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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 40 (1984), S. 1420-1422 
    ISSN: 1420-9071
    Keywords: Fetal development ; brain, human ; liver, human ; aldose metabolism ; sorbitol pathway
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Aldose reductase, sorbitol dehydrogenase, and glucose-6-phosphate dehydrogenase enzyme activities were studied in human foetal brain and liver at different periods of gestation. Aldose reductase activity in liver disappears after 16 weeks of gestation whereas sorbitol dehydrogenase keeps on increasing in liver as well as in brain. In utero, some glucose metabolism may be mediated through an active sorbitol pathway in human fetuses.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5987-6006 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A recently developed theory for angular distribution of electrons ejected by interaction of light with nonlinear molecules held fixed in space has been used to study ionization in a1 orbital of those systems which transform like the Td point symmetry group. Expressions for photoelectron angular distributions in the dipole approximation with the electric vector in the radiation beam both perpendicular and parallel to the molecular axis are derived. The properties of the two formulas, which are found to have completely different structures, have been studied. These expressions are shown to depend not only on all those quantities [i.e., the partial integrated cross-section σ¯, the asymmetry parameter β¯, and the polar angle θ of the propagation vector k (k,θ,φ) of the ejected electron] which are present in photoionization of an unoriented molecule, but involve in certain cases also the azimuthal angle φ, phase shifts of the continuum waves representing the outgoing electron, and the phase of the dipole transition amplitudes. Such fixed-molecule photoelectron angular distributions will therefore provide more stringent tests of theoretical models and probes of photoionization dynamics than the hitherto performed gas phase experiments on randomly oriented targets. They can also be used to identify the orientation of a molecule and/or geometry of a chemisorption site. The formulation presented here sets a frame work for the analysis of measurements and the calculations of spectra in those Td molecules which are fixed in space. We have applied it, as an example, to ionization in 4a1, 6a1, and 7a1 orbitals of oriented CF4, CCl4, and SiCl4, respectively. Without doing any dynamical calculations, using instead the experimentally measured values of σ¯ and β¯ as a function of the photon wavelength, the variations in the angular distributions with respect to the energy of the ejected electron as well as to the angles (θ,φ) and to the phases (which are treated as parameters) involved have been studied in detail. These distributions are found to have very rich and complicated structures arising from the spectral, angular, and/or phase variations of the angular momentum compositionof the photocurrent.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 5814-5821 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We have, in this paper, derived expressions for the partial photocurrent produced by ionization in the electric dipole approximation in an orbital of an oriented polyatomic molecule. The cross-section formulas, which are integrated over all directions of ejection of the photoelectron but differential with respect to the direction of the fixed molecular axis, are obtained in their simplest possible forms by taking full account of the transformation properties of the point symmetry group of the target and are thus applicable to photoionization in any oriented molecule belonging to one of the 32 point groups. The theory, as an example, has been applied to photoionization in a1 orbital of those oriented nonlinear systems whose point symmetry group is Td. This application shows that the singly differential, detection-integrated partial cross section for ionization by unpolarized, linearly or circularly polarized light in a1 orbital of a fixed Td molecule is (i) independent of the direction of its axis and (ii) equal to that averaged over all orientations of the target in space. Both conclusions are in agreement with recent experimental measurements on photoionization in 6a21 orbital of fixed CCl4. These results, in turn, are shown to mean that the variations with respect to the orientation of a molecule in space, found in theoretical calculations of photoelectron angular distribution for ionization in a1 valence orbitals of some of the Td targets, are due completely to the terms which stem from freezing both the molecular axis and the photoelectron detector in space. These terms completely vanish on integrating over all directions of propagation of the photoelectron, resulting in a current which is isotropic with respect to the orientation of the molecular axis in space. In such cases, it is therefore necessary to study the angular distribution of electrons ejected by photoionization in oriented molecules in order to obtain cross sections which will change with the direction of the target axis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 1608-1614 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The effect of attractive interactions on the behavior of polymers between surfaces is studied using Monte Carlo simulations. The molecules are modeled as fused sphere freely rotating chains with fixed bond lengths and bond angles; wall–fluid and fluid–fluid site–site interaction potentials are of the hard sphere plus Yukawa form. For athermal chains the density at the surface (relative to the bulk) is depleted at low densities and enhanced at high densities. The introduction of a fluid–fluid attraction causes a reduction of site density at the surface, and an introduction of a wall–fluid attraction causes an enhancement of site density at the surface, compared to when these interactions are absent. When the wall–fluid and fluid–fluid attractions are of comparable strength, however, the depletion mechanism due to the fluid–fluid attraction dominates. The center of mass profiles show the same trends as the site density profiles. Near the surface, the parallel and the perpendicular components of chain dimensions are different, which is explained in terms of a reorientation of chains. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 8509-8516 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A simple weighted-density-functional approach is developed for inhomogeneous fluids by approximating the excess free energy density functional by that of the corresponding uniform system evaluated at an effective density. This effective weighted density is obtained by a suitable local averaging procedure of the actual density distribution using a weight function which is evaluated only once at the bulk density, thus being decoupled from the weighted density. This approach does not involve any power series expansion or solution of any nonlinear differential equation at every point and each iteration, as is required in some of the analogous schemes. The new theory is applied to predict the structure of simple classical fluids, interacting with hard sphere, Coulombic as well as Yukawa potentials, under confinement in several geometries. The calculated results on the density profiles are shown to compare quite well with available simulation data. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 1579-1584 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A density functional theory is presented for the effect of attractions on the structure of polymers at surfaces. The theory treats the ideal gas functional exactly, and uses a weighted density approximation for the hard chain contribution to the excess free energy functional. The attractive interactions are treated using a van der Waals approximation. The theory is in good agreement with computer simulations for the density profiles at surfaces for a wide range of densities and temperatures, except for low polymer densities at low temperatures where it overestimates the depletion of chains from the surface. This deficiency is attributed to the neglect of liquid state correlations in the van der Waals term of the free energy functional. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 787-788 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: A mannose-specific agglutinin from garlic (Allium sativum) which forms part of a well conserved super-family of bulb lectins has been purified and crystallized by the hanging-drop vapour-diffusion technique, by equilibrating with a 20% solution of PEG 8000 in the presence of α-D-mannose. Crystals of the dimeric form of this protein are monoclinic C2 with unit-cell dimensions a = 203.2, b = 43.8, c = 79.3 Å and β = 112.4° and have two dimers in the asymmetric unit. Data have been collected to 2.4 Å resolution and the structure solved by molecular replacement using the coordinates of the snowdrop lectin as the search model.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 55 (1999), S. 1750-1758 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: It is difficult but not impossible to determine a macromolecular structure using X-ray data obtained from twinned crystals, providing it is noticed and corrected. For perfectly twinned crystals, the structure can probably only be solved by molecular replacement. It is possible to detect and characterize twinning from an analysis of the intensity statistics and crystal packing density. Tables of likely twinning operators and some examples are discussed here.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The crystal structures of 88 and 79% relative humidity forms of ribonuclease A, resulting from water-mediated transformations, have been refined employing the restrained least-squares method using X-ray data collected on an area detector to R = 0.173 for 15 326 observed reflections in the 10–1.5 Å resolution shell and R = 0.176 for 8534 observed reflections in the 10–1.8 Å shell, respectively. The comparison of these structures with those of the native, the phosphate-bound and the sulfate-bound forms demonstrates that the mobility of the ribonuclease A molecule involves hinge-bending movement of the two domains and local flexibility within them, particularly at the termini of regular secondary structures and in loops. The comparison also leads to the identification of 31 invariant water molecules in the hydration shell of the enzyme, many of which are involved in holding different parts of the molecule together and in stabilizing local structure. The conformational changes that accompany the partial removal of the surrounding water, particularly those observed in the 79% form, could be similar to those that occur during enzyme action.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physica A: Statistical Mechanics and its Applications 110 (1982), S. 565-579 
    ISSN: 0378-4371
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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