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  • Atomic, Molecular and Optical Physics  (6)
  • RecA  (5)
  • Stratum corneum  (3)
  • 1
    ISSN: 0022-2836
    Keywords: DNA complex ; RecA ; flow orientation ; pitch ; small-angle neutron scattering
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0022-2836
    Keywords: DNA-protein complex ; RecA ; genetic engineering ; linear dichroism ; recombination
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimie 73 (1991), S. 491-495 
    ISSN: 0300-9084
    Keywords: N-AcO-AAF ; RecA ; alternating GC sequences ; frameshift ; mutagenesis ; repetitive sequences
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimie 73 (1991), S. 219-226 
    ISSN: 0300-9084
    Keywords: RecA ; RecA-DNA complex ; linear dichroism ; recombination ; strand exchange
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 279 (1987), S. 281-282 
    ISSN: 1432-069X
    Keywords: Stratum corneum ; Desquamation ; Cell renewal time ; Dansyl chloride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-069X
    Keywords: Hematoxylin stainable protein ; Keratohyalin granules ; Membrane lining protein ; Stratum corneum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A monoclonal antibody (Ted-R-1) to the keratohyalin granules (KHGs) of the newborn rat epidermis was developed by immunizing mice with a pH 4.7 hematoxylin-stainable fraction of the extract in a 50 mM Tris-HCl buffer, pH 7.3, containing 10 μ/ml phenylmethylsulfonyl fluoride (PMSF) from the newborn rat whole epidermis. Using an indirect immunofluorescence technique, Ted-R-1 was located in two places: (a) the KHGs and (b) the cell membrane region of the stratum corneum. Under immunoelectron microscopy, the antigenic materials were located at the periphery of the KHGs. Immunoblotting analyses of the antigenic pH 4.7 fraction, the Tris-HCl extract from the stratum corneum, and the Tris-8M urea extract from freeze-dried whole skin demonstrated that there were 55 kd, 43 kd, and 78 kd polypeptides, respectively, with which Ted-R-1 reacts. No possitive spot was seen in the dermal extract. The major amino acids of the 55 kd protein were glycine (24.4%), serine (17.3%), glutamic acid (14.1%), and alanine (7.7%), while the histidine residue was only 3.1%. On the basis of its amino acid composition, the 55 kd protein is the third component of KHGs — in addition to histidine-rich and cystinerich proteins.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 285 (1993), S. 372-377 
    ISSN: 1432-069X
    Keywords: Stratum corneum ; Protease ; Desquamation ; Scaly skin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In order to identify the endogenous protease associated with stratum corneum (SC) desquamation, we examined properties of proteases in the stratum corneum of normal human skin. SC were obtained by tape stripping, washed in toluene and then dried. The proteolytic activity in SC was measured using peptidyl 4-methyl-coumaryl-7-amides (MCAs). The SC was dispersed uniformly in the reaction mixture with dimethylformamide and Triton X-100 and incubated with the peptidyl MCAs. The protease in the SC hydrolysed both Boc-Phe-Ser-Arg-MCA and Boc-Gln-Ala-Arg-MCA (substrates for trypsin) very effectively. The hydrolytic activity was inhibited by the serine protease inhibitors diisopropyl fluorophosphate (DFP), aprotinin, antipain and leupeptin, but not by chymostatin, a chymotrypsin inhibitor. These results show that one or more trypsin-like serine protease is present in the SC of normal human skin. Casein-acrylamide electrophoresis showed that the molecular weight of this serine protease was about 30 kDa. We have previously shown that cells dissociate from human SC sheets in a detergent mixture (N,N-dimethyldodecylamine oxide and sodium lauryl sulphate). This cell dissociation was inhibited by aprotinin and leupeptin. In addition, the proteolytic activity in the outer SC was higher than that in the inner SC, and the activity in the SC of scaly skin induced by SLS treatment was higher than that of untreated skin. These results strongly suggest that the trypsin-like serine protease described here is involved in SC desquamation.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 28 (1985), S. 459-479 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The role of electron correlation effects on the bond-length alternation in linear metalliclike systems, as modeled by cyclic polyenes CNHN, N = 2n = 4v + 2, v = 1,2,…, is examined using the coupled cluster approach in the localized Wannier basis formalism. A recently developed approximate coupled pair approach which accounts for connected quadruply excited clusters is employed together with various truncation schemes for the localized doubly-excited cluster components. It is found that for the physical value of the coupling constant, the electron correlation has only a very slight effect on the potential energy curves, yielding almost the same values for both the magnitude of the bond-length alternation and for the stabilization energy relative to the symmetric equidistant structures as the restricted Hartree-Fock theory. This is in contrast to a strongly correlated region where the correlation effects stabilize the undistorted non-alternating structures. Different mechanisms of the bond-length alternation or Peierl's distortion as implied by a simple Hückel Hamiltonian and by the Pariser-Parr-Pople Hamiltonian models are also pointed out.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 25 (1984), S. 423-443 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The problem of bond length alternation in linear extended systems with conjugated double bonds is examined on a simple cyclic polyene model using finite-order many-body perturbation theory. Three different partitionings of the model Hamiltonian are employed, namely the Hückel, Møller-Plesset, and Epstein-Nesbet partitionings. The dependence of correlation energy on bond length alternation is examined in each case, showing an almost constant behavior of Møller-Plesset and Epstein-Nesbet perturbation energies in contrast to a strong dependence on distortion, favoring undistorted structures, for the Hückel perturbation and UHF correlation energies. The origin of an unphysical character of the Hückel perturbation theory and the inappropriateness of the UHF approach for the problem considered are pointed out. The second- and third-order Møller-Plesset and also the second-order Epstein-Nesbet perturbation theories yield results which are similar to those obtained with the RHF method and which clearly favor the bond length alternating structures, leading to the bond length distortion of about 0.045 Å and to the stabilization energy per site (relative to the equidistant geometry) of about 0.03 eV.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 24 (1983), S. 707-727 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The applicability of the finite-order many-body perturbation theory to the electron correlation problem in extended one-dimensional systems is examined. The cyclic polyenes CNHN, N = 4ν + 2, ν = 1, 2, …, with the DNh geometry as described by both the Pariser-Parr-Pople and Hubbard Hamiltonians, are employed to model the metallic-like one-dimensional systems. The second-order perturbation theory contributions to the correlation energy are obtained with three different partitionings of the Hamiltonian (Hückel, M⊘ller-Plesset, and Epstein-Nesbet). The third- and fourth-order contributions are also calculated in special cases. A comparison with other methods is given wherever available. For the Hubbard Hamiltonian the asymptotic behavior of the perturbation theory expansion is examined numerically. It is shown that the finite-order perturbation expansion can provide reliable results for the correlation energy of one-dimensional systems even in the correlation region which corresponds to the spectroscopically determined physical value of the coupling constant.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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