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  • Male  (166)
  • American Association for the Advancement of Science (AAAS)  (166)
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  • American Association for the Advancement of Science (AAAS)  (166)
  • American Physical Society
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  • 2005-2009  (166)
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  • 101
    Publication Date: 2006-01-28
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Greg -- New York, N.Y. -- Science. 2006 Jan 27;311(5760):462-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16439639" target="_blank"〉PubMed〈/a〉
    Keywords: China/epidemiology ; Depression/epidemiology ; Depressive Disorder/*epidemiology ; Developing Countries ; Female ; Humans ; Male ; *Medicine, Chinese Traditional ; Mental Disorders/diagnosis/*epidemiology ; Stress, Psychological ; Suicide/psychology/statistics & numerical data
    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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  • 102
    Publication Date: 2006-06-03
    Description: Dominant mutations in superoxide dismutase cause amyotrophic lateral sclerosis (ALS), a progressive paralytic disease characterized by loss of motor neurons. With the use of mice carrying a deletable mutant gene, expression within motor neurons was shown to be a primary determinant of disease onset and of an early phase of disease progression. Diminishing the mutant levels in microglia had little effect on the early disease phase but sharply slowed later disease progression. Onset and progression thus represent distinct disease phases defined by mutant action within different cell types to generate non-cell-autonomous killing of motor neurons; these findings validate therapies, including cell replacement, targeted to the non-neuronal cells.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Boillee, Severine -- Yamanaka, Koji -- Lobsiger, Christian S -- Copeland, Neal G -- Jenkins, Nancy A -- Kassiotis, George -- Kollias, George -- Cleveland, Don W -- MC_U117581330/Medical Research Council/United Kingdom -- NS 27036/NS/NINDS NIH HHS/ -- R37 NS027036/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2006 Jun 2;312(5778):1389-92.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ludwig Institute for Cancer Research and Departments of Medicine and Neuroscience, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16741123" target="_blank"〉PubMed〈/a〉
    Keywords: Amyotrophic Lateral Sclerosis/*enzymology/genetics/pathology/physiopathology ; Animals ; Antigens, CD11b/genetics ; Disease Progression ; Female ; Humans ; Integrases/genetics ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Microglia/*metabolism ; Motor Neurons/*metabolism ; Mutation ; Superoxide Dismutase/genetics/*metabolism
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  • 103
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stewart, Jeffrey -- New York, N.Y. -- Science. 2006 May 5;312(5774):689-97; author reply 689-97.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16680824" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Choice Behavior ; Female ; *Game Theory ; Male ; Reproduction ; *Sexual Behavior, Animal ; *Social Behavior
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  • 104
    Publication Date: 2006-10-28
    Description: We characterized Apis mellifera in both native and introduced ranges using 1136 single-nucleotide polymorphisms genotyped in 341 individuals. Our results indicate that A. mellifera originated in Africa and expanded into Eurasia at least twice, resulting in populations in eastern and western Europe that are geographically close but genetically distant. A third expansion in the New World has involved the near-replacement of previously introduced "European" honey bees by descendants of more recently introduced A. m. scutellata ("African" or "killer" bees). Our analyses of spatial transects and temporal series in the New World revealed differential replacement of alleles derived from eastern versus western Europe, with admixture evident in all individuals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Whitfield, Charles W -- Behura, Susanta K -- Berlocher, Stewart H -- Clark, Andrew G -- Johnston, J Spencer -- Sheppard, Walter S -- Smith, Deborah R -- Suarez, Andrew V -- Weaver, Daniel -- Tsutsui, Neil D -- New York, N.Y. -- Science. 2006 Oct 27;314(5799):642-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Entomology, University of Illinois at Urbana-Champaign, 505 South Goodwin Avenue, IL 61801, USA. charlie@life.uiuc.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17068261" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Alleles ; Animal Migration ; Animals ; Asia ; Bees/classification/*genetics ; Biological Evolution ; Europe ; Female ; Genetics, Population ; Genotype ; Hybridization, Genetic ; Linkage Disequilibrium ; Male ; North America ; Phylogeny ; *Polymorphism, Single Nucleotide ; Population Dynamics ; Selection, Genetic ; Software ; South America ; Time
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  • 105
    Publication Date: 2006-04-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2006 Apr 21;312(5772):346.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16627702" target="_blank"〉PubMed〈/a〉
    Keywords: Humans ; Informed Consent ; Jurisprudence ; Male ; Missouri ; Ownership/*legislation & jurisprudence ; *Prostate ; Tissue Banks/*legislation & jurisprudence ; Universities/*legislation & jurisprudence
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  • 106
    Publication Date: 2006-09-02
    Description: Through the adoptive transfer of lymphocytes after host immunodepletion, it is possible to mediate objective cancer regression in human patients with metastatic melanoma. However, the generation of tumor-specific T cells in this mode of immunotherapy is often limiting. Here we report the ability to specifically confer tumor recognition by autologous lymphocytes from peripheral blood by using a retrovirus that encodes a T cell receptor. Adoptive transfer of these transduced cells in 15 patients resulted in durable engraftment at levels exceeding 10% of peripheral blood lymphocytes for at least 2 months after the infusion. We observed high sustained levels of circulating, engineered cells at 1 year after infusion in two patients who both demonstrated objective regression of metastatic melanoma lesions. This study suggests the therapeutic potential of genetically engineered cells for the biologic therapy of cancer.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2267026/" 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/PMC2267026/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Morgan, Richard A -- Dudley, Mark E -- Wunderlich, John R -- Hughes, Marybeth S -- Yang, James C -- Sherry, Richard M -- Royal, Richard E -- Topalian, Suzanne L -- Kammula, Udai S -- Restifo, Nicholas P -- Zheng, Zhili -- Nahvi, Azam -- de Vries, Christiaan R -- Rogers-Freezer, Linda J -- Mavroukakis, Sharon A -- Rosenberg, Steven A -- Z01 BC010763-01/Intramural NIH HHS/ -- Z01 SC003811-32/Intramural NIH HHS/ -- Z99 CA999999/Intramural NIH HHS/ -- New York, N.Y. -- Science. 2006 Oct 6;314(5796):126-9. Epub 2006 Aug 31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Surgery Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16946036" target="_blank"〉PubMed〈/a〉
    Keywords: *Adoptive Transfer ; Adult ; Antigens, Neoplasm/*immunology ; CD8-Positive T-Lymphocytes/*immunology ; Cancer Vaccines/therapeutic use ; Cells, Cultured ; Electroporation ; Female ; Genetic Engineering ; *Genetic Therapy ; HLA-A Antigens/immunology ; HLA-A2 Antigen ; Humans ; Interleukin-2/immunology/therapeutic use ; MART-1 Antigen ; Male ; Melanoma/immunology/secondary/*therapy ; Middle Aged ; Neoplasm Proteins/*immunology ; Receptors, Antigen, T-Cell, alpha-beta/*genetics/*immunology ; Transduction, Genetic ; Transgenes
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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2006 Jul 14;313(5784):158.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16840670" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Size ; Bone and Bones/*anatomy & histology ; Canada ; *Dinosaurs/anatomy & histology/growth & development ; Female ; *Fossils ; Longevity ; Male ; Mortality ; Paleontology
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  • 108
    Publication Date: 2006-05-20
    Description: Western scrub-jays (Aphelocoma californica) hide food caches for future consumption, steal others' caches, and engage in tactics to minimize the chance that their own caches will be stolen. We show that scrub-jays remember which individual watched them during particular caching events and alter their recaching behavior accordingly. We found no evidence to suggest that a storer's use of cache protection tactics is cued by the observer's behavior.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dally, Joanna M -- Emery, Nathan J -- Clayton, Nicola S -- New York, N.Y. -- Science. 2006 Jun 16;312(5780):1662-5. Epub 2006 May 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sub-department of Animal Behavior, University of Cambridge, Cambridge, CB3 8AA, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16709747" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Behavior, Animal ; Cues ; Female ; *Food ; Male ; *Memory ; Passeriformes/*physiology
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  • 109
    Publication Date: 2006-04-29
    Description: We surveyed an Anopheles gambiae population in a West African malaria transmission zone for naturally occurring genetic loci that control mosquito infection with the human malaria parasite, Plasmodium falciparum. The strongest Plasmodium resistance loci cluster in a small region of chromosome 2L and each locus explains at least 89% of parasite-free mosquitoes in independent pedigrees. Together, the clustered loci form a genomic Plasmodium-resistance island that explains most of the genetic variation for malaria parasite infection of mosquitoes in nature. Among the candidate genes in this chromosome region, RNA interference knockdown assays confirm a role in Plasmodium resistance for Anopheles Plasmodium-responsive leucine-rich repeat 1 (APL1), encoding a leucine-rich repeat protein that is similar to molecules involved in natural pathogen resistance mechanisms in plants and mammals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Riehle, Michelle M -- Markianos, Kyriacos -- Niare, Oumou -- Xu, Jiannong -- Li, Jun -- Toure, Abdoulaye M -- Podiougou, Belco -- Oduol, Frederick -- Diawara, Sory -- Diallo, Mouctar -- Coulibaly, Boubacar -- Ouatara, Ahmed -- Kruglyak, Leonid -- Traore, Sekou F -- Vernick, Kenneth D -- New York, N.Y. -- Science. 2006 Apr 28;312(5773):577-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Microbial and Plant Genomics and Department of Microbiology, University of Minnesota, St. Paul, MN 55108, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16645095" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Anopheles gambiae/*genetics/immunology/*parasitology ; Chromosome Mapping ; Female ; *Genes, Insect ; Genetic Linkage ; Genetic Variation ; Genome, Insect ; Humans ; Immunity, Innate/genetics ; Insect Proteins/*genetics/physiology ; Insect Vectors/genetics/*parasitology ; Malaria, Falciparum/parasitology ; Male ; Mali ; Oligonucleotide Array Sequence Analysis ; Pedigree ; Phenotype ; Plasmodium berghei/immunology/pathogenicity ; Plasmodium falciparum/immunology/*pathogenicity ; RNA Interference
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  • 110
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-01
    Description: Young people in their teens constitute the largest age group in the world, in a special stage recognized across the globe as the link in the life cycle between childhood and adulthood. Longitudinal studies in both developed and developing countries and better measurements of adolescent behavior are producing new insights. The physical and psychosocial changes that occur during puberty make manifest generational and early-childhood risks to development, in the form of individual differences in aspects such as growth, educational attainment, self-esteem, peer influences, and closeness to family. They also anticipate threats to adult health and well-being. Multidisciplinary approaches, especially links between the biological and the social sciences, as well as studies of socioeconomic and cultural diversity and determinants of positive outcomes, are needed to advance knowledge about this stage of development.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866186/" 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/PMC1866186/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Richter, Linda M -- 068599/Wellcome Trust/United Kingdom -- 077210/Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2006 Jun 30;312(5782):1902-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Child, Youth, Family, and Social Development, Human Sciences Research Council, Private Bag X07, Dalbridge 4014, South Africa. lrichter@hsrc.ac.za〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809526" target="_blank"〉PubMed〈/a〉
    Keywords: *Adolescent ; *Adolescent Behavior ; *Adolescent Development ; Child ; Child, Preschool ; Data Collection ; Early Intervention (Education) ; Family ; Female ; Humans ; Infant ; Infant, Newborn ; Life Style ; Longitudinal Studies ; Male ; Nutritional Physiological Phenomena ; Poverty ; Puberty ; Risk-Taking ; Sexual Behavior ; Smoking ; South Africa ; Violence
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  • 111
    Publication Date: 2006-04-15
    Description: Gamete recognition proteins can evolve at astonishing rates and lie at the heart of reproductive isolation and speciation in diverse taxa. However, the source of selection driving this evolution remains unknown. We report on how the sperm bindin genotype influences reproductive success under natural conditions. An interaction between genotype frequency and spawning density determines how sperm bindin genotype influences reproductive success. Common genotypes are selected under sperm-limited conditions, whereas rare genotypes are selected under conditions of intense sperm competition and sexual conflict. Variation in the evolutionary rates of bindin may reflect historic differences in sperm availability.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Levitan, Don R -- Ferrell, David L -- New York, N.Y. -- Science. 2006 Apr 14;312(5771):267-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Science, Florida State University, Tallahassee, Florida 32306-1100, USA. levitan@bio.fsu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16614223" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; *Evolution, Molecular ; Female ; Genotype ; Glycoproteins/*genetics/metabolism ; Male ; Ovum/physiology ; Polymorphism, Genetic ; Receptors, Cell Surface ; Reproduction ; *Selection, Genetic ; Sex Characteristics ; Species Specificity ; Spermatozoa/*physiology ; Strongylocentrotus/*genetics/*physiology
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  • 112
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Day, Troy -- Houle, David -- Rowe, Locke -- New York, N.Y. -- Science. 2006 May 5;312(5774):689-97; author reply 689-97.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16680819" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cooperative Behavior ; Female ; *Game Theory ; Male ; *Sexual Behavior, Animal ; *Social Behavior
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  • 113
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-15
    Description: Competitor species can have evolutionary effects on each other that result in ecological character displacement; that is, divergence in resource-exploiting traits such as jaws and beaks. Nevertheless, the process of character displacement occurring in nature, from the initial encounter of competitors to the evolutionary change in one or more of them, has not previously been investigated. Here we report that a Darwin's finch species (Geospiza fortis) on an undisturbed Galapagos island diverged in beak size from a competitor species (G. magnirostris) 22 years after the competitor's arrival, when they jointly and severely depleted the food supply. The observed evolutionary response to natural selection was the strongest recorded in 33 years of study, and close to the value predicted from the high heritability of beak size. These findings support the role of competition in models of community assembly, speciation, and adaptive radiations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Grant, Peter R -- Grant, B Rosemary -- New York, N.Y. -- Science. 2006 Jul 14;313(5784):224-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544-1003, USA. prgrant@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16840700" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Beak/*anatomy & histology ; *Biological Evolution ; Biomass ; Body Size ; Competitive Behavior ; Disasters ; Ecosystem ; Ecuador ; Feeding Behavior ; Female ; *Finches/anatomy & histology/physiology ; *Food ; Male ; Organ Size ; Population Density ; Population Dynamics ; *Seeds ; *Selection, Genetic ; Time Factors
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-12-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stone, Richard -- New York, N.Y. -- Science. 2006 Dec 1;314(5804):1380-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17138879" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Animals, Wild ; Breeding ; Cloning, Organism ; *Conservation of Natural Resources ; Ecosystem ; Female ; Male ; Population Dynamics ; *Ruminants/genetics ; Vietnam
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  • 115
    Publication Date: 2006-08-05
    Description: Human choices are remarkably susceptible to the manner in which options are presented. This so-called "framing effect" represents a striking violation of standard economic accounts of human rationality, although its underlying neurobiology is not understood. We found that the framing effect was specifically associated with amygdala activity, suggesting a key role for an emotional system in mediating decision biases. Moreover, across individuals, orbital and medial prefrontal cortex activity predicted a reduced susceptibility to the framing effect. This finding highlights the importance of incorporating emotional processes within models of human choice and suggests how the brain may modulate the effect of these biasing influences to approximate rationality.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2631940/" 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/PMC2631940/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉De Martino, Benedetto -- Kumaran, Dharshan -- Seymour, Ben -- Dolan, Raymond J -- 078865/Wellcome Trust/United Kingdom -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2006 Aug 4;313(5787):684-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Wellcome Department of Imaging Neuroscience, Institute of Neurology, University College London, 12 Queen Square, London WC1 3AR, UK. b.martino@fil.ion.ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16888142" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Amygdala/*physiology ; Brain Mapping ; *Choice Behavior ; Cognition ; *Emotions ; Female ; Gambling ; Games, Experimental ; Humans ; Magnetic Resonance Imaging ; Male ; Models, Psychological ; Prefrontal Cortex/*physiology
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  • 116
    Publication Date: 2006-01-21
    Description: Does geometry constitute a core set of intuitions present in all humans, regardless of their language or schooling? We used two nonverbal tests to probe the conceptual primitives of geometry in the Munduruku, an isolated Amazonian indigene group. Munduruku children and adults spontaneously made use of basic geometric concepts such as points, lines, parallelism, or right angles to detect intruders in simple pictures, and they used distance, angle, and sense relationships in geometrical maps to locate hidden objects. Our results provide evidence for geometrical intuitions in the absence of schooling, experience with graphic symbols or maps, or a rich language of geometrical terms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dehaene, Stanislas -- Izard, Veronique -- Pica, Pierre -- Spelke, Elizabeth -- New York, N.Y. -- Science. 2006 Jan 20;311(5759):381-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉INSERM-CEA Cognitive Neuroimaging Unit, Service Hospitalier Frederic Joliot, Commissariat a l'Energie Atomique, 91401 Orsay Cedex, France. dehaene@shfj.cea.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16424341" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Aged, 80 and over ; Analysis of Variance ; Brazil ; Child ; Child, Preschool ; *Comprehension ; Culture ; Female ; Humans ; Indians, South American/*psychology ; *Knowledge ; Language ; Male ; Maps as Topic ; *Mathematics ; Middle Aged
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  • 117
    Publication Date: 2006-04-15
    Description: Gene transcription may be regulated by remote enhancer or insulator regions through chromosome looping. Using a modification of chromosome conformation capture (3C) and fluorescence in situ hybridization, we found that one allele of the insulin-like growth factor 2 (Igf2)/H19 imprinting control region (ICR) on chromosome 7 colocalized with one allele of Wsb1/Nf1 on chromosome 11. Omission of CCCTC-binding factor (CTCF) or deletion of the maternal ICR abrogated this association and altered Wsb1/Nf1 gene expression. These findings demonstrate that CTCF mediates an interchromosomal association, perhaps by directing distant DNA segments to a common transcription factory, and the data provide a model for long-range allele-specific associations between gene regions on different chromosomes that suggest a framework for DNA recombination and RNA trans-splicing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ling, Jian Qun -- Li, Tao -- Hu, Ji Fan -- Vu, Thanh H -- Chen, Hui Ling -- Qiu, Xin Wen -- Cherry, Athena M -- Hoffman, Andrew R -- DK036054/DK/NIDDK NIH HHS/ -- DK065283/DK/NIDDK NIH HHS/ -- HD047013/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2006 Apr 14;312(5771):269-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Medical Service, Department of Veterans Affairs, Palo Alto Health Care System, and Department of Medicine, Stanford University, Palo Alto, CA 94304, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16614224" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Binding Sites ; Chromatin Immunoprecipitation ; Chromosomes, Mammalian/*genetics/metabolism ; DNA-Binding Proteins/*metabolism ; Epistasis, Genetic ; Female ; *Gene Expression Regulation ; Genomic Imprinting ; In Situ Hybridization, Fluorescence ; Insulin-Like Growth Factor II/genetics ; Male ; Mice ; Neurofibromin 1/genetics ; RNA, Long Noncoding ; RNA, Untranslated/genetics ; Regulatory Elements, Transcriptional ; Repressor Proteins/*metabolism ; Transcription, Genetic ; Ubiquitin-Protein Ligases/genetics
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  • 118
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-09-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lillard, Angeline -- Else-Quest, Nicole -- R01 HD036808/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2006 Sep 29;313(5795):1893-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Virginia P.O. Box 400400, Charlottesville, VA 22904, USA. lillard@virginia.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17008512" target="_blank"〉PubMed〈/a〉
    Keywords: *Achievement ; Child ; Child, Preschool ; *Cognition ; Education/*methods ; Female ; Humans ; Male ; *Social Behavior ; Teaching/*methods
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  • 119
    Publication Date: 2006-01-21
    Description: Mammalian X inactivation turns off one female X chromosome to enact dosage compensation between XX and XY individuals. X inactivation is known to be regulated in cis by Xite, Tsix, and Xist, but in principle the two Xs must also be regulated in trans to ensure mutually exclusive silencing. Here, we demonstrate that interchromosomal pairing mediates this communication. Pairing occurs transiently at the onset of X inactivation and is specific to the X-inactivation center. Deleting Xite and Tsix perturbs pairing and counting/choice, whereas their autosomal insertion induces de novo X-autosome pairing. Ectopic X-autosome interactions inhibit endogenous X-X pairing and block the initiation of X-chromosome inactivation. Thus, Tsix and Xite function both in cis and in trans. We propose that Tsix and Xite regulate counting and mutually exclusive choice through X-X pairing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xu, Na -- Tsai, Chia-Lun -- Lee, Jeannie T -- New York, N.Y. -- Science. 2006 Feb 24;311(5764):1149-52. Epub 2006 Jan 19.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Molecular Biology, Massachusetts General Hospital, Department of Genetics, Harvard Medical School Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16424298" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cell Line ; *Chromosome Pairing ; Female ; In Situ Hybridization, Fluorescence ; Male ; Mice ; Mice, Transgenic ; Models, Genetic ; Mutation ; RNA, Long Noncoding ; RNA, Untranslated/genetics/metabolism ; Regulatory Elements, Transcriptional ; Stem Cells ; Transgenes ; X Chromosome/genetics/*physiology ; *X Chromosome Inactivation
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  • 120
    Publication Date: 2006-12-23
    Description: Many species express endogenous cycles in physiology and behavior that allow anticipation of the seasons. The anatomical and cellular bases of these circannual rhythms have not been defined. Here, we provide strong evidence using an in vivo Soay sheep model that the circannual regulation of prolactin secretion, and its associated biology, derive from a pituitary-based timing mechanism. Circannual rhythm generation is seen as the product of the interaction between melatonin-regulated timer cells and adjacent prolactin-secreting cells, which together function as an intrapituitary "pacemaker-slave" timer system. These new insights open the way for a molecular analysis of long-term timing mechanisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lincoln, Gerald A -- Clarke, Iain J -- Hut, Roelof A -- Hazlerigg, David G -- G0600678/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2006 Dec 22;314(5807):1941-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Centre for Reproductive Biology, University of Edinburgh, Queen's Medical Research Institute, Edinburgh, Scotland. g.lincoln@hrsu.mrc.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17185605" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Clocks/*physiology ; Circadian Rhythm ; Cues ; Denervation ; Lactotrophs/physiology ; Male ; Melatonin/blood/*physiology ; Models, Biological ; Motor Activity ; Photoperiod ; Pineal Gland/innervation/physiology ; Pituitary Gland, Anterior/*physiology/secretion ; Prolactin/*secretion ; Seasons ; Sheep/blood/*physiology
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  • 121
    Publication Date: 2006-01-28
    Description: Cardio-facio-cutaneous (CFC) syndrome is a sporadic developmental disorder involving characteristic craniofacial features, cardiac defects, ectodermal abnormalities, and developmental delay. We demonstrate that heterogeneous de novo missense mutations in three genes within the mitogen-activated protein kinase (MAPK) pathway cause CFC syndrome. The majority of cases (18 out of 23) are caused by mutations in BRAF, a gene frequently mutated in cancer. Of the 11 mutations identified, two result in amino acid substitutions that occur in tumors, but most are unique and suggest previously unknown mechanisms of B-Raf activation. Furthermore, three of five individuals without BRAF mutations had missense mutations in either MEK1 or MEK2, downstream effectors of B-Raf. Our findings highlight the involvement of the MAPK pathway in human development and will provide a molecular diagnosis of CFC syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rodriguez-Viciana, Pablo -- Tetsu, Osamu -- Tidyman, William E -- Estep, Anne L -- Conger, Brenda A -- Cruz, Molly Santa -- McCormick, Frank -- Rauen, Katherine A -- HD048502/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2006 Mar 3;311(5765):1287-90. Epub 2006 Jan 26.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Comprehensive Cancer Center and Cancer Research Institute, University of California, San Francisco, CA 94115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16439621" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Multiple/*genetics ; Adolescent ; Adult ; Amino Acid Substitution ; Child ; Child, Preschool ; Craniofacial Abnormalities/genetics ; Extracellular Signal-Regulated MAP Kinases/metabolism ; Female ; *Germ-Line Mutation ; Growth Disorders/genetics ; Heart Defects, Congenital/genetics ; Humans ; Infant ; MAP Kinase Kinase 1/genetics ; MAP Kinase Kinase 2/genetics ; MAP Kinase Kinase Kinases/metabolism ; MAP Kinase Signaling System ; Male ; Mitogen-Activated Protein Kinases/genetics/*metabolism ; Mutation, Missense ; Phosphorylation ; Proto-Oncogene Proteins B-raf/genetics ; Skin Abnormalities/genetics ; Syndrome ; Transfection
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  • 122
    Publication Date: 2006-03-25
    Description: A cure for type 1 diabetes will probably require the provision or elicitation of new pancreatic islet beta cells as well as the reestablishment of immunological tolerance. A 2003 study reported achievement of both advances in the NOD mouse model by coupling injection of Freund's complete adjuvant with infusion of allogeneic spleen cells. It was concluded that the adjuvant eliminated anti-islet autoimmunity and the donor splenocytes differentiated into insulin-producing (presumably beta) cells, culminating in islet regeneration. Here, we provide data indicating that the recovered islets were all of host origin, reflecting that the diabetic NOD mice actually retain substantial beta cell mass, which can be rejuvenated/regenerated to reverse disease upon adjuvant-dependent dampening of autoimmunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nishio, Junko -- Gaglia, Jason L -- Turvey, Stuart E -- Campbell, Christopher -- Benoist, Christophe -- Mathis, Diane -- T32 CA09382/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2006 Mar 24;311(5768):1775-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Section on Immunology and Immunogenetics, Joslin Diabetes Center, and Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, and Harvard Stem Cell Institute, 1 Joslin Place, Boston, MA 02215, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16556845" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antibodies/immunology ; Autoimmunity ; Blood Glucose/analysis ; Cell Differentiation ; *Cell Transplantation ; Combined Modality Therapy ; Diabetes Mellitus, Type 1/immunology/pathology/*therapy ; Female ; Freund's Adjuvant/*therapeutic use ; Insulin-Secreting Cells/*cytology ; Islets of Langerhans/*cytology/pathology ; *Islets of Langerhans Transplantation ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Inbred NOD ; Polymorphism, Single Nucleotide ; Regeneration ; Spleen/*cytology/immunology
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  • 123
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-02-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ronald, Angelica -- Happe, Francesca -- Plomin, Robert -- New York, N.Y. -- Science. 2006 Feb 17;311(5763):952; author reply 952.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16484478" target="_blank"〉PubMed〈/a〉
    Keywords: Autistic Disorder/*genetics/psychology ; Behavior ; Female ; Humans ; Male ; Sex Characteristics ; Social Behavior
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  • 124
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-05-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Buss, David M -- New York, N.Y. -- Science. 2006 May 5;312(5774):689-97; author reply 689-97.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16680818" target="_blank"〉PubMed〈/a〉
    Keywords: Biological Evolution ; Female ; Humans ; Male ; Sex Characteristics ; *Sexual Behavior
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  • 125
    Publication Date: 2006-10-21
    Description: Age-related macular degeneration (AMD) is the most common cause of irreversible vision loss in the developed world and has a strong genetic predisposition. A locus at human chromosome 10q26 affects the risk of AMD, but the precise gene(s) have not been identified. We genotyped 581 AMD cases and 309 normal controls in a Caucasian cohort in Utah. We demonstrate that a single-nucleotide polymorphism, rs11200638, in the promoter region of HTRA1 is the most likely causal variant for AMD at 10q26 and is estimated to confer a population attributable risk of 49.3%. The HTRA1 gene encodes a secreted serine protease. Preliminary analysis of lymphocytes and retinal pigment epithelium from four AMD patients revealed that the risk allele was associated with elevated expression levels of HTRA1 mRNA and protein. We also found that drusen in the eyes of AMD patients were strongly immunolabeled with HTRA1 antibody. Together, these findings support a key role for HTRA1 in AMD susceptibility and identify a potential new pathway for AMD pathogenesis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yang, Zhenglin -- Camp, Nicola J -- Sun, Hui -- Tong, Zongzhong -- Gibbs, Daniel -- Cameron, D Joshua -- Chen, Haoyu -- Zhao, Yu -- Pearson, Erik -- Li, Xi -- Chien, Jeremy -- Dewan, Andrew -- Harmon, Jennifer -- Bernstein, Paul S -- Shridhar, Viji -- Zabriskie, Norman A -- Hoh, Josephine -- Howes, Kimberly -- Zhang, Kang -- CA98364/CA/NCI NIH HHS/ -- GCRC M01-RR00064/RR/NCRR NIH HHS/ -- P30EY014800/EY/NEI NIH HHS/ -- R01EY14428/EY/NEI NIH HHS/ -- R01EY14448/EY/NEI NIH HHS/ -- R01EY15771/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 2006 Nov 10;314(5801):992-3. Epub 2006 Oct 19.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17053109" target="_blank"〉PubMed〈/a〉
    Keywords: Aged ; Aging ; Alleles ; Case-Control Studies ; Chromosomes, Human, Pair 10/genetics ; Cohort Studies ; European Continental Ancestry Group/genetics ; Female ; *Genetic Predisposition to Disease ; Genotype ; Homozygote ; Humans ; Lymphocytes/enzymology ; Macular Degeneration/*genetics ; Male ; Middle Aged ; Pigment Epithelium of Eye/enzymology ; *Polymorphism, Single Nucleotide ; *Promoter Regions, Genetic ; RNA, Messenger/genetics/metabolism ; Retinal Drusen/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Serine Endopeptidases/analysis/*genetics/metabolism
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  • 126
    Publication Date: 2006-09-09
    Description: Paland and Lynch (Reports, 17 February 2006, p. 990) showed that in Daphnia pulex, the ratio of amino acid replacement to silent substitution in mitochondrial genes is higher in asexual lineages than in sexual lineages. If this base-composition bias is maintained by selection, it too should alter following transitions in reproductive mode. Analysis reveals no such change in the genomes of D. pulex.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Butlin, Roger -- New York, N.Y. -- Science. 2006 Sep 8;313(5792):1389; author reply 1389.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield S10 2TN, UK. r.k.butlin@sheffield.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16959991" target="_blank"〉PubMed〈/a〉
    Keywords: *Amino Acid Substitution ; Animals ; Base Composition ; DNA, Mitochondrial/*genetics ; Daphnia/*genetics/*physiology ; Female ; Genes, Mitochondrial ; Male ; Mutation ; *Reproduction, Asexual ; *Selection, Genetic
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  • 127
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-02-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nielsen, Rasmus -- New York, N.Y. -- Science. 2006 Feb 17;311(5763):960-1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Bioinformatics and Department of Biology, University of Copenhagen, Universitetsparken 15, 2100 Kbh O Denmark. rasmus@binf.ku.dk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16484481" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Daphnia/*genetics/*physiology ; Female ; Male ; Mutation ; Parthenogenesis ; *Recombination, Genetic ; *Selection, Genetic ; *Sex
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  • 128
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-03-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rubinoff, Daniel -- Haines, William P -- New York, N.Y. -- Science. 2006 Mar 10;311(5766):1377.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16527952" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Genitalia, Male/anatomy & histology ; Male ; Moths/*anatomy & histology/classification
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  • 129
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-09-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hagan, John -- Palloni, Alberto -- New York, N.Y. -- Science. 2006 Sep 15;313(5793):1578-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Sociology, Northwestern University, Evanston, IL 60208, and with the American Bar Foundation, Chicago, IL 60611, USA. j-hagan@northwestern.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16973863" target="_blank"〉PubMed〈/a〉
    Keywords: Data Collection ; Family ; Female ; Humans ; Male ; *Mortality ; Refugees ; Sudan ; Violence ; *Warfare
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  • 130
    Publication Date: 2006-09-02
    Description: Complex human social interaction is disrupted when the frontal lobe is damaged in disease, and in extreme cases patients are described as having acquired sociopathy. We compared, in macaques, the effects of lesions in subdivisions of the anterior cingulate and the orbitofrontal cortices believed to be anatomically homologous to those damaged in such patients. We show that the anterior cingulate gyrus in male macaques is critical for normal patterns of social interest in other individual male or female macaques. Conversely, the orbitofrontal cortex lesion had a marked effect only on responses to mildly fear-inducing stimuli. These results suggest that damage to the anterior cingulate gyrus may be the cause of changes in social interaction seen after frontal lobe damage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rudebeck, P H -- Buckley, M J -- Walton, M E -- Rushworth, M F S -- G0300665/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2006 Sep 1;313(5791):1310-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Experimental Psychology, University of Oxford, Oxford, OX1 3UD, UK. peter.rudebeck@psy.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16946075" target="_blank"〉PubMed〈/a〉
    Keywords: Analysis of Variance ; Animals ; Fear ; Female ; Frontal Lobe/physiology/surgery ; Gyrus Cinguli/*physiology/surgery ; Macaca ; Male ; Reaction Time ; *Social Behavior ; *Social Perception
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  • 131
    Publication Date: 2006-02-04
    Description: A strong, global commitment to expanded prevention programs targeted at sexual transmission and transmission among injecting drug users, started now, could avert 28 million new HIV infections between 2005 and 2015. This figure is more than half of the new infections that might otherwise occur during that period in 125 low- and middle-income countries. Although preventing these new infections would require investing about U.S.$122 billion over this period, it would reduce future needs for treatment and care. Our analysis suggests that it will cost about U.S.$3900 to prevent each new infection, but that this will produce a savings of U.S.$4700 in forgone treatment and care costs. Thus, greater spending on prevention now would not only prevent more than half the new infections that would occur from 2005 to 2015 but would actually produce a net financial saving as future costs for treatment and care are averted.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stover, John -- Bertozzi, Stefano -- Gutierrez, Juan-Pablo -- Walker, Neff -- Stanecki, Karen A -- Greener, Robert -- Gouws, Eleanor -- Hankins, Catherine -- Garnett, Geoff P -- Salomon, Joshua A -- Boerma, J Ties -- De Lay, Paul -- Ghys, Peter D -- New York, N.Y. -- Science. 2006 Mar 10;311(5766):1474-6. Epub 2006 Feb 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Futures Group/Constella, Glastonbury, CT 06033, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16456039" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/economics/*prevention & control ; Adult ; Child ; Cost Savings ; Developing Countries/economics ; Female ; Global Health ; HIV Infections/economics/*prevention & control ; Health Care Costs ; Health Policy ; Humans ; *Income ; Male ; Pregnancy ; Pregnancy Complications, Infectious/economics/prevention & control ; Preventive Health Services/*economics ; United States
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  • 132
    Publication Date: 2006-08-05
    Description: We analyzed longitudinal data on academic careers and conducted interviews with faculty members to determine the scope and causes of the gender gap in patenting among life scientists. Our regressions on a random sample of 4227 life scientists over a 30-year period show that women faculty members patent at about 40% of the rate of men. We found that the gender gap has improved over time but remains large.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ding, Waverly W -- Murray, Fiona -- Stuart, Toby E -- New York, N.Y. -- Science. 2006 Aug 4;313(5787):665-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Haas School of Business, University of California, Berkeley, CA 94720, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16888138" target="_blank"〉PubMed〈/a〉
    Keywords: Authorship ; Bibliometrics ; *Biological Science Disciplines ; Career Mobility ; Consultants ; Faculty/*statistics & numerical data ; Female ; Humans ; Industry ; Interviews as Topic ; Longitudinal Studies ; Male ; Patents as Topic/*statistics & numerical data ; Publishing ; Regression Analysis ; Sex Factors ; United States ; Universities ; Women, Working/*statistics & numerical data
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  • 133
    Publication Date: 2006-05-13
    Description: The DKC1 gene encodes a pseudouridine synthase that modifies ribosomal RNA (rRNA). DKC1 is mutated in people with X-linked dyskeratosis congenita (X-DC), a disease characterized by bone marrow failure, skin abnormalities, and increased susceptibility to cancer. How alterations in ribosome modification might lead to cancer and other features of the disease remains unknown. Using an unbiased proteomics strategy, we discovered a specific defect in IRES (internal ribosome entry site)-dependent translation in Dkc1(m) mice and in cells from X-DC patients. This defect results in impaired translation of messenger RNAs containing IRES elements, including those encoding the tumor suppressor p27(Kip1) and the antiapoptotic factors Bcl-xL and XIAP (X-linked Inhibitor of Apoptosis Protein). Moreover, Dkc1(m) ribosomes were unable to direct translation from IRES elements present in viral messenger RNAs. These findings reveal a potential mechanism by which defective ribosome activity leads to disease and cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoon, Andrew -- Peng, Guang -- Brandenburger, Yves -- Zollo, Ornella -- Xu, Wei -- Rego, Eduardo -- Ruggero, Davide -- New York, N.Y. -- Science. 2006 May 12;312(5775):902-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Human Genetics Program, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16690864" target="_blank"〉PubMed〈/a〉
    Keywords: *5' Untranslated Regions ; Animals ; Cell Cycle Proteins/chemistry/*genetics/physiology ; Cell Line ; Cells, Cultured ; Cyclin-Dependent Kinase Inhibitor p27/biosynthesis/genetics ; Dyskeratosis Congenita/*genetics ; Humans ; Insect Viruses/genetics ; Lymphocytes/metabolism ; Male ; Mice ; Nuclear Proteins/chemistry/*genetics/physiology ; Oligonucleotide Array Sequence Analysis ; Point Mutation ; Polyribosomes/metabolism ; *Protein Biosynthesis ; Proteomics ; Pseudouridine/metabolism ; RNA Viruses/genetics ; RNA, Messenger/*genetics/metabolism ; RNA, Ribosomal/metabolism ; Transfection ; X-Linked Inhibitor of Apoptosis Protein/biosynthesis/genetics ; bcl-X Protein/biosynthesis/genetics
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 134
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-08-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2006 Aug 18;313(5789):899.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16917030" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Animals ; China/epidemiology ; Humans ; *Influenza A Virus, H5N1 Subtype ; Influenza in Birds/epidemiology/virology ; Influenza, Human/epidemiology/*virology ; Internationality ; Male ; Poultry ; World Health Organization
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  • 135
    Publication Date: 2006-08-19
    Description: In 1988, the National Vietnam Veterans Readjustment Study (NVVRS) of a representative sample of 1200 veterans estimated that 30.9% had developed posttraumatic stress disorder (PTSD) during their lifetimes and that 15.2% were currently suffering from PTSD. The study also found a strong dose-response relationship: As retrospective reports of combat exposure increased, PTSD occurrence increased. Skeptics have argued that these results are inflated by recall bias and other flaws. We used military records to construct a new exposure measure and to cross-check exposure reports in diagnoses of 260 NVVRS veterans. We found little evidence of falsification, an even stronger dose-response relationship, and psychological costs that were lower than previously estimated but still substantial. According to our fully adjusted PTSD rates, 18.7% of the veterans had developed war-related PTSD during their lifetimes and 9.1% were currently suffering from PTSD 11 to 12 years after the war; current PTSD was typically associated with moderate impairment.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1584215/" 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/PMC1584215/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dohrenwend, Bruce P -- Turner, J Blake -- Turse, Nicholas A -- Adams, Ben G -- Koenen, Karestan C -- Marshall, Randall -- 5T32MH13043/MH/NIMH NIH HHS/ -- K08 MH070627/MH/NIMH NIH HHS/ -- K08 MH070627-01/MH/NIMH NIH HHS/ -- R01-MH059309/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2006 Aug 18;313(5789):979-82.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉New York State Psychiatric Institute, New York, NY 10032, USA. dohrenw@pi.cpmc.columbia.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16917066" target="_blank"〉PubMed〈/a〉
    Keywords: Humans ; Male ; Military Personnel/*psychology/statistics & numerical data ; Records as Topic ; Risk Assessment ; Stress Disorders, Post-Traumatic/diagnosis/*epidemiology ; United States/epidemiology ; Veterans/*psychology/statistics & numerical data ; Veterans Disability Claims ; *Vietnam Conflict
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  • 136
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carthew, Richard W -- R01 GM068743/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2006 Jul 21;313(5785):305-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Molecular Biology, and Cell Biology, Northwestern University, Evanston, IL 60208, USA. r-carthew@northwestern.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16857925" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA, Complementary ; Drosophila/genetics ; Drosophila melanogaster/genetics/metabolism ; Female ; *Gene Expression Regulation ; *Genome ; Germ Cells/metabolism/physiology ; Male ; Mice ; RNA/chemistry/*genetics/isolation & purification/*metabolism ; *RNA Interference ; RNA, Antisense/chemistry/metabolism ; RNA, Untranslated/chemistry/genetics/*metabolism ; Rats ; Retroelements ; Ribonucleoproteins/chemistry/isolation & purification/metabolism ; Spermatids/metabolism ; Spermatogenesis ; Testis/chemistry/cytology ; Transcription, Genetic
    Print ISSN: 0036-8075
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  • 137
    Publication Date: 2006-11-25
    Description: Incoming sensory information is often ambiguous, and the brain has to make decisions during perception. "Predictive coding" proposes that the brain resolves perceptual ambiguity by anticipating the forthcoming sensory environment, generating a template against which to match observed sensory evidence. We observed a neural representation of predicted perception in the medial frontal cortex, while human subjects decided whether visual objects were faces or not. Moreover, perceptual decisions about faces were associated with an increase in top-down connectivity from the frontal cortex to face-sensitive visual areas, consistent with the matching of predicted and observed evidence for the presence of faces.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Summerfield, Christopher -- Egner, Tobias -- Greene, Matthew -- Koechlin, Etienne -- Mangels, Jennifer -- Hirsch, Joy -- R21066129/PHS HHS/ -- New York, N.Y. -- Science. 2006 Nov 24;314(5803):1311-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Columbia University, 1190 Amsterdam Avenue, New York, NY 10027, USA. summerfd@paradox.columbia.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17124325" target="_blank"〉PubMed〈/a〉
    Keywords: Amygdala/physiology ; Brain Mapping ; Discrimination (Psychology) ; Face ; Female ; *Form Perception ; Frontal Lobe/*physiology ; Humans ; Magnetic Resonance Imaging ; Male ; *Mental Processes ; Models, Neurological ; Nerve Net/physiology ; Neurons/physiology ; Occipital Lobe/physiology ; Parietal Lobe/physiology ; Temporal Lobe/physiology ; Visual Cortex/physiology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 138
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2006 Jun 30;312(5782):1855.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809494" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Child ; Cluster Analysis ; Disease Outbreaks/veterinary ; Family Health ; Female ; Humans ; Indonesia/epidemiology ; *Influenza A Virus, H5N1 Subtype/genetics ; Influenza in Birds/epidemiology ; Influenza, Human/epidemiology/*transmission/virology ; Male ; Poultry
    Print ISSN: 0036-8075
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  • 139
    Publication Date: 2006-09-16
    Description: Herpes simplex virus-1 (HSV-1) encephalitis (HSE) is the most common form of sporadic viral encephalitis in western countries. Its pathogenesis remains unclear, as it affects otherwise healthy patients and only a small minority of HSV-1-infected individuals. Here, we elucidate a genetic etiology for HSE in two children with autosomal recessive deficiency in the intracellular protein UNC-93B, resulting in impaired cellular interferon-alpha/beta and -lambda antiviral responses. HSE can result from a single-gene immunodeficiency that does not compromise immunity to most pathogens, unlike most known primary immunodeficiencies. Other severe infectious diseases may also reflect monogenic disorders of immunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Casrouge, Armanda -- Zhang, Shen-Ying -- Eidenschenk, Celine -- Jouanguy, Emmanuelle -- Puel, Anne -- Yang, Kun -- Alcais, Alexandre -- Picard, Capucine -- Mahfoufi, Nora -- Nicolas, Nathalie -- Lorenzo, Lazaro -- Plancoulaine, Sabine -- Senechal, Brigitte -- Geissmann, Frederic -- Tabeta, Koichi -- Hoebe, Kasper -- Du, Xin -- Miller, Richard L -- Heron, Benedicte -- Mignot, Cyril -- de Villemeur, Thierry Billette -- Lebon, Pierre -- Dulac, Olivier -- Rozenberg, Flore -- Beutler, Bruce -- Tardieu, Marc -- Abel, Laurent -- Casanova, Jean-Laurent -- G0900867/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2006 Oct 13;314(5797):308-12. Epub 2006 Sep 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire de Genetique Humaine des Maladies Infectieuses, Universite de Paris Rene Descartes, INSERM, U550, Faculte de Medecine Necker, Paris 75015, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16973841" target="_blank"〉PubMed〈/a〉
    Keywords: Child, Preschool ; Cytokines/biosynthesis ; Encephalitis, Herpes Simplex/*genetics/immunology ; Female ; *Genetic Predisposition to Disease ; *Herpesvirus 1, Human/immunology ; Humans ; Infant ; Interferon-alpha/biosynthesis/immunology ; Interferon-beta/biosynthesis/immunology ; Interferon-gamma/biosynthesis/immunology ; Interferons/*biosynthesis/immunology ; Leukocytes, Mononuclear/immunology ; Male ; Membrane Transport Proteins/*deficiency/genetics/*physiology ; Mutation ; Pedigree ; Signal Transduction ; Toll-Like Receptor 3/agonists/physiology ; Toll-Like Receptors/agonists/physiology
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  • 140
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2006 Jun 30;312(5782):1855-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809493" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; China/epidemiology ; Humans ; *Influenza A Virus, H5N1 Subtype ; Influenza, Human/epidemiology/*virology ; Information Dissemination ; International Cooperation ; Male ; *Publishing ; Retraction of Publication as Topic
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  • 141
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-10-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lutz, Wolfgang -- Kritzinger, Sylvia -- Skirbekk, Vegard -- New York, N.Y. -- Science. 2006 Oct 20;314(5798):425.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉World Population Program, International Institute for Applied Systems Analysis (IIASA), Laxenburg, A-2361, Austria. lutz@iiasa.ac.at〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17053133" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Aged ; Aging ; *Ethnic Groups ; Europe ; European Union ; Female ; Forecasting ; Humans ; Male ; Middle Aged ; Politics ; *Social Identification
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  • 142
    Publication Date: 2006-03-25
    Description: Type 1 diabetes mellitus results from the autoimmune destruction of the beta cells of the pancreatic islets of Langerhans and is recapitulated in the nonobese diabetic strain of mice. In an attempt to rescue islet loss, diabetic mice were made normoglycemic by islet transplantation and immunization with Freund's complete adjuvant along with multiple injections of allogeneic male splenocytes. This treatment allowed for survival of transplanted islets and recovery of endogenous beta cell function in a proportion of mice, but with no evidence for allogeneic splenocyte-derived differentiation of new islet beta cells. Control of the autoimmune disease at a crucial time in diabetogenesis can result in recovery of beta cell function.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Suri, Anish -- Calderon, Boris -- Esparza, Thomas J -- Frederick, Katherine -- Bittner, Patrice -- Unanue, Emil R -- New York, N.Y. -- Science. 2006 Mar 24;311(5768):1778-80.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA. anish@pathology.wustl.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16556846" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmunity ; Blood Glucose/analysis ; Cell Count ; *Cell Transplantation ; Combined Modality Therapy ; Diabetes Mellitus, Type 1/*immunology/pathology/*therapy ; Female ; Freund's Adjuvant/*therapeutic use ; Insulin-Secreting Cells/cytology/*physiology ; Islets of Langerhans/pathology ; *Islets of Langerhans Transplantation ; Lymphocyte Culture Test, Mixed ; Male ; Mice ; Mice, Inbred NOD ; Spleen/*cytology/*immunology ; T-Lymphocytes/immunology
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  • 143
    Publication Date: 2006-12-23
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hanauer, David I -- Jacobs-Sera, Deborah -- Pedulla, Marisa L -- Cresawn, Steven G -- Hendrix, Roger W -- Hatfull, Graham F -- GM51975/GM/NIGMS NIH HHS/ -- RR16455/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2006 Dec 22;314(5807):1880-1.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Graduate Program in Composition and TESOL, Department of English, Indiana University of Pennsylvania, Indiana, PA 15705, USA. hanauer@iup.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17185586" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Authorship ; *Bacteriophages/genetics/isolation & purification ; Biomedical Research/*education ; Female ; Genome, Viral ; Genomics/*education ; Humans ; Male ; Mentors ; Pennsylvania ; Science/*education ; Sequence Analysis, DNA ; *Teaching ; Universities
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  • 144
    Publication Date: 2006-03-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2006 Mar 3;311(5765):1235-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16513958" target="_blank"〉PubMed〈/a〉
    Keywords: *Career Mobility ; Child ; Child Day Care Centers ; Female ; Humans ; Japan ; Male ; Parental Leave ; *Research Personnel ; Research Support as Topic ; *Science ; *Women, Working
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  • 145
    Publication Date: 2006-12-16
    Description: Sequencing of 81 entire human mitochondrial DNAs (mtDNAs) belonging to haplogroups M1 and U6 reveals that these predominantly North African clades arose in southwestern Asia and moved together to Africa about 40,000 to 45,000 years ago. Their arrival temporally overlaps with the event(s) that led to the peopling of Europe by modern humans and was most likely the result of the same change in climate conditions that allowed humans to enter the Levant, opening the way to the colonization of both Europe and North Africa. Thus, the early Upper Palaeolithic population(s) carrying M1 and U6 did not return to Africa along the southern coastal route of the "out of Africa" exit, but from the Mediterranean area; and the North African Dabban and European Aurignacian industries derived from a common Levantine source.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Olivieri, Anna -- Achilli, Alessandro -- Pala, Maria -- Battaglia, Vincenza -- Fornarino, Simona -- Al-Zahery, Nadia -- Scozzari, Rosaria -- Cruciani, Fulvio -- Behar, Doron M -- Dugoujon, Jean-Michel -- Coudray, Clotilde -- Santachiara-Benerecetti, A Silvana -- Semino, Ornella -- Bandelt, Hans-Jurgen -- Torroni, Antonio -- New York, N.Y. -- Science. 2006 Dec 15;314(5806):1767-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dipartimento di Genetica e Microbiologia, Universita di Pavia, Via Ferrata 1, 27100 Pavia, Italy.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17170302" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Asia ; Chromosomes, Human, Y/genetics ; Climate ; DNA, Mitochondrial/*genetics ; *Emigration and Immigration ; Europe ; Female ; Genetic Variation ; Geography ; *Haplotypes ; Humans ; Male ; Mediterranean Region ; Molecular Sequence Data ; Phylogeny ; *Population Dynamics ; Sequence Analysis, DNA ; Time
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  • 146
    Publication Date: 2006-06-24
    Description: Recent behavioral experiments aimed at understanding the evolutionary foundations of human cooperation have suggested that a willingness to engage in costly punishment, even in one-shot situations, may be part of human psychology and a key element in understanding our sociality. However, because most experiments have been confined to students in industrialized societies, generalizations of these insights to the species have necessarily been tentative. Here, experimental results from 15 diverse populations show that (i) all populations demonstrate some willingness to administer costly punishment as unequal behavior increases, (ii) the magnitude of this punishment varies substantially across populations, and (iii) costly punishment positively covaries with altruistic behavior across populations. These findings are consistent with models of the gene-culture coevolution of human altruism and further sharpen what any theory of human cooperation needs to explain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Henrich, Joseph -- McElreath, Richard -- Barr, Abigail -- Ensminger, Jean -- Barrett, Clark -- Bolyanatz, Alexander -- Cardenas, Juan Camilo -- Gurven, Michael -- Gwako, Edwins -- Henrich, Natalie -- Lesorogol, Carolyn -- Marlowe, Frank -- Tracer, David -- Ziker, John -- New York, N.Y. -- Science. 2006 Jun 23;312(5781):1767-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anthropology, Emory University, 1557 Dickey Drive, Atlanta, GA 30322, USA. jhenric@emory.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16794075" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Age Factors ; *Altruism ; *Biological Evolution ; Cooperative Behavior ; Cross-Cultural Comparison ; *Cultural Evolution ; Educational Status ; Female ; Games, Experimental ; Humans ; Male ; Melanesia ; *Punishment ; Regression Analysis ; Sex Factors ; Siberia ; Social Behavior ; Socioeconomic Factors ; South America ; United States
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  • 147
    Publication Date: 2006-07-01
    Description: On the basis of analysis of ancient DNA from early European farmers, Haak et al. (Reports, 11 November 2005, p. 1016) argued for the Paleolithic ancestry of modern Europeans. We stress that the study is more limited in scope than the authors claim, in part because not all of the skeletal samples date to the time of the Neolithic transition in a given area of Europe.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ammerman, Albert J -- Pinhasi, Ron -- Banffy, Eszter -- New York, N.Y. -- Science. 2006 Jun 30;312(5782):1875; author reply 1875.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Classics, Colgate University, Hamilton, New York, USA. Aammerman@mail.colgate.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809513" target="_blank"〉PubMed〈/a〉
    Keywords: Agriculture/*history ; Culture ; DNA, Mitochondrial/*genetics/history ; Europe ; European Continental Ancestry Group/*genetics/history ; Female ; History, Ancient ; Humans ; Male ; Sample Size
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  • 148
    Publication Date: 2006-07-15
    Description: The size and age structures for four assemblages of North American tyrannosaurs-Albertosaurus, Tyrannosaurus, Gorgosaurus, and Daspletosaurus-reveal a pronounced, bootstrap-supported pattern of age-specific mortality characterized by relatively high juvenile survivorship and increased mortality at midlife and near the maximum life span. Such patterns are common today in wild populations of long-lived birds and mammals. Factors such as predation and entrance into the breeding population may have influenced tyrannosaur survivorship. This survivorship pattern can explain the rarity of juvenile specimens in museum collections.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Erickson, Gregory M -- Currie, Philip J -- Inouye, Brian D -- Winn, Alice A -- New York, N.Y. -- Science. 2006 Jul 14;313(5784):213-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Science, Florida State University, Tallahassee, FL 32306, USA. gerickson@bio.fsu.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16840697" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Size ; Bone Development ; Bone and Bones/*anatomy & histology ; Canada ; *Dinosaurs/anatomy & histology/growth & development/physiology ; Female ; Fibula/anatomy & histology ; *Fossils ; Life Tables ; Longevity ; Male ; Metatarsal Bones/anatomy & histology ; Mortality ; Paleontology ; Regression Analysis ; Reproduction
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  • 149
    Publication Date: 2006-02-14
    Description: The molecular mechanisms that maintain totipotency of the germline are not well understood. Here, we show that two conserved translational regulators, MEX-3 and GLD-1, are essential for maintaining totipotency in the Caenorhabditis elegans germline. In mex-3 gld-1 mutants, germ cells transdifferentiate into various somatic cell types such as muscles or neurons. Our findings implicate RNA regulation in the maintenance of totipotency, suggest that multiple mechanisms maintain totipotency at different stages of germline development, and establish a genetically tractable model for studying the development of teratomas.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ciosk, Rafal -- DePalma, Michael -- Priess, James R -- New York, N.Y. -- Science. 2006 Feb 10;311(5762):851-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. rafal.ciosk@fmi.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16469927" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caenorhabditis elegans/*cytology/genetics/physiology ; Caenorhabditis elegans Proteins/genetics/*metabolism ; Cell Differentiation ; Cytoplasmic Granules/ultrastructure ; Female ; Germ Cells/chemistry/*cytology/*physiology ; Male ; Meiosis ; Mitosis ; Muscle Cells/cytology ; Mutation ; Neurons/cytology ; Pachytene Stage ; RNA, Helminth/genetics/metabolism ; RNA, Messenger/genetics/metabolism ; RNA-Binding Proteins/genetics/*metabolism ; Teratoma
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  • 150
    Publication Date: 2006-10-21
    Description: Human memory is a polygenic trait. We performed a genome-wide screen to identify memory-related gene variants. A genomic locus encoding the brain protein KIBRA was significantly associated with memory performance in three independent, cognitively normal cohorts from Switzerland and the United States. Gene expression studies showed that KIBRA was expressed in memory-related brain structures. Functional magnetic resonance imaging detected KIBRA allele-dependent differences in hippocampal activations during memory retrieval. Evidence from these experiments suggests a role for KIBRA in human memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Papassotiropoulos, Andreas -- Stephan, Dietrich A -- Huentelman, Matthew J -- Hoerndli, Frederic J -- Craig, David W -- Pearson, John V -- Huynh, Kim-Dung -- Brunner, Fabienne -- Corneveaux, Jason -- Osborne, David -- Wollmer, M Axel -- Aerni, Amanda -- Coluccia, Daniel -- Hanggi, Jurgen -- Mondadori, Christian R A -- Buchmann, Andreas -- Reiman, Eric M -- Caselli, Richard J -- Henke, Katharina -- de Quervain, Dominique J-F -- P30AG19610/AG/NIA NIH HHS/ -- R01MH057899/MH/NIMH NIH HHS/ -- U01-HL086528-01/HL/NHLBI NIH HHS/ -- U24NS051872/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2006 Oct 20;314(5798):475-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Psychiatry Research, University of Zurich, Zurich 8057, Switzerland. papas@bli.unizh.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17053149" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Alleles ; Animals ; Attention ; Brain/*physiology ; Brain Chemistry ; Calcium-Binding Proteins/genetics ; Cohort Studies ; Female ; Gene Expression ; Genotype ; Haplotypes ; Hippocampus/chemistry/*physiology ; Humans ; Intracellular Signaling Peptides and Proteins ; Magnetic Resonance Imaging ; Male ; Membrane Proteins/genetics ; *Memory ; Mice ; Middle Aged ; Phosphoproteins ; *Polymorphism, Single Nucleotide ; Proteins/analysis/*genetics/*physiology ; Reverse Transcriptase Polymerase Chain Reaction ; Switzerland ; United States
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  • 151
    Publication Date: 2006-07-11
    Description: Natural populations of beach mice exhibit a characteristic color pattern, relative to their mainland conspecifics, driven by natural selection for crypsis. We identified a derived, charge-changing amino acid mutation in the melanocortin-1 receptor (Mc1r) in beach mice, which decreases receptor function. In genetic crosses, allelic variation at Mc1r explains 9.8% to 36.4% of the variation in seven pigmentation traits determining color pattern. The derived Mc1r allele is present in Florida's Gulf Coast beach mice but not in Atlantic coast mice with similar light coloration, suggesting that different molecular mechanisms are responsible for convergent phenotypic evolution. Here, we link a single mutation in the coding region of a pigmentation gene to adaptive quantitative variation in the wild.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hoekstra, Hopi E -- Hirschmann, Rachel J -- Bundey, Richard A -- Insel, Paul A -- Crossland, Janet P -- P40-RR14279/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2006 Jul 7;313(5783):101-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA. hoekstra@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16825572" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Biological ; Alleles ; Amino Acid Substitution ; Animals ; Cell Line ; Crosses, Genetic ; Cyclic AMP/metabolism ; Female ; Florida ; Gene Frequency ; Genotype ; Hair ; Hair Color/*genetics ; Humans ; Male ; Molecular Sequence Data ; *Mutation ; Peromyscus/*genetics ; Phenotype ; Pigmentation/*genetics ; Polymorphism, Single Nucleotide ; Principal Component Analysis ; Receptor, Melanocortin, Type 1/chemistry/*genetics/metabolism ; Sequence Analysis, DNA
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  • 152
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-04-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2006 Mar 31;311(5769):1850.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16574833" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Culture Techniques ; Cell Differentiation ; Ectoderm/cytology ; Endoderm/cytology ; Female ; Male ; Mesoderm/cytology ; Mice ; Multipotent Stem Cells/*cytology ; Pluripotent Stem Cells/cytology ; Spermatogonia/*cytology ; Stem Cell Transplantation ; Teratoma/pathology
    Print ISSN: 0036-8075
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  • 153
    Publication Date: 2006-09-02
    Description: Comparisons of recent with historical samples of chromosome inversion frequencies provide opportunities to determine whether genetic change is tracking climate change in natural populations. We determined the magnitude and direction of shifts over time (24 years between samples on average) in chromosome inversion frequencies and in ambient temperature for populations of the fly Drosophila subobscura on three continents. In 22 of 26 populations, climates warmed over the intervals, and genotypes characteristic of low latitudes (warm climates) increased in frequency in 21 of those 22 populations. Thus, genetic change in this fly is tracking climate warming and is doing so globally.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balanya, Joan -- Oller, Josep M -- Huey, Raymond B -- Gilchrist, George W -- Serra, Luis -- New York, N.Y. -- Science. 2006 Sep 22;313(5794):1773-5. Epub 2006 Aug 31.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetics, Faculty of Biology, University of Barcelona, Diagonal 645, Barcelona 08071, Spain. jbalanya@ub.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16946033" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Chromosome Inversion ; *Climate ; Drosophila/*genetics ; Europe ; Female ; Genome, Insect ; Geography ; Greenhouse Effect ; Male ; South America ; Temperature ; Time Factors ; United States
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  • 154
    Publication Date: 2006-11-25
    Description: Chong et al., Nishio et al., and Suri et al. (Reports, 24 March 2006, pp. 1774, 1775, and 1778) confirmed that treating nonobese diabetic (NOD) mice with an immune adjuvant and semisyngenic spleen cells can reverse the disease but found that spleen cells did not contribute to the observed recovery of pancreatic islets. We show that islet regeneration predominately originates from endogenous cells but that introduced spleen cells can also contribute to islet recovery.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Faustman, Denise L -- Tran, Simon D -- Kodama, Shohta -- Lodde, Beatrijs M -- Szalayova, Ildiko -- Key, Sharon -- Toth, Zsuzsanna E -- Mezey, Eva -- New York, N.Y. -- Science. 2006 Nov 24;314(5803):1243; author reply 1243.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Massachusetts General Hospital, Charlestown, MA 02129, USA. faustman@helix.mgh.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17124308" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Glucose/analysis ; Cell Differentiation ; *Cell Transplantation ; Combined Modality Therapy ; Diabetes Mellitus, Type 1/immunology/*therapy ; Female ; Freund's Adjuvant/*therapeutic use ; Insulin/secretion ; Insulin-Secreting Cells/*cytology/metabolism ; Islets of Langerhans/*cytology ; Islets of Langerhans Transplantation ; Male ; Mice ; Mice, Inbred NOD ; Regeneration ; Spleen/*cytology
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  • 155
    Publication Date: 2006-08-26
    Description: Analogous to learning and memory storage, long-term potentiation (LTP) is divided into induction and maintenance phases. Testing the hypothesis that the mechanism of LTP maintenance stores information requires reversing this mechanism in vivo and finding out whether long-term stored information is lost. This was not previously possible. Recently however, persistent phosphorylation by the atypical protein kinase C isoform, protein kinase Mzeta (PKMz), has been found to maintain late LTP in hippocampal slices. Here we show that a cell-permeable PKMz inhibitor, injected in the rat hippocampus, both reverses LTP maintenance in vivo and produces persistent loss of 1-day-old spatial information. Thus, the mechanism maintaining LTP sustains spatial memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pastalkova, Eva -- Serrano, Peter -- Pinkhasova, Deana -- Wallace, Emma -- Fenton, Andre Antonio -- Sacktor, Todd Charlton -- MH57068/MH/NIMH NIH HHS/ -- R01 MH53576/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2006 Aug 25;313(5790):1141-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Physiology, Pharmacology, and Neurology, Robert F. Furchgott Center for Neural and Behavioral Science, SUNY Downstate Medical Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16931766" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Avoidance Learning ; Conditioning (Psychology) ; Dentate Gyrus/drug effects/physiology ; Electric Stimulation ; Excitatory Postsynaptic Potentials/drug effects ; Heat-Shock Proteins/administration & dosage/pharmacology ; Hippocampus/drug effects/*physiology ; Long-Term Potentiation/drug effects/*physiology ; Male ; Memory/drug effects/*physiology ; Perforant Pathway ; Protein Kinase C/antagonists & inhibitors/metabolism ; Rats ; Rats, Long-Evans ; Staurosporine/pharmacology ; Time Factors
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  • 156
    Publication Date: 2006-06-17
    Description: Coordinated control of energy metabolism and glucose homeostasis requires communication between organs and tissues. We identified a neuronal pathway that participates in the cross talk between the liver and adipose tissue. By studying a mouse model, we showed that adenovirus-mediated expression of peroxisome proliferator-activated receptor (PPAR)-g2 in the liver induces acute hepatic steatosis while markedly decreasing peripheral adiposity. These changes were accompanied by increased energy expenditure and improved systemic insulin sensitivity. Hepatic vagotomy and selective afferent blockage of the hepatic vagus revealed that the effects on peripheral tissues involve the afferent vagal nerve. Furthermore, an antidiabetic thiazolidinedione, a PPARg agonist, enhanced this pathway. This neuronal pathway from the liver may function to protect against metabolic perturbation induced by excessive energy storage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Uno, Kenji -- Katagiri, Hideki -- Yamada, Tetsuya -- Ishigaki, Yasushi -- Ogihara, Takehide -- Imai, Junta -- Hasegawa, Yutaka -- Gao, Junhong -- Kaneko, Keizo -- Iwasaki, Hiroko -- Ishihara, Hisamitsu -- Sasano, Hironobu -- Inukai, Kouichi -- Mizuguchi, Hiroyuki -- Asano, Tomoichiro -- Shiota, Masakazu -- Nakazato, Masamitsu -- Oka, Yoshitomo -- New York, N.Y. -- Science. 2006 Jun 16;312(5780):1656-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Molecular Metabolism and Diabetes, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16778057" target="_blank"〉PubMed〈/a〉
    Keywords: Adipose Tissue/innervation/*metabolism ; Afferent Pathways/physiology ; Animals ; Blood Glucose/analysis ; Dietary Fats/administration & dosage ; Efferent Pathways/physiology ; *Energy Metabolism ; Fatty Liver/pathology ; Glucose/metabolism ; Glucose Tolerance Test ; Hypoglycemic Agents/pharmacology ; Insulin/blood/*physiology ; Insulin Resistance ; Lipolysis ; Liver/*innervation/*metabolism/pathology ; Male ; Mice ; Mice, Inbred C57BL ; Muscle, Skeletal/metabolism ; Oxygen Consumption ; PPAR gamma/genetics/metabolism ; Rats ; Rats, Sprague-Dawley ; Sympathetic Nervous System/physiology ; Vagotomy ; Vagus Nerve/*physiology ; Weight Gain
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  • 157
    Publication Date: 2006-07-01
    Description: In the Drosophila germline, repeat-associated small interfering RNAs (rasiRNAs) ensure genomic stability by silencing endogenous selfish genetic elements such as retrotransposons and repetitive sequences. Whereas small interfering RNAs (siRNAs) derive from both the sense and antisense strands of their double-stranded RNA precursors, rasiRNAs arise mainly from the antisense strand. rasiRNA production appears not to require Dicer-1, which makes microRNAs (miRNAs), or Dicer-2, which makes siRNAs, and rasiRNAs lack the 2',3' hydroxy termini characteristic of animal siRNA and miRNA. Unlike siRNAs and miRNAs, rasiRNAs function through the Piwi, rather than the Ago, Argonaute protein subfamily. Our data suggest that rasiRNAs protect the fly germline through a silencing mechanism distinct from both the miRNA and RNA interference pathways.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vagin, Vasily V -- Sigova, Alla -- Li, Chengjian -- Seitz, Herve -- Gvozdev, Vladimir -- Zamore, Phillip D -- GM62862/GM/NIGMS NIH HHS/ -- GM65236/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2006 Jul 21;313(5785):320-4. Epub 2006 Jun 29.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809489" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Argonaute Proteins ; Drosophila Proteins/genetics/metabolism ; Drosophila melanogaster/*genetics/metabolism ; Female ; Germ Cells/*physiology ; Male ; Mutation ; Oligonucleotide Array Sequence Analysis ; Ovary/cytology ; Peptide Initiation Factors/genetics/metabolism ; Periodic Acid/pharmacology ; Phosphates/analysis ; Proteins/genetics/metabolism ; *RNA Interference ; RNA, Antisense/chemistry/*genetics/metabolism ; RNA, Messenger/genetics/metabolism ; RNA, Small Interfering/chemistry/*genetics/metabolism ; RNA-Induced Silencing Complex ; Repetitive Sequences, Nucleic Acid ; Retroelements ; Terminal Repeat Sequences ; Testis/cytology
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  • 158
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-08-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McNally, Richard J -- New York, N.Y. -- Science. 2006 Aug 18;313(5789):923-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, Harvard University, Cambridge, MA 02138, USA. rjm@ wjh.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16917047" target="_blank"〉PubMed〈/a〉
    Keywords: Humans ; Male ; Military Personnel/*psychology/statistics & numerical data ; Prevalence ; Records as Topic ; Stress Disorders, Post-Traumatic/*epidemiology ; United States/epidemiology ; Veterans/*psychology/statistics & numerical data ; *Vietnam Conflict
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  • 159
    Publication Date: 2006-04-15
    Description: The molecular organization of presynaptic active zones during calcium influx-triggered neurotransmitter release is the focus of intense investigation. The Drosophila coiled-coil domain protein Bruchpilot (BRP) was observed in donut-shaped structures centered at active zones of neuromuscular synapses by using subdiffraction resolution STED (stimulated emission depletion) fluorescence microscopy. At brp mutant active zones, electron-dense projections (T-bars) were entirely lost, Ca2+ channels were reduced in density, evoked vesicle release was depressed, and short-term plasticity was altered. BRP-like proteins seem to establish proximity between Ca2+ channels and vesicles to allow efficient transmitter release and patterned synaptic plasticity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kittel, Robert J -- Wichmann, Carolin -- Rasse, Tobias M -- Fouquet, Wernher -- Schmidt, Manuela -- Schmid, Andreas -- Wagh, Dhananjay A -- Pawlu, Christian -- Kellner, Robert R -- Willig, Katrin I -- Hell, Stefan W -- Buchner, Erich -- Heckmann, Manfred -- Sigrist, Stephan J -- New York, N.Y. -- Science. 2006 May 19;312(5776):1051-4. Epub 2006 Apr 13.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉European Neuroscience Institute Gottingen, Grisebachstrasse 5, 37077 Gottingen, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16614170" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Calcium Channels/*metabolism ; Drosophila ; Drosophila Proteins/genetics/*physiology ; Female ; Larva ; Male ; Models, Neurological ; Mutation ; Nerve Tissue Proteins/metabolism/*physiology ; Presynaptic Terminals/metabolism ; Synapses/metabolism/*physiology/ultrastructure ; Synaptic Vesicles/*metabolism
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  • 160
    Publication Date: 2006-09-02
    Description: Two randomized field experiments tested a social-psychological intervention designed to improve minority student performance and increase our understanding of how psychological threat mediates performance in chronically evaluative real-world environments. We expected that the risk of confirming a negative stereotype aimed at one's group could undermine academic performance in minority students by elevating their level of psychological threat. We tested whether such psychological threat could be lessened by having students reaffirm their sense of personal adequacy or "self-integrity." The intervention, a brief in-class writing assignment, significantly improved the grades of African American students and reduced the racial achievement gap by 40%. These results suggest that the racial achievement gap, a major social concern in the United States, could be ameliorated by the use of timely and targeted social-psychological interventions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Geoffrey L -- Garcia, Julio -- Apfel, Nancy -- Master, Allison -- New York, N.Y. -- Science. 2006 Sep 1;313(5791):1307-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Colorado, Muenzinger Psychology Building, Boulder, CO 80309-0345, USA. cohen.geoff@gmail.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16946074" target="_blank"〉PubMed〈/a〉
    Keywords: *Achievement ; Adolescent ; African Americans/*psychology ; Double-Blind Method ; Educational Measurement ; *Educational Status ; Female ; Humans ; Male ; Minority Groups/*psychology ; *Psychology, Social ; *Self Concept ; *Social Perception ; Social Values ; Stereotyping ; Stress, Psychological ; United States
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  • 161
    Publication Date: 2006-08-19
    Description: Congenital myasthenic syndromes (CMSs) are a group of inherited disorders of neuromuscular transmission characterized by fatigable muscle weakness. One major subgroup of patients shows a characteristic "limb girdle" pattern of muscle weakness, in which the muscles have small, simplified neuromuscular junctions but normal acetylcholine receptor and acetylcholinesterase function. We showed that recessive inheritance of mutations in Dok-7, which result in a defective structure of the neuromuscular junction, is a cause of CMS with proximal muscle weakness.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Beeson, David -- Higuchi, Osamu -- Palace, Jackie -- Cossins, Judy -- Spearman, Hayley -- Maxwell, Susan -- Newsom-Davis, John -- Burke, Georgina -- Fawcett, Peter -- Motomura, Masakatsu -- Muller, Juliane S -- Lochmuller, Hanns -- Slater, Clarke -- Vincent, Angela -- Yamanashi, Yuji -- G117/490/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2006 Sep 29;313(5795):1975-8. Epub 2006 Aug 17.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Neurosciences Group, Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford OX3 9DS, UK. dbeeson@hammer.imm.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16917026" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Line ; Cells, Cultured ; Female ; *Frameshift Mutation ; Genes, Recessive ; Humans ; Male ; Muscle Fibers, Skeletal/metabolism ; Muscle Proteins/*genetics/physiology ; Muscle Weakness/physiopathology ; Mutation ; Myasthenic Syndromes, Congenital/*genetics/pathology/physiopathology ; Neuromuscular Junction/*pathology/*physiopathology ; Pedigree ; Polymerase Chain Reaction ; Receptor Protein-Tyrosine Kinases/physiology ; Receptors, Cholinergic/metabolism/physiology ; Sequence Analysis, DNA ; Synaptic Transmission
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  • 162
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mejia, Robin -- New York, N.Y. -- Science. 2006 Jul 21;313(5785):288-90.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16857915" target="_blank"〉PubMed〈/a〉
    Keywords: Confidence Intervals ; *Data Collection/methods ; Data Interpretation, Statistical ; Developing Countries ; Female ; Human Rights Abuses/legislation & jurisprudence/*statistics & numerical data ; Humans ; Interviews as Topic ; Male ; Models, Statistical ; Sierra Leone ; War Crimes/legislation & jurisprudence/*statistics & numerical data ; Warfare
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  • 163
    Publication Date: 2006-07-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Jon -- New York, N.Y. -- Science. 2006 Jul 28;313(5786):487-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16873656" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/drug therapy/*epidemiology ; Anti-HIV Agents/supply & distribution/therapeutic use ; Argentina/epidemiology ; Delivery of Health Care ; *Disease Outbreaks ; Female ; HIV Infections/complications/drug therapy/*epidemiology ; Health Education ; *Heterosexuality ; Homosexuality, Male ; Humans ; Male ; *National Health Programs ; Quality of Health Care ; Substance Abuse, Intravenous/complications
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  • 164
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-01
    Description: As Europe ages, the proportion of people who work will decline unless older individuals remain in the labor force. Such reform could be part of a more general redistribution of work. If a greater share of the population worked, then the average number of hours worked per week could be reduced. This could particularly help younger people and increase Europe's low birth rates. The challenges facing Germany, Europe's most populous country, are highlighted, but statistics are also given for five other European countries and, for comparison, the United States. Social science research is needed to provide policy-relevant knowledge about life-course options.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vaupel, James W -- Loichinger, Elke -- AG-08761/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2006 Jun 30;312(5782):1911-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Rostocker Zentrum for the Study of Demographic Change and Max Planck Institute for Demographic Research, Konrad-Zuse-Strasse 1, D-18057 Rostock, Germany. jwv@demogr.mpg.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16809529" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Aged ; *Aging ; Birth Rate ; Employment/*statistics & numerical data ; Europe ; Female ; Germany ; Humans ; Income ; Longevity ; Male ; Middle Aged ; *Population Dynamics ; Retirement ; United States ; Women, Working
    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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  • 165
    Publication Date: 2006-07-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Jon -- New York, N.Y. -- Science. 2006 Jul 28;313(5786):477-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16873647" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/drug therapy/epidemiology/prevention & ; control/transmission ; Anti-HIV Agents/supply & distribution/therapeutic use ; Disease Outbreaks ; Female ; HIV Infections/drug therapy/*epidemiology/*prevention & control/transmission ; Health Services Accessibility ; Homosexuality, Male ; Humans ; Male ; Mexico/epidemiology ; Pregnancy ; Pregnancy Complications, Infectious/epidemiology ; Prevalence ; Preventive Health Services ; Quality of Health Care ; Transients and Migrants
    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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  • 166
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2006-07-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Jon -- New York, N.Y. -- Science. 2006 Jul 28;313(5786):477.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16873646" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/epidemiology/transmission ; Central America/epidemiology ; Disease Outbreaks ; Female ; HIV Infections/*epidemiology/transmission ; Humans ; Male ; Mexico/epidemiology
    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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