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  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 55 (1999), S. 1463-1466 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of environmental contamination and toxicology 60 (1998), S. 773-780 
    ISSN: 1432-0800
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Herpesvirus saimiri (H. saimiri) can transform T lymphocytes and cause lymphoid tumors in rabbits and New World monkeys. H. saimiri-immortalized T cells express IL-2 and IL-4. The putative oncogenes of a group C strain of H. saimiri have been mapped to a region of the unique L-DNA which includes genes encoding four U-like small nuclear RNAs (HSUR1-HSUR4). Jurkat T cells express a 70 kD RNA binding factor (AUBF70) which binds HSUR2. Here we examined AUBF70 expression in resting and mitogenstimulated human peripheral blood T cells and its sequence specificity and subcellular distribution. Band-shift assays demonstrated that resting human T cells express low amounts of AUBF70 which is induced by mitogen treatment. IL-2 and IL-4 mRNAs were co-induced with AUBF70 suggesting that AUBF70 is a positive regulator of lymphokine gene expression. Normal resting, mitogen-stimulated, and leukemic Jurkat T cells all express AUBF70 with virtually identical V8 proteolytic enzyme digestion patterns. Northern blots demonstrated that HSUR1 and HSUR2 are localized both in the nucleus and cytoplasm. HSUR2 accumulate in the cytoplasm in the presence of actinomycin D, which is consistent with re-transport of HSURs to the nucleus by (an) unstable factor(s). We hypothesize that HSUR1 and 2 transport AUBF70 from the cytoplasm to the nucleus; in the nucleus, AUBF70 binds and stabilizes lymphokine transcripts. Increased stability of lymphokine mRNAs could contribute to oncogenic transformation induced by H. saimiri.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1434-6036
    Keywords: PACS. 61.12.-q Neutron diffraction and scattering - 64.70.Rh Commensurate-incommensurate transitions - 77.22.Ch Permittivity (dielectric function)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: We report a combined experimental study by means of elastic neutron scattering and dielectric measurements of a partially deuterated and brominated BCCD (Betaine Calcium Chloride Dihydrate) crystal. The lowest-temperature phase is one-dimensional modulated and characterized by the coexistence of different commensurate domains (with = 1/4, 4/17, 2/9 and 1/5 on cooling), but with a clear predominance of the five-fold phase. A huge global thermal hysteresis of the wave-vector of the modulation, attaining values of about 9 K in the incommensurate phase and up to 15 K in the “harmless” low temperature part of the phase diagram, is observed up to . The role of lattice defects on this phenomenon is discussed. Similarly to the behaviour of the pure compound, the structural modulation evolves on cooling towards a soliton regime (growth of third and fifth-order satellite peaks), probably with respect to a non-stabilized non-modulated ferroelectric phase. The critical temperatures deduced from dielectric constant and pyroelectric current measurements are in very good agreement with those obtained from neutron scattering. The dielectric anomaly observed in at K, and known as the “ -anomaly”, could not be related with any special feature detected in the neutron data, and in particular no correlation between this anomaly and the appearance of the soliton regime can be established.
    Type of Medium: Electronic Resource
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