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  • Articles: DFG German National Licenses  (11)
  • Physics  (9)
  • Apoptosis  (2)
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  • Articles: DFG German National Licenses  (11)
Material
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 279 (1995), S. 379-383 
    ISSN: 1432-0878
    Keywords: NADPH-diaphorase ; Myenteric plexus-Ileum ; Proximal colon ; Age ; Programmed cell survival and cell death ; Apoptosis ; Rat (Sprague Dawley)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The effect of age on the distribution of NADPH-diaphorase-containing neurones was investigated in the myenteric plexus of ileum and proximal colon of embryonic day-19 rats, as well as in rats at postnatal day 4, 6 months and 26 months. The mean percentage of NADPH-diaphorase-stained neurones per ganglion was established using protein gene product 9.5 (protein found in most if not all neurones)-immunostained neurones as 100%. The results revealed that there was a significant relative increase in NADPH-diaphorase-positive neurones with increasing age in the myenteric plexus of proximal colon with nearly all protein gene product 9.5-immunoreactive neurones staining for NADPH-diaphorase in 26-month-old rats. This was in marked contrast with the ileum, where no significant relative increase in NADPH-diaphorase-positive neurones was seen in aged rats. The implications of these findings in relation to programmed cell survival and cell death are discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 279 (1995), S. 379-383 
    ISSN: 1432-0878
    Keywords: Key words: NADPH-diaphorase ; Myenteric plexus ; Ileum ; Proximal colon ; Age ; Programmed cell survival and cell death ; Apoptosis ; Rat (Sprague Dawley)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The effect of age on the distribution of NADPH-diaphorase-containing neurones was investigated in the myenteric plexus of ileum and proximal colon of embryonic day-19 rats, as well as in rats at postnatal day 4, 6 months and 26 months. The mean percentage of NADPH-diaphorase-stained neurones per ganglion was established using protein gene product 9.5(protein found in most if not all neurones)-immunostained neu- rones as 100%. The results revealed that there was a significant relative increase in NADPH-diaphorase-positive neurones with increasing age in the myenteric plexus of proximal colon with nearly all protein gene product 9.5-immunoreactive neurones staining for NADPH-diaphorase in 26-month-old rats. This was in marked contrast with the ileum, where no significant relative increase in NADPH-diaphorase-positive neurones was seen in aged rats. The implications of these findings in relation to programmed cell survival and cell death are discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 10 (1972), S. 1521-1527 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Stress and birefringence relaxation have been measured for two polyurethane block polymers at several temperatures to 140°C. Superposition of the stress curves is possible, but the existence of multiple relaxation mechanisms makes such a process of questionable validity. Simple superposition of the birefringence relaxation was not possible. The time and temperature dependence of the stress-optical coefficient implies different mechanisms for mechanical and optical relaxation process. Analysis of the birefringence data requires consideration of nonorientational sources of birefringence.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2401-2412 
    ISSN: 0887-6266
    Keywords: nylon 2 4 ; chain folding ; lamellar crystals ; structure and morphology ; crystallization ; electron microscopy ; Brill transformation ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain-folded lamellar crystals of nylon 2 4 have been prepared from dilute solution by addition of poor solvent. Two crystal structures are observed at room temperature: a monoclinic form I, precipitated at elevated temperature, and a less-defined, orthorhombic form II, precipitated at room temperature. The unit cell parameters for both forms are similar to those reported for its isomer, nylon 3. Nylon 2 4 form II is a liquid-crystal-like or disordered phase, consisting of hydrogen-bonded sheets in poor register in the hydrogen bond direction. Form I crystals have two characteristic interchain spacings of 0.41 nm and 0.39 nm at room temperature and on heating, exhibit a structural transformation and a Brill temperature (250°C) characteristic of many other even-even nylons. Nylon 2 4 is a member of the nylon 2 Y and nylon 2N 2(N+1) families, and the form I crystals show behavior commensurate with both. We propose they contain a proportion of intersheet hydrogen bonds at room temperature, similar to that for the nylon 2 Y family, and the short dimethylene alkane segments mean that the structure consists of hydrogen-bonded a-sheets, with an amide unit in each fold, similar to that of nylon 4 6. The fold geometry and sheet structure is compared with chain-folded apβ-sheet polypeptides and nylon 3. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. B Polym. Phys. 36: 2401-2412, 1998
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 35 (1997), S. 675-688 
    ISSN: 0887-6266
    Keywords: nylons ; lamellar crystals ; diffraction ; Brill transition temperatures ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Four members of the even-even nylon 2 Y series, for Y = 6, 8, 10, and 12, have been crystallized in the form of chain-folded lamellar single crystals from 1,4-butanediol and studied by transmission electron microscopy (imaging and diffraction), x-ray diffraction, and thermal analysis. The structures of these 2 Y nylons are different from those of nylon 6 6 and many other even-even nylons. At room temperature, two strong diffraction signals are observed at spacings 0.42 and 0.39 nm, respectively; these values differ from the 0.44 and 0.37 nm diffraction signals observed for nylon 6 6 and most even-even nylons at ambient temperature. Detailed analyses of the diffraction patterns show that all these 2 Y nylons have triclinic unit cells. The diamine alkane segments of 2 Y nylons are too short to sustain chain folds; thus, the chain folds must be in the diacid alkane segments in all cases. On heating the crystals from room temperature to the melt, the triclinic structures transform into pseudohexagonal structures and the two diffraction signals meet at the Brill transition temperature which occurs significantly below the melting point. The room temperature structures of these 2 Y nylons are similar to the unit cell of nylon 6 6 at elevated temperature, but below its Brill temperature. The room temperature structures and behavior on heating of the nylon 2 Y family is noticeably different from that of the even-even nylon X 4 family, although the only difference between these families of polyamides is the relative disposition of the amide groups within the chains. The results show that in order to understand the structure, behavior and properties of crystalline nylons, especially as a function of temperature, the detailed stereochemistry needs to be taken into account. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys, 35: 675-688, 1997
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1153-1165 
    ISSN: 0887-6266
    Keywords: even-odd nylons ; lamellar crystals ; structure ; hydrogen-bonding schemes ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nylon 6 9 has been shown to have structures with interchain hydrogen bonds in both two and in three directions. Chain-folded lamellar crystals were studied using transmission electron microscopy and sedimented crystal mats and uniaxially oriented fibers studied by X-ray diffraction. The principal room-temperature structure shows the two characteristic (interchain) diffraction signals at spacings of 0.43 and 0.38 nm, typical of α-phase nylons; however, nylon 6 9 is unable to form the α-phase hydrogen-bonded sheets without serious distortion of the all-trans polymeric backbone. Our structure has c and c* noncoincident and two directions of hydrogen bonding. Optimum hydrogen bonding can only occur if consecutive pairs of amide units alternate between two crystallographic planes. The salient features of our model offer a possible universal solution for the crystalline state of all odd-even nylons. The nylon 6 9 room-temperature structure has a C-centered monoclinic unit cell (β = 108°) with the hydrogen bonds along the C-face diagonals; this structure bears a similarity to that recently proposed for nylons 6 5 and X3. On heating nylon 6 9 lamellar crystals and fibers, the two characteristic diffraction signals converge and meet at 0.42 nm at the Brill temperature, TB · TB for nylon 6 9 lamellar crystals is slightly below the melting point (Tm), whereas TB for nylon 6 9 fibers is ≅ 100°C below Tm. Above TB, nylon 6 9 has a hexagonal unit cell; the alkane segments exist in a mobile phase and equivalent hydrogen bonds populate the three principal (hexagonal) directions. A structure with perturbed hexagonal symmetry, which bears a resemblance to the reported γ-phase for nylons, can be obtained by quenching from the crystalline growth phase (above TB) to room temperature. We propose that this structure is a “quenched-in” perturbed form of the nylon 6 9 high-temperature hexagonal phase and has interchain hydrogen bonds in all three principal crystallographic directions. In this respect it differs importantly from the γ-phase models. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1153-1165, 1998
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 2135-2157 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of low-molecular-weight miscible additives on the sub-Tg (β) relaxation process in bisphenol-A polycarbonate (BPAPC) was studied using high-resolution carbon-13 solid-state NMR. The trend of the spin-lattice relaxation times T1 at 50 MHz suggests that strong intermolecular interactions occur upon mixing when BPAPC is physically stiffened by the antiplasticizing diluent, diphenylphthalate. The values of 13C T1 at 15 MHz in d-chloroform solutions for similar BPAPC-diluent mixtures suggest that diluent effects on the megahertz mobility of the polymer occur exclusively in the solid state. These results are explained using equilibrium thermodynamics, in the Ehrenfest sense, at the second-order glass transition temperature Tg. Theory predicts that the temperature dependence of the Flory-Huggins interaction parameter ∂χ/∂T changes abruptly as the polymer-diluent blends are cooled below Tg from the molten state. The difference between ∂χ/∂T in the liquid and glassy states is the major factor which determines the diluent concentration dependence of Tg. A method is developed to estimate the relative magnitudes of χ for polymerdiluent blends in the glassy state.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 2319-2338 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A series of polyurethane block polymers based on hydroxybutyl-terminated polydimethyl-siloxane soft segments of molecular weight 2000 were synthesized. The hard segments consisted of 4,4′-methylenediphenylene diisocyanate (MDI) which was chain extended with either 1,4-butanediol (BD) or N-methyldiethanolamine (MDEA). The MDEA-extended materials were ionized by using 1,3-propane sultone. The weight fraction of hard segments was in the range 0.13-0.39. The morphology and properties of these polyurethane elastomers were studied by a variety of techniques. All of these short-segment block copolymers showed nearly complete phase separation. The zwitterionomer materials exhibited ionic aggregation within the hard domains. Hard-segment crystallinity or ionic aggregation did not affect the morphology. Hard-domain cohesion was found to be a more important factor than hard-domain volume fraction in determining the tensile and viscoelastic properties of these elastomers.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 1389-1401 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nafion membranes neutralized with Ni2+ have been examined by extended x-ray absorption fine-structure (EXAFS) and x-ray absorption near-edge-structure (XANES) spectroscopy. The results indicate that in both the dry and water-soaked membranes, the nickel is in an octahedral site with six oxygen atoms as nearest neighbors. The degree of disorder in the Ni—O distance is comparable to that in ionic crystals in both the dry and hydrated materials. A contribution from a second shell of neighbors is very weak in the dry samples but, surprisingly, this contribution is strongly accentuated in the hydrated membranes. The data indicate that this contribution is due to neighboring Ni2+ cations. Thus the water absorption seems to enhance the local ordering of the cation environment. The local structure does not depend strongly on the concentration of ionic groups in the materials.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 2073-2093 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Extended x-ray absorption fine-structure (EXAFS) measurements were used to determine the near-neighbor environment of the neutralizing cation in several ionomer system. The observed structure is compared to that existing in analogous low-molecular-weight crystalline salts. A wide variety in the degree of local order was observed between different systems even though all exhibit similar small-angle x-ray scattering curves indicating the existence of ionic microdomains.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
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