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  • American Association for the Advancement of Science (AAAS)
  • Hindawi
  • 2015-2019  (2)
  • 1985-1989  (3)
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  • 1
    Publication Date: 2019
    Description: 〈p〉Manley 〈i〉et al.〈/i〉 (〈i〉Science Advances〈/i〉, 16 September 2016, p. e1501814) report the splitting of a transverse acoustic phonon branch below 〈i〉T〈/i〉〈i〉〈sub〉C〈/sub〉〈/i〉 in the relaxor ferroelectric Pb[(Mg〈sub〉1/3〈/sub〉Nb〈sub〉2/3〈/sub〉)〈sub〉1–〈i〉x〈/i〉〈/sub〉Ti〈i〉〈sub〉x〈/sub〉〈/i〉]O〈sub〉3〈/sub〉 with 〈i〉x〈/i〉 = 0.30 using neutron scattering methods. Manley 〈i〉et al.〈/i〉 argue that this splitting occurs because these phonons hybridize with local, harmonic lattice vibrations associated with polar nanoregions. We show that splitting is absent when the measurement is made using a different neutron wavelength, and we suggest an alternative interpretation.〈/p〉
    Electronic ISSN: 2375-2548
    Topics: Natural Sciences in General
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  • 2
    Publication Date: 2015-07-18
    Description: Immune systems distinguish "self" from "nonself" to maintain homeostasis and must differentially gate access to allow colonization by potentially beneficial, nonpathogenic microbes. Plant roots grow within extremely diverse soil microbial communities but assemble a taxonomically limited root-associated microbiome. We grew isogenic Arabidopsis thaliana mutants with altered immune systems in a wild soil and also in recolonization experiments with a synthetic bacterial community. We established that biosynthesis of, and signaling dependent on, the foliar defense phytohormone salicylic acid is required to assemble a normal root microbiome. Salicylic acid modulates colonization of the root by specific bacterial families. Thus, plant immune signaling drives selection from the available microbial communities to sculpt the root microbiome.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lebeis, Sarah L -- Paredes, Sur Herrera -- Lundberg, Derek S -- Breakfield, Natalie -- Gehring, Jase -- McDonald, Meredith -- Malfatti, Stephanie -- Glavina del Rio, Tijana -- Jones, Corbin D -- Tringe, Susannah G -- Dangl, Jeffery L -- F32-GM103156/GM/NIGMS NIH HHS/ -- K12GM000678/GM/NIGMS NIH HHS/ -- T32 GM067553-06/GM/NIGMS NIH HHS/ -- T32 GM07092-34/GM/NIGMS NIH HHS/ -- Howard Hughes Medical Institute/ -- New York, N.Y. -- Science. 2015 Aug 21;349(6250):860-4. doi: 10.1126/science.aaa8764. Epub 2015 Jul 16.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Microbiology, University of Tennessee, Knoxville, TN 37996-0845, USA. Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. slebeis@utk.edu dangl@email.unc.edu. ; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Howard Hughes Medical Institute, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. ; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. ; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. ; Joint Genome Institute, U.S. Department of Energy, Walnut Creek, CA, USA. ; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Carolina Center for Genome Sciences, University of North Carolina, Chapel Hill, NC 27599-3280, USA. ; Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Howard Hughes Medical Institute, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Bioinformatics and Computational Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Carolina Center for Genome Sciences, University of North Carolina, Chapel Hill, NC 27599-3280, USA. Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599-3280, USA. slebeis@utk.edu dangl@email.unc.edu.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/26184915" target="_blank"〉PubMed〈/a〉
    Keywords: Arabidopsis/genetics/immunology/microbiology ; Bacteria/classification/isolation & purification ; Bacterial Processes ; Microbiota/drug effects/*physiology ; Plant Growth Regulators/genetics/pharmacology/*physiology ; Plant Roots/genetics/*immunology/*microbiology ; Salicylic Acid/*metabolism/pharmacology ; *Soil Microbiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-06-05
    Description: The body plan of Drosophila is determined to a large extent by homeotic genes, which specify the identity and spatial arrangement of the body segments. Homeotic genes share a characteristic DNA segment, the homeo box, which encodes a defined domain of the homeotic proteins. The homeo domain seems to mediate the binding to specific DNA sequences, whereby the homeotic proteins exert a gene regulatory function. By isolating the normal Antennapedia gene, fusing its protein-coding sequences to an inducible promoter, and reintroducing this fusion gene into the germline of flies, it has been possible to transform head structures into thoracic structures and to alter the body plan in a predicted way. Sequence homologies suggest that similar genetic mechanisms may control development in higher organisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gehring, W J -- New York, N.Y. -- Science. 1987 Jun 5;236(4806):1245-52.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2884726" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Base Sequence ; Blastoderm/ultrastructure ; Drosophila/embryology/*genetics ; Embryonic and Fetal Development ; *Genes, Homeobox ; Mutation ; Ovum/ultrastructure
    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: 1988-01-08
    Description: Segmentation genes control cell identities during early pattern formation in Drosophila. One of these genes, fushi tarazu (ftz), is now shown also to control cell fate during neurogenesis. Early in development, ftz is expressed in a striped pattern at the blastoderm stage. Later, it is transiently expressed in a specific subset of neuronal precursor cells, neurons (such as aCC, pCC, RP1, and RP2), and glia in the developing central nervous system (CNS). The function of ftz in the CNS was determined by creating ftz mutant embryos that express ftz in the blastoderm stripes but not in the CNS. In the absence of ftz CNS expression, some neurons appear normal (for example, the aCC, pCC, and RP1), whereas the RP2 neuron extends its growth cone along an abnormal pathway, mimicking its sibling (RP1), suggesting a transformation in neuronal identity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Doe, C Q -- Hiromi, Y -- Gehring, W J -- Goodman, C S -- New York, N.Y. -- Science. 1988 Jan 8;239(4836):170-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biological Sciences, Stanford University, CA 94305.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/2892267" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Drosophila melanogaster/*embryology/genetics ; Gene Expression Regulation ; Genes, Homeobox ; Morphogenesis ; Nervous System/*embryology ; Neuroglia/cytology/physiology ; Neurons/cytology/physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 1987-01-01
    Print ISSN: 0142-0453
    Topics: Chemistry and Pharmacology
    Published by Hindawi
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