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  • Articles  (90)
  • Pregnancy  (54)
  • Disease Models, Animal
  • 2010-2014  (31)
  • 1980-1984  (59)
  • 1950-1954
  • 2013  (31)
  • 1981  (59)
  • Science. 211(4477): 6, 8.  (1)
  • Science. 211(4477): 76-7.  (1)
  • Science. 211(4477): 82-4.  (1)
  • Science. 211(4478): 177-80.  (1)
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  • Science. 211(4480): 351-8.  (1)
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  • Science. 212(4495): 648-9.  (1)
  • 25
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  • Articles  (90)
Years
  • 2010-2014  (31)
  • 1980-1984  (59)
  • 1950-1954
Year
Journal
  • 1
    Publication Date: 2013-04-27
    Description: Secondary bacterial pneumonia leads to increased morbidity and mortality from influenza virus infections. What causes this increased susceptibility, however, is not well defined. Host defense from infection relies not only on immune resistance mechanisms but also on the ability to tolerate a given level of pathogen burden. Failure of either resistance or tolerance can contribute to disease severity, making it hard to distinguish their relative contribution. We employ a coinfection mouse model of influenza virus and Legionella pneumophila in which we can separate resistance and tolerance. We demonstrate that influenza virus can promote susceptibility to lethal bacterial coinfection, even when bacterial infection is controlled by the immune system. We propose that this failure of host defense is due to impaired ability to tolerate tissue damage.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933032/" 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/PMC3933032/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Jamieson, Amanda M -- Pasman, Lesley -- Yu, Shuang -- Gamradt, Pia -- Homer, Robert J -- Decker, Thomas -- Medzhitov, Ruslan -- AI R01 055502/AI/NIAID NIH HHS/ -- R01 046688/PHS HHS/ -- R01 AI046688/AI/NIAID NIH HHS/ -- R01 AI055502/AI/NIAID NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2013 Jun 7;340(6137):1230-4. doi: 10.1126/science.1233632. Epub 2013 Apr 25.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Immunobiology, Yale University School of Medicine, New Haven, CT 06520, USA. amanda_jamieson@brown.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23618765" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caspase 1 ; Coinfection/*immunology/pathology ; Disease Models, Animal ; Host-Pathogen Interactions/immunology ; Interleukin-1beta/metabolism ; *Legionella pneumophila ; Legionnaires' Disease/*immunology/pathology ; Lung/microbiology/pathology/virology ; Mice ; Mice, Inbred C57BL ; *Orthomyxoviridae ; Orthomyxoviridae Infections/*immunology/pathology ; Pneumonia, Bacterial/*immunology/pathology ; Toll-Like Receptor 2/metabolism ; Toll-Like Receptor 3/metabolism ; Toll-Like Receptor 4/metabolism ; Tumor Necrosis Factor-alpha/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-12-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 2013 Dec 20;342(6165):1436. doi: 10.1126/science.342.6165.1436-a.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24357287" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Line ; Cell Separation ; Cloning, Organism/*methods ; Female ; Humans ; *Induced Pluripotent Stem Cells ; Nuclear Transfer Techniques ; Pregnancy ; *Research Embryo Creation ; Surrogate Mothers
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  • 3
    Publication Date: 2013-11-30
    Description: Hypercholesterolemia is a risk factor for estrogen receptor (ER)-positive breast cancers and is associated with a decreased response of tumors to endocrine therapies. Here, we show that 27-hydroxycholesterol (27HC), a primary metabolite of cholesterol and an ER and liver X receptor (LXR) ligand, increases ER-dependent growth and LXR-dependent metastasis in mouse models of breast cancer. The effects of cholesterol on tumor pathology required its conversion to 27HC by the cytochrome P450 oxidase CYP27A1 and were attenuated by treatment with CYP27A1 inhibitors. In human breast cancer specimens, CYP27A1 expression levels correlated with tumor grade. In high-grade tumors, both tumor cells and tumor-associated macrophages exhibited high expression levels of the enzyme. Thus, lowering circulating cholesterol levels or interfering with its conversion to 27HC may be a useful strategy to prevent and/or treat breast cancer.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899689/" 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/PMC3899689/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nelson, Erik R -- Wardell, Suzanne E -- Jasper, Jeff S -- Park, Sunghee -- Suchindran, Sunil -- Howe, Matthew K -- Carver, Nicole J -- Pillai, Ruchita V -- Sullivan, Patrick M -- Sondhi, Varun -- Umetani, Michihisa -- Geradts, Joseph -- McDonnell, Donald P -- K99CA172357/CA/NCI NIH HHS/ -- R37 DK048807/DK/NIDDK NIH HHS/ -- R37DK048807/DK/NIDDK NIH HHS/ -- T32 CA059365/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 2013 Nov 29;342(6162):1094-8. doi: 10.1126/science.1241908.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC 27710, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24288332" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Breast Neoplasms/blood/*metabolism/*pathology ; Cell Line, Tumor ; Cholestanetriol 26-Monooxygenase/antagonists & inhibitors/metabolism ; Disease Models, Animal ; Female ; Humans ; Hydroxycholesterols/antagonists & inhibitors/blood/*metabolism ; Hypercholesterolemia/blood/*metabolism ; Lung Neoplasms/secondary ; Mice ; Tumor Cells, Cultured
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2013-03-02
    Description: Prenatal infection and exposure to traumatizing experiences during peripuberty have each been associated with increased risk for neuropsychiatric disorders. Evidence is lacking for the cumulative impact of such prenatal and postnatal environmental challenges on brain functions and vulnerability to psychiatric disease. Here, we show in a translational mouse model that combined exposure to prenatal immune challenge and peripubertal stress induces synergistic pathological effects on adult behavioral functions and neurochemistry. We further demonstrate that the prenatal insult markedly increases the vulnerability of the pubescent offspring to brain immune changes in response to stress. Our findings reveal interactions between two adverse environmental factors that have individually been associated with neuropsychiatric disease and support theories that mental illnesses with delayed onsets involve multiple environmental hits.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Giovanoli, Sandra -- Engler, Harald -- Engler, Andrea -- Richetto, Juliet -- Voget, Mareike -- Willi, Roman -- Winter, Christine -- Riva, Marco A -- Mortensen, Preben B -- Feldon, Joram -- Schedlowski, Manfred -- Meyer, Urs -- New York, N.Y. -- Science. 2013 Mar 1;339(6123):1095-9. doi: 10.1126/science.1228261.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, 8603 Schwerzenbach, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23449593" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cytokines/immunology ; Disease Models, Animal ; Female ; Humans ; Mental Disorders/*immunology ; Mice ; Mice, Inbred C57BL ; Poly I-C/immunology/pharmacology ; Pregnancy ; Prenatal Exposure Delayed Effects/*immunology/virology ; Puberty/*immunology ; Stress, Physiological/*immunology
    Print ISSN: 0036-8075
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2013-05-21
    Description: Lazic criticizes the statistical analyses used to support the conclusions in our mouse model. His theory-biased criticism is disproportionate in view of the robustness of our findings (even if different statistical methods are applied) and falls short in explaining the postpubertal onset of effects.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Giovanoli, Sandra -- Meyer, Urs -- New York, N.Y. -- Science. 2013 May 17;340(6134):811. doi: 10.1126/science.1238060.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Physiology and Behavior Laboratory, Swiss Federal Institute of Technology (ETH) Zurich, Schwerzenbach, Switzerland.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23687030" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Humans ; Mental Disorders/*immunology ; Pregnancy ; Prenatal Exposure Delayed Effects/*immunology ; Puberty/*immunology ; Stress, Physiological/*immunology
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  • 6
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-05-21
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weiss, Robin A -- Stoye, Jonathan P -- MC_U117512710/Medical Research Council/United Kingdom -- New York, N.Y. -- Science. 2013 May 17;340(6134):820-1. doi: 10.1126/science.1235148.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Division of Infection and Immunity, University College London, Gower Street, London WC1E 6BT, UK. rweiss@ucl.ac.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23687035" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; DNA, Viral/genetics ; Endogenous Retroviruses/*genetics ; Female ; Genome, Human/*genetics ; Humans ; Placenta/virology ; Pregnancy ; Promoter Regions, Genetic ; Proviruses/*genetics ; Transcription, Genetic
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  • 7
    Publication Date: 2013-07-03
    Description: Oxygen deprivation followed by reoxygenation causes pathological responses in many disorders, including ischemic stroke, heart attacks, and reperfusion injury. Key aspects of ischemia-reperfusion can be modeled by a Caenorhabditis elegans behavior, the O2-ON response, which is suppressed by hypoxic preconditioning or inactivation of the O2-sensing HIF (hypoxia-inducible factor) hydroxylase EGL-9. From a genetic screen, we found that the cytochrome P450 oxygenase CYP-13A12 acts in response to the EGL-9-HIF-1 pathway to facilitate the O2-ON response. CYP-13A12 promotes oxidation of polyunsaturated fatty acids into eicosanoids, signaling molecules that can strongly affect inflammatory pain and ischemia-reperfusion injury responses in mammals. We propose that roles of the EGL-9-HIF-1 pathway and cytochrome P450 in controlling responses to reoxygenation after anoxia are evolutionarily conserved.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3969381/" 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/PMC3969381/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ma, Dengke K -- Rothe, Michael -- Zheng, Shu -- Bhatla, Nikhil -- Pender, Corinne L -- Menzel, Ralph -- Horvitz, H Robert -- GM24663/GM/NIGMS NIH HHS/ -- R01 GM024663/GM/NIGMS NIH HHS/ -- R37 GM024663/GM/NIGMS NIH HHS/ -- T32 GM007484/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2013 Aug 2;341(6145):554-8. doi: 10.1126/science.1235753. Epub 2013 Jun 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Biology, McGovern Institute for Brain Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23811225" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caenorhabditis elegans/genetics/*metabolism ; Caenorhabditis elegans Proteins/*metabolism ; Disease Models, Animal ; Eicosanoids/metabolism ; Evolution, Molecular ; Fatty Acids, Unsaturated/metabolism ; Hypoxia-Inducible Factor 1/*metabolism ; Oxygen/*metabolism ; Reperfusion Injury/*metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2013-08-10
    Description: Tree-building with diverse data maximizes explanatory power. Application of molecular clock models to ancient speciation events risks a bias against detection of fast radiations subsequent to the Cretaceous-Paleogene (K-Pg) event. Contrary to Springer et al., post-K-Pg placental diversification does not require "virus-like" substitution rates. Even constraining clade ages to their model, the explosive model best explains placental evolution.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉O'Leary, Maureen A -- Bloch, Jonathan I -- Flynn, John J -- Gaudin, Timothy J -- Giallombardo, Andres -- Giannini, Norberto P -- Goldberg, Suzann L -- Kraatz, Brian P -- Luo, Zhe-Xi -- Meng, Jin -- Ni, Xijun -- Novacek, Michael J -- Perini, Fernando A -- Randall, Zachary -- Rougier, Guillermo W -- Sargis, Eric J -- Silcox, Mary T -- Simmons, Nancy B -- Spaulding, Michelle -- Velazco, Paul M -- Weksler, Marcelo -- Wible, John R -- Cirranello, Andrea L -- New York, N.Y. -- Science. 2013 Aug 9;341(6146):613. doi: 10.1126/science.1238162.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anatomical Sciences, HSC T-8 (040), Stony Brook University, Stony Brook, NY 11794-8081, USA. maureen.oleary@stonybrook.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23929968" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Female ; *Fossils ; *Mammals ; *Phylogeny ; Pregnancy
    Print ISSN: 0036-8075
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  • 9
    Publication Date: 2013-07-28
    Description: Gram-negative bacteria including Escherichia coli, Citrobacter rodentium, Salmonella typhimurium, and Shigella flexneri are sensed in an ill-defined manner by an intracellular inflammasome complex that activates caspase-11. We show that macrophages loaded with synthetic lipid A, E. coli lipopolysaccharide (LPS), or S. typhimurium LPS activate caspase-11 independently of the LPS receptor Toll-like receptor 4 (TLR4). Consistent with lipid A triggering the noncanonical inflammasome, LPS containing a divergent lipid A structure antagonized caspase-11 activation in response to E. coli LPS or Gram-negative bacteria. Moreover, LPS-mutant E. coli failed to activate caspase-11. Tlr4(-/-) mice primed with TLR3 agonist polyinosinic:polycytidylic acid [poly(I:C)] to induce pro-caspase-11 expression were as susceptible as wild-type mice were to sepsis induced by E. coli LPS. These data unveil a TLR4-independent mechanism for innate immune recognition of LPS.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kayagaki, Nobuhiko -- Wong, Michael T -- Stowe, Irma B -- Ramani, Sree Ranjani -- Gonzalez, Lino C -- Akashi-Takamura, Sachiko -- Miyake, Kensuke -- Zhang, Juan -- Lee, Wyne P -- Muszynski, Artur -- Forsberg, Lennart S -- Carlson, Russell W -- Dixit, Vishva M -- New York, N.Y. -- Science. 2013 Sep 13;341(6151):1246-9. doi: 10.1126/science.1240248. Epub 2013 Jul 25.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiological Chemistry, Genentech, South San Francisco, CA 94080, USA. kayagaki@gene.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23887873" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caspases/biosynthesis ; Cholera Toxin/immunology ; Disease Models, Animal ; Escherichia coli/immunology ; Escherichia coli Infections/genetics/immunology ; *Immunity, Innate ; Inflammasomes/*immunology ; Lipid A/genetics/*immunology ; Macrophages/*immunology ; Mice ; Mice, Mutant Strains ; Mutation ; Salmonella Infections/immunology ; Salmonella typhimurium/immunology ; Sepsis/immunology ; Toll-Like Receptor 4/*immunology
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  • 10
    Publication Date: 2013-08-10
    Description: O'Leary et al. (Research Article, 8 February 2013, p. 662) examined mammalian relationships and divergence times and concluded that a single placental ancestor crossed the Cretaceous-Paleogene (K-Pg) boundary. This conclusion relies on phylogenetic analyses that fail to discriminate between homology and homoplasy and further implies virus-like rates of nucleotide substitution in early Paleocene placentals.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Springer, Mark S -- Meredith, Robert W -- Teeling, Emma C -- Murphy, William J -- New York, N.Y. -- Science. 2013 Aug 9;341(6146):613. doi: 10.1126/science.1238025.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, University of California, Riverside, CA 92521, USA. mark.springer@ucr.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23929967" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Female ; *Fossils ; *Mammals ; *Phylogeny ; Pregnancy
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 11
    Publication Date: 2013-05-25
    Description: The emergence of the H7N9 influenza virus in humans in Eastern China has raised concerns that a new influenza pandemic could occur. Here, we used a ferret model to evaluate the infectivity and transmissibility of A/Shanghai/2/2013 (SH2), a human H7N9 virus isolate. This virus replicated in the upper and lower respiratory tracts of the ferrets and was shed at high titers for 6 to 7 days, with ferrets showing relatively mild clinical signs. SH2 was efficiently transmitted between ferrets via direct contact, but less efficiently by airborne exposure. Pigs were productively infected by SH2 and shed virus for 6 days but were unable to transmit the virus to naive pigs or ferrets. Under appropriate conditions, human-to-human transmission of the H7N9 virus may be possible.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhu, H -- Wang, D -- Kelvin, D J -- Li, L -- Zheng, Z -- Yoon, S-W -- Wong, S-S -- Farooqui, A -- Wang, J -- Banner, D -- Chen, R -- Zheng, R -- Zhou, J -- Zhang, Y -- Hong, W -- Dong, W -- Cai, Q -- Roehrl, M H A -- Huang, S S H -- Kelvin, A A -- Yao, T -- Zhou, B -- Chen, X -- Leung, G M -- Poon, L L M -- Webster, R G -- Webby, R J -- Peiris, J S M -- Guan, Y -- Shu, Y -- HSN266200700005C/PHS HHS/ -- New York, N.Y. -- Science. 2013 Jul 12;341(6142):183-6. doi: 10.1126/science.1239844. Epub 2013 May 23.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Joint Influenza Research Centre [Shantou University Medical College/University of Hong Kong], Shantou University, Shantou, PR China.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23704376" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Communicable Diseases, Emerging/*transmission/*virology ; Disease Models, Animal ; Ferrets ; Humans ; Influenza, Human/pathology/*transmission/*virology ; Orthomyxoviridae/classification/genetics/*pathogenicity ; Respiratory System/pathology/virology ; Sus scrofa
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  • 12
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-02-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoder, Anne D -- New York, N.Y. -- Science. 2013 Feb 8;339(6120):656-8. doi: 10.1126/science.1233999.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology, Duke University, Durham, NC 27708, USA. anne.yoder@duke.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23393254" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Female ; *Fossils ; *Mammals ; *Phylogeny ; Pregnancy
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  • 13
    Publication Date: 2013-05-21
    Description: Giovanoli et al. (Reports, 1 March 2013, p. 1095) applied an immune challenge to pregnant females, and therefore to all offspring, and subsequently applied stress to offspring on a per cage basis. The data, however, were analyzed as a completely randomized design, which is inappropriate given these restrictions on randomization. This will increase both false positives and false negatives.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lazic, Stanley E -- New York, N.Y. -- Science. 2013 May 17;340(6134):811. doi: 10.1126/science.1237793.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉In Silico Lead Discovery, Novartis Institutes for Biomedical Research, Basel, Switzerland. stan.lazic@cantab.net〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23687029" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Humans ; Mental Disorders/*immunology ; Pregnancy ; Prenatal Exposure Delayed Effects/*immunology ; Puberty/*immunology ; Stress, Physiological/*immunology
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  • 14
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-12-21
    Description: 〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084614/" 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/PMC4084614/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holland, William L -- Scherer, Philipp E -- P01 DK088761/DK/NIDDK NIH HHS/ -- R01 DK055758/DK/NIDDK NIH HHS/ -- R01 DK099110/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2013 Dec 20;342(6165):1460-1. doi: 10.1126/science.1249077.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Touchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, TX 75390-8549, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24357309" target="_blank"〉PubMed〈/a〉
    Keywords: Adiponectin/*biosynthesis/chemistry/pharmacology ; Animals ; Anti-Inflammatory Agents, Non-Steroidal/chemistry/pharmacology ; Anti-Obesity Agents/chemistry/*pharmacology/therapeutic use ; Apoptosis/drug effects ; Ceramidases/metabolism ; Diabetes Mellitus, Experimental/drug therapy ; Disease Models, Animal ; Hypoglycemic Agents/chemistry/*pharmacology/therapeutic use ; Insulin Resistance ; Mice ; Molecular Mimicry ; *Molecular Targeted Therapy ; Obesity/drug therapy ; Piperidines/chemistry/*pharmacology/therapeutic use ; Receptors, Adiponectin/*agonists
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  • 15
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-09-14
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Underwood, Emily -- New York, N.Y. -- Science. 2013 Sep 13;341(6151):1164-7. doi: 10.1126/science.341.6151.1164.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24030995" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autistic Disorder/*diagnosis/*immunology ; Brain/embryology/*immunology ; California ; Child, Preschool ; Female ; Fetal Proteins/*immunology ; Humans ; *Immunologic Tests ; Maternal-Fetal Exchange/immunology ; Pregnancy
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  • 16
    Publication Date: 2013-08-31
    Description: The lateral habenula (LHb) has recently emerged as a key brain region in the pathophysiology of depression. However, the molecular mechanism by which LHb becomes hyperactive in depression remains unknown. Through a quantitative proteomic screen, we found that expression of the beta form of calcium/calmodulin-dependent protein kinase type II (betaCaMKappaIotaIota) was significantly up-regulated in the LHb of animal models of depression and down-regulated by antidepressants. Increasing beta-, but not alpha-, CaMKII in the LHb strongly enhanced the synaptic efficacy and spike output of LHb neurons and was sufficient to produce profound depressive symptoms, including anhedonia and behavioral despair. Down-regulation of betaCaMKII levels, blocking its activity or its target molecule the glutamate receptor GluR1 reversed the depressive symptoms. These results identify betaCaMKII as a powerful regulator of LHb neuron function and a key molecular determinant of depression.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932364/" 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/PMC3932364/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Li, Kun -- Zhou, Tao -- Liao, Lujian -- Yang, Zhongfei -- Wong, Catherine -- Henn, Fritz -- Malinow, Roberto -- Yates, John R 3rd -- Hu, Hailan -- P41 GM103533/GM/NIGMS NIH HHS/ -- R01 MH067880/MH/NIMH NIH HHS/ -- R01 MH091119/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2013 Aug 30;341(6149):1016-20. doi: 10.1126/science.1240729.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institute of Neuroscience and State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, P R China.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23990563" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Antidepressive Agents/pharmacology ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/antagonists & ; inhibitors/*biosynthesis/genetics ; Depressive Disorder, Major/*enzymology/genetics/psychology ; Disease Models, Animal ; Gene Knockdown Techniques ; Habenula/drug effects/*enzymology ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Neurons/drug effects/enzymology ; Promoter Regions, Genetic ; Proteomics ; Rats ; Rats, Sprague-Dawley
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  • 17
    Publication Date: 2013-11-16
    Description: Mitochondrial dysfunction contributes to numerous health problems, including neurological and muscular degeneration, cardiomyopathies, cancer, diabetes, and pathologies of aging. Severe mitochondrial defects can result in childhood disorders such as Leigh syndrome, for which there are no effective therapies. We found that rapamycin, a specific inhibitor of the mechanistic target of rapamycin (mTOR) signaling pathway, robustly enhances survival and attenuates disease progression in a mouse model of Leigh syndrome. Administration of rapamycin to these mice, which are deficient in the mitochondrial respiratory chain subunit Ndufs4 [NADH dehydrogenase (ubiquinone) Fe-S protein 4], delays onset of neurological symptoms, reduces neuroinflammation, and prevents brain lesions. Although the precise mechanism of rescue remains to be determined, rapamycin induces a metabolic shift toward amino acid catabolism and away from glycolysis, alleviating the buildup of glycolytic intermediates. This therapeutic strategy may prove relevant for a broad range of mitochondrial diseases.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055856/" 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/PMC4055856/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Johnson, Simon C -- Yanos, Melana E -- Kayser, Ernst-Bernhard -- Quintana, Albert -- Sangesland, Maya -- Castanza, Anthony -- Uhde, Lauren -- Hui, Jessica -- Wall, Valerie Z -- Gagnidze, Arni -- Oh, Kelly -- Wasko, Brian M -- Ramos, Fresnida J -- Palmiter, Richard D -- Rabinovitch, Peter S -- Morgan, Philip G -- Sedensky, Margaret M -- Kaeberlein, Matt -- R01 AG039390/AG/NIA NIH HHS/ -- T32 AG000057/AG/NIA NIH HHS/ -- T32 ES007032/ES/NIEHS NIH HHS/ -- T32AG000057/AG/NIA NIH HHS/ -- T32ES007032/ES/NIEHS NIH HHS/ -- New York, N.Y. -- Science. 2013 Dec 20;342(6165):1524-8. doi: 10.1126/science.1244360. Epub 2013 Nov 14.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology, University of Washington, Seattle, WA 98195, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24231806" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Brain/drug effects/enzymology/pathology ; Disease Models, Animal ; Electron Transport Complex I/genetics/metabolism ; Glycolysis/drug effects ; Leigh Disease/*drug therapy/genetics/pathology ; Mice ; Mice, Knockout ; Mice, Mutant Strains ; Mitochondria/drug effects/enzymology ; Mitochondrial Diseases/*drug therapy/genetics/pathology ; *Molecular Targeted Therapy ; Multiprotein Complexes/*antagonists & inhibitors ; Neuroprotective Agents/*therapeutic use ; Sirolimus/*therapeutic use ; TOR Serine-Threonine Kinases/*antagonists & inhibitors
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  • 18
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-11-10
    Description: During embryonic development, many cells are born far from their final destination and must travel long distances. To become motile and invasive, embryonic epithelial cells undergo a process of mesenchymal conversion known as epithelial-to-mesenchymal transition (EMT). Likewise, EMT can be seen in cancer cells as they leave the primary tumor and disseminate to other parts of the body to colonize distant organs and form metastases. In addition, through the reverse process (mesenchymal-to-epithelial transition), both normal and carcinoma cells revert to the epithelial phenotype to, respectively, differentiate into organs or form secondary tumors. The parallels in phenotypic plasticity in normal morphogenesis and cancer highlight the importance of studying the embryo to understand tumor progression and to aid in the design of improved therapeutic strategies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nieto, M Angela -- New York, N.Y. -- Science. 2013 Nov 8;342(6159):1234850. doi: 10.1126/science.1234850.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Instituto de Neurociencias Consejo Superior de Investigaciones Cientificas (CSIC)-Universidad Miguel Hernandez (UMH), Avenida Ramon y Cajal s/n, 03550 San Juan de Alicante, Spain.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24202173" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Carcinoma/*pathology ; Cell Movement ; Disease Models, Animal ; Embryonic Stem Cells/*physiology ; *Epithelial-Mesenchymal Transition ; Humans ; Mice ; Neoplasms/drug therapy/*pathology ; Neoplastic Stem Cells/drug effects/*physiology
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  • 19
    Publication Date: 2013-01-19
    Description: Environmental stressors during childhood and adolescence influence postnatal brain maturation and human behavioral patterns in adulthood. Accordingly, excess stressors result in adult-onset neuropsychiatric disorders. We describe an underlying mechanism in which glucocorticoids link adolescent stressors to epigenetic controls in neurons. In a mouse model of this phenomenon, a mild isolation stress affects the mesocortical projection of dopaminergic neurons in which DNA hypermethylation of the tyrosine hydroxylase gene is elicited, but only when combined with a relevant genetic risk for neuropsychiatric disorders. These molecular changes are associated with several neurochemical and behavioral deficits that occur in this mouse model, all of which are blocked by a glucocorticoid receptor antagonist. The biology and phenotypes of the mouse models resemble those of psychotic depression, a common and debilitating psychiatric disease.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617477/" 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/PMC3617477/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Niwa, Minae -- Jaaro-Peled, Hanna -- Tankou, Stephanie -- Seshadri, Saurav -- Hikida, Takatoshi -- Matsumoto, Yurie -- Cascella, Nicola G -- Kano, Shin-ichi -- Ozaki, Norio -- Nabeshima, Toshitaka -- Sawa, Akira -- K99 MH094408/MH/NIMH NIH HHS/ -- K99MH-094408/MH/NIMH NIH HHS/ -- MH-069853/MH/NIMH NIH HHS/ -- MH-084018/MH/NIMH NIH HHS/ -- MH-085226/MH/NIMH NIH HHS/ -- MH-088753/MH/NIMH NIH HHS/ -- MH-092443/MH/NIMH NIH HHS/ -- MH-094268/MH/NIMH NIH HHS/ -- R01 MH092443/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2013 Jan 18;339(6117):335-9. doi: 10.1126/science.1226931.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemical Pharmacology, Meijo University Graduate School of Pharmaceutical Sciences, Nagoya, Japan.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23329051" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; *Adolescent Behavior ; *Adolescent Development ; Affective Disorders, Psychotic/genetics/*metabolism ; Animals ; Disease Models, Animal ; Dopaminergic Neurons/*metabolism ; *Epigenesis, Genetic ; Glucocorticoids/*metabolism ; Humans ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Nerve Tissue Proteins/genetics/metabolism ; Stress, Psychological/genetics/*metabolism
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  • 20
    Publication Date: 2013-06-08
    Description: Recent examples have highlighted how stem cells have the capability to initiate morphogenesis in vitro; that is, to generate complex structures in culture that closely parallel their in vivo counterparts. Lgr5, the receptor for the Wnt-agonistic R-spondins, marks stem cells in multiple adult organs of mice and humans. In R-spondin-based three-dimensional cultures, these Lgr5 stem cells can grow into ever-expanding epithelial organoids that retain their original organ identity. Single Lgr5 stem cells derived from the intestine can be cultured to build epithelial structures that retain hallmarks of the in vivo epithelium. Here, we review the mechanisms that support this notable example of self-organization and discuss applications of this technology for stem cell research, disease modeling (e.g., for colorectal cancer and cystic fibrosis), and regenerative medicine.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sato, Toshiro -- Clevers, Hans -- New York, N.Y. -- Science. 2013 Jun 7;340(6137):1190-4. doi: 10.1126/science.1234852.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Gastroenterology, Keio University School of Medicine, Tokyo, Japan. t.sato@a7.keio.jp〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23744940" target="_blank"〉PubMed〈/a〉
    Keywords: Adult Stem Cells/*physiology ; Animals ; Cell Count ; *Cell Culture Techniques ; Disease Models, Animal ; Ephrin-B1/metabolism ; Humans ; Intestinal Mucosa/physiology ; Intestine, Small/*growth & development ; Mice ; *Morphogenesis ; Receptors, G-Protein-Coupled/genetics ; *Regenerative Medicine ; Stem Cell Niche ; Wnt Proteins/metabolism
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  • 21
    Publication Date: 2013-11-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Marshall, Eliot -- New York, N.Y. -- Science. 2013 Nov 8;342(6159):680. doi: 10.1126/science.342.6159.680.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24202151" target="_blank"〉PubMed〈/a〉
    Keywords: DNA/blood ; Down Syndrome/*diagnosis ; Female ; Genetic Testing/*legislation & jurisprudence ; Humans ; Intellectual Property ; Male ; Patents as Topic/*legislation & jurisprudence ; Pregnancy ; Prenatal Diagnosis/*methods ; San Francisco
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  • 22
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-08-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pennisi, Elizabeth -- New York, N.Y. -- Science. 2013 Aug 23;341(6148):833-6. doi: 10.1126/science.341.6148.833.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23970676" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Caspase 9/genetics/*metabolism ; DNA, Bacterial/*genetics ; Disease Models, Animal ; Food Microbiology ; Gene Knockout Techniques/methods ; Gene Targeting/*methods ; Genome/genetics ; Humans ; Mice ; Rats ; *Streptococcus Phages ; Streptococcus thermophilus/*genetics/*immunology/virology
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  • 23
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2013-03-09
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Jon -- New York, N.Y. -- Science. 2013 Mar 8;339(6124):1134. doi: 10.1126/science.339.6124.1134.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23471378" target="_blank"〉PubMed〈/a〉
    Keywords: Anti-HIV Agents/*therapeutic use ; *Convalescence ; *Early Medical Intervention ; Female ; HIV/isolation & purification ; HIV Infections/*blood/*drug therapy/transmission ; Humans ; Infant, Newborn ; Infectious Disease Transmission, Vertical/prevention & control ; Pregnancy ; United States
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  • 24
    Publication Date: 2013-03-02
    Description: Human birth defects are a major public health burden: The Center for Disease Control estimates that 1 of every 33 United States newborns presents with a birth defect, and worldwide the estimate approaches 6% of all births. Among the most common and debilitating of human birth defects are those affecting the formation of the neural tube, the precursor to the central nervous system. Neural tube defects (NTDs) arise from a complex combination of genetic and environmental interactions. Although substantial advances have been made in the prevention and treatment of these malformations, NTDs remain a substantial public health problem, and we are only now beginning to understand their etiology. Here, we review the process of neural tube development and how defects in this process lead to NTDs, both in humans and in the animal models that serve to inform our understanding of these processes. The insights we are gaining will help generate new intervention strategies to tackle the clinical challenges and to alleviate the personal and societal burdens that accompany these defects.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3677196/" 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/PMC3677196/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Wallingford, John B -- Niswander, Lee A -- Shaw, Gary M -- Finnell, Richard H -- 5R01GM074104/GM/NIGMS NIH HHS/ -- P01 HD067244/HD/NICHD NIH HHS/ -- P01HD067244/HD/NICHD NIH HHS/ -- R01 GM074104/GM/NIGMS NIH HHS/ -- R01NS050249/NS/NINDS NIH HHS/ -- R01NS058979/NS/NINDS NIH HHS/ -- R01NS076465/NS/NINDS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2013 Mar 1;339(6123):1222002. doi: 10.1126/science.1222002.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, The University of Texas at Austin, Austin, TX 78712, USA. wallingford@austin.utexas.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23449594" target="_blank"〉PubMed〈/a〉
    Keywords: Amphibians/abnormalities ; Animals ; Disease Models, Animal ; Embryo, Nonmammalian/abnormalities ; Folic Acid/administration & dosage/metabolism ; Folic Acid Deficiency/complications/genetics ; Humans ; Mutation ; Neural Tube Defects/*genetics/*prevention & control/therapy ; Primary Prevention
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  • 25
    Publication Date: 2013-02-09
    Description: To discover interordinal relationships of living and fossil placental mammals and the time of origin of placentals relative to the Cretaceous-Paleogene (K-Pg) boundary, we scored 4541 phenomic characters de novo for 86 fossil and living species. Combining these data with molecular sequences, we obtained a phylogenetic tree that, when calibrated with fossils, shows that crown clade Placentalia and placental orders originated after the K-Pg boundary. Many nodes discovered using molecular data are upheld, but phenomic signals overturn molecular signals to show Sundatheria (Dermoptera + Scandentia) as the sister taxon of Primates, a close link between Proboscidea (elephants) and Sirenia (sea cows), and the monophyly of echolocating Chiroptera (bats). Our tree suggests that Placentalia first split into Xenarthra and Epitheria; extinct New World species are the oldest members of Afrotheria.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉O'Leary, Maureen A -- Bloch, Jonathan I -- Flynn, John J -- Gaudin, Timothy J -- Giallombardo, Andres -- Giannini, Norberto P -- Goldberg, Suzann L -- Kraatz, Brian P -- Luo, Zhe-Xi -- Meng, Jin -- Ni, Xijun -- Novacek, Michael J -- Perini, Fernando A -- Randall, Zachary S -- Rougier, Guillermo W -- Sargis, Eric J -- Silcox, Mary T -- Simmons, Nancy B -- Spaulding, Michelle -- Velazco, Paul M -- Weksler, Marcelo -- Wible, John R -- Cirranello, Andrea L -- New York, N.Y. -- Science. 2013 Feb 8;339(6120):662-7. doi: 10.1126/science.1229237.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anatomical Sciences, School of Medicine, HSC T-8 (040), Stony Brook University, Stony Brook, NY 11794-8081, USA. maureen.oleary@stonybrook.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23393258" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; *Biological Evolution ; Dentition ; Ecosystem ; Extinction, Biological ; Female ; *Fossils ; *Mammals/anatomy & histology/classification/genetics ; Paleodontology ; *Phylogeny ; Phylogeography ; Placenta ; Pregnancy ; Sequence Alignment ; Time ; Xenarthra/anatomy & histology/classification/genetics
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  • 26
    Publication Date: 2013-09-21
    Description: Opioid receptor antagonists increase hyperalgesia in humans and animals, which indicates that endogenous activation of opioid receptors provides relief from acute pain; however, the mechanisms of long-term opioid inhibition of pathological pain have remained elusive. We found that tissue injury produced mu-opioid receptor (MOR) constitutive activity (MOR(CA)) that repressed spinal nociceptive signaling for months. Pharmacological blockade during the posthyperalgesia state with MOR inverse agonists reinstated central pain sensitization and precipitated hallmarks of opioid withdrawal (including adenosine 3',5'-monophosphate overshoot and hyperalgesia) that required N-methyl-D-aspartate receptor activation of adenylyl cyclase type 1. Thus, MOR(CA) initiates both analgesic signaling and a compensatory opponent process that generates endogenous opioid dependence. Tonic MOR(CA) suppression of withdrawal hyperalgesia may prevent the transition from acute to chronic pain.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440417/" 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/PMC4440417/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Corder, G -- Doolen, S -- Donahue, R R -- Winter, M K -- Jutras, B L -- He, Y -- Hu, X -- Wieskopf, J S -- Mogil, J S -- Storm, D R -- Wang, Z J -- McCarson, K E -- Taylor, B K -- 5K02DA19656/DA/NIDA NIH HHS/ -- F31 DA032496/DA/NIDA NIH HHS/ -- F31DA032496/DA/NIDA NIH HHS/ -- HD02528/HD/NICHD NIH HHS/ -- K02 DA019656/DA/NIDA NIH HHS/ -- P30 HD002528/HD/NICHD NIH HHS/ -- R01 NS045954/NS/NINDS NIH HHS/ -- R01NS45954/NS/NINDS NIH HHS/ -- UL1 TR000117/TR/NCATS NIH HHS/ -- New York, N.Y. -- Science. 2013 Sep 20;341(6152):1394-9. doi: 10.1126/science.1239403.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Physiology, University of Kentucky, Lexington, KY 40536, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24052307" target="_blank"〉PubMed〈/a〉
    Keywords: Acute Pain/metabolism ; Adenosine Monophosphate/metabolism ; Adenylyl Cyclases/metabolism ; Animals ; Chronic Pain/*metabolism ; Disease Models, Animal ; Freund's Adjuvant/pharmacology ; Hyperalgesia/chemically induced/*metabolism ; Isoflurane/pharmacology ; Male ; Mice ; Naltrexone/analogs & derivatives/pharmacology ; Nociceptive Pain/*metabolism ; Receptors, N-Methyl-D-Aspartate/metabolism ; Receptors, Opioid, mu/agonists/antagonists & inhibitors/*metabolism ; Spinal Cord/drug effects/metabolism ; Substance Withdrawal Syndrome/metabolism
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  • 27
    Publication Date: 2013-09-21
    Description: Soluble beta-amyloid (Abeta) oligomers impair synaptic plasticity and cause synaptic loss associated with Alzheimer's disease (AD). We report that murine PirB (paired immunoglobulin-like receptor B) and its human ortholog LilrB2 (leukocyte immunoglobulin-like receptor B2), present in human brain, are receptors for Abeta oligomers, with nanomolar affinity. The first two extracellular immunoglobulin (Ig) domains of PirB and LilrB2 mediate this interaction, leading to enhanced cofilin signaling, also seen in human AD brains. In mice, the deleterious effect of Abeta oligomers on hippocampal long-term potentiation required PirB, and in a transgenic model of AD, PirB not only contributed to memory deficits present in adult mice, but also mediated loss of synaptic plasticity in juvenile visual cortex. These findings imply that LilrB2 contributes to human AD neuropathology and suggest therapeutic uses of blocking LilrB2 function.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853120/" 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/PMC3853120/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kim, Taeho -- Vidal, George S -- Djurisic, Maja -- William, Christopher M -- Birnbaum, Michael E -- Garcia, K Christopher -- Hyman, Bradley T -- Shatz, Carla J -- 5P50AG005134/AG/NIA NIH HHS/ -- 5R01AG041507/AG/NIA NIH HHS/ -- 5T32EY020485/EY/NEI NIH HHS/ -- EY02858/EY/NEI NIH HHS/ -- K08 NS069811/NS/NINDS NIH HHS/ -- K08NS069811/NS/NINDS NIH HHS/ -- NS069375/NS/NINDS NIH HHS/ -- R01 AG041507/AG/NIA NIH HHS/ -- R01 EY002858/EY/NEI NIH HHS/ -- R01 MH071666/MH/NIMH NIH HHS/ -- T32 EY020485/EY/NEI NIH HHS/ -- T32 MH020016/MH/NIMH NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2013 Sep 20;341(6152):1399-404. doi: 10.1126/science.1242077.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biology and Bio-X, James H. Clark Center, Stanford University, Stanford, CA 94305, USA. tkim808@stanford.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24052308" target="_blank"〉PubMed〈/a〉
    Keywords: Alzheimer Disease/*physiopathology ; Amyloid beta-Peptides/*metabolism/pharmacology ; Animals ; Disease Models, Animal ; Female ; HEK293 Cells ; Hippocampus/physiopathology ; Humans ; Long-Term Potentiation ; Male ; Membrane Glycoproteins/genetics/*physiology ; Mice ; Mice, Transgenic ; *Neuronal Plasticity ; Peptide Fragments/*metabolism/pharmacology ; Receptors, Immunologic/genetics/*physiology ; Synapses/*physiology
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  • 28
    Publication Date: 2013-06-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Couzin-Frankel, Jennifer -- New York, N.Y. -- Science. 2013 Jun 7;340(6137):1160-1. doi: 10.1126/science.340.6137.1160.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23744922" target="_blank"〉PubMed〈/a〉
    Keywords: Adult ; Birth Weight ; Body Composition ; Diet ; Female ; *Fetal Development ; *Health ; Heart Diseases/epidemiology ; Humans ; Infant, Low Birth Weight/growth & development ; Infant, Newborn ; Insulin Resistance ; Male ; Maternal Nutritional Physiological Phenomena ; Placenta/*anatomy & histology ; Pregnancy ; Uterus/*metabolism
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  • 29
    Publication Date: 2013-06-01
    Description: Vaccines are among the greatest successes in the history of public health. However, past strategies for vaccine development are unlikely to succeed in the future against major global diseases such as AIDS, tuberculosis, and malaria. For such diseases, the correlates of protection are poorly defined and the pathogens evade immune detection and/or exhibit extensive genetic variability. Recent advances have heralded in a new era of vaccine discovery. However, translation of these advances into vaccines remains impeded by lack of understanding of key vaccinology principles in humans. We review these advances toward vaccine discovery and suggest that for accelerating successful vaccine development, new human immunology-based clinical research initiatives be implemented with the goal of elucidating and more effectively generating vaccine-induced protective immune responses.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026248/" 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/PMC4026248/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Koff, Wayne C -- Burton, Dennis R -- Johnson, Philip R -- Walker, Bruce D -- King, Charles R -- Nabel, Gary J -- Ahmed, Rafi -- Bhan, Maharaj K -- Plotkin, Stanley A -- UM1 AI100663/AI/NIAID NIH HHS/ -- New York, N.Y. -- Science. 2013 May 31;340(6136):1232910. doi: 10.1126/science.1232910.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉International AIDS Vaccine Initiative (IAVI), New York, NY 10004, USA. wkoff@iavi.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23723240" target="_blank"〉PubMed〈/a〉
    Keywords: Acquired Immunodeficiency Syndrome/prevention & control ; Adjuvants, Immunologic/administration & dosage ; Animals ; Antigens/genetics/immunology/isolation & purification ; *Communicable Disease Control ; Disease Models, Animal ; Drug Delivery Systems ; Humans ; Malaria/prevention & control ; Tuberculosis/prevention & control ; Vaccines/administration & dosage/*immunology
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  • 30
    Publication Date: 2013-05-21
    Description: Several progeroid disorders, including Hutchinson-Gilford progeria syndrome (HGPS) and restrictive dermopathy (ZMPSTE24 deficiency), arise when a farnesylated and methylated form of prelamin A accumulates at the nuclear envelope. Here, we found that a hypomorphic allele of isoprenylcysteine carboxyl methyltransferase (ICMT) increased body weight, normalized grip strength, and prevented bone fractures and death in Zmpste24-deficient mice. The reduced ICMT activity caused prelamin A mislocalization within the nucleus and triggered prelamin A-dependent activation of AKT-mammalian target of rapamycin (mTOR) signaling, which abolished the premature senescence of Zmpste24-deficient fibroblasts. ICMT inhibition increased AKT-mTOR signaling and proliferation and delayed senescence in human HGPS fibroblasts but did not reduce the levels of misshapen nuclei in mouse and human cells. Thus, targeting ICMT might be useful for treating prelamin A-associated progeroid disorders.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295631/" 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/PMC4295631/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ibrahim, Mohamed X -- Sayin, Volkan I -- Akula, Murali K -- Liu, Meng -- Fong, Loren G -- Young, Stephen G -- Bergo, Martin O -- P01 HL090553/HL/NHLBI NIH HHS/ -- R01 AG035626/AG/NIA NIH HHS/ -- R01 HL086683/HL/NHLBI NIH HHS/ -- R01 HL089781/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 2013 Jun 14;340(6138):1330-3. doi: 10.1126/science.1238880. Epub 2013 May 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Sahlgrenska Cancer Center, Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, S-41390 Gothenburg, Sweden.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23686339" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Aging/genetics ; Cell Nucleus/metabolism ; Disease Models, Animal ; Fibroblasts/metabolism ; *Gene Knockout Techniques ; Hand Strength ; Humans ; Lamin Type A ; Membrane Proteins/genetics/*metabolism ; Metalloendopeptidases/genetics/*metabolism ; Methylation ; Mice ; Mice, Mutant Strains ; Nuclear Proteins/metabolism ; Progeria/physiopathology/*therapy ; Protein Methyltransferases/*genetics/*metabolism ; Protein Precursors/metabolism ; TOR Serine-Threonine Kinases/metabolism ; Weight Gain/genetics
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  • 31
    Publication Date: 2013-06-08
    Description: Dysfunctions in frontostriatal brain circuits have been implicated in neuropsychiatric disorders, including those characterized by the presence of repetitive behaviors. We developed an optogenetic approach to block repetitive, compulsive behavior in a mouse model in which deletion of the synaptic scaffolding gene, Sapap3, results in excessive grooming. With a delay-conditioning task, we identified in the mutants a selective deficit in behavioral response inhibition and found this to be associated with defective down-regulation of striatal projection neuron activity. Focused optogenetic stimulation of the lateral orbitofrontal cortex and its terminals in the striatum restored the behavioral response inhibition, restored the defective down-regulation, and compensated for impaired fast-spiking neuron striatal microcircuits. These findings raise promising potential for the design of targeted therapy for disorders involving excessive repetitive behavior.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876800/" 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/PMC3876800/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Burguiere, Eric -- Monteiro, Patricia -- Feng, Guoping -- Graybiel, Ann M -- R01 HD028341/HD/NICHD NIH HHS/ -- R01 MH081201/MH/NIMH NIH HHS/ -- R01 MH097104/MH/NIMH NIH HHS/ -- R37 HD028341/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 2013 Jun 7;340(6137):1243-6. doi: 10.1126/science.1232380.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉McGovern Institute for Brain Research and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23744950" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Compulsive Behavior/*therapy ; Corpus Striatum/*physiopathology ; Disease Models, Animal ; Frontal Lobe/*physiopathology ; Gene Deletion ; Gene Targeting ; Grooming ; Male ; Mice ; Nerve Tissue Proteins/*genetics ; Neurons/physiology ; Optogenetics/*methods
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  • 32
    Publication Date: 1981-08-14
    Description: Two maternally derived chromosome sets and both maternal histocompatibility antigen haplotypes were identified in the tissues of a malformed triploid acardiac twin that developed within the same chorion as its normal twin. These findings indicate that the twins arose as a result of independent fertilizations, by two different spermatozoa, of a normal haploid ovum and its diploid first-meiotic-division polar body.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bieber, F R -- Nance, W E -- Morton, C C -- Brown, J A -- Redwine, F O -- Jordan, R L -- Mohanakumar, T -- New York, N.Y. -- Science. 1981 Aug 14;213(4509):775-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7196086" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Severe Teratoid/*genetics ; Female ; Fertilization ; HLA Antigens/genetics ; Heart Defects, Congenital/*genetics ; Humans ; Infant, Newborn ; Karyotyping ; Male ; Meiosis ; Polyploidy ; Pregnancy ; *Twins
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  • 33
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1981 May 8;212(4495):610.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7194507" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cattle ; *Embryo Transfer ; Female ; Humans ; Pregnancy
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  • 34
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-29
    Description: A summary of 111 studies identified in a survey of the world literature on familial resemblances in measured intelligence reveals a profile of average correlations consistent with a polygenic mode of inheritance. There is, however, a marked degree of heterogeneity of the correlations within familial groupings, which is not moderated by sex of familial pairing or by type of intelligence test used.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bouchard, T J Jr -- McGue, M -- 5 T32 MH14647/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1981 May 29;212(4498):1055-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7195071" target="_blank"〉PubMed〈/a〉
    Keywords: *Family ; Female ; *Genetics, Medical ; Humans ; *Intelligence ; Intelligence Tests ; Male ; Pregnancy ; Sex Factors ; Twins
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  • 35
    Publication Date: 1981-10-09
    Description: The serum of lactating rats that have never been infected with the protozoan parasite Trypanosoma lewisi contains a rheumatoid factor-like immunoglobulin M (IgM). This IgM amplifies a specific immunoglobulin G (IgG) response to the parasite and accounts for the unusual resistance of previously uninfected lactating rats and their suckling pups to infection with T. lewisi. A similar rheumatoid factor-like IgM, which is induced late in the usual course of infection with T. lewisi in nonlactating rats, amplifies an earlier IgM response and terminates the infection. To our knowledge, this is the first description of a rheumatoid factor, which is classified as an autoimmune antibody, acting in a protective manner.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Clarkson, A B Jr -- Mellow, G H -- New York, N.Y. -- Science. 1981 Oct 9;214(4517):186-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7025211" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Suckling/immunology ; Antigen-Antibody Complex ; Female ; Immunoglobulin G ; Immunoglobulin M/*immunology ; *Lactation ; Pregnancy ; Rats ; Rheumatoid Factor/*immunology ; Trypanosoma lewisi/immunology ; Trypanosomiasis/*immunology
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  • 36
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-03-20
    Description: Gender identity depends largely on postnatal environmental influences, while sex-dimorphic behavior and temperamental sex differences appear to be modified by prenatal sex hormones. A role of the prenatal endocrine milieu in the development of erotic partner preference, as in hetero-, homo-, or bisexual orientation, or of cognitive sex differences has not been conclusively demonstrated.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ehrhardt, A A -- Meyer-Bahlburg, H F -- New York, N.Y. -- Science. 1981 Mar 20;211(4488):1312-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209510" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adrenal Hyperplasia, Congenital/metabolism/psychology ; Adult ; Androgens/pharmacology ; Behavior/drug effects ; Child ; Cognition/drug effects ; Embryo, Mammalian/drug effects ; Estrogens/pharmacology ; Female ; *Gender Identity ; Gonadal Steroid Hormones/*pharmacology ; Humans ; *Identification (Psychology) ; Male ; Pregnancy ; Pregnancy Complications/drug therapy ; Progestins/pharmacology/therapeutic use ; Sexual Behavior/*drug effects
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  • 37
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-30
    Description: Malformations associated with the fetal hydantoin syndrome have been reproduced in a mouse model. The occurrence of these defects was correlated with maternal serum concentrations, but not with maternal or fetal genotype or the presence of a seizure disorder.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Finnell, R H -- New York, N.Y. -- Science. 1981 Jan 30;211(4481):483-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7455686" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Models, Animal ; Epilepsy/drug therapy ; Female ; Mice ; Mice, Neurologic Mutants/physiology ; Phenytoin/*adverse effects ; *Teratogens
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  • 38
    Publication Date: 1981-09-04
    Description: Ovaries removed from New Zealand White rabbits were perfused and exposed to gonadotropin in vitro. The ova ovulated in vitro (N = 56) were recovered and cultured and then transferred to the oviducts of six previously mated Dutch Belted hosts. Twelve of the resulting 36 offspring (33.3 percent) were white. In control matings between 12 Dutch Belted females (six randomly selected and the six hosts) and New Zealand White males, only one of 80 (1.2 percent) offspring was white. These data indicate that ova ovulated in vitro can be transferred to the oviduct of a host rabbit where they may be fertilized and after implantation may develop into viable embryos.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kobayashi, Y -- Santulli, R -- Wright, K H -- Wallach, E E -- HD-05948/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1981 Sep 4;213(4512):1127-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268420" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chorionic Gonadotropin/*pharmacology ; Embryo Transfer ; Female ; *Fertilization in Vitro ; Ovary/drug effects/*physiology ; *Ovulation/drug effects ; Pregnancy ; Rabbits
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  • 39
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-10
    Description: Ninety-two cases of brain tumor in children less than 10 years old were compared with 92 matched controls for parental occupational history. Cases were more likely than controls to show material occupations involving chemical exposure, paternal occupations involving solvents, and employment of father in the aircraft industry. These three factors were not affected by adjustment for the potential confounding variables examined in this study.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Peters, F M -- Preston-Martin, S -- Yu, M C -- P01CA17054/CA/NCI NIH HHS/ -- R01CA20571/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Jul 10;213(4504):235-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244631" target="_blank"〉PubMed〈/a〉
    Keywords: Air Pollutants/*adverse effects ; Air Pollutants, Occupational/*adverse effects ; Brain Neoplasms/*chemically induced ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Male ; *Maternal-Fetal Exchange ; Pregnancy ; Respiration ; Risk ; Skin Absorption ; Solvents
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 40
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-09-04
    Description: Recovery of visual acuity was studied in six long-term monocularly deprived cats after removal of the nondeprived eye or reverse lid suture. Although both manipulations improved visual acuity, removal of the nondeprived eye was associated with more rapid recovery and higher find acuity than in reverse suture. These results are in agreement with the known electrophysiological effects of these recovery conditions and are also similar to the effects of reverse occlusion or loss of the nonamblyopic eye in human amblyopes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, D C -- EYO 7005/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1981 Sep 4;213(4512):1137-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268422" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Amblyopia/physiopathology ; Animals ; Cats ; Disease Models, Animal ; Form Perception/physiology ; Visual Acuity ; Visual Cortex/growth & development/*physiology ; Visual Perception/*physiology
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  • 41
    Publication Date: 1981-10-30
    Description: Viruses classified by immunologic criteria as equine herpesvirus 1 cause respiratory disease and abortion in horses. Restriction endonuclease analyses of the DNA's of viruses from animals with respiratory disease and from aborted fetuses show that the patterns for respiratory viruses, while similar to each other, are entirely different from the patterns for fetal viruses. It is therefore proposed that the DNA restriction endonuclease patterns of fetal and respiratory viruses analyzed in this study be designated as prototypic of equine herpesvirus 1 and 4, respectively.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Studdert, M J -- Simpson, T -- Roizman, B -- CA 08494/CA/NCI NIH HHS/ -- CA 09241/CA/NCI NIH HHS/ -- CA 19264/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Oct 30;214(4520):562-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6270790" target="_blank"〉PubMed〈/a〉
    Keywords: Abortion, Veterinary/*microbiology ; Animals ; DNA Restriction Enzymes ; DNA, Viral/genetics ; Female ; Fetus/microbiology ; Herpesviridae/*genetics ; Herpesvirus 1, Equid/*genetics ; Horse Diseases/*microbiology ; Horses ; Pregnancy
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  • 42
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-06-12
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sun, M -- New York, N.Y. -- Science. 1981 Jun 12;212(4500):1253.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233217" target="_blank"〉PubMed〈/a〉
    Keywords: Abortion, Induced ; *Amniocentesis ; Congenital Abnormalities/diagnosis ; Federal Government ; Female ; Humans ; Legislation, Medical ; Pregnancy ; United States
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  • 43
    Publication Date: 1981-07-31
    Description: Erythrocytes infected with the late stages of the human malarial parasite Plasmodium falciparum became attached to a subpopulation of cultured human endothelial cells by knoblike protrusions on the surface of the infected erythrocytes. Infected erythrocytes did not bind to cultured fibroblasts; uninfected erythrocytes did not bind to either endothelial cells or fibroblasts. The results suggest a specific receptor-ligand interaction between endothelial cells and a component, components, in the knobs of the infected erythrocytes.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Udeinya, I J -- Schmidt, J A -- Aikawa, M -- Miller, L H -- Green, I -- New York, N.Y. -- Science. 1981 Jul 31;213(4507):555-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7017935" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Aotus trivirgatus ; Cells, Cultured ; Endothelium/microbiology ; Erythrocytes/*microbiology/ultrastructure ; Female ; Humans ; Microscopy, Electron ; Plasmodium falciparum/*pathogenicity ; Pregnancy ; Umbilical Veins
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  • 44
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-10-23
    Description: The classic procedures for testing potential carcinogens in animals have basically not changed in the past 50 years. Considerable knowledge of the mechanisms of carcinogenesis has accrued in the last 20 years, particularly concepts on the metabolic activation of chemicals to reactive electrophilic compounds that can interact with nucleophilic including DNA. These developments, in turn, have yielded a framework for integrating into carcinogen testing the determination of genetic effects of chemicals. A systematic decision point approach to carcinogen testing has been developed which entails a sequential decision-making process as specific tests are performed and evaluated prior to initiation of higher order, more complex tests. Compared to conventional bioassays in rodents, this approach provides knowledge based on mechanisms of carcinogenesis, yields a substantial amount of data at minimal cost, and forms a solid base for eventual heath risk assessment.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Weisburger, J H -- Williams, G M -- New York, N.Y. -- Science. 1981 Oct 23;214(4519):401-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7291981" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Assay ; *Carcinogens ; Disease Models, Animal ; *Drug Evaluation, Preclinical ; Mutagenicity Tests ; Mutagens ; Neoplasms, Experimental/*etiology ; Research Design
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  • 45
    Publication Date: 1981-02-27
    Description: Rats exposed to ethanol throughout their gestation were found to have abnormally distributed mossy fibers in temporal regions of the hippocampus. This demonstrates that prenatal exposure to ethanol causes alterations in neuronal circuitry that persist to maturity. Such defects may play a role in the mental retardation often observed in children with fetal alcohol syndrome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉West, J R -- Hodges, C A -- Black, A C Jr -- AA-03884/AA/NIAAA NIH HHS/ -- New York, N.Y. -- Science. 1981 Feb 27;211(4485):957-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466371" target="_blank"〉PubMed〈/a〉
    Keywords: Abnormalities, Drug-Induced/*etiology ; Animals ; Ethanol/*pharmacology ; Female ; Hippocampus/abnormalities/drug effects/*embryology ; Pregnancy ; Pregnancy, Animal/*drug effects ; Rats
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  • 46
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-02
    Description: Rat pups nursed by pregnant dams grow as fast as pups reared by dams that are not pregnant. Moreover, litters that were in utero during a lactation are as numerous at birth and grow as fast as pups developing in a nonlactating, pregnant mother. These litters continue to grow as fast as pups born to nonlactating dams whether or not the first litter remains after the birth of the second litter. When pregnant and lactating dams have a restricted food supply, some dams are capable of extending the duration of their pregnancies by over 2 weeks past that of nonlactating, pregnant dams. This facultative prolongation of pregnancy apparently allows females to carry normal litters to term.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Woodside, B -- Wilson, R -- Chee, P -- Leon, M -- New York, N.Y. -- Science. 1981 Jan 2;211(4477):76-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7444451" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/*physiology ; Energy Intake ; Energy Metabolism ; Female ; *Lactation ; Litter Size ; Pregnancy ; *Pregnancy, Animal ; Rats/*physiology
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  • 47
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-31
    Description: An established line of mesenchymal cells from the human embryonic palate is highly sensitive to the stimulatory effect of epidermal growth factor on growth, labeled thymidine incorporation, and ornithine decarboxylase activity. The results suggest that epidermal growth factor may play a key role in development of various human embryonic and fetal tissues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yoneda, T -- Pratt, R M -- New York, N.Y. -- Science. 1981 Jul 31;213(4507):563-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7017936" target="_blank"〉PubMed〈/a〉
    Keywords: Cell Division/drug effects ; Cell Line ; DNA Replication/drug effects ; Embryo, Mammalian ; Epidermal Growth Factor/*pharmacology ; Female ; Humans ; Insulin/pharmacology ; Kinetics ; Organ Specificity ; Ornithine Decarboxylase/metabolism ; Palate/drug effects/*physiology ; Peptides/*pharmacology ; Pregnancy
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  • 48
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-17
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zack, B G -- New York, N.Y. -- Science. 1981 Jul 17;213(4505):291.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244615" target="_blank"〉PubMed〈/a〉
    Keywords: *Abortion, Spontaneous ; *Beginning of Human Life ; *Embryo, Mammalian ; Female ; Humans ; *Jurisprudence ; *Life ; *Personhood ; Pregnancy ; United States
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  • 49
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-01
    Description: Lead acetate (0.02 or 0.5 percent) was administered to dams throughout the lactation period with half of the litters continuing on lead after weaning. Drug thresholds for d-amphetamine were determined by using the drug-discrimination learning paradigm. All the offspring that had been exposed to lead were less sensitive to the stimulus properties of d-amphetamine irrespective of whether or not they had continued on lead after weaning.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zenick, H -- Goldsmith, M -- New York, N.Y. -- Science. 1981 May 1;212(4494):569-71.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209554" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal/drug effects ; Dextroamphetamine/*pharmacology ; Discrimination Learning/*physiology ; Disease Models, Animal ; Female ; Fetus/drug effects ; Lead Poisoning/*physiopathology ; Male ; Pregnancy ; Rats
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  • 50
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-30
    Description: When presented a novel olfactory stimulus while suckling a passive dam, 11- to 14-day-old rat pups acquire a conditioned preference for that stimulus. The magnitude of the conditioned preference is greater if the pups received milk while suckling than if they did not. The results indicate that infants are capable of learning while suckling and that milk delivery plays a role in this associative process.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Brake, S C -- MH 32429/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1981 Jan 30;211(4481):506-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7192882" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Population Groups/*physiology ; Animals ; Animals, Suckling/*physiology ; Association Learning/physiology ; Behavior, Animal/*physiology ; Conditioning (Psychology) ; Female ; *Lactation ; Pregnancy ; Rats ; Smell
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  • 51
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-06-26
    Description: Pregnant rats were intubated with alcohol (ethanol, 3 grams per kilogram) twice daily throughout gestation. Control animals received solutions of isocaloric sucrose. At birth, offspring were placed with untreated surrogate dams. Beginning at 6 months of age, the offspring were tested for their thermogenic responsiveness to various drugs and to cold. Prenatal exposure to alcohol resulted in tolerance to alcohol and cross-tolerance to pentobarbital and diazepam but did not affect responsiveness to cold. This pattern of effects suggest that prenatal exposure to alcohol produces specific long-term effects on the neural mechanisms underlying drug tolerance.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Abel, E L -- Bush, R -- Dintcheff, B A -- New York, N.Y. -- Science. 1981 Jun 26;212(4502):1531-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233243" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chlorpromazine/pharmacology ; Dextroamphetamine/pharmacology ; Diazepam/pharmacology ; Drug Hypersensitivity ; Drug Tolerance ; Ethanol/*pharmacology ; Female ; Fetus/*drug effects ; Morphine/pharmacology ; Pentobarbital/pharmacology ; Pregnancy ; Rats
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  • 52
    Publication Date: 1981-07-10
    Description: Rats treated with chloramphenicol from days 7 to 21 of intrauterine life (50 milligrams per kilogram per day, injected subcutaneously into the mothers) or in the first 3 days of extrauterine life (50 to 100 milligrams per kilogram per day) were trained for avoidance conditioning when 60 days old. The acquisition of the avoidance response was impaired to a highly significant degree in all the treated groups.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bertolini, A -- Poggioli, R -- New York, N.Y. -- Science. 1981 Jul 10;213(4504):238-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244633" target="_blank"〉PubMed〈/a〉
    Keywords: Aging ; Animals ; Avoidance Learning/*drug effects ; Brain/drug effects/embryology/*growth & development ; Chloramphenicol/*pharmacology ; Female ; Male ; Maternal-Fetal Exchange ; Pregnancy ; Rats ; Sex Factors
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  • 53
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-13
    Description: Extraction of fibronectin from two human tissues, lung parenchyma and placental villi, was facilitated by the incorporation of heparin into extraction media. The effect of heparin was additive to the effect of urea which is known to extract fibronectin. These experiments provide further evidence that fibronectin and glycosaminoglycans are associated in connective tissues and the use of heparin forms the basis for a simple method for extraction and quantitation of tissue fibronectin.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bray, B A -- Mandl, I -- Turino, G M -- HL 15832/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1981 Nov 13;214(4522):793-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7292011" target="_blank"〉PubMed〈/a〉
    Keywords: Dermatan Sulfate ; Female ; Fibronectins/*isolation & purification ; *Heparin ; Heparitin Sulfate ; Humans ; Lung/analysis ; Placenta/analysis ; Pregnancy ; Urea
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  • 54
    Publication Date: 1981-12-04
    Description: When pregnant rats were fed a 50 percent galactose diet there was a striking reduction in oocyte number in the offspring. The most prominent effects were noted after exposure to galactose during the premeiotic stages of oogenesis. Prenatal exposure to galactose or its metabolites may contribute to the premature ovarian failure characteristic of human galactosemia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chen, Y T -- Mattison, D R -- Feigenbaum, L -- Fukui, H -- Schulman, J D -- New York, N.Y. -- Science. 1981 Dec 4;214(4525):1145-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302587" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Dietary Carbohydrates/*physiology ; Female ; Fetus/drug effects/physiology ; Galactose/*pharmacology ; Maternal-Fetal Exchange ; Oocytes/drug effects/*physiology ; Ovum/*physiology ; Pregnancy ; Rats ; Rats, Inbred Strains
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  • 55
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-01
    Description: Administration of tyrosine, the amino acid precursor of catecholamines, increased blood pressure 38 to 49 percent in rats made acutely hypotensive by hemorrhage; other large neutral amino acids were ineffective. Tyrosine's effect was abolished by adrenalectomy, suggesting that, in hypotensive animals, it acts by accelerating the peripheral synthesis and release of catecholamines.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Conlay, L A -- Maher, T J -- Wurtman, R J -- AM-14228/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1981 May 1;212(4494):559-60.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209553" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenalectomy ; Animals ; Blood Pressure/*drug effects ; Catecholamines/metabolism ; Disease Models, Animal ; Hypotension/*drug therapy/physiopathology ; Male ; Rats ; Tyrosine/*pharmacology/therapeutic use
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  • 56
    Publication Date: 1981-09-04
    Description: Adult mice were administered the common parasite Toxocara canis or lead or both. The parasite clearly altered mouse performance on tests of exploration, activity, learning, and motor coordination; behavioral effects in mice receiving lead alone were less general. Consequence of Toxocara administration appeared attenuated in animals receiving both agents. Parasite larvae were found in the central nervous system in all infected mice.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dolinsky, Z S -- Burright, R G -- Donovick, P J -- Glickman, L T -- Babish, J -- Summers, B -- Cypess, R H -- 08-K4AI00301A-03/AI/NIAID NIH HHS/ -- 08R1AI1478A-03/AI/NIAID NIH HHS/ -- 5S07RR0749-04/RR/NCRR NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1981 Sep 4;213(4512):1142-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268424" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Ascariasis/*complications ; Behavior, Animal/*physiology ; Brain/parasitology ; Disease Models, Animal ; Lead Poisoning/*complications/physiopathology ; Male ; Mice ; Toxocariasis/*complications/physiopathology
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  • 57
    Publication Date: 1981-05-01
    Description: Female prairie voles (Microtus ochrogaster) exposed to a single drop of male urine on the upper lip showed changes in concentrations of luteinizing hormone-releasing hormone (LHRH) and norepinephrine in olfactory bulb tissue; no such changes occurred in dopamine concentration. The changes were measured in the posterior but not the anterior olfactory bulb tissue of females within 1 hour after they were exposed to urine. These females also showed rapid increases in serum concentrations of luteinizing hormone. Females exposed to water on the upper lip showed none of these changes. These results suggest that in this species LHRH and norepinephrine in the olfactory bulb may mediate luteinizing hormone release in response to external (pheromonal) chemical cues.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Dluzen, D E -- Ramirez, V D -- Carter, C S -- Getz, L L -- HDO9328/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1981 May 1;212(4494):573-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7010608" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Arvicolinae/*physiology ; Estrus ; Female ; Gonadotropin-Releasing Hormone/*metabolism ; Humans ; Luteinizing Hormone/blood ; Male ; Norepinephrine/*metabolism ; Olfactory Bulb/*metabolism ; Pheromones/*urine ; Pregnancy ; Reproduction ; Rodentia/*physiology ; Stress, Psychological/physiopathology
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  • 58
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-30
    Description: The opiate antagonist naloxone has been used to treat cats subjected to cervical spinal trauma. In contrast to saline-treated controls, naloxone treatment significantly improved the hypotension observed after cervical spinal injury. More critically, naloxone therapy significantly improved neurologic recovery. These findings implicate endorphins in the pathophysiology of spinal cord injury and indicate that narcotic antagonists may have a therapeutic role in this condition.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Faden, A I -- Jacobs, T P -- Holaday, J W -- New York, N.Y. -- Science. 1981 Jan 30;211(4481):493-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7455690" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Pressure/*drug effects ; Cats ; Disease Models, Animal ; Endorphins/antagonists & inhibitors ; Naloxone/pharmacology/*therapeutic use ; Spinal Cord/blood supply ; Spinal Cord Injuries/*drug therapy/physiopathology
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  • 59
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-13
    Description: When young rats are exposed to white fluorescent light the concentration of calcium in their serum decreases. This effect is prevented by shielding the occiput, by inhibiting corticosterone synthesis, and by exogenous melatonin. Furthermore, the expected hypocalcemic response to cortisol injection is prevented by melatonin. Light-induced hypocalcemia may result from increased calcium uptake by bone when the blocking effect of melatonin decreases after pineal inhibition by transcranial illumination.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hakanson, D O -- Bergstrom, W H -- New York, N.Y. -- Science. 1981 Nov 13;214(4522):807-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6895262" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Animals, Newborn/*radiation effects ; Disease Models, Animal ; Female ; Humans ; Hydrocortisone/antagonists & inhibitors ; Hypocalcemia/etiology/*prevention & control ; Infant, Newborn ; Jaundice, Neonatal/therapy ; Light ; Male ; Melatonin/*pharmacology ; Phototherapy/adverse effects ; Rats ; Spectrum Analysis ; Time Factors
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  • 60
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-04-17
    Description: Sexually receptive female Spermophilus beldingi (Rodentia: Sciuridae) usually mate with several different males. The paternity of 27 litters born in 1977 and 1978 was ascertained by combining field observations of mating with laboratory paternity exclusion analyses. Most of the litters (78 percent) were multiply sired, usually by two or three males. This may be the highest frequency of multiple paternity ever directly demonstrated in a natural population.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hanken, J -- Sherman, P W -- New York, N.Y. -- Science. 1981 Apr 17;212(4492):351-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7209536" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Female ; Male ; Pregnancy ; Sciuridae/*physiology ; *Sexual Behavior, Animal
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  • 61
    Publication Date: 1981-06-19
    Description: Concentrations of estradiol and progesterone in blood collected during the 12.5-day gestation period of the Virginia opossum were not significantly different from those during equivalent days of the estrous cycle. Progesterone was correlated with an index of corpora luteral mass. Ratio of estradiol to progesterone were highest 3 to 4 days before estrus and on the day of parturition.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Harder, J D -- Fleming, M W -- New York, N.Y. -- Science. 1981 Jun 19;212(4501):1400-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233228" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Corpus Luteum/physiology ; Estradiol/*blood ; Estrus ; Female ; Opossums/*physiology ; Pregnancy ; *Pregnancy, Animal ; Progesterone/*blood ; Species Specificity
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  • 62
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-22
    Description: Long-term oral administration of the long-acting opiate 1-alpha-acetylmethadol (LAAM) to female rats beginning on the day of conception interfered with the dams' ability to carry litters to term. When treatment was initiated 3 weeks prior to mating this effect was not observed. Daily administration of the opiate antagonist naloxone from day 14 of gestation through term, to precipitate withdrawal in utero, resulted in increased stillbirths, decreased pup weight and size, and weight loss 24 hours after birth. These data question the validity of animal experiments which purport to be models for methadone maintenance programs but in which treatment is started immediately prior to or soon after conception. They also suggest that withdrawal in utero may be responsible for many of the adverse effects of opiates on human and animal development.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lichtblau, L -- Sparber, S B -- DA 01880/DA/NIDA NIH HHS/ -- New York, N.Y. -- Science. 1981 May 22;212(4497):943-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7195068" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Drug Tolerance ; Embryo Implantation/drug effects ; Female ; Fetal Death/*etiology ; Humans ; Litter Size/drug effects ; Methadone/*analogs & derivatives ; Methadyl Acetate/*adverse effects/antagonists & inhibitors ; Naloxone/pharmacology ; Opioid-Related Disorders/*complications ; Pregnancy ; Pregnancy, Animal/*drug effects ; Rats ; Substance Withdrawal Syndrome/*complications
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 63
    Publication Date: 1981-01-09
    Description: Phosphorus-31 nuclear magnetic resonance (NMR) measurements with small surface coils have been used to observe phosphorus metabolism of perfused hearts within localized regions. The method allows for direct, noninvasive, sequential assessment of the altered regional metabolism resulting from myocardial infarction and its response to drug treatment, which cannot be observed by conventional techniques.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nunnally, R L -- Bottomley, P A -- GM 17172/GM/NIGMS NIH HHS/ -- HL 17655-06/HL/NHLBI NIH HHS/ -- HL 22080/HL/NHLBI NIH HHS/ -- New York, N.Y. -- Science. 1981 Jan 9;211(4478):177-80.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7444460" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chlorpromazine/therapeutic use ; Coronary Circulation/drug effects ; Disease Models, Animal ; Magnetic Resonance Spectroscopy/*methods ; Myocardial Infarction/*diagnosis/drug therapy/metabolism ; Phosphorus/*metabolism ; Phosphorus Isotopes ; Rabbits ; Verapamil/therapeutic use
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  • 64
    Publication Date: 1981-08-21
    Description: Sunlight photodegradation of 2,2', 4,4', 5,5' -hexabromobiphenyl, the major component of Firemaster, gave a mixture that produces severe hyperkeratosis of the rabbit ear. This component in its pure state does not cause hyperkeratosis. One or more of the four major photolysis products must be responsible for this activity. A similar photodegradation pattern was observed for 2,2', 3,4,4', 5,5' -heptabromobiphenyl, the second largest component of Firemaster.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Patterson, D G -- Hill, R H -- Needham, L L -- Orti, D L -- Kimbrough, R D -- Liddle, J A -- New York, N.Y. -- Science. 1981 Aug 21;213(4510):901-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6266016" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biphenyl Compounds/radiation effects ; Chemical Industry ; Disease Models, Animal ; Environmental Exposure ; Keratosis/*chemically induced ; Michigan ; Photochemistry ; *Polybrominated Biphenyls/radiation effects ; Rabbits ; Sunlight
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  • 65
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-20
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rakic, P -- EY 02593/EY/NEI NIH HHS/ -- New York, N.Y. -- Science. 1981 Nov 20;214(4523):928-31.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7302569" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/ultrastructure ; Brain/embryology/*growth & development ; Female ; Functional Laterality ; Geniculate Bodies/embryology/growth & development ; Macaca mulatta ; Microscopy, Electron ; Pregnancy ; Retina/physiology ; Synapses/physiology ; Visual Cortex/embryology/growth & development ; *Visual Perception
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  • 66
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-16
    Description: According to one hypothesis, the paroxysmal depolarizing shift observed in the penicillin model of epilepsy results from a giant excitatory postsynaptic potential. This hypothesis has recently been questioned, primarily because it has never been subjected to rigorous experimental examination. Four quantitative predictions were derived from this hypothesis and tested in CA3 pyramidal neurons of the hippocampus. The four critical predictions concern the behavior of the paroxysmal depolarizing shift under current- and voltage-clamp conditions as a function of membrane potential. The experiments confirmed all four predictions.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Johnston, D -- Brown, T H -- NS11535/NS/NINDS NIH HHS/ -- NS15772/NS/NINDS NIH HHS/ -- RR-05471-17/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Jan 16;211(4479):294-7.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7444469" target="_blank"〉PubMed〈/a〉
    Keywords: Action Potentials ; Animals ; Disease Models, Animal ; Electric Conductivity ; Epilepsy/*physiopathology ; Guinea Pigs ; Hippocampus/*physiopathology ; In Vitro Techniques ; Membrane Potentials ; Penicillin G ; Synaptic Membranes/physiology
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  • 67
    Publication Date: 1981-03-06
    Description: The human demyelinative disorder central pontine myelinolysis may be an iatrogenic disease caused by a rapid rise in serum sodium, usually when hyponatremia is corrected. Rats treated with hypertonic saline after 3 days of vasopressin-induced hyponatremia had demyelinative lesions in the corpus striatum, lateral hemispheric white matter, cerebral cortex, hippocampal fimbria, anterior commissure, thalamus, brainstem tegmentum, and cerebellum. Thus, rapid correction of hyponatremia can lead to demyelinative lesions and may be the cause of central pontine myelinolysis in man.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kleinschmidt-DeMasters, B K -- Norenberg, M D -- New York, N.Y. -- Science. 1981 Mar 6;211(4486):1068-70.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466381" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood-Brain Barrier ; Brain Diseases/*etiology ; Demyelinating Diseases/*etiology/pathology ; Disease Models, Animal ; Hyponatremia/*complications ; Male ; Pons/*pathology ; Rats
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  • 68
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-05-08
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1981 May 8;212(4495):648-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7221549" target="_blank"〉PubMed〈/a〉
    Keywords: *Abortion, Legal ; *Beginning of Human Life ; *Embryo, Mammalian ; *Embryo, Nonmammalian ; Federal Government ; Female ; Legislation as Topic ; *Life ; *Personhood ; Pregnancy ; United States ; Value of Life
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  • 69
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holden, C -- New York, N.Y. -- Science. 1981 Jul 24;213(4506):421.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244639" target="_blank"〉PubMed〈/a〉
    Keywords: *Abortion, Legal ; *Ethics, Medical ; Female ; Humans ; Legislation, Medical ; Pregnancy ; United States
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  • 70
    Publication Date: 1981-08-21
    Description: Hippocampi of seizure-sensitive and seizure-resistant Mongolian gerbils were examined in search of structural correlates of seizure behavior. In animals with well-established seizure histories, differences were found in both presynaptic and postsynaptic structures. Seizing animals had less dense dendritic spines, a greater proportion of mossy tuft area devoted to presynaptic vesicles, and a smaller proportion devoted to spines. The possible relationship of these findings to epilepsy is discussed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Paul, L A -- Fried, I -- Watanabe, K -- Forsythe, A B -- Scheibel, A B -- 5-507-RR05756-06/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Aug 21;213(4510):924-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256289" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Disease Models, Animal ; Gerbillinae/*anatomy & histology/physiology ; Hippocampus/*anatomy & histology/ultrastructure ; Microscopy, Electron ; Seizures/pathology/*physiopathology
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  • 71
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-10
    Description: Female rats are masculinized in utero by male littermates sharing the same uterine horn. Increased anogenital distances in neonatal females and mounting behavior in adult females are related to the presence of males on the caudal side of the females in the uterine horn. Contrary to current beliefs, interamniotic diffusion may not be responsible for the exchange of masculinizing agents among fetuses. Since uterine blood flow in the rat is from the direction of the cervix toward the ovary, masculinizing hormones secreted by fetal males may be carried via the uterine vasculature to female littermates located further downstream.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Meisel, R L -- Ward, I L -- HD-04688/HD/NICHD NIH HHS/ -- K2-MH00049/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 1981 Jul 10;213(4504):239-42.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244634" target="_blank"〉PubMed〈/a〉
    Keywords: Androgens/*physiology ; Animals ; Castration ; Estradiol/pharmacology ; Female ; Fetus/*physiology ; Male ; Posture ; Pregnancy ; Progesterone/pharmacology ; Rats ; *Sex Characteristics/drug effects ; Sexual Behavior, Animal/drug effects ; Uterus/physiology
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  • 72
    Publication Date: 1981-09-18
    Description: Spontaneous diabetes occurring in "BB" rats (derived from a colony of outbred Wistar rats) is the result of destruction of pancreatic islets by infiltrating mononuclear cells (insulitis) and may be a disease very similar to human juvenile onset diabetes. Both diseases probably have an autoimmune etiology. Evidence is presented that islets transplanted to diabetic BB rats are destroyed by the original disease process. Inoculation of bone marrow from normal (nondiabetes-susceptible) rat donors into neonatal BB recipients usually prevented the development of hyperglycemia.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Naji, A -- Silvers, W K -- Bellgrau, D -- Barker, C F -- AM19525/AM/NIADDK NIH HHS/ -- AM26007/AM/NIADDK NIH HHS/ -- CA18640/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1981 Sep 18;213(4514):1390-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6791286" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Autoimmune Diseases/*immunology ; Bone Marrow Transplantation ; Diabetes Mellitus, Experimental/*immunology ; Disease Models, Animal ; Graft Rejection ; Immune Tolerance ; Islets of Langerhans/*immunology ; Islets of Langerhans Transplantation ; Rats
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  • 73
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-02
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Paigen, B -- New York, N.Y. -- Science. 1981 Jan 2;211(4477):6, 8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7444447" target="_blank"〉PubMed〈/a〉
    Keywords: Dicyclomine ; Doxylamine/*adverse effects ; Drug Combinations/adverse effects ; Female ; Humans ; New York ; Pregnancy ; Pyridines/*adverse effects ; Pyridoxine/*adverse effects ; *Teratogens ; United States ; United States Food and Drug Administration ; Water Pollutants/*adverse effects ; Water Pollutants, Chemical/*adverse effects
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  • 74
    Publication Date: 1981-02-13
    Description: Intravenous infusion of tyrosine (1, 2, or 4 milligrams per kilogram) for 20 to 30 minutes caused dose-dependent increases in the ventricular fibrillation threshold in normal dogs. Administration of valine, a neutral amino acid that competes with tyrosine for uptake at the blood-brain barrier, in a dose equimolar to the most effective dose of tyrosine, slightly decreased the ventricular fibrillation threshold when given alone and significantly blocked elevation of the ventricular fibrillation threshold after tyrosine infusion. Hence, tyrosine, presumably acting in the central nervous system, can protect against certain ventricular arrhythmias.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Scott, N A -- DeSilva, R A -- Lown, B -- Wurtman, R J -- 21384-08/PHS HHS/ -- AM-14228/AM/NIADDK NIH HHS/ -- New York, N.Y. -- Science. 1981 Feb 13;211(4483):727-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7455710" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood-Brain Barrier ; Catecholamines/metabolism ; Disease Models, Animal ; Dogs ; Tyrosine/antagonists & inhibitors/metabolism/*therapeutic use ; Valine/pharmacology ; Ventricular Fibrillation/*prevention & control
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  • 75
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-06-26
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, R J -- New York, N.Y. -- Science. 1981 Jun 26;212(4502):1485.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7015515" target="_blank"〉PubMed〈/a〉
    Keywords: Antiemetics/*therapeutic use ; Clinical Trials as Topic ; Dicyclomine ; Doxylamine/*therapeutic use ; Drug Combinations/therapeutic use ; Female ; Humans ; Infant Mortality ; Infant, Newborn ; Pregnancy ; Pregnancy Complications/*drug therapy ; Pyridines/*therapeutic use ; Pyridoxine/*therapeutic use
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  • 76
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-20
    Description: When two small doses of ethanol were administered to pregnant mice during the gastrulation stage of embryogenesis, the embryos developed craniofacial malformations closely resembling those seen in the human fetal alcohol syndrome. Striking histological changes appeared in the developing brain (neuroectoderm) within 24 hours of exposure. Decreased development of the neural plate and its derivatives apparently accounts for the craniofacial malformations. The critical exposure period is equivalent to the third week in human pregnancy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sulik, K K -- Johnston, M C -- Webb, M A -- DE 02668/DE/NIDCR NIH HHS/ -- DE 05906/DE/NIDCR NIH HHS/ -- RR 05333/RR/NCRR NIH HHS/ -- New York, N.Y. -- Science. 1981 Nov 20;214(4523):936-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6795717" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Child ; Disease Models, Animal ; Embryo, Mammalian/*drug effects/ultrastructure ; Ethanol/*pharmacology ; Eye Abnormalities ; Female ; Fetal Alcohol Spectrum Disorders/*physiopathology ; Humans ; Mice ; Mice, Inbred C57BL ; Microscopy, Electron, Scanning ; Pregnancy
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  • 77
    Publication Date: 1981-05-08
    Description: Normal pregnancies have been established in four women with tubal infertility by fertilization in vitro, embryo culture, and embryo transfer after stimulation of follicular growth with clomiphene citrate. In three of these women the time of oocyte maturation was controlled by human chorionic gonadotropin. This procedure for the control of ovulatory response has many advantages when compared with the previously successful method of using the natural ovulatory cycle.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Trounson, A O -- Leeton, J F -- Wood, C -- Webb, J -- Wood, J -- New York, N.Y. -- Science. 1981 May 8;212(4495):681-2.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7221556" target="_blank"〉PubMed〈/a〉
    Keywords: Chorionic Gonadotropin/*pharmacology ; Clomiphene/*pharmacology ; *Embryo Transfer ; Female ; *Fertilization in Vitro ; Humans ; Infertility, Female/therapy ; Ovulation/*drug effects ; Pregnancy
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  • 78
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-31
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1981 Jul 31;213(4507):494, 496.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244648" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Beginning of Human Life ; Ethics, Medical ; Female ; *Fertilization ; Fetus ; Humans ; *Life ; Male ; *Personhood ; Pregnancy ; Value of Life
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  • 79
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-10
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉New York, N.Y. -- Science. 1981 Jul 10;213(4504):154-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244627" target="_blank"〉PubMed〈/a〉
    Keywords: *Beginning of Human Life ; Ethics ; Female ; *Fertilization ; Humans ; *Life ; Male ; Ovum/physiology ; *Personhood ; Pregnancy ; Spermatozoa/physiology
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  • 80
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-08-07
    Description: The eye can be visualized ultrasonically in more than 90 percent of fetuses 16 through 42 weeks of gestational age. Slow eye movements are present by 16 weeks. Rapid eye movements begin at 23 weeks and become more frequent between 24 and 35 weeks. Eye inactivity becomes more common after 36 weeks and is associated with sustained diaphragmatic excursions implying a "quiet sleep" state. Pathologic eye movements were seen in four fetuses with dysmorphic brain structure.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Birnholz, J C -- New York, N.Y. -- Science. 1981 Aug 7;213(4508):679-81.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7256272" target="_blank"〉PubMed〈/a〉
    Keywords: Brain/abnormalities/embryology ; Eye/*embryology ; *Eye Movements ; Female ; Gestational Age ; Humans ; Pregnancy ; Sleep/physiology ; Ultrasonics
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  • 81
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-12-11
    Description: Genetic material has been successfully transferred into the genomes of newborn mice by injection of that material into pronuclei of fertilized eggs. Initial results indicated two patterns of processing the injected DNA: one in which the material was not integrated into the host genome, and another in which the injected genes became associated with high molecular weight DNA. These patterns are maintained through further development to adulthood. The evidence presented indicates the covalent association of injected DNA with host sequences, and transmission of such linked sequences in a Mendelian distribution to two succeeding generations of progeny.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gordon, J W -- Ruddle, F H -- GMO7959-01/GM/NIGMS NIH HHS/ -- GMO9966/GM/NIGMS NIH HHS/ -- New York, N.Y. -- Science. 1981 Dec 11;214(4526):1244-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6272397" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Nucleus/*metabolism ; Crosses, Genetic ; DNA Restriction Enzymes ; DNA, Recombinant/*metabolism ; Embryo, Mammalian/*physiology ; Female ; *Genes ; Genetic Linkage ; Herpesviridae/enzymology ; Male ; Mice ; Nucleic Acid Hybridization ; Ovum/*physiology ; *Plasmids ; Pregnancy ; Sex Ratio ; Simian virus 40/enzymology ; Thymidine Kinase/*genetics
    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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  • 82
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-11-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kolata, G B -- New York, N.Y. -- Science. 1981 Nov 6;214(4521):642-3, 645.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7197392" target="_blank"〉PubMed〈/a〉
    Keywords: Abortion, Spontaneous/chemically induced ; *Ethanol ; Female ; Humans ; Infant, Low Birth Weight ; Infant, Newborn ; Pregnancy ; Pregnancy Complications/*chemically induced
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 83
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-07-24
    Description: Perinatal morbidity and mortality are associated with colonization of the chorionic surface of the placenta by Ureaplasma urealyticum or Mycoplasma hominis or both. These organisms are more strongly associated with unfavourable gestational outcome than group B streptococci. Chlamydia trachomatis does not appear to be important in the etiology of reproductive casualties. The mechanisms linking the mycoplasmas to perinatal disorders and death are not clear but merit investigation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kundsin, R B -- Driscoll, S G -- Pelletier, P A -- HD 10984/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1981 Jul 24;213(4506):474-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7244646" target="_blank"〉PubMed〈/a〉
    Keywords: Critical Care ; Female ; *Fetal Death ; Humans ; *Infant Mortality ; Infant, Newborn ; Infant, Newborn, Diseases/*microbiology ; Mycoplasma/*pathogenicity ; Mycoplasma Infections/*complications ; Placenta/microbiology ; Pregnancy ; Ureaplasma/*pathogenicity
    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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  • 84
    Publication Date: 1981-07-10
    Description: Thyrotropin-releasing hormone significantly improved cardiovascular function when it was injected intravenously into conscious rats subjected to experimental endotoxic or hemorrhagic shock. Because thyrotropin-releasing hormone appears to be a "physiologic: opiate antagonist without effects on pain responsiveness, it may provide therapeutic benefits in the treatment of shock or acute hypotension.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holaday, J W -- D'Amato, R J -- Faden, A I -- New York, N.Y. -- Science. 1981 Jul 10;213(4504):216-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6787704" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blood Pressure/*drug effects ; Disease Models, Animal ; Endotoxins ; Heart Rate/drug effects ; Male ; Rats ; Shock, Hemorrhagic/*physiopathology ; Shock, Septic/*physiopathology ; Thyrotropin-Releasing Hormone/*pharmacology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 85
    Publication Date: 1981-01-02
    Description: Clonidine and L-alpha-methylnoradrenaline (but not D-alpha-methylnoradrenaline) increase the release of a substance with beta-endorphin immunoreactivity from slices of brainstem of spontaneously hypertensive rats, but not that of normotensive rats. It was reported earlier that opiate antagonists inhibit the hypotensive action of clonidine and alpha-methyldopa in spontaneously hypertensive but not in normotensive rats and that beta-endorphin has hypotensive effects of its own. Together, these findings indicate that release of beta-endorphin by central alpha-receptor agonists may contribute to the antihypertensive action of these drugs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kunos, G -- Farsang, C -- Ramirez-Gonzales, M D -- New York, N.Y. -- Science. 1981 Jan 2;211(4477):82-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6108611" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenergic alpha-Agonists/*pharmacology ; Animals ; Brain Stem/*metabolism ; Clonidine/pharmacology ; Disease Models, Animal ; Endorphins/*metabolism ; Hypertension/*physiopathology ; Immunoassay ; Male ; Naloxone/pharmacology ; Nordefrin/pharmacology ; Rats
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 86
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-08-28
    Description: Seizures were produced in rat pups by ambient hyperthermia. Seizure threshold temperatures, measured rectally and intracerebrally, increased between 2 and 10 days of age. Electrocortical paroxysmal discharges were confirmed in hyperthermic 6- and 10-day-old pups. The increasing resistance to hyperthermic seizures with maturation and the electroencephalographic changes induced by hyperthermia are similar to those in young children.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holtzman, D -- Obana, K -- Olson, J -- NS 16256/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1981 Aug 28;213(4511):1034-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7268407" target="_blank"〉PubMed〈/a〉
    Keywords: Age Factors ; Animals ; Brain/physiopathology ; Disease Models, Animal ; Electroencephalography ; Fever/*complications ; Rats ; Seizures/*physiopathology ; Seizures, Febrile/*physiopathology
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 87
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-03-27
    Description: In ovariectomized rats treated with progesterone, implantation was induced by a minute dose of 17 beta-estradiol. Twenty-four hours later, the concentrations of estradiol receptor in nuclear and cytosol fractions prepared from the endometrium surrounding the blastocyst and the inter-implantation areas remained very low. This indicates that estrogen was not secreted by the blastocyst. The higher receptor content in cytosol from inter-implantation sites may reflect modifications accompanying the decidual reaction since our results show that there is no translocation of the receptor to the nuclei. The choice of the dye used to reveal the implantation sites is critical, since Trypan blue but not Evans blue binds steroids and thereby interferes with receptor measurements.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Martel, D -- Psychoyos, A -- New York, N.Y. -- Science. 1981 Mar 27;211(4489):1454-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7466405" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Blastocyst/secretion ; Castration ; Cell Nucleus/analysis ; Cytoplasm/analysis ; *Embryo Implantation ; Endometrium/*analysis ; Estradiol/pharmacology ; Estrogens/secretion ; Evans Blue/metabolism ; Female ; Pregnancy ; Progesterone ; Rats ; Receptors, Estrogen/*analysis ; Trypan Blue/metabolism
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 88
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-12-04
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Russell, E S -- New York, N.Y. -- Science. 1981 Dec 4;214(4525):1074, 1076.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6946561" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cats ; Disease Models, Animal ; Dogs ; *Genetic Engineering ; *Genetics, Medical ; Humans ; Mice ; Mutation ; Rats
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    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 89
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-01-23
    Description: About 17,000 bovine pregnancies were produced by superovulation and embryo transfer in North America in 1979. The major use of these techniques is to increase the reproductive rate of valuable cows. Other applications include circumventing infertility, exporting embryos, and testing potential carriers for Mendelian recessive alleles. Cryopreservation of embryos is beginning to be used commercially, and sexing embryos before transfer may soon become routine.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Seidel, G E Jr -- New York, N.Y. -- Science. 1981 Jan 23;211(4480):351-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7194504" target="_blank"〉PubMed〈/a〉
    Keywords: Animal Husbandry/*methods ; Animals ; Cattle/*physiology ; *Embryo Transfer ; Female ; Industry ; *Ovulation ; Pregnancy ; *Pregnancy, Animal ; Reproduction ; Time Factors
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 90
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1981-06-19
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Smith, R J -- New York, N.Y. -- Science. 1981 Jun 19;212(4501):1372-3.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7233224" target="_blank"〉PubMed〈/a〉
    Keywords: *Abortion, Induced ; *Ethics, Medical ; Federal Government ; Female ; Humans ; Legislation, Medical ; Personhood ; Pregnancy ; United States
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    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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