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  • Articles  (57)
  • Elsevier  (49)
  • American Association for the Advancement of Science (AAAS)  (8)
  • Inter-Research
  • 2015-2019
  • 1985-1989  (51)
  • 1955-1959  (6)
  • 1925-1929
  • 1987  (51)
  • 1956  (6)
  • Chemistry and Pharmacology  (50)
  • Geography  (7)
  • Law
Collection
  • Articles  (57)
Years
  • 2015-2019
  • 1985-1989  (51)
  • 1955-1959  (6)
  • 1925-1929
Year
Journal
  • 1
    Publication Date: 1987-11-01
    Print ISSN: 0006-2952
    Electronic ISSN: 1873-2968
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Published by Elsevier
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  • 2
    Publication Date: 1987-04-01
    Print ISSN: 0191-2615
    Electronic ISSN: 1879-2367
    Topics: Architecture, Civil Engineering, Surveying , Geography , Economics
    Published by Elsevier
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  • 3
    Publication Date: 1987-12-01
    Print ISSN: 0040-1625
    Electronic ISSN: 1873-5509
    Topics: Geography , Sociology , Technology
    Published by Elsevier
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  • 4
    Publication Date: 1987-11-06
    Description: The stable rotation and sharp radio pulses of PSR 1937+21 make this pulsar a clock whose long-term frequency stability approaches and may exceed that of the best atomic clocks. Improvements in measurement techniques now permit pulse arrival times to be determined in 1 hour at the Arecibo radio telescope with uncertainties of about 300 nanoseconds relative to atomic time. Measurements taken approximately every 2 weeks since November 1982 yield estimates of fractional frequency stability that continue to improve with increasing averaging time. The pulsar's frequency stability is at least as good as 6 x 10(-14) for averaging times longer than 4 months, and over the longest intervals the measurements appear to be limited by the stability of the reference atomic docks. The data yield a firm upper limit of 7 x 10(-36) gram per cubic centimeter for the energy density of a cosmic background of gravitational radiation at frequencies of about 0.23 cycle per year. This limit corresponds to approximately 4 x 10(-7) of the density required to close the universe.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rawley, L A -- Taylor, J H -- Davis, M M -- Allan, D W -- New York, N.Y. -- Science. 1987 Nov 6;238(4828):761-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17814704" target="_blank"〉PubMed〈/a〉
    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
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-03-13
    Description: On the basis of well-established principles of evolutionary biology and microbiology, I conclude that (i) the deliberate introduction of a novel bacterial strain to the environment is not substantially more dangerous than the accidental release of a smaller number of cells; (ii) distant organisms are less (rather than more) likely to yield dangerous hybrids than more closely related ones; and (iii) the complex attribute of pathogenicity is not likely to emerge from genetic alterations in nonpathogens. If these conclusions are correct, most engineered bacteria need not be regulated more strictly than the bacterial strains that have been tested in the field in the past. The only exceptions would be strains derived from cells, or appropriate genes, of microbes pathogenic for plants or animals. Microbiologists not only recognize the need to handle pathogens with caution: they have long accepted regulations, such as those governing transportation, that reinforce that recognition. It is remarkable that we can still be arguing, on the basis of analogies rather than firm scientific principles or evidence, about hypothetical disasters from kinds of organisms that are being produced in hundreds or thousands of laboratories without a trace of demonstrable harm. RAC required 6 years to adjust its initially conservative guidelines to the emerging understanding of the scientific realities, while maintaining public confidence. Since the level of public concern is not nearly as great today, EPA should be able to relax its excessive restrictions much more quickly. Even better would be a return to having RAC, or a single successor group, evaluate the problems of danger for all classes of engineered bacteria, since the applicable shared principles outweigh any specialized differences in the nature or use of the specific strains. But the regulations are unlikely to be unified in this way, or to be divested of unproductive restrictions, without broad encouragement from the scientific community-including, hopefully, many ecologists. The agenda has been set for too long by apocalyptic activists. To protect this promising field of research and technological application the scientific community must take initiative in helping the public and decision-makers to distinguish reasonable probabilities from remote fantasies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, B D -- New York, N.Y. -- Science. 1987 Mar 13;235(4794):1329b-35b.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17829976" target="_blank"〉PubMed〈/a〉
    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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  • 6
    Publication Date: 1987-05-01
    Description: The mechanisms whereby insulin increases diacylglycerol in BC3H-1 myocytes were examined. When [3H]arachidonate labeling of phospholipids was used as an indicator of phospholipase C activation, transient increases in [3H]diacylglycerol were observed between 0.5 and 10 minutes after the onset of insulin treatment. With [3H]glycerol labeling as an indicator of de novo phospholipid synthesis, [3H]diacylglycerol was increased maximally at 1 minute and remained elevated for 20 minutes. [3H]Glycerol-labeled diacylglycerol was largely derived directly from phosphatidic acid. Insulin increased de novo phosphatidic acid synthesis within 5 to 10 seconds; within 1 minute, this synthesis was 60 times greater than that of controls. Thus, the initial increase in diacylglycerol is due to both increased hydrolysis of phospholipids and a burst of de novo phosphatidic acid synthesis. After 5 to 10 minutes, de novo phosphatidic acid synthesis continues as a major source of diacylglycerol. Both phospholipid effects of insulin seem important for generating diacylglycerol and other phospholipid-derived intracellular signaling substances.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Farese, R V -- Konda, T S -- Davis, J S -- Standaert, M L -- Pollet, R J -- Cooper, D R -- AM18608/AM/NIADDK NIH HHS/ -- HD22248/HD/NICHD NIH HHS/ -- New York, N.Y. -- Science. 1987 May 1;236(4801):586-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3107122" target="_blank"〉PubMed〈/a〉
    Keywords: Arachidonic Acid ; Arachidonic Acids/metabolism ; Cell Line ; Diglycerides/*metabolism ; Enzyme Activation ; Glycerides/*metabolism ; Glycerol/metabolism ; Insulin/*pharmacology ; Kinetics ; Muscles/drug effects/*metabolism ; Phosphatidic Acids/*biosynthesis ; Phosphatidylinositols/metabolism ; Phospholipids/metabolism ; Type C Phospholipases/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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  • 7
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-12-18
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, D L -- New York, N.Y. -- Science. 1987 Dec 18;238(4834):1633-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3120316" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; *Carcinogens ; *Diet ; *Haplorhini ; Humans ; *Paleontology
    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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  • 8
    Publication Date: 1987-06-26
    Description: Quantitative autoradiography of brain glucose metabolism has been combined with digital image processing to represent the brain as a three-dimensional (3-D) reconstruction of brain energy use. Autoradiographs contain enormous amounts of potentially useful data, but conventional analyses, based on tedious manual methods, can sample and analyze only a small portion of this information. Computer 3-D reconstruction provides a mechanism for observing and analyzing all the data; therefore, a system of computer programs was developed for this purpose. The programs use digital imaging methods for image registration, superimpose whole brain data sets, and allow resampling of the 3-D data in arbitrary planes for pixel-by-pixel comparisons among multiple 3-D sets. These programs operate on the mathematical properties of the images alone, obviating the need for manual image alignment. Various statistical analyses can be applied to the data directly to study the patterns of metabolic changes in different experiments. The system is applied to data from experiments on the influence of injectable anesthetics on cerebral glucose metabolism.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hibbard, L S -- McGlone, J S -- Davis, D W -- Hawkins, R A -- AA06023/AA/NIAAA NIH HHS/ -- NS16389/NS/NINDS NIH HHS/ -- NS16737/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1987 Jun 26;236(4809):1641-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3603004" target="_blank"〉PubMed〈/a〉
    Keywords: Anesthetics/pharmacology ; Animals ; Autoradiography ; Brain/drug effects/*metabolism ; *Energy Metabolism/drug effects ; Glucose/metabolism ; *Image Processing, Computer-Assisted ; Rats
    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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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 1987-08-07
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, J C -- New York, N.Y. -- Science. 1987 Aug 7;237(4815):669-72.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17758579" target="_blank"〉PubMed〈/a〉
    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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  • 10
    Publication Date: 1987-05-29
    Description: The epithelial cell layer of human amnion membrane can be removed while the basement membrane and stromal surfaces remain morphologically intact. Such a preparation has been used as a substratum for the in vitro culture of dissociated neurons. Embryonic motor neurons from chick ciliary ganglion attached to both surfaces but grew extensive neurites only on the basement membrane. On cross sections of rolled amnion membranes, regenerating axons of cultured neurons were guided along pathways of basement membrane that were immunoreactive with an antibody to laminin. In addition, when rolled amnion membranes were implanted into a lesion cavity between the rat septum and hippocampus, cholinergic neurons extended axons through the longitudinally oriented implant into the hippocampus. Thus, this amnion preparation can serve as a bridge to promote axonal regeneration in vivo in damaged adult brain.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, G E -- Blaker, S N -- Engvall, E -- Varon, S -- Manthorpe, M -- Gage, F H -- AM30051/AM/NIADDK NIH HHS/ -- CA28896/CA/NCI NIH HHS/ -- NS16349/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1987 May 29;236(4805):1106-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3576223" target="_blank"〉PubMed〈/a〉
    Keywords: *Amnion ; Animals ; Axons/*growth & development ; Basement Membrane ; Chick Embryo ; Humans ; In Vitro Techniques ; Motor Neurons/growth & development ; Rats
    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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