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  • 101
    Publication Date: 2005-01-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Timothy M -- Cleveland, Don W -- R37 NS027036/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2005 Jan 21;307(5708):361-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ludwig Institute for Cancer Research and the Department of Medicine and Neurosciences, University of California, San Diego, La Jolla, CA 92093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15661995" target="_blank"〉PubMed〈/a〉
    Keywords: Amyotrophic Lateral Sclerosis/*drug therapy ; Animals ; Anti-Bacterial Agents/pharmacology/*therapeutic use ; Brain/metabolism ; Ceftriaxone/pharmacology/*therapeutic use ; Clinical Trials as Topic ; Drug Evaluation, Preclinical ; Excitatory Amino Acid Transporter 2/genetics/metabolism ; Glutamic Acid/metabolism ; Humans ; Mice ; Motor Neurons/physiology ; Neurodegenerative Diseases/*drug therapy ; Spinal Cord/metabolism ; Synapses/physiology ; Synaptic Transmission ; beta-Lactams/pharmacology/*therapeutic use
    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: 2005-11-15
    Description: The invasion of Europe by the western corn rootworm, North America's most destructive corn pest, is ongoing and represents a serious threat to European agriculture. Because this pest was initially introduced in Central Europe, it was believed that subsequent outbreaks in Western Europe originated from this area. Using model-based Bayesian analyses of the genetic variability of the western corn rootworm, we demonstrate that this belief is false: There have been at least three independent introductions from North America during the past two decades. This result raises questions about changing circumstances that have enabled a sudden burst of transatlantic introductions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Miller, Nicholas -- Estoup, Arnaud -- Toepfer, Stefan -- Bourguet, Denis -- Lapchin, Laurent -- Derridj, Sylvie -- Kim, Kyung Seok -- Reynaud, Philippe -- Furlan, Lorenzo -- Guillemaud, Thomas -- New York, N.Y. -- Science. 2005 Nov 11;310(5750):992.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biologie des Populations en Interaction, Unite Mixte de Recherche (UMR) 1112 Institute National de la Recherche Agronomique (INRA)-Universite de Nice-Sophia Antipolis, 400 Route des Chappes, 06903 Sophia Antipolis Cedex, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16284172" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bayes Theorem ; *Beetles/genetics ; Computer Simulation ; Europe ; Genetic Variation ; Insect Control ; Microsatellite Repeats ; North America ; Population Dynamics ; United States ; *Zea mays
    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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  • 103
    Publication Date: 2005-07-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉de Ruiter, Peter C -- Wolters, Volkmar -- Moore, John C -- Winemiller, Kirk O -- New York, N.Y. -- Science. 2005 Jul 1;309(5731):68-71.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Environmental Sciences, Copernicus Research Institute for Sustainable Development and Innovation, Utrecht University, 3508 TC Utrecht, Netherlands. p.deruiter@geo.uu.nl〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15994518" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; Body Size ; *Ecosystem ; Fishes ; *Food Chain ; Population Density ; Population Dynamics ; Predatory Behavior ; Time Factors
    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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  • 104
    Publication Date: 2005-02-12
    Description: The microenvironments of the thymus are generated by thymic epithelial cells (TECs) and are essential for inducing immune self-tolerance or developing T cells. However, the molecular mechanisms that underlie the differentiation of TECs and thymic compartmentalization are not fully understood. Here we show that deficiency in the tumor necrosis factor receptor-associated factor (TRAF) 6 results in disorganized distribution of medullary TECs (mTECs) and the absence of mature mTECs. Engraftment of thymic stroma of TRAF6(-/-) embryos into athymic nude mice induced autoimmunity. Thus, TRAF6 directs the development of thymic stroma and represents a critical point of regulation for self-tolerance and autoimmunity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Akiyama, Taishin -- Maeda, Shiori -- Yamane, Sayaka -- Ogino, Kaori -- Kasai, Michiyuki -- Kajiura, Fumiko -- Matsumoto, Mitsuru -- Inoue, Jun-ichiro -- New York, N.Y. -- Science. 2005 Apr 8;308(5719):248-51. Epub 2005 Feb 10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Cellular and Molecular Biology, Institute of Medical Science, University of Tokyo, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15705807" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmunity ; Cell Line ; Epithelial Cells/immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Nude ; Organ Culture Techniques ; Proto-Oncogene Proteins/physiology ; *Self Tolerance ; T-Lymphocytes/immunology ; TNF Receptor-Associated Factor 6/immunology/*physiology ; Thymus Gland/cytology/embryology/*immunology ; Transcription Factor RelB ; Transcription Factors/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 105
    Publication Date: 2005-12-03
    Description: Proper chromosome segregation requires the attachment of sister kinetochores to microtubules from opposite spindle poles to form bi-oriented chromosomes on the metaphase spindle. The chromosome passenger complex containing Survivin and the kinase Aurora B regulates this process from the centromeres. We report that a de-ubiquitinating enzyme, hFAM, regulates chromosome alignment and segregation by controlling both the dynamic association of Survivin with centromeres and the proper targeting of Survivin and Aurora B to centromeres. Survivin is ubiquitinated in mitosis through both Lys(48) and Lys(63) ubiquitin linkages. Lys(63) de-ubiquitination mediated by hFAM is required for the dissociation of Survivin from centromeres, whereas Lys(63) ubiquitination mediated by the ubiquitin binding protein Ufd1 is required for the association of Survivin with centromeres. Thus, ubiquitinaton regulates dynamic protein-protein interactions and chromosome segregation independently of protein degradation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vong, Queenie P -- Cao, Kan -- Li, Hoi Y -- Iglesias, Pablo A -- Zheng, Yixian -- GM56312/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2005 Dec 2;310(5753):1499-504.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Embryology, Carnegie Institution of Washington and Howard Hughes Medical Institute, 3520 San Martin Drive, Baltimore, MD 21218, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16322459" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; Aurora Kinase B ; Aurora Kinases ; Centromere/*metabolism ; Chromosomal Proteins, Non-Histone/metabolism ; Chromosome Segregation/*physiology ; Egg Proteins/metabolism ; Endopeptidases/metabolism ; HeLa Cells ; Humans ; Inhibitor of Apoptosis Proteins ; Lysine/metabolism ; Microtubule-Associated Proteins/metabolism ; Molecular Sequence Data ; Neoplasm Proteins/metabolism ; Protein Binding ; Protein-Serine-Threonine Kinases/metabolism ; Ubiquitin/*metabolism ; Ubiquitin Thiolesterase ; Xenopus ; Xenopus Proteins/*metabolism
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 106
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lawler, Andrew -- New York, N.Y. -- Science. 2005 Apr 29;308(5722):610-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15860595" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astronauts ; *Biological Science Disciplines ; Humans ; *Research/economics ; Research Support as Topic ; *Space Flight ; *Spacecraft ; United States ; *United States National Aeronautics and Space ; Administration/economics/organization & administration
    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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  • 107
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Delfino, Massimo -- New York, N.Y. -- Science. 2005 Apr 1;308(5718):49-50; author reply 49-50.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15818797" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; *Amphibians/classification/physiology ; Animals ; *Biodiversity ; Biological Evolution ; Climate ; *Ecosystem ; Environment ; Population Dynamics ; Time
    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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  • 108
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-07-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Buzsaki, Gyorgy -- New York, N.Y. -- Science. 2005 Jul 22;309(5734):568-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Molecular and Behavioral Neuroscience, Rutgers University, Newark, NJ 07102, USA. buzsaki@axon.rutgers.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16040697" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain Mapping ; Cues ; Electrophysiology ; Hippocampus/cytology/*physiology ; Interneurons/physiology ; Memory/*physiology ; Nerve Net/*physiology ; Neural Inhibition ; Neurons/*physiology ; Orientation/*physiology ; Perception/physiology ; Pyramidal Cells/*physiology ; Rats ; Space Perception/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 109
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kaiser, Jocelyn -- New York, N.Y. -- Science. 2005 Mar 11;307(5715):1544-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15761128" target="_blank"〉PubMed〈/a〉
    Keywords: Advisory Committees ; Animals ; *Clinical Trials as Topic ; Genetic Diseases, X-Linked/*therapy ; *Genetic Therapy/adverse effects ; Genetic Vectors ; Haplorhini ; Humans ; Infant ; Leukemia, T-Cell/etiology ; Mice ; Oncogenes ; Retroviridae/genetics ; Severe Combined Immunodeficiency/*therapy ; United States
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 110
    Publication Date: 2005-04-23
    Description: We addressed the question of bottom-up versus top-down control of marine ecosystem trophic interactions by using annual fish catch data and satellite-derived (SeaWiFS) chlorophyll a measurements for the continental margin of western North America. Findings reveal a marked alongshore variation in retained primary production that is highly correlated with the alongshore variation in resident fish yield. The highest productivity occurs off the coasts of Washington and southern British Columbia. Zooplankton data for coastal British Columbia confirm strong bottom-up trophic linkages between phytoplankton, zooplankton, and resident fish, extending to regional areas as small as 10,000 square kilometers.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ware, Daniel M -- Thomson, Richard E -- New York, N.Y. -- Science. 2005 May 27;308(5726):1280-4. Epub 2005 Apr 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Aquatic Ecosystem Associates, 3674 Planta Road, Nanaimo, BC V9T 1M2, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15845876" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Migration ; Animals ; Biodiversity ; Biomass ; Chlorophyll/analysis ; Climate ; *Ecosystem ; *Fishes/physiology ; Food Chain ; North America ; Pacific Ocean ; *Phytoplankton/physiology ; Population Density ; *Seawater/chemistry ; *Zooplankton/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 111
    Publication Date: 2005-07-26
    Description: A key unresolved question in population ecology concerns the relationship between a population's size and its growth rate. We estimated this relationship for 1780 time series of mammals, birds, fish, and insects. We found that rates of population growth are high at low population densities but, contrary to previous predictions, decline rapidly with increasing population size and then flatten out, for all four taxa. This produces a strongly concave relationship between a population's growth rate and its size. These findings have fundamental implications for our understanding of animals' lives, suggesting in particular that many animals in these taxa will be found living at densities above the carrying capacity of their environments.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sibly, Richard M -- Barker, Daniel -- Denham, Michael C -- Hone, Jim -- Pagel, Mark -- New York, N.Y. -- Science. 2005 Jul 22;309(5734):607-10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Animal and Microbial Sciences, University of Reading, Whiteknights, Reading RG6 6AJ, UK. r.m.sibly@reading.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16040705" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; *Birds ; Conservation of Natural Resources ; Databases, Factual ; *Ecosystem ; Environment ; *Fishes ; *Insects ; Logistic Models ; *Mammals ; Mathematics ; Models, Biological ; Phylogeny ; Population Density ; Population Dynamics ; Population Growth ; Regression Analysis
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 112
    Publication Date: 2005-01-22
    Description: The Karoo basin of South Africa exposes a succession of Upper Permian to Lower Triassic terrestrial strata containing abundant terrestrial vertebrate fossils. Paleomagnetic/magnetostratigraphic and carbon-isotope data allow sections to be correlated across the basin. With this stratigraphy, the vertebrate fossil data show a gradual extinction in the Upper Permian punctuated by an enhanced extinction pulse at the Permian-Triassic boundary interval, particularly among the dicynodont therapsids, coinciding with negative carbon-isotope anomalies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ward, Peter D -- Botha, Jennifer -- Buick, Roger -- De Kock, Michiel O -- Erwin, Douglas H -- Garrison, Geoffrey H -- Kirschvink, Joseph L -- Smith, Roger -- New York, N.Y. -- Science. 2005 Feb 4;307(5710):709-14. Epub 2005 Jan 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of Washington, Seattle, WA 98195, USA. argo@u.washington.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15661973" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; Carbon Isotopes/analysis ; *Ecosystem ; Environment ; *Fossils ; Geologic Sediments ; Magnetics ; Plants ; South Africa ; Time ; *Vertebrates
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  • 113
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-09-24
    Description: The notion that a trade-off exists between immunity and reproduction is now a central concept in theories of sexual selection. However, whether such a trade-off exists between immunity and gamete viability has not been established. Here we show that genetic variance for high levels of an immune response required to fight bacterial infections is associated with genetic variance for low sperm viability. These data have implications for our understanding of sexual selection mechanisms and of reproductive costs in male longevity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Simmons, Leigh W -- Roberts, Benjamin -- New York, N.Y. -- Science. 2005 Sep 23;309(5743):2031.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Evolutionary Biology Research Group, School of Animal Biology (M092), University of Western Australia, Crawley, WA 6009, Australia. lsimmons@cyllene.uwa.edu.au〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16179472" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Survival ; Female ; Genetic Variation ; Gryllidae/genetics/*immunology/*physiology ; Hemocytes/immunology ; Immunity, Cellular ; Male ; Micrococcus/*immunology ; Muramidase/metabolism ; Phenotype ; Reproduction ; Spermatozoa/*physiology
    Print ISSN: 0036-8075
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  • 114
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-02-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Simmons, Nancy B -- New York, N.Y. -- Science. 2005 Jan 28;307(5709):527-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Vertebrate Zoology, American Museum of Natural History, New York, NY 10024, USA. simmons@amnh.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15681371" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Chiroptera/anatomy & histology/*classification/*genetics/physiology ; Echolocation ; Flight, Animal ; Fossils ; *Phylogeny ; Predatory Behavior
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  • 115
    Publication Date: 2005-02-26
    Description: Apical membrane antigen 1 from Plasmodium is a leading malaria vaccine candidate. The protein is essential for host-cell invasion, but its molecular function is unknown. The crystal structure of the three domains comprising the ectoplasmic region of the antigen from P. vivax, solved at 1.8 angstrom resolution, shows that domains I and II belong to the PAN motif, which defines a superfamily of protein folds implicated in receptor binding. We also mapped the epitope of an invasion-inhibitory monoclonal antibody specific for the P. falciparum ortholog and modeled this to the structure. The location of the epitope and current knowledge on structure-function correlations for PAN domains together suggest a receptor-binding role during invasion in which domain II plays a critical part. These results are likely to aid vaccine and drug design.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pizarro, Juan Carlos -- Vulliez-Le Normand, Brigitte -- Chesne-Seck, Marie-Laure -- Collins, Christine R -- Withers-Martinez, Chrislaine -- Hackett, Fiona -- Blackman, Michael J -- Faber, Bart W -- Remarque, Edmond J -- Kocken, Clemens H M -- Thomas, Alan W -- Bentley, Graham A -- MC_U117532063/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2005 Apr 15;308(5720):408-11. Epub 2005 Feb 24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Unite d'Immunologie Structurale, Centre National de la Recherche Scientifique, URA 2185, Institut Pasteur, 25 rue du Docteur Roux, 75724 Paris, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15731407" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Motifs ; Amino Acid Sequence ; Animals ; Antibodies, Monoclonal/immunology ; Antigens, Protozoan/*chemistry/immunology ; Binding Sites ; Crystallization ; Crystallography, X-Ray ; Epitope Mapping ; Epitopes ; Heparin/metabolism ; Malaria Vaccines ; Membrane Proteins/*chemistry/immunology ; Models, Molecular ; Molecular Sequence Data ; Plasmodium falciparum/chemistry/immunology ; Plasmodium vivax/chemistry/*immunology ; Protein Conformation ; Protein Folding ; Protein Structure, Secondary ; Protein Structure, Tertiary ; Protozoan Proteins/*chemistry/immunology ; Recombinant Proteins/chemistry ; Sequence Alignment
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  • 116
    Publication Date: 2005-07-23
    Description: Many large animal species have a high risk of extinction. This is usually thought to result simply from the way that species traits associated with vulnerability, such as low reproductive rates, scale with body size. In a broad-scale analysis of extinction risk in mammals, we find two additional patterns in the size selectivity of extinction risk. First, impacts of both intrinsic and environmental factors increase sharply above a threshold body mass around 3 kilograms. Second, whereas extinction risk in smaller species is driven by environmental factors, in larger species it is driven by a combination of environmental factors and intrinsic traits. Thus, the disadvantages of large size are greater than generally recognized, and future loss of large mammal biodiversity could be far more rapid than expected.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cardillo, Marcel -- Mace, Georgina M -- Jones, Kate E -- Bielby, Jon -- Bininda-Emonds, Olaf R P -- Sechrest, Wes -- Orme, C David L -- Purvis, Andy -- New York, N.Y. -- Science. 2005 Aug 19;309(5738):1239-41. Epub 2005 Jul 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Biology, Imperial College London, Silwood Park, Ascot SL5 7PY, UK. m.cardillo@imperial.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16037416" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; Biological Evolution ; *Body Size ; Body Weight ; Conservation of Natural Resources ; *Ecosystem ; *Environment ; Female ; Homing Behavior ; Humans ; *Mammals/physiology ; Models, Biological ; Models, Statistical ; Population Density ; Population Dynamics ; Pregnancy ; Pregnancy, Animal ; Regression Analysis ; Risk ; Weaning
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  • 117
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-09-06
    Description: Recent work indicates that the posttranscriptional control of eukaryotic gene expression is much more elaborate and extensive than previously thought, with essentially every step of messenger RNA (mRNA) metabolism being subject to regulation in an mRNA-specific manner. Thus, a comprehensive understanding of eukaryotic gene expression requires an appreciation for how the lives of mRNAs are influenced by a wide array of diverse regulatory mechanisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moore, Melissa J -- New York, N.Y. -- Science. 2005 Sep 2;309(5740):1514-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, Howard Hughes Medical Institute, Brandeis University, 415 South Street, Waltham, MA 02454. mmoore@brandeis.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16141059" target="_blank"〉PubMed〈/a〉
    Keywords: Active Transport, Cell Nucleus ; Animals ; Cell Nucleus/metabolism ; Cytoplasm/metabolism ; Cytoplasmic Granules/chemistry ; Eukaryotic Cells/*metabolism ; *Gene Expression Regulation ; Protein Biosynthesis ; RNA Processing, Post-Transcriptional ; RNA, Messenger/analysis/biosynthesis/*metabolism ; Ribonucleoproteins/metabolism
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  • 118
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-01-22
    Description: The epidemic of obesity-associated diabetes is a major crisis in modern societies, in which food is plentiful and exercise is optional. The biological basis of this problem has been explored from evolutionary and mechanistic perspectives. Evolutionary theories, focusing on the potential survival advantages of "thrifty" genes that are now maladaptive, are of great interest but are inherently speculative and difficult to prove. Mechanistic studies have revealed numerous fat-derived molecules and a link to inflammation that, together, are hypothesized to underlie the obesity-diabetes connection and thereby represent prospective targets for therapeutic intervention.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lazar, Mitchell A -- New York, N.Y. -- Science. 2005 Jan 21;307(5708):373-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, and The Penn Diabetes Center, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6149, USA. lazar@mail.med.upenn.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15662001" target="_blank"〉PubMed〈/a〉
    Keywords: Adipocytes/metabolism ; Adipose Tissue/metabolism ; Animals ; Biological Evolution ; Cytokines/metabolism ; Diabetes Mellitus, Type 2/epidemiology/*etiology/physiopathology ; Epigenesis, Genetic ; Fetal Nutrition Disorders/physiopathology ; Glucose/metabolism ; Humans ; Immunity, Innate ; Inflammation/physiopathology ; Insulin/physiology ; Insulin Resistance ; Leptin/blood/genetics/physiology ; Lipid Metabolism ; Macrophages/immunology/metabolism ; Obesity/*complications/epidemiology/genetics/physiopathology ; Phenotype ; Proteins/metabolism
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  • 119
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dobson, Andrew P -- New York, N.Y. -- Science. 2005 Oct 28;310(5748):628-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544-1003, USA. dobber@princeton.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16254175" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chiroptera/physiology/*virology ; Communicable Diseases, Emerging/*transmission/virology ; *Disease Reservoirs ; Humans ; *SARS Virus ; Severe Acute Respiratory Syndrome/*transmission/virology ; Viverridae/virology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 120
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-05-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Poucet, Bruno -- Save, Etienne -- New York, N.Y. -- Science. 2005 May 6;308(5723):799-800.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Neurobiology and Cognition, CNRS-Universite Aix-Marseille, Centre Saint-Charles, 13331 Marseille Cedex 3, France. bpoucet@up.univ-mrs.fr〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15879197" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Brain Mapping ; Cues ; Environment ; Form Perception ; Hippocampus/*cytology/*physiology ; Learning ; Memory/*physiology ; Orientation ; Pattern Recognition, Visual ; Pyramidal Cells/*physiology ; Rats ; Space Perception
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  • 121
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-12
    Description: Despite spending weeks at sea as larvae, potentially scattered over many kilometers, young coral reef fish find suitable settlement habitat and in some cases return to their natal reefs. We report that some dominant families of larval reef fish use the sounds made by fish and shrimp resident on reefs to help them locate and settle on reefs and that some fish groups use specific components of the reef sound to guide their behavior. These findings could offer potential for active management of reef fisheries.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Simpson, Stephen D -- Meekan, Mark -- Montgomery, John -- McCauley, Rob -- Jeffs, Andrew -- New York, N.Y. -- Science. 2005 Apr 8;308(5719):221.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Biological Sciences, University of Edinburgh, Edinburgh, EH9 3JT, UK. s.simpson@ed.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15821083" target="_blank"〉PubMed〈/a〉
    Keywords: *Animal Communication ; Animals ; Anthozoa ; Ecosystem ; Fishes/embryology/*physiology ; *Homing Behavior ; Oceans and Seas ; Sound
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  • 122
    Publication Date: 2005-08-20
    Description: The molecular machinery that governs circadian rhythmicity is based on clock proteins organized in regulatory feedback loops. Although posttranslational modification of clock proteins is likely to finely control their circadian functions, only limited information is available to date. Here, we show that BMAL1, an essential transcription factor component of the clock mechanism, is SUMOylated on a highly conserved lysine residue (Lys259) in vivo. BMAL1 shows a circadian pattern of SUMOylation that parallels its activation in the mouse liver. SUMOylation of BMAL1 requires and is induced by CLOCK, the heterodimerization partner of BMAL1. Ectopic expression of a SUMO-deficient BMAL1 demonstrates that SUMOylation plays an important role in BMAL1 circadian expression and clock rhythmicity. This reveals an additional level of regulation within the core mechanism of the circadian clock.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cardone, Luca -- Hirayama, Jun -- Giordano, Francesca -- Tamaru, Teruya -- Palvimo, Jorma J -- Sassone-Corsi, Paolo -- New York, N.Y. -- Science. 2005 Aug 26;309(5739):1390-4. Epub 2005 Aug 18.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut de Genetique et de Biologie Moleculaire et Cellulaire, 1 rue Laurent Fries, 67404 Illkirch, Strasbourg, France.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16109848" target="_blank"〉PubMed〈/a〉
    Keywords: ARNTL Transcription Factors ; Animals ; Basic Helix-Loop-Helix Transcription Factors ; CLOCK Proteins ; COS Cells ; Cell Cycle Proteins ; Cell Line ; *Circadian Rhythm ; Dimerization ; Ethylmaleimide/pharmacology ; Gene Expression Regulation ; Liver/metabolism ; Lysine/metabolism ; Mice ; Mutation ; Nuclear Proteins/genetics/metabolism ; Period Circadian Proteins ; Phosphorylation ; Recombinant Fusion Proteins/metabolism ; SUMO-1 Protein/*metabolism ; Trans-Activators/genetics/metabolism ; Transcription Factors/chemistry/genetics/*metabolism
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  • 123
    Publication Date: 2005-07-30
    Description: To study adaptation, it is essential to identify multiple adaptive mutations and to characterize their molecular, phenotypic, selective, and ecological consequences. Here we describe a genomic screen for adaptive insertions of transposable elements in Drosophila. Using a pilot application of this screen, we have identified an adaptive transposable element insertion, which truncates a gene and apparently generates a functional protein in the process. The insertion of this transposable element confers increased resistance to an organophosphate pesticide and has spread in D. melanogaster recently.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Aminetzach, Yael T -- Macpherson, J Michael -- Petrov, Dmitri A -- New York, N.Y. -- Science. 2005 Jul 29;309(5735):764-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Stanford University, 371 Serra Mall, Stanford, CA 94305, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16051794" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptation, Physiological ; Alleles ; Amino Acid Substitution ; Animals ; Azinphosmethyl/pharmacology ; Base Sequence ; Choline/metabolism ; Crosses, Genetic ; *DNA Transposable Elements ; Drosophila/drug effects/genetics/physiology ; Drosophila Proteins/chemistry/*genetics/physiology ; Drosophila melanogaster/drug effects/*genetics/physiology ; *Evolution, Molecular ; Exons ; Female ; Gene Expression ; *Genes, Insect ; Haplotypes ; Insecticide Resistance/*genetics ; Insecticides/pharmacology ; Introns ; Long Interspersed Nucleotide Elements ; Molecular Sequence Data ; Mutation ; Polymorphism, Genetic ; Recombination, Genetic ; Selection, Genetic
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  • 124
    Publication Date: 2005-09-24
    Description: Herbivore-damaged plants release complex mixtures of volatiles that attract natural enemies of the herbivore. To study the relevance of individual components of these mixtures for predator attraction, we manipulated herbivory-induced volatiles through genetic engineering. Metabolic engineering of terpenoids, which dominate the composition of many induced plant volatile bouquets, holds particular promise. By switching the subcellular localization of the introduced sesquiterpene synthase to the mitochondria, we obtained transgenic Arabidopsis thaliana plants emitting two new isoprenoids. These altered plants attracted carnivorous predatory mites (Phytoseiulus persimilis) that aid the plants' defense mechanisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kappers, Iris F -- Aharoni, Asaph -- van Herpen, Teun W J M -- Luckerhoff, Ludo L P -- Dicke, Marcel -- Bouwmeester, Harro J -- New York, N.Y. -- Science. 2005 Sep 23;309(5743):2070-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Entomology, Wageningen University, Post Office Box 8031, 6700 EH Wageningen, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16179482" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arabidopsis/enzymology/*genetics/growth & development/*metabolism ; Fragaria/enzymology/genetics ; Gene Targeting ; Genes, Plant ; *Genetic Engineering ; Hydro-Lyases/*genetics/metabolism ; *Mites/physiology ; Mitochondria/enzymology ; *Pest Control, Biological ; Pheromones ; Plants, Genetically Modified ; Predatory Behavior ; Sesquiterpenes/*metabolism ; Terpenes/metabolism ; Transformation, Genetic
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  • 125
    Publication Date: 2005-09-24
    Description: Mammalian tooth crowns have precise functional requirements but cannot be substantially remodeled after eruption. In developing teeth, epithelial signaling centers, the enamel knots, form at future cusp positions and are the first signs of cusp patterns that distinguish species. We report that ectodin, a secreted bone morphogenetic protein (BMP) inhibitor, is expressed as a "negative" image of mouse enamel knots. Furthermore, we show that ectodin-deficient mice have enlarged enamel knots, highly altered cusp patterns, and extra teeth. Unlike in normal teeth, excess BMP accelerates patterning in ectodin-deficient teeth. We propose that ectodin is critical for robust spatial delineation of enamel knots and cusps.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kassai, Yoshiaki -- Munne, Pauliina -- Hotta, Yuhei -- Penttila, Enni -- Kavanagh, Kathryn -- Ohbayashi, Norihiko -- Takada, Shinji -- Thesleff, Irma -- Jernvall, Jukka -- Itoh, Nobuyuki -- New York, N.Y. -- Science. 2005 Sep 23;309(5743):2067-70.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Genetic Biochemistry, Kyoto University Graduate School of Pharmaceutical Sciences, Kyoto 606-8501, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16179481" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Body Patterning ; Bone Morphogenetic Protein 4 ; Bone Morphogenetic ; Proteins/biosynthesis/genetics/metabolism/pharmacology/*physiology ; Cell Cycle Proteins/biosynthesis/genetics/physiology ; Chimera ; Cyclin-Dependent Kinase Inhibitor p21 ; Dental Enamel/embryology ; Gene Expression Regulation, Developmental ; Hedgehog Proteins ; Heterozygote ; Mice ; Mice, Inbred C57BL ; Microscopy, Confocal ; Molar/embryology/metabolism ; Mutation ; *Odontogenesis ; Organ Culture Techniques ; Tooth Crown/*embryology ; Trans-Activators/biosynthesis/genetics
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  • 126
    Publication Date: 2005-09-17
    Description: A small number of mammalian signaling pathways mediate a myriad of distinct physiological responses to diverse cellular stimuli. Temporal control of the signaling module that contains IkappaB kinase (IKK), its substrate inhibitor of NF-kappaB (IkappaB), and the key inflammatory transcription factor NF-kappaB can allow for selective gene activation. We have demonstrated that different inflammatory stimuli induce distinct IKK profiles, and we examined the underlying molecular mechanisms. Although tumor necrosis factor-alpha (TNFalpha)-induced IKK activity was rapidly attenuated by negative feedback, lipopolysaccharide (LPS) signaling and LPS-specific gene expression programs were dependent on a cytokine-mediated positive feedback mechanism. Thus, the distinct biological responses to LPS and TNFalpha depend on signaling pathway-specific mechanisms that regulate the temporal profile of IKK activity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Werner, Shannon L -- Barken, Derren -- Hoffmann, Alexander -- GM071573/GM/NIGMS NIH HHS/ -- GM72024/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2005 Sep 16;309(5742):1857-61.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Signaling Systems Laboratory, Department of Chemistry and Biochemistry, 9500 Gilman Drive, Mailcode 0375, La Jolla, CA 92093-0375, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16166517" target="_blank"〉PubMed〈/a〉
    Keywords: Algorithms ; Animals ; Autocrine Communication ; Cell Line ; Cells, Cultured ; Computer Simulation ; Cytokines/genetics ; Feedback, Physiological ; Gene Expression Profiling ; *Gene Expression Regulation ; I-kappa B Kinase ; I-kappa B Proteins/metabolism ; Lipopolysaccharides/immunology/metabolism/pharmacology ; Mice ; Models, Biological ; NF-kappa B/deficiency/metabolism ; Oligonucleotide Array Sequence Analysis ; Protein-Serine-Threonine Kinases/*metabolism ; Receptors, Immunologic/metabolism ; Signal Transduction ; Toll-Like Receptor 4 ; Transcriptional Activation ; Tumor Necrosis Factor-alpha/deficiency/immunology/metabolism/pharmacology
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  • 127
    Publication Date: 2005-03-19
    Description: The adherence of Candida glabrata to host cells is mediated, at least in part, by the EPA genes, a family of adhesins encoded at subtelomeric loci, where they are subject to transcriptional silencing. We show that normally silent EPA genes are expressed during murine urinary tract infection (UTI) and that the inducing signal is the limitation of nicotinic acid (NA), a precursor of nicotinamide adenine dinucleotide (NAD+). C. glabrata is an NA auxotroph, and NA-induced EPA expression is likely the result of a reduction in NAD+ availability for the NAD+-dependent histone deacetylase Sir2p. The adaptation of C. glabrata to the host, therefore, involves a loss of metabolic capacity and exploitation of the resulting auxotrophy to signal a particular host environment.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Domergue, Renee -- Castano, Irene -- De Las Penas, Alejandro -- Zupancic, Margaret -- Lockatell, Virginia -- Hebel, J Richard -- Johnson, David -- Cormack, Brendan P -- 2PO1DK49720/DK/NIDDK NIH HHS/ -- R01AI46223/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2005 May 6;308(5723):866-70. Epub 2005 Mar 17.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15774723" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Candida glabrata/*genetics/growth & development/*pathogenicity/physiology ; Candidiasis/*microbiology ; Cell Adhesion ; Culture Media ; Female ; Gene Expression Regulation, Fungal ; *Gene Silencing ; Genes, Fungal ; Histone Deacetylases/genetics/metabolism ; Lectins/*genetics ; Mice ; Mice, Inbred BALB C ; Mice, Inbred CBA ; NAD/metabolism ; Niacin/administration & dosage/*metabolism/pharmacology/urine ; Niacinamide/pharmacology/urine ; Sirtuins/genetics/metabolism ; Transcription, Genetic ; Urinary Bladder/microbiology ; Urinary Tract Infections/*microbiology ; Urine/microbiology ; Urothelium/microbiology ; Virulence
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  • 128
    Publication Date: 2005-03-05
    Description: Unexpected, biologically salient stimuli elicit a short-latency, phasic response in midbrain dopaminergic (DA) neurons. Although this signal is important for reinforcement learning, the information it conveys to forebrain target structures remains uncertain. One way to decode the phasic DA signal would be to determine the perceptual properties of sensory inputs to DA neurons. After local disinhibition of the superior colliculus in anesthetized rats, DA neurons became visually responsive, whereas disinhibition of the visual cortex was ineffective. As the primary source of visual afferents, the limited processing capacities of the colliculus may constrain the visual information content of phasic DA responses.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dommett, Eleanor -- Coizet, Veronique -- Blaha, Charles D -- Martindale, John -- Lefebvre, Veronique -- Walton, Natalie -- Mayhew, John E W -- Overton, Paul G -- Redgrave, Peter -- New York, N.Y. -- Science. 2005 Mar 4;307(5714):1476-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychology, University of Sheffield, Sheffield, S10 2TP, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15746431" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bicuculline/pharmacology ; Dopamine/*metabolism ; Electrochemistry ; Evoked Potentials, Visual ; Habituation, Psychophysiologic ; Neostriatum/physiology ; Neural Inhibition ; Neurons/*physiology ; *Photic Stimulation ; Rats ; *Reaction Time ; Reinforcement (Psychology) ; Reward ; Substantia Nigra/*physiology ; Superior Colliculi/*physiology ; Ventral Tegmental Area/*physiology ; Visual Cortex/physiology ; Visual Pathways/physiology
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  • 129
    Publication Date: 2005-02-26
    Description: Many pathogenic bacteria use a type III secretion nanomachine (an injectisome) to deliver virulence proteins into the cytosol of their eukaryotic host cells. Most injectisomes possess a stiff needlelike structure of a genetically defined length. We found that a minimal needle length was required for efficient functioning of the Yersinia enterocolitica injectisome. This minimal needle length correlated with the length of the major adhesin at the bacterial surface. The needle may be required for triggering type III secretion, and its length may have evolved to match specific structures at the bacterial and host cell surfaces.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Mota, Luis Jaime -- Journet, Laure -- Sorg, Isabel -- Agrain, Celine -- Cornelis, Guy R -- New York, N.Y. -- Science. 2005 Feb 25;307(5713):1278.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biozentrum, Universitat Basel, 4056 Basel, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15731447" target="_blank"〉PubMed〈/a〉
    Keywords: Adhesins, Bacterial/chemistry/*metabolism ; Animals ; Bacterial Outer Membrane Proteins/metabolism ; Bacterial Proteins/chemistry/genetics/metabolism ; Cell Line ; Macrophages/metabolism/microbiology ; Mice ; Plasmids ; Protein-Serine-Threonine Kinases/metabolism ; Virulence ; Virulence Factors/metabolism ; Yersinia enterocolitica/genetics/*metabolism/*pathogenicity
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  • 130
    Publication Date: 2005-12-24
    Description: Epimorphic regeneration requires the presence or creation of pluripotent cells capable of reproducing lost organs. Zebrafish fin regeneration is mediated by the creation of blastema cells. Here, we characterize the devoid of blastema (dob) mutant that fails fin regeneration during initial steps, forms abnormal regeneration epithelium, and does not form blastema. This mutation has no impact on embryonic survival. Dob results from an fgf20a null mutation, Y148S. Fgf20a is expressed during initiation of fin regeneration at the epithelial-mesenchymal boundary and later overlaps with the blastema marker msxb. Thus, fgf20a has a regeneration-specific requirement, initiating fin regeneration, and controlling blastema formation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Whitehead, Geoffrey G -- Makino, Shinji -- Lien, Ching-Ling -- Keating, Mark T -- New York, N.Y. -- Science. 2005 Dec 23;310(5756):1957-60.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Cell Biology, Harvard Medical School, Department of Cardiology, Children's Hospital, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16373575" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Extremities ; Fibroblast Growth Factors/*physiology ; Homeodomain Proteins/biosynthesis ; Male ; Mesoderm ; Mutation ; Regeneration/genetics/*physiology ; Temperature ; Wound Healing ; Zebrafish ; Zebrafish Proteins/biosynthesis/*physiology
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  • 131
    Publication Date: 2005-01-18
    Description: Organogenesis begins with specification of a progenitor cell population, the size of which provides a foundation for the organ's final dimensions. Here, we present a new mechanism for regulating the number of progenitor cells by limiting their density within a competent region. We demonstrate that retinoic acid signaling restricts cardiac specification in the zebrafish embryo. Reduction of retinoic acid signaling causes formation of an excess of cardiomyocytes, via fate transformations that increase cardiac progenitor density within a multipotential zone. Thus, retinoic acid signaling creates a balance between cardiac and noncardiac identities, thereby refining the dimensions of the cardiac progenitor pool.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Keegan, Brian R -- Feldman, Jessica L -- Begemann, Gerrit -- Ingham, Philip W -- Yelon, Deborah -- New York, N.Y. -- Science. 2005 Jan 14;307(5707):247-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Developmental Genetics Program, Skirball Institute of Biomolecular Medicine, and Department of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15653502" target="_blank"〉PubMed〈/a〉
    Keywords: Aldehyde Oxidoreductases/genetics/metabolism ; Animals ; Blastomeres/cytology/physiology ; Blastula/cytology/physiology ; Cell Count ; Cell Differentiation ; Cell Proliferation ; Embryo, Nonmammalian/cytology/physiology ; Gastrula/physiology ; Heart/*embryology ; Mesoderm/cytology ; Myocytes, Cardiac/cytology/*physiology ; Receptors, Retinoic Acid/antagonists & inhibitors ; Retinal Dehydrogenase ; Retinoids/pharmacology ; *Signal Transduction ; Stem Cells/cytology/*physiology ; Tretinoin/*metabolism ; Zebrafish
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  • 132
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    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-15
    Description: Only recently have we begun to characterize fine-scale recombination rates in mammals. In her Perspective, Przeworski discusses the work by Myers et al. in which linkage disequilibrium data have been used to produce a high-resolution recombination map for most of the human genome. More than 25,000 putative hotspots have been identified, as well as the first motifs that appear to influence their intensity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Przeworski, Molly -- New York, N.Y. -- Science. 2005 Oct 14;310(5746):247-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Human Genetics, University of Chicago, 920 East 57th Street, 507F CLSC, Chicago, IL 60637, USA. mfp@uchicago.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16224010" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Chromosome Mapping ; Chromosomes, Human, X ; Female ; *Genome, Human ; Humans ; Male ; Recombination, Genetic/*genetics
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  • 133
    Publication Date: 2005-06-11
    Description: Repetitive microsatellites mutate at relatively high rates and may contribute to the rapid evolution of species-typical traits. We show that individual alleles of a repetitive polymorphic microsatellite in the 5' region of the prairie vole vasopressin 1a receptor (avpr1a) gene modify gene expression in vitro. In vivo, we observe that this regulatory polymorphism predicts both individual differences in receptor distribution patterns and socio-behavioral traits. These data suggest that individual differences in gene expression patterns may be conferred via polymorphic microsatellites in the cis-regulatory regions of genes and may contribute to normal variation in behavioral traits.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hammock, Elizabeth A D -- Young, Larry J -- MH56897/MH/NIMH NIH HHS/ -- MH64692/MH/NIMH NIH HHS/ -- MH67397/MH/NIMH NIH HHS/ -- RR00165/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 2005 Jun 10;308(5728):1630-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Psychiatry and Behavioral Sciences, Center for Behavioral Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15947188" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Anxiety ; Arvicolinae/*genetics/physiology/psychology ; Base Sequence ; *Behavior, Animal ; Brain/metabolism ; *Gene Expression Regulation ; Genes, Reporter ; Genetic Variation ; Genotype ; Grooming ; Male ; *Microsatellite Repeats ; Molecular Sequence Data ; Odors ; Pair Bond ; Paternal Behavior ; Receptors, Vasopressin/*genetics/metabolism ; *Social Behavior
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  • 134
    Publication Date: 2005-02-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Doumbo, Ogobara K -- New York, N.Y. -- Science. 2005 Feb 4;307(5710):679-81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Epidemiology of Parasitic Diseases (DEAP), Faculty of Medicine, Pharmacy and Odonto-Stomatology, University of Bamako, Mali, BP 1805, Bamako, Mali. okd@mrtcbko.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15692036" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anopheles/parasitology ; Antimalarials/therapeutic use ; Biomedical Research/*ethics ; Clinical Trials as Topic/*ethics ; Delivery of Health Care ; Developing Countries ; *Ethics, Research ; Family ; Female ; Human Experimentation/*ethics ; Humans ; *Informed Consent ; Insect Vectors/parasitology ; *Malaria/drug therapy/prevention & control/transmission ; Mali ; Pregnancy ; Pregnancy Complications, Parasitic/prevention & control
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  • 135
    Publication Date: 2005-03-19
    Description: Recognizing a deficiency of indispensable amino acids (IAAs) for protein synthesis is vital for dietary selection in metazoans, including humans. Cells in the brain's anterior piriform cortex (APC) are sensitive to IAA deficiency, signaling diet rejection and foraging for complementary IAA sources, but the mechanism is unknown. Here we report that the mechanism for recognizing IAA-deficient foods follows the conserved general control (GC) system, wherein uncharged transfer RNA induces phosphorylation of eukaryotic initiation factor 2 (eIF2) via the GC nonderepressing 2 (GCN2) kinase. Thus, a basic mechanism of nutritional stress management functions in mammalian brain to guide food selection for survival.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hao, Shuzhen -- Sharp, James W -- Ross-Inta, Catherine M -- McDaniel, Brent J -- Anthony, Tracy G -- Wek, Ronald C -- Cavener, Douglas R -- McGrath, Barbara C -- Rudell, John B -- Koehnle, Thomas J -- Gietzen, Dorothy W -- GM49164/GM/NIGMS NIH HHS/ -- NS043231/NS/NINDS NIH HHS/ -- NS33347/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2005 Mar 18;307(5716):1776-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Veterinary Medicine, Department of Anatomy, Physiology and Cell Biology, University of California, Davis, CA 95616, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15774759" target="_blank"〉PubMed〈/a〉
    Keywords: Acylation ; Amino Acids, Essential/*administration & dosage/analysis/*deficiency ; Animals ; Diet ; Eating ; Eukaryotic Initiation Factor-2/*metabolism ; *Food ; Food Preferences ; Leucine/administration & dosage/*analogs & derivatives/pharmacology ; Mice ; Mice, Inbred C57BL ; Olfactory Pathways/*metabolism ; Phosphorylation ; Protein Kinases/*metabolism ; Protein-Serine-Threonine Kinases ; RNA, Transfer/*metabolism ; Rats ; Stereoisomerism ; Threonine/administration & dosage ; eIF-2 Kinase/metabolism
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  • 136
    Publication Date: 2005-03-05
    Description: The serpentinite-hosted Lost City hydrothermal field is a remarkable submarine ecosystem in which geological, chemical, and biological processes are intimately interlinked. Reactions between seawater and upper mantle peridotite produce methane- and hydrogen-rich fluids, with temperatures ranging from 〈40 degrees to 90 degrees C at pH 9 to 11, and carbonate chimneys 30 to 60 meters tall. A low diversity of microorganisms related to methane-cycling Archaea thrive in the warm porous interiors of the edifices. Macrofaunal communities show a degree of species diversity at least as high as that of black smoker vent sites along the Mid-Atlantic Ridge, but they lack the high biomasses of chemosynthetic organisms that are typical of volcanically driven systems.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kelley, Deborah S -- Karson, Jeffrey A -- Fruh-Green, Gretchen L -- Yoerger, Dana R -- Shank, Timothy M -- Butterfield, David A -- Hayes, John M -- Schrenk, Matthew O -- Olson, Eric J -- Proskurowski, Giora -- Jakuba, Mike -- Bradley, Al -- Larson, Ben -- Ludwig, Kristin -- Glickson, Deborah -- Buckman, Kate -- Bradley, Alexander S -- Brazelton, William J -- Roe, Kevin -- Elend, Mitch J -- Delacour, Adelie -- Bernasconi, Stefano M -- Lilley, Marvin D -- Baross, John A -- Summons, Roger E -- Sylva, Sean P -- New York, N.Y. -- Science. 2005 Mar 4;307(5714):1428-34.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉School of Oceanography, University of Washington, Seattle, WA 98195, USA. kelley@ocean.washington.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15746419" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Archaea/classification/*growth & development/isolation & purification/metabolism ; Bacteria/classification/*growth & development/isolation & purification/metabolism ; Biodiversity ; Biomass ; *Carbonates ; Colony Count, Microbial ; *Ecosystem ; Environment ; Fishes ; *Geologic Sediments/chemistry/microbiology ; Hot Temperature ; Hydrogen/analysis/metabolism ; Hydrogen-Ion Concentration ; *Invertebrates ; Lipids/analysis ; Methane/analysis/metabolism ; Phylogeny ; *Seawater
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  • 137
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-09-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Du Pasquier, Louis -- New York, N.Y. -- Science. 2005 Sep 16;309(5742):1826-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Zoology and Evolutionary Biology, University of Basel, Vesalgasse 1, CH-4051 Basel, Switzerland. dupasquier@dial.eunet.ch〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16166509" target="_blank"〉PubMed〈/a〉
    Keywords: *Alternative Splicing ; Animals ; Axons/physiology ; Binding Sites ; Biological Evolution ; Cell Adhesion Molecules ; Drosophila Proteins/chemistry/*genetics/*immunology/metabolism ; Drosophila melanogaster/*genetics/*immunology ; Genetic Variation ; Hemocytes/immunology/*metabolism ; Humans ; Immunity, Innate ; Immunoglobulins/chemistry ; Membrane Proteins ; Neurons/metabolism ; Protein Isoforms/chemistry/genetics/metabolism ; Proteins/genetics/physiology ; Receptors, Antigen/immunology/metabolism ; Vertebrates/physiology
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  • 138
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-08-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wickner, Reed B -- New York, N.Y. -- Science. 2005 Aug 5;309(5736):874.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16081716" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; China ; History, Ancient ; Scrapie/*history ; Sheep
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  • 139
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-12-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Antebi, Adam -- New York, N.Y. -- Science. 2005 Dec 23;310(5756):1911-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16373563" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/genetics/*physiology ; Animals ; Caenorhabditis elegans ; Caenorhabditis elegans Proteins/genetics/*physiology ; Forkhead Transcription Factors ; Longevity/genetics/physiology ; MicroRNAs/*physiology ; Nuclear Proteins/genetics/*physiology ; RNA, Helminth/*physiology ; Repressor Proteins/genetics/*physiology ; Signal Transduction ; Transcription Factors/physiology
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  • 140
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-11-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harcourt, A H -- New York, N.Y. -- Science. 2005 Nov 25;310(5752):1276-8; author reply 1276-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16311317" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Size ; *Databases, Factual ; Ecosystem ; Environment ; *Mammals/anatomy & histology/physiology ; Population Density ; Reproduction ; Risk
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  • 141
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-11-30
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Putland, David -- New York, N.Y. -- Science. 2005 Nov 25;310(5752):1276-8; author reply 1276-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16315350" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Body Size ; Conservation of Natural Resources ; Ecosystem ; Environment ; *Mammals/anatomy & histology/classification/physiology ; Phylogeny ; Population Density ; Risk
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  • 142
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-12-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kennedy, Donald -- New York, N.Y. -- Science. 2005 Dec 23;310(5756):1869.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16373537" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Brain Diseases ; Greenhouse Effect ; Humans ; Research
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  • 143
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Arlinghaus, Robert -- Cooke, Steven J -- New York, N.Y. -- Science. 2005 Mar 11;307(5715):1561-3; author reply 1561-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15765561" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Conservation of Natural Resources ; Ecosystem ; *Fisheries ; *Fishes ; Fresh Water ; Internationality ; Population Dynamics ; *Recreation ; Seawater ; United States
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  • 144
    Publication Date: 2005-09-17
    Description: The spike protein (S) of SARS coronavirus (SARS-CoV) attaches the virus to its cellular receptor, angiotensin-converting enzyme 2 (ACE2). A defined receptor-binding domain (RBD) on S mediates this interaction. The crystal structure at 2.9 angstrom resolution of the RBD bound with the peptidase domain of human ACE2 shows that the RBD presents a gently concave surface, which cradles the N-terminal lobe of the peptidase. The atomic details at the interface between the two proteins clarify the importance of residue changes that facilitate efficient cross-species infection and human-to-human transmission. The structure of the RBD suggests ways to make truncated disulfide-stabilized RBD variants for use in the design of coronavirus vaccines.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Fang -- Li, Wenhui -- Farzan, Michael -- Harrison, Stephen C -- AI061601/AI/NIAID NIH HHS/ -- CA13202/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2005 Sep 16;309(5742):1864-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Laboratory of Molecular Medicine, 320 Longwood Avenue, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16166518" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Amino Acid Substitution ; Animals ; Antibodies, Viral/immunology ; Binding Sites ; Carboxypeptidases/*chemistry/metabolism ; Cell Line ; Crystallography, X-Ray ; Disease Outbreaks ; Epitopes ; Glycosylation ; Humans ; Hydrophobic and Hydrophilic Interactions ; Membrane Glycoproteins/*chemistry/genetics/immunology/*metabolism ; Models, Molecular ; Molecular Sequence Data ; Mutation ; Peptidyl-Dipeptidase A ; Protein Conformation ; Protein Structure, Tertiary ; Receptors, Virus/*chemistry/metabolism ; SARS Virus/*chemistry/genetics/physiology ; Severe Acute Respiratory Syndrome/transmission/*virology ; Species Specificity ; Spike Glycoprotein, Coronavirus ; Viral Envelope Proteins/*chemistry/genetics/immunology/*metabolism ; Viral Vaccines ; Viverridae/virology
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  • 145
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-26
    Description: The function of an organ is dependent on its cellular constituents as well as on their assembly into a cohesive unit. The developing gut faces unique challenges as one of the longest and largest organs in the body and also because it is constantly interfacing with external factors through the diet. Its location deep within the body has until recently hampered investigation into its formation. The patterning of the gut along its longitudinal, dorsoventral, left-right, and radial axes is one of the fascinating issues that pertain to the development, function, and homeostasis of this understudied organ.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stainier, Didier Y R -- New York, N.Y. -- Science. 2005 Mar 25;307(5717):1902-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Biophysics, Programs in Developmental Biology, Genetics and Human Genetics, University of California, San Francisco, San Francisco, CA 94143-2711, USA. didier_stainier@biochem.ucsf.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15790841" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Body Patterning ; Diet ; Digestive System/*embryology/microbiology ; Digestive System Abnormalities ; Digestive System Physiological Phenomena ; Endoderm/physiology ; Epigenesis, Genetic ; Gene Expression Regulation, Developmental ; Genes, Homeobox ; Humans ; Intestinal Mucosa/cytology/embryology ; Intestines/abnormalities/*embryology/microbiology/physiology ; Mesoderm/physiology ; Morphogenesis ; Signal Transduction ; Stem Cells/physiology
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  • 146
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-26
    Description: The intestinal epithelium follows the paradigms of stem cell biology established for other self-renewing tissues. With a unique topology, it constitutes a two-dimensional structure folded into valleys and hills: the proliferative crypts and the differentiated villi. Its unprecedented self-renewal rate appears reflected in a high susceptibility to malignant transformation. The molecular mechanisms that control homeostatic self-renewal and those that underlie colorectal cancer are remarkably symmetrical. Here, we discuss the biology of the intestinal epithelium, emphasizing the roles played by Wnt, bone morphogenic protein, and Notch signaling cascades in epithelial self-renewal and cancer.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Radtke, Freddy -- Clevers, Hans -- New York, N.Y. -- Science. 2005 Mar 25;307(5717):1904-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Ludwig Institute for Cancer Research, Lausanne Branch, University of Lausanne, Chemin de Boveresses 155, CH-1066 Epalinges, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15790842" target="_blank"〉PubMed〈/a〉
    Keywords: Adenomatous Polyposis Coli/genetics/metabolism/pathology ; Animals ; Bone Morphogenetic Proteins/metabolism ; Cell Transformation, Neoplastic ; Colorectal Neoplasms/*etiology/genetics/pathology/physiopathology ; Colorectal Neoplasms, Hereditary Nonpolyposis/genetics/metabolism/pathology ; Helix-Loop-Helix Motifs ; Humans ; Intercellular Signaling Peptides and Proteins/metabolism ; Intestinal Mucosa/*cytology/embryology/*physiology ; Membrane Proteins/metabolism ; Mutation ; Receptors, Notch ; Signal Transduction ; Stem Cells/cytology/physiology ; Wnt Proteins
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  • 147
    Publication Date: 2005-04-16
    Description: Ebola virus (EboV) causes rapidly fatal hemorrhagic fever in humans and there is currently no effective treatment. We found that the infection of African green monkey kidney (Vero) cells by vesicular stomatitis viruses bearing the EboV glycoprotein (GP) requires the activity of endosomal cysteine proteases. Using selective protease inhibitors and protease-deficient cell lines, we identified an essential role for cathepsin B (CatB) and an accessory role for cathepsin L (CatL) in EboV GP-dependent entry. Biochemical studies demonstrate that CatB and CatL mediate entry by carrying out proteolysis of the EboV GP subunit GP1 and support a multistep mechanism that explains the relative contributions of these enzymes to infection. CatB and CatB/CatL inhibitors diminish the multiplication of infectious EboV-Zaire in cultured cells and may merit investigation as anti-EboV drugs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chandran, Kartik -- Sullivan, Nancy J -- Felbor, Ute -- Whelan, Sean P -- Cunningham, James M -- R01 AI059371/AI/NIAID NIH HHS/ -- R01 AI059371-01A1/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2005 Jun 10;308(5728):1643-5. Epub 2005 Apr 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15831716" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cathepsin B/antagonists & inhibitors/*metabolism ; Cathepsin L ; Cathepsins/antagonists & inhibitors/*metabolism ; Cell Line ; Cells, Cultured ; Cercopithecus aethiops ; Cysteine Endopeptidases/*metabolism ; Cysteine Proteinase Inhibitors/pharmacology ; Ebolavirus/metabolism/*physiology ; Endosomes/*metabolism ; Hydrogen-Ion Concentration ; Mice ; Vero Cells ; Vesicular stomatitis Indiana virus/genetics/physiology ; Viral Envelope Proteins/*metabolism ; Virion/physiology
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  • 148
    Publication Date: 2005-10-22
    Description: Blood calcium concentration is maintained within a narrow range despite large variations in dietary input and body demand. The Transient Receptor Potential ion channel TRPV5 has been implicated in this process. We report here that TRPV5 is stimulated by the mammalian hormone klotho. Klotho, a beta-glucuronidase, hydrolyzes extracellular sugar residues on TRPV5, entrapping the channel in the plasma membrane. This maintains durable calcium channel activity and membrane calcium permeability in kidney. Thus, klotho activates a cell surface channel by hydrolysis of its extracellular N-linked oligosaccharides.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chang, Q -- Hoefs, S -- van der Kemp, A W -- Topala, C N -- Bindels, R J -- Hoenderop, J G -- New York, N.Y. -- Science. 2005 Oct 21;310(5747):490-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, Netherlands.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16239475" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Calcium/metabolism ; Calcium Channels/genetics/*metabolism ; Cell Line ; Cell Membrane/metabolism ; Cells, Cultured ; Glucuronidase/antagonists & inhibitors/metabolism ; Glycosylation ; Humans ; Hydrolysis ; Kidney/cytology/metabolism ; Membrane Proteins/*metabolism ; Mice ; Mice, Inbred C57BL ; Mutation ; Patch-Clamp Techniques ; Protein Transport ; Rabbits ; Sodium/metabolism ; TRPV Cation Channels/genetics/*metabolism ; Transfection
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  • 149
    Publication Date: 2005-02-19
    Description: We describe several fossils referable to Gomphos elkema from deposits close to the Paleocene-Eocene boundary at Tsagan Khushu, Mongolia. Gomphos shares a suite of cranioskeletal characters with extant rabbits, hares, and pikas but retains a primitive dentition and jaw compared to its modern relatives. Phylogenetic analysis supports the position of Gomphos as a stem lagomorph and excludes Cretaceous taxa from the crown radiation of placental mammals. Our results support the hypothesis that rodents and lagomorphs radiated during the Cenozoic and diverged from other placental mammals close to the Cretaceous-Tertiary boundary.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Asher, Robert J -- Meng, Jin -- Wible, John R -- McKenna, Malcolm C -- Rougier, Guillermo W -- Dashzeveg, Demberlyn -- Novacek, Michael J -- New York, N.Y. -- Science. 2005 Feb 18;307(5712):1091-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Museum fur Naturkunde, Humboldt Universitat, Invalidenstrasse 43, 10115 Berlin, Germany. robert.asher@museum.hu-berlin.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15718468" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Foot Bones/anatomy & histology ; *Fossils ; Jaw/anatomy & histology ; *Lagomorpha/anatomy & histology/classification ; Leg Bones/anatomy & histology ; *Mammals/anatomy & histology/classification ; Mongolia ; Paleodontology ; Phylogeny ; Rodentia/anatomy & histology/classification ; Skull/anatomy & histology ; Spine/anatomy & histology
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  • 150
    Publication Date: 2005-09-06
    Description: Noncoding RNA molecules (ncRNAs) have been implicated in numerous biological processes including transcriptional regulation and the modulation of protein function. Yet, in spite of the apparent abundance of ncRNA, little is known about the biological role of the projected thousands of ncRNA genes present in the human genome. To facilitate functional analysis of these RNAs, we have created an arrayed library of short hairpin RNAs (shRNAs) directed against 512 evolutionarily conserved putative ncRNAs and, via cell-based assays, we have begun to determine their roles in cellular pathways. Using this system, we have identified an ncRNA repressor of the nuclear factor of activated T cells (NFAT), which interacts with multiple proteins including members of the importin-beta superfamily and likely functions as a specific regulator of NFAT nuclear trafficking.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Willingham, A T -- Orth, A P -- Batalov, S -- Peters, E C -- Wen, B G -- Aza-Blanc, P -- Hogenesch, J B -- Schultz, P G -- New York, N.Y. -- Science. 2005 Sep 2;309(5740):1570-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry, Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16141075" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; DNA-Binding Proteins/*antagonists & inhibitors ; Humans ; Mice ; NFATC Transcription Factors ; Nuclear Proteins/*antagonists & inhibitors ; *RNA Interference ; RNA, Long Noncoding ; RNA, Untranslated/antagonists & inhibitors/genetics/*physiology ; Transcription Factors/*antagonists & inhibitors ; beta Karyopherins/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 151
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-09-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hauser, Marc D -- New York, N.Y. -- Science. 2005 Sep 2;309(5740):1498-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Departments of Psychology, Organismic and Evolutionary Biology, and Biological Anthropology, Harvard University, Cambridge, MA 02138, USA. mdh@wjh.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16141053" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Behavior, Animal ; Conservation of Natural Resources ; Evolution, Molecular ; *Feeding Behavior ; Genome ; Pan troglodytes/genetics/*psychology
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  • 152
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-11-19
    Description: Cells are inherently sensitive to local mesoscale, microscale, and nanoscale patterns of chemistry and topography. We review current approaches to control cell behavior through the nanoscale engineering of materials surfaces. Far-reaching implications are emerging for applications including medical implants, cell supports, and materials that can be used as instructive three-dimensional environments for tissue regeneration.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stevens, Molly M -- George, Julian H -- New York, N.Y. -- Science. 2005 Nov 18;310(5751):1135-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Materials and Institute for Biomedical Engineering, Imperial College of Science, Technology, and Medicine, Prince Consort Road, London SW7 2BP, UK. m.stevens@imperial.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16293749" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biocompatible Materials ; Cell Membrane/*physiology ; *Cell Physiological Phenomena ; Extracellular Matrix/*physiology ; Forecasting ; Humans ; Nanotechnology/*trends ; Surface Properties ; Tissue Engineering/trends
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 153
    Publication Date: 2005-12-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wilmut, Ian -- West, Michael D -- Lanza, Robert P -- Gearhart, John D -- Smith, Austin -- Colman, Alan -- Trounson, Alan O -- Campbell, Keith H -- New York, N.Y. -- Science. 2005 Dec 23;310(5756):1903. Epub 2005 Dec 13.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16352868" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blastocyst/cytology ; Cell Line ; *Cloning, Organism ; Embryo, Mammalian/*cytology ; Humans ; Nuclear Transfer Techniques ; *Stem Cells
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 154
    Publication Date: 2005-09-10
    Description: Recent studies have shown multiple differences between humans and apes in sialic acid (Sia) biology, including Siglecs (Sia-recognizing-Ig-superfamily lectins). Comparisons with the chimpanzee genome indicate that human SIGLEC11 emerged through human-specific gene conversion by an adjacent pseudogene. Conversion involved 5 cent untranslated sequences and the Sia-recognition domain. This human protein shows reduced binding relative to the ancestral form but recognizes oligosialic acids, which are enriched in the brain. SIGLEC11 is expressed in human but not in chimpanzee brain microglia. Further studies will determine if this event was related to the evolution of Homo.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hayakawa, Toshiyuki -- Angata, Takashi -- Lewis, Amanda L -- Mikkelsen, Tarjei S -- Varki, Nissi M -- Varki, Ajit -- R01GM32373/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2005 Sep 9;309(5741):1693.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Glycobiology Research and Training Center, University of California at San Diego, La Jolla, CA 92093, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16151003" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Evolution ; Brain/*metabolism ; Exons ; *Gene Conversion ; Humans ; Lectins/*genetics/metabolism ; Membrane Proteins/*genetics/metabolism ; Microglia/*metabolism ; Pan troglodytes/genetics/metabolism ; Phylogeny ; Pongo pygmaeus/genetics/metabolism ; Pseudogenes ; Regulatory Sequences, Nucleic Acid ; Sialic Acids/metabolism
    Print ISSN: 0036-8075
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  • 155
    Publication Date: 2005-11-15
    Description: Rapid global warming of 5 degrees to 10 degrees C during the Paleocene-Eocene Thermal Maximum (PETM) coincided with major turnover in vertebrate faunas, but previous studies have found little floral change. Plant fossils discovered in Wyoming, United States, show that PETM floras were a mixture of native and migrant lineages and that plant range shifts were large and rapid (occurring within 10,000 years). Floral composition and leaf shape and size suggest that climate warmed by approximately 5 degrees C during the PETM and that precipitation was low early in the event and increased later. Floral response to warming and/or increased atmospheric CO2 during the PETM was comparable in rate and magnitude to that seen in postglacial floras and to the predicted effects of anthropogenic carbon release and climate change on future vegetation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wing, Scott L -- Harrington, Guy J -- Smith, Francesca A -- Bloch, Jonathan I -- Boyer, Douglas M -- Freeman, Katherine H -- New York, N.Y. -- Science. 2005 Nov 11;310(5750):993-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Paleobiology, Smithsonian Museum of Natural History, 10th Street and Constitution Avenue, NW, Washington, DC 20560, USA. wings@si.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16284173" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biodiversity ; Carbon Isotopes/analysis ; *Climate ; *Ecosystem ; *Fossils ; Geologic Sediments ; *Greenhouse Effect ; Oxygen Isotopes/analysis ; Plant Development ; Plant Leaves/anatomy & histology ; *Plants/anatomy & histology/classification ; Rain ; Temperature ; Time Factors ; Wyoming
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  • 156
    Publication Date: 2005-07-16
    Description: Whole-genome sequencing of the protozoan pathogen Trypanosoma cruzi revealed that the diploid genome contains a predicted 22,570 proteins encoded by genes, of which 12,570 represent allelic pairs. Over 50% of the genome consists of repeated sequences, such as retrotransposons and genes for large families of surface molecules, which include trans-sialidases, mucins, gp63s, and a large novel family (〉1300 copies) of mucin-associated surface protein (MASP) genes. Analyses of the T. cruzi, T. brucei, and Leishmania major (Tritryp) genomes imply differences from other eukaryotes in DNA repair and initiation of replication and reflect their unusual mitochondrial DNA. Although the Tritryp lack several classes of signaling molecules, their kinomes contain a large and diverse set of protein kinases and phosphatases; their size and diversity imply previously unknown interactions and regulatory processes, which may be targets for intervention.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉El-Sayed, Najib M -- Myler, Peter J -- Bartholomeu, Daniella C -- Nilsson, Daniel -- Aggarwal, Gautam -- Tran, Anh-Nhi -- Ghedin, Elodie -- Worthey, Elizabeth A -- Delcher, Arthur L -- Blandin, Gaelle -- Westenberger, Scott J -- Caler, Elisabet -- Cerqueira, Gustavo C -- Branche, Carole -- Haas, Brian -- Anupama, Atashi -- Arner, Erik -- Aslund, Lena -- Attipoe, Philip -- Bontempi, Esteban -- Bringaud, Frederic -- Burton, Peter -- Cadag, Eithon -- Campbell, David A -- Carrington, Mark -- Crabtree, Jonathan -- Darban, Hamid -- da Silveira, Jose Franco -- de Jong, Pieter -- Edwards, Kimberly -- Englund, Paul T -- Fazelina, Gholam -- Feldblyum, Tamara -- Ferella, Marcela -- Frasch, Alberto Carlos -- Gull, Keith -- Horn, David -- Hou, Lihua -- Huang, Yiting -- Kindlund, Ellen -- Klingbeil, Michele -- Kluge, Sindy -- Koo, Hean -- Lacerda, Daniela -- Levin, Mariano J -- Lorenzi, Hernan -- Louie, Tin -- Machado, Carlos Renato -- McCulloch, Richard -- McKenna, Alan -- Mizuno, Yumi -- Mottram, Jeremy C -- Nelson, Siri -- Ochaya, Stephen -- Osoegawa, Kazutoyo -- Pai, Grace -- Parsons, Marilyn -- Pentony, Martin -- Pettersson, Ulf -- Pop, Mihai -- Ramirez, Jose Luis -- Rinta, Joel -- Robertson, Laura -- Salzberg, Steven L -- Sanchez, Daniel O -- Seyler, Amber -- Sharma, Reuben -- Shetty, Jyoti -- Simpson, Anjana J -- Sisk, Ellen -- Tammi, Martti T -- Tarleton, Rick -- Teixeira, Santuza -- Van Aken, Susan -- Vogt, Christy -- Ward, Pauline N -- Wickstead, Bill -- Wortman, Jennifer -- White, Owen -- Fraser, Claire M -- Stuart, Kenneth D -- Andersson, Bjorn -- AI045039/AI/NIAID NIH HHS/ -- AI45038/AI/NIAID NIH HHS/ -- AI45061/AI/NIAID NIH HHS/ -- R01 AI031077/AI/NIAID NIH HHS/ -- R01 AI031077-11/AI/NIAID NIH HHS/ -- U01 AI045038/AI/NIAID NIH HHS/ -- U01 AI045039/AI/NIAID NIH HHS/ -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2005 Jul 15;309(5733):409-15.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Parasite Genomics, Institute for Genomic Research, Rockville, MD 20850, USA. nelsayed@tigr.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16020725" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chagas Disease/drug therapy/parasitology ; DNA Repair ; DNA Replication ; DNA, Mitochondrial/genetics ; DNA, Protozoan/genetics ; Genes, Protozoan ; *Genome, Protozoan ; Humans ; Meiosis ; Membrane Proteins/chemistry/genetics/physiology ; Multigene Family ; Protozoan Proteins/chemistry/*genetics/physiology ; Recombination, Genetic ; Repetitive Sequences, Nucleic Acid ; Retroelements ; *Sequence Analysis, DNA ; Signal Transduction ; Telomere/genetics ; Trypanocidal Agents/pharmacology/therapeutic use ; Trypanosoma cruzi/chemistry/*genetics/physiology
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  • 157
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Eric -- New York, N.Y. -- Science. 2005 Oct 7;310(5745):32.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16210505" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Conservation of Natural Resources/*legislation & jurisprudence ; *Ecosystem ; Environment ; Public Policy ; United States ; United States Government Agencies
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 158
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-12-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Dec 16;310(5755):1758.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16357238" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cricetinae ; Humans ; Mice ; PrPC Proteins/*chemistry ; PrPSc Proteins/*chemistry/*pathogenicity ; Prion Diseases/*etiology ; Protein Folding
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  • 159
    Publication Date: 2005-12-13
    Description: Sir2 (silent information regulator 2) is a nicotinamide adenine dinucleotide-dependent deacetylase required for longevity due to calorie restriction in yeast and Drosophila. In mammals, calorie restriction induces a complex pattern of physiological and behavioral changes. Here we report that the mammalian Sir2 ortholog, Sirt1, is required for the induction of a phenotype by calorie restriction in mice.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, Danica -- Steele, Andrew D -- Lindquist, Susan -- Guarente, Leonard -- AG11119/AG/NIA NIH HHS/ -- New York, N.Y. -- Science. 2005 Dec 9;310(5754):1641.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16339438" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Caloric Restriction ; Eating ; Mice ; Mice, Knockout ; *Motor Activity ; Movement ; Sirtuin 1 ; Sirtuins/genetics/*physiology
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  • 160
    Publication Date: 2005-04-23
    Description: Obligate Acacia ant plants house mutualistic ants as a defense mechanism and provide them with extrafloral nectar (EFN). Ant/plant mutualisms are widespread, but little is known about the biochemical basis of their species specificity. Despite its importance in these and other plant/animal interactions, little attention has been paid to the control of the chemical composition of nectar. We found high invertase (sucrose-cleaving) activity in Acacia EFN, which thus contained no sucrose. Sucrose, a disaccharide common in other EFNs, usually attracts nonsymbiotic ants. The EFN of the ant acacias was therefore unattractive to such ants. The Pseudomyrmex ants that are specialized to live on Acacia had almost no invertase activity in their digestive tracts and preferred sucrose-free EFN. Our results demonstrate postsecretory regulation of the carbohydrate composition of nectar.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Heil, M -- Rattke, J -- Boland, W -- New York, N.Y. -- Science. 2005 Apr 22;308(5721):560-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Bioorganic Chemistry, Max-Planck-Institute for Chemical Ecology, Hans-Knoll-Strasse 8, D-07745 Jena, Germany. Heil_Martin@web.de〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15845855" target="_blank"〉PubMed〈/a〉
    Keywords: Acacia/chemistry/*enzymology/physiology ; Animals ; Ants/enzymology/*physiology ; Biological Evolution ; Feeding Behavior ; Hydrolysis ; Species Specificity ; Sucrose/analysis/*metabolism ; *Symbiosis ; beta-Fructofuranosidase/*metabolism
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  • 161
    Publication Date: 2005-10-15
    Description: Observation of actions performed by others activates monkey ventral premotor cortex, where action meaning, but not object identity, is coded. In a functional MRI (fMRI) study, we investigated whether other monkey frontal areas respond to actions performed by others. Observation of a hand grasping objects activated four frontal areas: rostral F5 and areas 45B, 45A, and 46. Observation of an individual grasping an object also activated caudal F5, which indicates different degrees of action abstraction in F5. Observation of shapes activated area 45, but not premotor F5. Convergence of object and action information in area 45 may be important for full comprehension of actions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nelissen, Koen -- Luppino, Giuseppe -- Vanduffel, Wim -- Rizzolatti, Giacomo -- Orban, Guy A -- New York, N.Y. -- Science. 2005 Oct 14;310(5746):332-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratorium voor Neuro-en Psychofysiologie, Katholieke Universiteit Leuven Medical School, Leuven, Belgium.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16224029" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Frontal Lobe/*physiology ; Humans ; *Interpersonal Relations ; Macaca mulatta ; Magnetic Resonance Imaging ; Male ; Motion Perception/*physiology ; Motor Activity ; Neurons/physiology ; Videotape Recording
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  • 162
    Publication Date: 2005-07-30
    Description: The open oceans comprise most of the biosphere, yet patterns and trends of species diversity there are enigmatic. Here, we derive worldwide patterns of tuna and billfish diversity over the past 50 years, revealing distinct subtropical "hotspots" that appeared to hold generally for other predators and zooplankton. Diversity was positively correlated with thermal fronts and dissolved oxygen and a nonlinear function of temperature (approximately 25 degrees C optimum). Diversity declined between 10 and 50% in all oceans, a trend that coincided with increased fishing pressure, superimposed on strong El Nino-Southern Oscillation-driven variability across the Pacific. We conclude that predator diversity shows a predictable yet eroding pattern signaling ecosystem-wide changes linked to climate and fishing.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Worm, Boris -- Sandow, Marcel -- Oschlies, Andreas -- Lotze, Heike K -- Myers, Ransom A -- New York, N.Y. -- Science. 2005 Aug 26;309(5739):1365-9. Epub 2005 Jul 28.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Biology Department, Dalhousie University, Halifax, NS, Canada B3H 4J1. bworm@dal.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16051749" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Climate ; *Ecosystem ; Fisheries ; Oceans and Seas ; Oxygen/analysis ; *Perciformes ; Population Density ; *Predatory Behavior ; Regression Analysis ; Seasons ; Temperature ; Time Factors ; *Tuna ; Zooplankton
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  • 163
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-11-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Nov 18;310(5751):1103.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16293730" target="_blank"〉PubMed〈/a〉
    Keywords: Acetamides/economics/supply & distribution ; Animals ; Antiviral Agents/economics ; Birds ; Disease Outbreaks/economics/*prevention & control ; Health Planning ; Health Services Accessibility ; Humans ; *Influenza A Virus, H5N1 Subtype ; Influenza in Birds/prevention & control ; Influenza, Human/economics/*epidemiology/prevention & control ; International Cooperation ; Oseltamivir ; World Health Organization
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  • 164
    Publication Date: 2005-04-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Helgen, Kristofer M -- Groves, Colin P -- New York, N.Y. -- Science. 2005 Apr 8;308(5719):199; author reply 199.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15821069" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Birds/classification ; Climate ; India ; Mammals/classification ; Sri Lanka
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  • 165
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-16
    Description: Earth's climate can change substantially on time scales of 1000 years or so, but given the time it takes for an ice sheet to grow or melt, it has been unclear whether continental ice sheets-and hence global sea levels-mirror these rapid changes. In his Perspective, Henderson discusses the report by Thompson and Goldstein, who have used a new correction method to date coral samples that are up to 250,000 years old. The corals can be used to deduce past sea levels. The resulting sea-level record shows that sea levels have varied on millennial time scales even during times of high sea level and relative climate stability.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Henderson, Gideon M -- New York, N.Y. -- Science. 2005 Apr 15;308(5720):361-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Earth Sciences, University of Oxford, Oxford OX1 3PR, United Kingdom. gideon.henderson@earth.ox.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15831744" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Anthozoa/chemistry ; Climate ; *Fossils ; Ice ; Oceans and Seas ; Seasons ; *Seawater ; Temperature ; Thorium/analysis ; Time ; Uranium/analysis
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  • 166
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-12-03
    Description: The self-renewing ability of a stem cell is controlled by its specialized micro-environment or niche, whereas epigenetic regulation of gene expression by chromatin remodeling factors underlies cell fate determination. Here we report that the adenosine triphosphate-dependent chromatin remodeling factors ISWI and DOM control germline stem cell and somatic stem cell self-renewal in the Drosophila ovary, respectively. The iswi mutant germline stem cells are lost rapidly because of defects in responding to bone morphogenetic protein niche signals and in repressing differentiation, whereas the dom mutant somatic stem cells are lost because of defective self-renewal. This work demonstrates that different stem cell types can use different chromatin remodeling factors to control cell self-renewal.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xi, Rongwen -- Xie, Ting -- 1R01 GM64428-01/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2005 Dec 2;310(5753):1487-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, MO 64110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16322456" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphatases/*physiology ; Animals ; Bone Morphogenetic Proteins/metabolism ; Cell Division/physiology ; Chromatin Assembly and Disassembly/*physiology ; Drosophila/cytology/enzymology ; Drosophila Proteins/*physiology ; Female ; Gene Expression Regulation ; Mutagenesis ; Ovary/cytology ; Stem Cells/*physiology ; Transcription Factors/*physiology
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  • 167
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Oct 14;310(5746):209.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16223989" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Birds ; *Disease Outbreaks/prevention & control/veterinary ; Europe ; Health Planning ; Humans ; *Influenza A virus ; *Influenza Vaccines ; Influenza in Birds/epidemiology/transmission ; Influenza, Human/*epidemiology/prevention & control/virology ; *Politics ; *Public Health ; Turkey ; United States/epidemiology
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  • 168
    Publication Date: 2005-01-18
    Description: Dendritic cells (DCs) and macrophages are critical to innate and adaptive immunity to the intestinal bacterial microbiota. Here, we identify a myeloid-derived mucosal DC in mice, which populates the entire lamina propria of the small intestine. Lamina propria DCs were found to depend on the chemokine receptor CX3CR1 to form transepithelial dendrites, which enable the cells to directly sample luminal antigens. CX3CR1 was also found to control the clearance of entero-invasive pathogens by DCs. Thus, CX3CR1-dependent processes, which control host interactions of specialized DCs with commensal and pathogenic bacteria, may regulate immunological tolerance and inflammation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Niess, Jan Hendrik -- Brand, Stephan -- Gu, Xiubin -- Landsman, Limor -- Jung, Steffen -- McCormick, Beth A -- Vyas, Jatin M -- Boes, Marianne -- Ploegh, Hidde L -- Fox, James G -- Littman, Dan R -- Reinecker, Hans-Christian -- AI33856/AI/NIAID NIH HHS/ -- DK33506/DK/NIDDK NIH HHS/ -- DK54427/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2005 Jan 14;307(5707):254-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Gastrointestinal Unit, Massachusetts General Hospital and Harvard Medical School, 55 Fruit Street, Boston, MA 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15653504" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chemokine CX3CL1 ; Chemokines, CX3C/metabolism ; Dendritic Cells/cytology/*immunology/microbiology ; Escherichia coli/*immunology/isolation & purification ; Gene Deletion ; Green Fluorescent Proteins/metabolism ; Ileum/cytology/immunology ; *Immunity, Mucosal ; Intestinal Mucosa/*immunology/microbiology ; Intestine, Small/immunology/microbiology ; Lymphoid Tissue/cytology/immunology ; Membrane Proteins/metabolism ; Mice ; Mice, Transgenic ; Peyer's Patches/immunology/microbiology ; Phagocytosis ; Receptors, Chemokine/genetics/metabolism/*physiology ; Salmonella Infections, Animal/*immunology/microbiology ; Salmonella typhimurium/*immunology/isolation & purification
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  • 169
    Publication Date: 2005-08-06
    Description: Functional imaging methods monitor neural activity by measuring hemodynamic signals. These are more closely related to local field potentials (LFPs) than to action potentials. We simultaneously recorded electrical and hemodynamic responses in the cat visual cortex. Increasing stimulus strength enhanced spiking activity, high-frequency LFP oscillations, and hemodynamic responses. With constant stimulus intensity, the hemodynamic response fluctuated; these fluctuations were only loosely related to action potential frequency but tightly correlated to the power of LFP oscillations in the gamma range. These oscillations increase with the synchrony of synaptic events, which suggests a close correlation between hemodynamic responses and neuronal synchronization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Niessing, Jorn -- Ebisch, Boris -- Schmidt, Kerstin E -- Niessing, Michael -- Singer, Wolf -- Galuske, Ralf A W -- New York, N.Y. -- Science. 2005 Aug 5;309(5736):948-51.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Max Planck Institute for Brain Research, 60528 Frankfurt/M., Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16081740" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Brain Mapping ; Cats ; Electric Stimulation ; Electroencephalography ; Evoked Potentials, Visual ; *Hemodynamics ; Neurons/physiology ; Oxygen/blood ; Photic Stimulation ; Visual Cortex/*physiology
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  • 170
    Publication Date: 2005-10-15
    Description: A proposed strategy to aid in controlling the growing burden of vector-borne disease is population replacement, in which a natural vector population is replaced by a population with a reduced capacity for disease transmission. An important component of such a strategy is the drive system, which serves to spread a desired genotype into the targeted field population. Endosymbiotic Wolbachia bacteria are potential transgene drivers, but infections do not naturally occur in some important mosquito vectors, notably Aedes aegypti. In this work, stable infections of wAlbB Wolbachia were established in A. aegypti and caused high rates of cytoplasmic incompatibility (that is, elimination of egg hatch). Laboratory cage tests demonstrated the ability of wAlbB to spread into an A. aegypti population after seeding of an uninfected population with infected females, reaching infection fixation within seven generations.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Xi, Zhiyong -- Khoo, Cynthia C H -- Dobson, Stephen L -- AI-51533/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2005 Oct 14;310(5746):326-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Entomology, University of Kentucky, Lexington, KY 40546, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16224027" target="_blank"〉PubMed〈/a〉
    Keywords: Aedes/*microbiology ; Animals ; Crosses, Genetic ; Cytoplasm ; Female ; Insect Vectors/microbiology ; Male ; Pest Control, Biological ; Reproduction ; Wolbachia/*physiology
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  • 171
    Publication Date: 2005-02-12
    Description: The steroid hormone estrogen regulates many functionally unrelated processes in numerous tissues. Although it is traditionally thought to control transcriptional activation through the classical nuclear estrogen receptors, it also initiates many rapid nongenomic signaling events. We found that of all G protein-coupled receptors characterized to date, GPR30 is uniquely localized to the endoplasmic reticulum, where it specifically binds estrogen and fluorescent estrogen derivatives. Activating GPR30 by estrogen resulted in intracellular calcium mobilization and synthesis of phosphatidylinositol 3,4,5-trisphosphate in the nucleus. Thus, GPR30 represents an intracellular transmembrane estrogen receptor that may contribute to normal estrogen physiology as well as pathophysiology.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Revankar, Chetana M -- Cimino, Daniel F -- Sklar, Larry A -- Arterburn, Jeffrey B -- Prossnitz, Eric R -- 1 S10 RR14668/RR/NCRR NIH HHS/ -- AI36357/AI/NIAID NIH HHS/ -- EB00264/EB/NIBIB NIH HHS/ -- P20 RR11830/RR/NCRR NIH HHS/ -- R24 CA88339/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2005 Mar 11;307(5715):1625-30. Epub 2005 Feb 10.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology and Physiology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15705806" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antisense Elements (Genetics) ; Calcium/metabolism ; Cell Line ; Cell Line, Tumor ; Cell Membrane/metabolism ; Cell Nucleus/metabolism ; Endoplasmic Reticulum/*metabolism ; Estradiol/metabolism ; Estrogen Receptor alpha/metabolism ; Estrogens/*metabolism ; Humans ; Nuclear Envelope/metabolism ; Phosphatidylinositol 3-Kinases/metabolism ; Phosphatidylinositol Phosphates/metabolism ; Protein Transport ; Receptor, Epidermal Growth Factor/metabolism ; Receptors, Estrogen/*metabolism ; Receptors, G-Protein-Coupled/*metabolism ; Recombinant Fusion Proteins/metabolism ; *Signal Transduction ; Transfection
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  • 172
    Publication Date: 2005-07-30
    Description: Animals alter their behavioral patterns in an experience-dependent manner. Olfactory imprinting is a process in which the exposure of animals to olfactory cues during specific and restricted time windows leaves a permanent memory ("olfactory imprint") that shapes the animal's behavior upon encountering the olfactory cues at later times. We found that Caenorhabditis elegans displays olfactory imprinting behavior that is mediated by a single pair of interneurons. To function in olfactory imprinting, this interneuron pair must express a G protein-coupled chemoreceptor family member encoded by the sra-11 gene. Our study provides insights into the cellular and molecular basis of olfactory imprinting and reveals a function for a chemosensory receptor family member in interneurons.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Remy, Jean-Jacques -- Hobert, Oliver -- NS039996-05/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2005 Jul 29;309(5735):787-90.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratoire NMDA CNRS UMR 6156, Institut de Biologie du Developpement (IBDM), 13288 Marseille Cedex 9, France. remy@ibdm.univ-mrs.fr.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16051801" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Genetically Modified ; Benzaldehydes ; Caenorhabditis elegans/genetics/growth & development/*physiology ; Caenorhabditis elegans Proteins/genetics/*physiology ; Cues ; Food ; Gene Expression Regulation ; Genes, Helminth ; Genes, Homeobox ; Interneurons/*physiology ; Memory/physiology ; Movement ; Neurons, Afferent/physiology ; *Odors ; Oviposition ; Receptors, G-Protein-Coupled/genetics/*physiology ; Serotonin/pharmacology ; Smell/*physiology
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  • 173
    Publication Date: 2005-02-26
    Description: Uncontrolled releases of Tigris and Euphrates River waters after the 2003 war have partially restored some former marsh areas in southern Iraq, but restoration is failing in others because of high soil and water salinities. Nearly 20% of the original 15,000-square-kilometer marsh area was reflooded by March 2004, but the extent of marsh restoration is unknown. High-quality water, nonsaline soils, and the densest native vegetation were found in the only remaining natural marsh, the Al-Hawizeh, located on the Iranian border. Although substantially reduced in area and under current threat of an Iranian dike, it has the potential to be a native repopulation center for the region. Rapid reestablishment, high productivity, and reproduction of native flora and fauna in reflooded former marsh areas indicate a high probability for successful restoration, provided the restored wetlands are hydraulically designed to allow sufficient flow of noncontaminated water and flushing of salts through the ecosystem.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Richardson, Curtis J -- Reiss, Peter -- Hussain, Najah A -- Alwash, Azzam J -- Pool, Douglas J -- New York, N.Y. -- Science. 2005 Feb 25;307(5713):1307-11.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Duke University Wetland Center, Nicholas School of Environment and Earth Sciences, Duke University, Box 90333, Durham, NC 27708, USA. curtr@duke.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15731454" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; *Conservation of Natural Resources ; *Ecosystem ; *Fresh Water ; Iraq ; Metals/analysis ; Plant Development ; Rivers ; Sodium Chloride ; Soil ; Water Movements ; Xenobiotics/analysis
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  • 174
    Publication Date: 2005-09-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Sep 2;309(5740):1475.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16141040" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Bioterrorism ; New York ; *United States Government Agencies ; Virus Diseases/*veterinary
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  • 175
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2005 Mar 25;307(5717):1852.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15790815" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Vessels/*anatomy & histology ; Bone and Bones/*blood supply/*cytology ; DNA/analysis ; Dinosaurs/*anatomy & histology ; *Fossils ; Montana ; Osteocytes/*cytology ; Proteins/analysis ; Time
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  • 176
    Publication Date: 2005-04-16
    Description: Microglial cells represent the immune system of the mammalian brain and therefore are critically involved in various injuries and diseases. Little is known about their role in the healthy brain and their immediate reaction to brain damage. By using in vivo two-photon imaging in neocortex, we found that microglial cells are highly active in their presumed resting state, continually surveying their microenvironment with extremely motile processes and protrusions. Furthermore, blood-brain barrier disruption provoked immediate and focal activation of microglia, switching their behavior from patroling to shielding of the injured site. Microglia thus are busy and vigilant housekeepers in the adult brain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nimmerjahn, Axel -- Kirchhoff, Frank -- Helmchen, Fritjof -- New York, N.Y. -- Science. 2005 May 27;308(5726):1314-8. Epub 2005 Apr 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Abteilung Zellphysiologie, Max Planck Institut fur Medizinische Forschung, Jahnstrasse 29, 69120 Heidelberg, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15831717" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Astrocytes/physiology/ultrastructure ; Bicuculline/pharmacology ; Blood-Brain Barrier ; Brain Injuries/physiopathology ; Capillaries/injuries ; Cell Movement ; Cell Surface Extensions/*physiology/ultrastructure ; GABA Antagonists/pharmacology ; Green Fluorescent Proteins ; Lasers ; Lipopolysaccharides/pharmacology ; Mice ; Mice, Transgenic ; Microglia/cytology/*physiology/*ultrastructure ; Microscopy, Fluorescence ; Neocortex/*cytology/*physiology ; Pseudopodia/physiology ; Sodium Channel Blockers/pharmacology ; Tetrodotoxin/pharmacology
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  • 177
    Publication Date: 2005-01-08
    Description: Epilepsy afflicts 1% of humans and 5% of dogs. We report a canine epilepsy mutation and evidence for the existence of repeat-expansion disease outside humans. A canid-specific unstable dodecamer repeat in the Epm2b (Nhlrc1) gene recurrently expands, causing a fatal epilepsy and contributing to the high incidence of canine epilepsy. Tracing the repeat origins revealed two successive events, starting 50 million years ago, unique to canid evolution. A genetic test, presented here, will allow carrier and presymptomatic diagnosis and disease eradication. Clinicopathologic characterization establishes affected animals as a model for Lafora disease, the most severe teenage-onset human epilepsy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lohi, Hannes -- Young, Edwin J -- Fitzmaurice, Susan N -- Rusbridge, Clare -- Chan, Elayne M -- Vervoort, Mike -- Turnbull, Julie -- Zhao, Xiao-Chu -- Ianzano, Leonarda -- Paterson, Andrew D -- Sutter, Nathan B -- Ostrander, Elaine A -- Andre, Catherine -- Shelton, G Diane -- Ackerley, Cameron A -- Scherer, Stephen W -- Minassian, Berge A -- New York, N.Y. -- Science. 2005 Jan 7;307(5706):81.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15637270" target="_blank"〉PubMed〈/a〉
    Keywords: Alleles ; Animals ; Chromosome Mapping ; Cloning, Molecular ; *DNA Repeat Expansion ; Dog Diseases/*genetics ; Dogs/*genetics ; Female ; Lafora Disease/genetics/*veterinary ; Male ; Muscle, Skeletal/metabolism ; Pedigree ; Polymerase Chain Reaction ; RNA, Messenger/genetics/metabolism ; Sequence Analysis, DNA
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  • 178
    Publication Date: 2005-02-19
    Description: The sex pheromone of the German cockroach, Blattella germanica, has been characterized as gentisyl quinone isovalerate. This cockroach is a major cause of allergic disease and serves as a mechanical vector of pathogens, making it one of the most important residential and food-associated pests worldwide. The sex pheromone-producing gland in adult females was identified in 1993, but thermal instability of the pheromone made characterization difficult. Now, using a new preparative gas chromatography approach coupled with electroantennographic detection, we have isolated and characterized the pheromone, which we term blattellaquinone, and confirmed the identification by chemical synthesis. The synthetic pheromone was active in behavioral assays and highly effective in field trapping tests, which suggest that it may provide a new tool in cockroach population detection, monitoring, and control.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nojima, Satoshi -- Schal, Coby -- Webster, Francis X -- Santangelo, Richard G -- Roelofs, Wendell L -- New York, N.Y. -- Science. 2005 Feb 18;307(5712):1104-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Entomology, New York Agricultural Experiment Station, Cornell University, Geneva, NY 14456, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15718472" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/drug effects ; Blattellidae/*chemistry/physiology ; Chromatography, Gas ; Chromatography, High Pressure Liquid ; Electrodes ; Female ; Gas Chromatography-Mass Spectrometry ; Magnetic Resonance Spectroscopy ; Male ; Mass Spectrometry ; Molecular Structure ; Molecular Weight ; Quinones/chemical synthesis/*chemistry/*isolation & purification/pharmacology ; Sense Organs/drug effects/physiology ; Sex Attractants/chemical synthesis/*chemistry/*isolation & ; purification/pharmacology
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  • 179
    Publication Date: 2005-02-01
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Stokstad, Erik -- New York, N.Y. -- Science. 2005 Jan 28;307(5709):507.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15681361" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/drug effects/embryology ; Female ; Humans ; Maximum Allowable Concentration ; National Academy of Sciences (U.S.) ; Perchlorates/administration & dosage/*toxicity ; Pregnancy ; Rats ; Risk Assessment ; Thyroid Gland/drug effects ; Thyroid Hormones/metabolism ; Toxicity Tests ; United States ; United States Environmental Protection Agency ; Water Pollutants, Chemical/administration & dosage/*toxicity ; *Water Supply
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  • 180
    Publication Date: 2005-10-22
    Description: Infection of mice with an attenuated Creutzfeldt-Jakob disease agent (SY-CJD) interferes with superinfection by a more virulent human-derived CJD agent (FU-CJD) and does not require pathological prion protein (PrPres). Using a rapid coculture system, we found that a neural cell line free of immune system cells similarly supported substantial CJD agent interference without PrPres. In addition, SY-CJD prevented superinfection by sheep-derived Chandler (Ch) and 22L scrapie agents. However, only 22L and not Ch prevented FU-CJD infection, even though both scrapie strains provoked abundant PrPres. This relationship between particular strains of sheep- and human-derived agents is likely to affect their prevalence and epidemic spread.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nishida, Noriuki -- Katamine, Shigeru -- Manuelidis, Laura -- NS12674/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2005 Oct 21;310(5747):493-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Yale Medical School, New Haven, CT 06510, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16239476" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; Coculture Techniques ; *Creutzfeldt-Jakob Syndrome ; Humans ; Mice ; Neurons/metabolism/*physiology ; PrPSc Proteins/metabolism/*pathogenicity ; Prions/metabolism/*pathogenicity/*physiology ; Scrapie ; Sheep ; Species Specificity ; Virulence
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  • 181
    Publication Date: 2005-02-01
    Description: Neuronal gene transcription is repressed in non-neuronal cells by the repressor element 1 (RE-1)-silencing transcription factor/neuron-restrictive silencer factor (REST/NRSF) complex. To understand how this silencing is achieved, we examined a family of class-C RNA polymerase II (RNAPII) carboxyl-terminal domain (CTD) phosphatases [small CTD phosphatases (SCPs) 1 to 3], whose expression is restricted to non-neuronal tissues. We show that REST/NRSF recruits SCPs to neuronal genes that contain RE-1 elements, leading to neuronal gene silencing in non-neuronal cells. Phosphatase-inactive forms of SCP interfere with REST/NRSF function and promote neuronal differentiation of P19 stem cells. Likewise, small interfering RNA directed to the single Drosophila SCP unmasks neuronal gene expression in S2 cells. Thus, SCP activity is an evolutionarily conserved transcriptional regulator that acts globally to silence neuronal genes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yeo, Michele -- Lee, Soo-Kyung -- Lee, Bora -- Ruiz, Esmeralda C -- Pfaff, Samuel L -- Gill, Gordon N -- DK13149/DK/NIDDK NIH HHS/ -- NS37116/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 2005 Jan 28;307(5709):596-600.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, University of California, 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/15681389" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basic Helix-Loop-Helix Transcription Factors ; Cell Differentiation ; Cell Line ; Chromatin Immunoprecipitation ; DNA-Binding Proteins/metabolism ; Down-Regulation ; Drosophila/genetics/metabolism ; Drosophila Proteins/genetics/metabolism ; Gene Expression Profiling ; Gene Expression Regulation ; *Gene Silencing ; Humans ; In Situ Hybridization ; Mice ; Nerve Tissue Proteins/metabolism ; Neurons/cytology/*physiology ; Nuclear Proteins ; Phosphoprotein Phosphatases/genetics/*metabolism ; Phosphorylation ; RNA Interference ; Regulatory Sequences, Nucleic Acid ; Repressor Proteins/*metabolism ; TCF Transcription Factors ; Transcription Factor 7-Like 1 Protein ; Transcription Factors/*metabolism ; Tretinoin/pharmacology
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  • 182
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-07-16
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Jul 15;309(5733):370-1.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16020707" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Asia/epidemiology ; Birds/virology ; *Disease Outbreaks/veterinary ; *Global Health ; Humans ; *Influenza A virus ; *Influenza in Birds/*epidemiology/virology ; Influenza, Human/*epidemiology/virology ; Poultry/virology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 183
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lotem, Arnon -- Winkler, David W -- New York, N.Y. -- Science. 2005 Apr 15;308(5720):353-6; author reply 353-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15834973" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Communication ; Animals ; *Behavior, Animal ; Cues ; *Cultural Evolution ; *Knowledge ; *Terminology as Topic
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  • 184
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lowe, John B -- 1P01CA71932/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2005 Mar 11;307(5715):1570-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, University of Michigan Medical School, Ann Arbor, MI 48109-2216, USA. johnlowe@umich.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15761143" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Substitution ; Animals ; Cell Membrane/*metabolism ; Drosophila Proteins/chemistry/genetics/*metabolism ; Drosophila melanogaster/genetics/*metabolism ; Endoplasmic Reticulum/enzymology/metabolism ; Fucose/metabolism ; Fucosyltransferases/chemistry/genetics/*metabolism ; Guanosine Diphosphate Fucose/metabolism ; Ligands ; Membrane Proteins/*metabolism ; Molecular Chaperones/chemistry/genetics/*metabolism ; Mutation ; Protein Folding ; Protein Transport ; RNA Interference ; Receptors, Cell Surface/*metabolism ; Receptors, Notch ; Recombinant Fusion Proteins/metabolism ; Signal Transduction
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  • 185
    Publication Date: 2005-10-29
    Description: Hypothalamic neurons that express neuropeptide Y (NPY) and agouti-related protein (AgRP) are thought to be critical regulators of feeding behavior and body weight. To determine whether NPY/AgRP neurons are essential in mice, we targeted the human diphtheria toxin receptor to the Agrp locus, which allows temporally controlled ablation of NPY/AgRP neurons to occur after an injection of diphtheria toxin. Neonatal ablation of NPY/AgRP neurons had minimal effects on feeding, whereas their ablation in adults caused rapid starvation. These results suggest that network-based compensatory mechanisms can develop after the ablation of NPY/AgRP neurons in neonates but do not readily occur when these neurons become essential in adults.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Luquet, Serge -- Perez, Francisco A -- Hnasko, Thomas S -- Palmiter, Richard D -- K01 DA026504/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 2005 Oct 28;310(5748):683-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Biochemistry, University of Washington, Box 357370, Seattle, WA 98195, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16254186" target="_blank"〉PubMed〈/a〉
    Keywords: Aging/physiology ; Agouti-Related Protein ; Animals ; Animals, Newborn ; Arcuate Nucleus of Hypothalamus/cytology ; Body Weight/physiology ; Diphtheria Toxin ; Feeding Behavior/*physiology ; Heparin-binding EGF-like Growth Factor ; Humans ; Intercellular Signaling Peptides and Proteins ; Mice ; Neurons/metabolism/*physiology ; Neuropeptide Y/*metabolism ; Proteins/*metabolism ; Receptors, Cell Surface/genetics
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  • 186
    Publication Date: 2005-04-30
    Description: Mammalian Toll-like receptors (TLRs) play an important role in the innate recognition of pathogens by dendritic cells (DCs). Although TLRs are clearly involved in the detection of bacteria and viruses, relatively little is known about their function in the innate response to eukaryotic microorganisms. Here we identify a profilin-like molecule from the protozoan parasite Toxoplasma gondii that generates a potent interleukin-12 (IL-12) response in murine DCs that is dependent on myeloid differentiation factor 88. T. gondii profilin activates DCs through TLR11 and is the first chemically defined ligand for this TLR. Moreover, TLR11 is required in vivo for parasite-induced IL-12 production and optimal resistance to infection, thereby establishing a role for the receptor in host recognition of protozoan pathogens.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yarovinsky, Felix -- Zhang, Dekai -- Andersen, John F -- Bannenberg, Gerard L -- Serhan, Charles N -- Hayden, Matthew S -- Hieny, Sara -- Sutterwala, Fayyaz S -- Flavell, Richard A -- Ghosh, Sankar -- Sher, Alan -- 1R01AI045806-01A1/AI/NIAID NIH HHS/ -- AI05093/AI/NIAID NIH HHS/ -- R01-AI59440/AI/NIAID NIH HHS/ -- R01-GM38765/GM/NIGMS NIH HHS/ -- Intramural NIH HHS/ -- Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2005 Jun 10;308(5728):1626-9. Epub 2005 Apr 28.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Immunobiology Section, Laboratory of Parasitic Diseases; National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA. fyarovinsky@niaid.nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15860593" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Proteins, Signal Transducing ; Amino Acid Motifs ; Amino Acid Sequence ; Animals ; Antigens, Differentiation/genetics/metabolism ; Contractile Proteins/chemistry/*immunology/isolation & purification/metabolism ; Dendritic Cells/*immunology ; Genes, Protozoan ; Immunity, Innate ; Interleukin-12/biosynthesis/blood ; Ligands ; Membrane Glycoproteins/metabolism ; Mice ; Mice, Inbred C57BL ; Microfilament Proteins/chemistry/*immunology/isolation & purification/metabolism ; Molecular Sequence Data ; Myeloid Differentiation Factor 88 ; NF-kappa B/metabolism ; Profilins ; Protozoan Proteins/chemistry/*immunology/isolation & purification/metabolism ; Receptors, Cell Surface/*metabolism ; Receptors, Immunologic/genetics/metabolism ; Recombinant Proteins/immunology ; Signal Transduction ; Toll-Like Receptors ; Toxoplasma/genetics/*immunology ; Toxoplasmosis, Animal/*immunology ; Transfection
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  • 187
    Publication Date: 2005-06-11
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Jun 10;308(5728):1531-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15947147" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anopheles/*microbiology/*parasitology/physiology ; Feeding Behavior ; Humans ; *Hypocreales ; Insect Vectors/microbiology/parasitology ; Longevity ; Malaria/parasitology/transmission ; *Pest Control, Biological ; Plasmodium chabaudi/*growth & development ; Spores, Fungal ; Tanzania
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  • 188
    Publication Date: 2005-06-04
    Description: Despite the greater information content of genomic DNA, ancient DNA studies have largely been limited to the amplification of mitochondrial sequences. Here we describe metagenomic libraries constructed with unamplified DNA extracted from skeletal remains of two 40,000-year-old extinct cave bears. Analysis of approximately 1 megabase of sequence from each library showed that despite significant microbial contamination, 5.8 and 1.1% of clones contained cave bear inserts, yielding 26,861 base pairs of cave bear genome sequence. Comparison of cave bear and modern bear sequences revealed the evolutionary relationship of these lineages. The metagenomic approach used here establishes the feasibility of ancient DNA genome sequencing programs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Noonan, James P -- Hofreiter, Michael -- Smith, Doug -- Priest, James R -- Rohland, Nadin -- Rabeder, Gernot -- Krause, Johannes -- Detter, J Chris -- Paabo, Svante -- Rubin, Edward M -- T32 HL07279/HL/NHLBI NIH HHS/ -- U1 HL66681B/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2005 Jul 22;309(5734):597-9. Epub 2005 Jun 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉United States Department of Energy Joint Genome Institute, Walnut Creek, CA 94598, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15933159" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cloning, Molecular ; Computational Biology ; DNA/genetics/history ; Dogs/genetics ; *Genome ; Genomic Library ; History, Ancient ; Molecular Sequence Data ; Phylogeny ; Sequence Alignment ; *Sequence Analysis, DNA ; Ursidae/*genetics
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  • 189
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-15
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, Constance -- New York, N.Y. -- Science. 2005 Oct 14;310(5746):215.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16223996" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Wild ; *Conservation of Natural Resources/legislation & jurisprudence ; Kenya ; Politics
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  • 190
    Publication Date: 2005-10-22
    Description: Cell-cell interactions and cross-talk between signaling pathways specify Caenorhabditis elegans vulval precursor cells (VPCs) to adopt a spatial pattern: a central "1 degrees " VPC, in which epidermal growth factor receptor (EGFR)-mitogen-activated protein kinase (MAPK) activity is high and LIN-12/Notch activity is low, flanked by two "2 degrees " VPCs, in which LIN-12/Notch activity is high and EGFR-MAPK activity is low. Here, we identify a microRNA gene, mir-61, as a direct transcriptional target of LIN-12 and show that expression of mir-61 promotes the 2 degrees fate. We also identify vav-1, the ortholog of the Vav oncogene, as a target of mir-61, and show that down-regulation of VAV-1 promotes lin-12 activity in specifying the 2 degrees fate. Our results suggest that lin-12, mir-61, and vav-1 form a feedback loop that helps maximize lin-12 activity in the presumptive 2 degrees VPCs.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010395/" 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/PMC3010395/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoo, Andrew S -- Greenwald, Iva -- CA095389/CA/NCI NIH HHS/ -- R01 CA095389/CA/NCI NIH HHS/ -- R01 CA095389-01A1/CA/NCI NIH HHS/ -- R01 CA095389-02/CA/NCI NIH HHS/ -- R01 CA095389-03/CA/NCI NIH HHS/ -- R01 CA095389-04/CA/NCI NIH HHS/ -- R01 CA095389-05/CA/NCI NIH HHS/ -- R01 CA095389-06A1/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2005 Nov 25;310(5752):1330-3. Epub 2005 Oct 20.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Integrated Program in Cellular, Molecular, and Biophysical Studies, Howard Hughes Medical Institute, Columbia University College of Physicians and Surgeons, 701 West 168th Street, Room 720, New York, NY 10032, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16239437" target="_blank"〉PubMed〈/a〉
    Keywords: 3' Untranslated Regions ; Animals ; Animals, Genetically Modified ; Caenorhabditis elegans/*cytology/*genetics/growth & development/metabolism ; Caenorhabditis elegans Proteins/*genetics/*metabolism ; Computational Biology ; Down-Regulation ; Feedback, Physiological ; Female ; Gene Expression Regulation, Developmental ; Genes, Helminth ; Membrane Proteins/genetics/*metabolism ; MicroRNAs/*genetics/*metabolism ; Proto-Oncogene Proteins c-vav/*genetics/metabolism ; Receptors, Notch ; Regulatory Sequences, Nucleic Acid ; Signal Transduction ; Stem Cells/*cytology/metabolism ; Transcription, Genetic ; Vulva/cytology/growth & development
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  • 191
    Publication Date: 2005-11-29
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2005 Nov 25;310(5752):1256-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16311302" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; China/epidemiology ; Humans ; *Immunization Programs ; Influenza A Virus, H5N1 Subtype/*immunology ; *Influenza Vaccines ; Influenza in Birds/epidemiology/mortality/*prevention & control/virology ; Influenza, Human/epidemiology/mortality ; Population Surveillance ; *Poultry ; Vaccination/*veterinary
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  • 192
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-04-02
    Description: A fossil mammal from the Late Jurassic Morrison Formation, Colorado, has highly specialized teeth similar to those of xenarthran and tubulidentate placental mammals and different from the generalized insectivorous or omnivorous dentitions of other Jurassic mammals. It has many forelimb features specialized for digging, and its lumbar vertebrae show xenarthrous articulations. Parsimony analysis suggests that this fossil represents a separate basal mammalian lineage with some dental and vertebral convergences to those of modern xenarthran placentals, and reveals a previously unknown ecomorph of early mammals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Luo, Zhe-Xi -- Wible, John R -- New York, N.Y. -- Science. 2005 Apr 1;308(5718):103-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Carnegie Museum of Natural History, Pittsburgh, PA 15213, USA. luoz@carnegiemnh.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15802602" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Bone and Bones/anatomy & histology ; Colorado ; Dentition ; Diet ; Forelimb/anatomy & histology ; *Fossils ; Humerus/anatomy & histology ; Lumbar Vertebrae/anatomy & histology ; Mammals/*anatomy & histology/*classification/physiology ; Mandible/anatomy & histology ; Molar/anatomy & histology ; Paleodontology ; Phylogeny ; Scapula/anatomy & histology
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  • 193
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-11-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2005 Nov 18;310(5751):1112-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16293738" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Disease Outbreaks ; Global Health ; Health Planning ; Humans ; Influenza A Virus, H5N1 Subtype/*pathogenicity ; Influenza, Human/*epidemiology/transmission ; Risk Assessment ; Virulence
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  • 194
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-10-22
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Normile, Dennis -- New York, N.Y. -- Science. 2005 Oct 21;310(5747):426-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16239454" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Migration ; Animals ; Animals, Wild/*virology ; Antibodies, Viral/blood ; Asia/epidemiology ; Birds/*virology ; Carrier State/veterinary ; Commerce ; Disease Outbreaks/*veterinary ; Disease Reservoirs ; Europe/epidemiology ; Influenza A virus/classification/immunology/*isolation & ; purification/pathogenicity ; Influenza in Birds/*epidemiology/*transmission ; Population Surveillance ; Poultry/virology
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  • 195
    Publication Date: 2005-12-03
    Description: We present a detailed history of glacial to Holocene radiocarbon in the deep western North Atlantic from deep-sea corals and paired benthic-planktonic foraminifera. The deglaciation is marked by switches between radiocarbon-enriched and -depleted waters, leading to large radiocarbon gradients in the water column. These changes played an important role in modulating atmospheric radiocarbon. The deep-ocean record supports the notion of a bipolar seesaw with increased Northern-source deep-water formation linked to Northern Hemisphere warming and the reverse. In contrast, the more frequent radiocarbon variations in the intermediate/deep ocean are associated with roughly synchronous changes at the poles.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Robinson, Laura F -- Adkins, Jess F -- Keigwin, Lloyd D -- Southon, John -- Fernandez, Diego P -- Wang, S-L -- Scheirer, Daniel S -- New York, N.Y. -- Science. 2005 Dec 2;310(5753):1469-73. Epub 2005 Nov 3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉California Institute of Technology, MS 100-23, 1200 East California Boulevard, Pasadena, CA 91125, USA. laurar@gps.caltech.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16322451" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Anthozoa ; Atlantic Ocean ; Carbon Isotopes ; Carbon Radioisotopes ; *Climate ; *Eukaryota ; *Ice Cover ; Time ; Zooplankton
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  • 196
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Balter, Michael -- New York, N.Y. -- Science. 2005 Mar 4;307(5714):1386.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15746392" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Anthropology ; Archaeology ; Australia ; *Bone and Bones ; *Hominidae ; Indonesia ; Paleontology
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  • 197
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-03-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yuspa, Stuart H -- Epstein, Ervin H Jr -- New York, N.Y. -- Science. 2005 Mar 18;307(5716):1727-8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Cellular Carcinogenesis and Tumor Promotion, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA. sy12j@nih.gov〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15774745" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carcinoma, Squamous Cell/etiology/genetics/pathology/*physiopathology ; Cell Adhesion Molecules/metabolism ; Cell Transformation, Neoplastic ; Collagen Type VII/chemistry/*genetics/*physiology ; Disease Susceptibility ; Epidermolysis Bullosa Dystrophica/complications/*genetics/metabolism/pathology ; Genes, ras ; Humans ; I-kappa B Proteins/genetics/metabolism ; Keratinocytes/*metabolism/pathology ; Mice ; Mutation ; Neoplasm Invasiveness ; Protein Structure, Tertiary ; Skin Neoplasms/etiology/genetics/pathology/*physiopathology ; Transduction, Genetic ; Transforming Growth Factor beta/metabolism
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  • 198
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-02-05
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Storch, David -- Marquet, Pablo A -- Gaston, Kevin J -- New York, N.Y. -- Science. 2005 Feb 4;307(5710):684-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Theoretical Study, Charles University, 110 00-CZ Praha 1, Czech Republic.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15692039" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; Biomass ; *Ecosystem ; Environment ; Fractals ; Models, Biological ; Plants ; Population Dynamics ; Population Growth ; Stochastic Processes ; Temperature
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  • 199
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-09-06
    Description: Small RNA guides--microRNAs, small interfering RNAs, and repeat-associated small interfering RNAs, 21 to 30 nucleotides in length--shape diverse cellular pathways, from chromosome architecture to stem cell maintenance. Fifteen years after the discovery of RNA silencing, we are only just beginning to understand the depth and complexity of how these RNAs regulate gene expression and to consider their role in shaping the evolutionary history of higher eukaryotes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zamore, Phillip D -- Haley, Benjamin -- GM62862-01/GM/NIGMS NIH HHS/ -- GM65236-01/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 2005 Sep 2;309(5740):1519-24.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA. phillip.zamore@umassmed.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16141061" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Binding Sites ; Cell Nucleus/genetics ; History, 20th Century ; Humans ; MicroRNAs/chemistry/history/*physiology ; Models, Genetic ; Molecular Biology/history ; *RNA Interference ; RNA, Messenger/chemistry/metabolism ; RNA, Small Interfering/chemistry/history/*physiology ; Stem Cells/cytology
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  • 200
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-01-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Enserink, Martin -- New York, N.Y. -- Science. 2005 Jan 7;307(5706):33.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15637249" target="_blank"〉PubMed〈/a〉
    Keywords: Africa ; Animals ; Antimalarials/economics/*supply & distribution/therapeutic use ; Artemisinins/economics/*supply & distribution/therapeutic use ; Clinical Trials as Topic ; Drug Costs ; Drug Design ; Drug Evaluation, Preclinical ; Drug Resistance ; Drug Therapy, Combination ; Drug Utilization ; Genetic Engineering ; Heterocyclic Compounds, 1-Ring/chemistry/pharmacology ; Humans ; Malaria/*drug therapy ; Peroxides/chemistry/pharmacology ; Plasmodium falciparum/drug effects ; Spiro Compounds/chemistry/pharmacology ; World Health Organization
    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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