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  • 11
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Section 44 (1988), S. 1391-1393 
    ISSN: 0584-8539
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica A: Statistical Mechanics and its Applications 207 (1994), S. 37-45 
    ISSN: 0378-4371
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy Section 39 (1983), S. 251-260 
    ISSN: 0584-8539
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 575 (1994), S. 85-92 
    ISSN: 0375-9474
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Vacuum 42 (1991), S. 1085 
    ISSN: 0042-207X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 25 (2007), S. 505-506 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] To the editor: We are writing in response to the correspondence by Autumn Fiester entitled “Why the omega-3 piggy should not go to market” in your December issue (Nat. Biotechnol. 24, 1472–1473, 2006). We feel that her critique of our paper on the transgenic omega-3 pig ignored ...
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 555 (Sept. 2007), p. 459-465 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Molded polyurethane foams for car seats are based on petrochemical polyols ofmolecular weight 4000-6000 and copolymer polyols containing micron size polymeric particles.Copolymer polyols (CPP) typically constitute 30% of the mixture with the base polyol. They helpcell opening, increase load bearing and tear strength of the foams, but they are relatively expensive.Hyperbranched polyols of petrochemical origin were used in molded foams.[1] They are solid inthe pure form and due to high crosslinking density could be incorporated at low concentration inconjunction with copolymer polyols. Instead, we have made hyperbranched polyols which could bea total replacement for CPP in molded foams. Six hyperbranched polyols with primary andsecondary hydroxyl groups and different hydroxyl numbers were prepared from soybean oil andtested in flexible foams. Novel polyols were liquid even at very high molecular weights and couldcompletely replace copolymer polyols. Functionality of these polyols increased linearly withmolecular weight to very high values, resulting eventually in their high crosslinking power. Theeffects of the type of hydroxyl groups (primary vs. secondary), hydroxyl number (from 85 to 135mg KOH/g), and concentration (7.5-30%) in the mixture with the base polyol on foam propertieswere analyzed. It was found that hyperbranched polyols could replace copolymer polyolscompletely but their effect on cell morphology and mechanical properties varied with the type ofpolyol and concentration
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 133 (1997), S. 214-223 
    ISSN: 1432-2072
    Keywords: Key words Diazepam dependence in rat ; Flumazenil precipitated abstinence ; PK 11195 precipitated abstinence ; Slow release of diazepam
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The abilities of the central (CBR) and the peripheral (PBR) benzodiazepine receptor antagonists, flumazenil (FLU) and PK 11195 (PK), to precipitate an abstinence syndrome in diazepam (DZ)-dependent rats have been evaluated. Female rats were exposed for 5 weeks to DZ slowly released from SC implanted silastic capsules (90 mg/capsule per week) and thereafter they were challenged in weekly intervals with IV injections of FLU (10, 20, 40 mg/kg) or PK (5, 10, 20 mg/kg), respectively. The maximum abstinence scores tended to increase with the dose of FLU but not with the dose of PK. Although FLU and PK precipitated some common abstinence signs, there were marked differences between these antagonists. FLU evoked dose-related tonic-clonic and clonic convulsions (five out of six rats), whereas PK (10 mg/kg) induced convulsions in only one rat (out of five); tachypnea tended to increase with the dose of both FLU and PK; twitches and jerks, backing and writhing had a significant regression on the dose of FLU; rearing tended to decrease with the dose of PK whereas FLU-evoked head bobbing and PK-evoked twitches and jerks had inverse U-shaped dose-response curves. In comparison to FLU, similar doses of PK (10 and 20 mg/kg) induced a lower precipitated abstinence score (P〈0.05) and a less intense tachypnea (P〈0.05).The data indicate that the chronic continuous exposure to DZ (and/or its active metabolites) affects both CBR and PBR in the rat; however, the abstinence syndromes produced by the CBR and PBR antagonists, FLU and PK, differ in overall intensities and in the diversity of evoked abstinence signs.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    Transport in porous media 41 (2000), S. 263-285 
    ISSN: 1573-1634
    Keywords: network model ; electrical resistivity ; capillary pressure ; pore geometry ; wettability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Technology
    Notes: Abstract In order to model petrophysical properties of hydrocarbon reservoir rocks, the underlying physics occurring in realistic rock pore structures must be captured. Experimental evidence showing variations of wetting occurring within a pore, and existence of the so-called 'non-Archie' behaviour, has led to numerical models using pore shapes with crevices (for example, square, elliptic, star-like shapes, etc.). This paper presents theoretical derivations and simulation results of a new pore space network model for the prediction of petrophysical properties of reservoir rocks. The effects of key pore geometrical factors such as pore shape, pore size distribution and pore co-ordination number (pore connectivity) have been incorporated into the theoretical model. In particular, the model is used to investigate the effects of wettability and saturation history on electrical resistivity and capillary pressure characteristics. The petrophysical characteristics were simulated for reservoir rock samples. The use of the more realistic grain boundary pore (GBP) shape allows simulation of the generic behaviour of sandstone rocks, with various wetting scenarios. The predictions are in close agreement with electrical resistivity and capillary pressure characteristics observed in experiments.
    Type of Medium: Electronic Resource
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  • 20
    ISSN: 1572-994X
    Keywords: FAdV ; ORF RTL1 transcript ; splicing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two transcription products were found for the open reading frame (ORF) RTL1 located near the right terminus of the fowl adenovirus type-8 genome. The larger transcript, which was transcribed mostly during the early stage of the virus infection, contains the complete sequence (933 nucleotides) of the predicted ORF from the genomic DNA sequence encoding a 311 amino acid (aa) polypeptide. In contrast, the shorter transcript, which was more predominant at the late stage of the infection, was missing 580 nucleotides (from nucleotide 117 to 696). A premature stop codon was introduced at 210 nucleotides downstream from the start codon and the shorter transcript would encode a 70 aa polypeptide. This observation indicates that the ORF RTL1 may produce two different proteins, which function differently at different stages of the virus infection. Another possibility is that the virus may use alternative splicing as a mechanism to control the expression of the ORF, since the spliced transcript was prematurely terminated at the late stage of the infection.
    Type of Medium: Electronic Resource
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