalin (MCPH1) regulates brain size and has evolved under strong positive selection in the human evolutionary lineage. We show that one genetic variant of Microcephalin in modern humans, which arose approximately 37,000 years ago, increased in frequency too rapidly to be compatible with neutral drift. This indicates that it has spread under strong positive selection, although the exact nature of the selection is unknown. The finding that an important brain gene has continued to evolve adaptively in anatomically modern humans suggests the ongoing evolutionary plasticity of the human brain. It also makes Microcephalin an attractive candidate locus for studying the genetics of human variation in brain-related phenotypes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Evans, Patrick D -- Gilbert, Sandra L -- Mekel-Bobrov, Nitzan -- Vallender, Eric J -- Anderson, Jeffrey R -- Vaez-Azizi, Leila M -- Tishkoff, Sarah A -- Hudson, Richard R -- Lahn, Bruce T -- New York, N.Y. -- Science. 2005 Sep 9;309(5741):1717-20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16151009" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Biological ; African Continental Ancestry Group/genetics ; Alleles ; Amino Acid Substitution ; Asian Continental Ancestry Group/genetics ; *Biological Evolution ; Brain/*anatomy & histology/physiology ; European Continental Ancestry Group/genetics ; Exons ; Gene Conversion ; Gene Frequency ; Genetic Variation ; Genotype ; Haplotypes ; Humans ; Linkage Disequilibrium ; Microcephaly/genetics ; Nerve Tissue Proteins/*genetics ; Organ Size ; Polymorphism, Genetic ; Recombination, Genetic ; *Selection, Genetic ; Sequence Analysis, DNA ; Time
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 10
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    Legionella effectors that promote nonlytic release from protozoa (2004)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 2004-02-28
    Description: Legionella pneumophila, the bacterial agent of legionnaires' disease, replicates intracellularly within a specialized vacuole of mammalian and protozoan host cells. Little is known about the specialized vacuole except that the Icm/Dot type IV secretion system is essential for its formation and maintenance. The Legionella genome database contains two open reading frames encoding polypeptides (LepA and LepB) with predicted coiled-coil regions and weak homology to SNAREs; these are delivered to host cells by an Icm/Dot-dependent mechanism. Analysis of mutant strains suggests that the Lep proteins may enable the Legionella to commandeer a protozoan exocytic pathway for dissemination of the pathogen.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, John -- de Felipe, Karim Suwwan -- Clarke, Margaret -- Lu, Hao -- Anderson, O Roger -- Segal, Gil -- Shuman, Howard A -- NIH-R01 AI23549/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2004 Feb 27;303(5662):1358-61.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology, College of Physicians and Surgeons, Columbia University, 701 West 168th Street, New York, NY 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/14988561" target="_blank"〉PubMed〈/a〉
    Keywords: Acanthamoeba/*microbiology/physiology/ultrastructure ; Animals ; Bacterial Proteins/genetics/metabolism/*physiology ; Cell Line ; Colony Count, Microbial ; Cyclic AMP/metabolism ; Dictyostelium/*microbiology/physiology/ultrastructure ; Exocytosis ; Genome, Bacterial ; Humans ; Legionella pneumophila/*genetics/growth & development/pathogenicity/*physiology ; Lysosomes/physiology ; Macrophages/microbiology/ultrastructure ; Mutation ; Open Reading Frames ; Phagosomes/physiology ; Recombinant Fusion Proteins/metabolism ; Vacuoles/microbiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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