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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 41 (1935), S. 468-482 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 42 (1935), S. 397-416 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 43 (1936), S. 343-358 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of cancer research and clinical oncology 43 (1936), S. 54-65 
    ISSN: 1432-1335
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0827
    Keywords: Endochondral mineralization ; Cartilage ; Alkaline phosphatase ; In vitro ; Levamisole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Isolated mesenchymal limb bud cells from day-12 mouse embryos grown at high density in organoid culture at the medium/air interphase differentiate into chondrocytes and form cartilage nodules. Upon addition of β-glycerophosphate (β-GP), cartilage undergoes endochondral mineralization. This β-GP-induced mineralization was investigated by measuring the calcium content in the cultures and the activity of alkaline phosphatase (AP) in the cell mass and the medium. Calcium incorporation depended on the amount of β-GP added. After continuous treatment, mineralization began on day 8 of the culture period and increased linearly until day 15. In long-term cultures, periodical treatment for 6 days caused an increase in mineralization the older the cultures were, but the slope of increase was proportionately less steep. Treatment at the latest period on days 19–24 resulted in a markedly reduced mineralization. After short-term treatment (48 hours), mineralization increased also the older the cultures were and proceeded during further cultivation in β-GP-free medium. This kinetic behavior indicates a dependency of mineralization on cartilage maturation in this in vitro system. AP activity increased enormously and nearly logarithmically in the cell mass in β-GP-free medium, whereas β-GP treatment inhibited this drastic increase. In the medium, considerable activities of AP were also measurable from day 10 onward. It increased in β-GP-free medium up to day 14, but was diminished after mineralization had been induced. Levamisole inhibited AP activity dose dependently when added directly to the enzyme-containing medium (100% inhibition at 10-3 M). Added to the cultures from day 7 to 14, it partially inhibited AP activity and mineralization at 5×10-5 M; mineralization was totally inhibited at 10-3 M, but AP activity was still present. This high concentration was cytotoxic, as revealed ultrastructurally and by GAG estimation. This in vitro system comprises cartilage development and maturation, β-GP-inducible endochondral mineralization, and final degenerative changes; it may be an appropriate model for investigations on endochondral mineralization.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 225 (1994), S. 124-130 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 102 (1995), S. 5088-5093 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Thin films of monolithium phthalocyanine (PcLi) were prepared by vacuum deposition on cleaved mica. The highly anisotropic spin diffusion in these films was studied by electron spin resonance (ESR). Using averaging techniques, we succeeded in the detection of films as thin as 100 nm using pulsed ESR and 2 nm with cw ESR. The electronic relaxation is shown to depend on the substrate temperatures Ts during film deposition which determine the morphology of the films. We find relaxation rates of films which are faster by a factor of 20 (T1e−1) to 30 (T2e−1) than those of single crystals. At ambient temperature, a low-dimensional spin exchange mechanism is proposed for the single crystal. At low temperatures, in single crystals the electronic relaxation rates T1e−1 and T2e−1 hint at a reduced exchange with increased dimensionality d(approximately-greater-than)1. This holds for the films at all temperatures and is explained by different crystal structures of single crystals and films. A generally applicable relaxation model is developed which describes the transition from one-dimensional to three-dimensional spin propagation. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 5735-5741 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We present correlated temperature dependent reflection and conductivity measurements on crystals and films of the undeuterated (h8) and the partly deuterated (d6) (2,5-dimethyl- dicyanoquinonediimine)2Cu radical anion salt. Using thin optical fibers, it was possible to study individual needle like crystals of a diameter of only a few μm. The temperature dependence of the reflectivity of single (d6) needles in the visible and the near-infrared region shows a "dip'', which coincides with the phase transition in the conductivity. To interpret our data, we extended the commonly used models for the conductivity from Drude and Epstein, so that we are able to deal with reflection and conductivity in terms of one consistent model. For the (d6) films, a metal–insulator phase transition has been proved by reflection and conductivity. With the assumption of a broad distribution of different phase transition temperatures for the crystallites of the films, the observed spectra of films can also be treated with the model used for the crystals. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 104 (1996), S. 4198-4203 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The deuterated dicyanoquinonediimine salt Cu(2-CD3,5-CD3-DCNQI)2, (d6), a highly conductive organic metal, exhibits a phase transition from the metallic to the insulating state at Tc≈60 K. In a wide temperature range we observe an anticoincidence of high conductivity and electron spin resonance (ESR). These experiments were performed simultaneously in our ESR apparatus equipped for application of He pressure up to 200 bar. Near Tc there is a coexistence of conducting (ESR-silent) and insulating (ESR-detectable) domains. This correlation of ESR and conductivity σ points to a percolation limited conductivity. Upper and lower limits of the size of the domains are given. Light shifts Tc to lower temperatures, pressure to higher ones. This could be due to shrinking of the lattice which induces the phase transition when critical structural parameters are approached. This is most probably explained by a simultaneous development of a charge density wave (CDW) and a spin pairing within the DCNQI stack together with the trimerization of the lattice. Systematic measurements by variation of temperature, pressure, and light led to phase diagrams of (d6) and to the understanding of the mechanism of the phase transitions. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 105 (1996), S. 6538-6545 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Phase transitions in the radical ion salts of Cu(2,5-dimethyl-dicyanoquinonediimine)2 (Cu(DCNQI)2) can be achieved either by "external'' pressure or by "internal'' pressure. The latter is introduced by chemical modifications at the DCNQI-molecules (e.g., deuteration) or by alloying deuterated Cu(2,5-(CD3)2-DCNQI)2 (d6) with undeuterated Cu(2,5-(CH3)2-DCNQI)2 (h8), giving the mixture (h8/d6) in different ratios. In this work we present simultaneous conductivity (σ) and electron spin resonance (ESR) experiments on differently deuterated Cu(DCNQI)2-systems and on alloys (h8/d6) under external pressure. The anticoincidence of σ and ESR allows the determination of phase transition temperatures even in the absence of electrical contacts. For each system an individual phase diagram is established. Introducing an effective pressure peff=p0+p with p0 being the "internal'' (chemical) pressure, a general phase diagram could be constructed by determining the individual p0 value for all systems. For the alloys (h8/d6) the relation ∂p0/∂q=5.0 bar/% (q is the percentage of d6) could be evaluated. The occurrence of a phase transition is associated with a change in the lattice parameters. For that, a structural model of a v-shaped temperature dependence of the unit cell volume V is suggested. For thermodynamic considerations, V is used as order parameter. If this order parameter V crosses critical values Vcbig and Vcsmall from above (cooling) or below (heating), phase transitions from conducting to insulating phases or vice versa are induced. This model explains the phase transition temperatures, the re-entry and the hysteresis effects of all systems qualitatively. © 1996 American Institute of Physics.
    Type of Medium: Electronic Resource
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