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  • Wiley-Blackwell  (166)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 7 (1987), S. 110-115 
    ISSN: 0886-1544
    Keywords: microtubules ; antitubulin ; particle translocalion ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Microtubules have been demonstrated to be a substrate for organelle transport and particle translocation in vitro and in vivo. Subsequent to a previous report of inhibition of axonal transport of exogenous tracers in vivo using antiserum NS-20 against tubulin (Johnston et al: Brain Res. 1986), we now show disruption of particle movement in extruded squid axoplnsm using this unique immunological probe. Using video-enhanced contract-differential interference contrast (AVEC-DIC) microscopy, we examined the properties of particle movement along microtubules and demonstrated that bolh the velocity of particle movement and the numbers of particles moving are decreased in the presence of NS-20 antiserum or NS-20 affinity-purified antibodies but. not in the presence of another antiserum against tubulin. The amount of microtubule substrate does not change in the presence of any of the antisera. In conclusion, we suggest that NS-20 antibodies bind near or at a site on the tubulin molecule which is critical in the mechanism of particle transport, and provide a direct immunological probe to examine the mechanism of microtubule involvement in axonal transport.
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 2175-2183 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previous work by a number of researchers has noted the presence of anhydride during the imidization step of polyimide polymer processing from diester-diacids and diamines. This has been often, and incorrectly, dismissed as being due to the reversion of the intermediate amide-acid. Comparison of the relative rates of reactions among model compounds demonstrates the intermediacy of anhydride in the imidization reaction. When creation of the anhydride is blocked, the production of amide-acid is greatly slowed. Infrared and NMR observations of mixtures of monomers confirm the production of anhydride as a necessary intermediate in the imidization reaction occuring during the production of polyimide polymers from diester diacids.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 29 (1994), S. 280-290 
    ISSN: 0886-1544
    Keywords: mitosis ; phosphorylation ; protein phosphatase ; okadaic acid ; mitotic apparatus ; sea urchin ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: A protein component of isolated mitotic apparatus having a relative molecular mass of 62,000 (p62) is a substrate of a calcium/calmodulin dependent protein kinase, and the phosphorylation of p62 in vitro correlates directly with microtubule disassembly. In vivo experiments have determined the phosphorylation of p62 increases after fertilization; maximum incorporation of phosphate occurs during late metaphase/early anaphase and decreases thereafter. Because the level of p62 is constant throughout the cell cycle [Johnston and Sloboda, 1992: J. Cell Biol. 119:843-54] the decrease in phosphorylation of p62 observed after anaphase onset is most likely due to the action of a phosphatase. By examination of the relative amount of phosphorylated p62 which remained radiolabeled as a function of time using a standard in vitro phosphorylation assay, the activity of a phosphoprotein phosphatase capable of dephosphorylating p62 in the isolated mitotic apparatus was observed. To characterize the p62 phosphatase, okadaic acid and calyculin A were used to inhibit the dephosphorylation of p62 in vitro. It was found that specific concentrations of okadaic acid (50-500 nM) and of calyculin A (10-100 nM) were effective at inhibiting the dephosphorylation of p62 in vitro. Lower concentrations of either inhibitor had a negligible effect on dephosphorylation of p62. These data indicate the presence of phosphoprotein phosphatase type 1 activity associated with mitotic apparatus isolated from sea urchin embryos using the procedures described here. The implications of these findings relative to our understanding of the regulation of mitosis and cytokinesis are discussed. © 1994 Wiley-Liss, Inc.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 76 (1912), S. 201-273 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Die Darstellung von Eisendisulfid wurde ausgeführt 1. durch Einwirkung von Schwefelwasserstoff auf Ferrisalze oder von Schwefel und Schwefelwasserstoff auf Ferrosalze; 2. durch Addition von Schwefel aus Lösung an amorphes Ferrosulfid oder Pyrrhotin; 3. durch die Einwirkung löslicher Polysulfide auf Ferrosalze; 4. durch Einwirkung löslicher Thiosulfate auf Ferrosalze nach der Gleichung: \documentclass{article}\pagestyle{empty}\begin{document}$$ 4{\rm M}_2 {\rm S}_2 {\rm O}_3 + {\rm FeX}_2 = 3{\rm Me}_2 {\rm SO}_4 + {\rm FeS}_2 + {\rm 2MX} + {\rm 3s}{\rm .} $$\end{document}. Die ersten drei Methoden können allgemein bezeichnet werden als Einwirkung von Schwefel auf Ferrosulfid: (a) in saurer Lösung, (b) in fast neutraler Lösung, und (c) in alkalischer Lösung, da wir bei 1. annehmen können, daß sich zuerst Ferrosulfid durch Einwirkung von Schwefelwasserstoff auf Ferrosalz bildet und da wir bei 3. wissen, daß Polysulfide zuerst ein Gemisch von Ferrosulfid und Schwefel fallen. Markasit erhielt man mit Sicherheit nur nach Methode 1; niedere Temperatur und freie Säure begünstigen seine Bildung. Eine Lösung mit etwa 1 % freier Schwefelsaure bei 100° gibt reinen Markasit. Weniger saure Lösungen bei höherer Temperatur geben Gemische von Markasit und Pyrit. Die anderen Verfahren liefern Pyrit, der unter gewissen Bedingungen mit amorphem Disulfid gemischt sein kann. Es ist möglich, daß etwas Markasit nach Methode 4 gebildet wird.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 76 (1912), S. 274-302 
    ISSN: 0863-1778
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1. Mit einer neuen verbesserten Form des Pyknometers haben wir die Dichte von Salzen und anderen Substanzen mit einer Genauigkeit von 3-4 Einheiten in der vierten Dezimale, d. h. bis auf etwa 0.02% bestimmt. In vielen Fällen jedoch ist eine derartige Genauigkeit nicht notwendig, da die durch die Inhomogenität des Materiales bedingten Dichteänderungen bedeutend größer sein können.
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  • 6
    ISSN: 0899-0042
    Keywords: chiral HPLC ; resolution ; absolute configuration ; X-ray analysis ; GABAB antagonist ; GABAB receptor affinity ; phaclofen ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phaclofen, which is the phosphonic acid analogue of the GABAB agonist (RS)-3-(4-chlorophenyl)-4-aminobutyric acid (baclofen), is a GABAB antagonist. As part of our studies on the structural requirements for activation and blockade of GABAB receptors, we have resolved phaclofen using chiral chromatographic techniques. The absolute stereochemistry of (-)-(R)-phaclofen was established by X-ray crystallographic analysis. (-)-(R)-Phaclofen was shown to inhibit the binding of [3H]-(R)-baclofen to GABAB receptor sites on rat cerebellar membranes (IC50 = 76 ± 13 μM), whereas (+)-(S)-phaclofen was inactive in this binding assay (IC50 〉 1000 μM). (-)-(R)-Phaclofen (200 μM) was equipotent with (RS)-phaclofen (400 μM) in antagonizing the action of baclofen in rat cerebral cortical slices, while (+)-(S)-phaclofen (200 μM) was inactive. The structural similarity of the agonist (R)-baclofen and the antagonist (-)-(R)-phaclofen suggests that these ligands interact with the GABAB receptor sites in a similar manner. Thus, it may be concluded that the different pharmacological effects of these compounds essentially result from the different spatial and proteolytic properties of their acid groups. © 1994 Wiley-Liss, Inc.
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  • 7
    ISSN: 0935-6304
    Keywords: Terpenoid analysis ; Douglas-fir ; Sapwood ; Capillary gas chromatography ; Solvent extraction ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to investigate the relationship between terpenoid content and black bear foraging preference, an analytical method was required to quantify mono- and sesquiterpenoids present in Douglas-fir sapwood. Sapwood samples were scraped from trees, immediately frozen in liquid nitrogen, and then homogenized. A simple extraction requiring no clean-up step was performed with ethyl acetate. Extracts were analyzed by gas chromatography with mass selective detection versus external standards. The recoveries of 22 terpenoids from fortified controls were approximately 90% with good precision (relative standard deviations of approximately 10%).
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Biomaterials 6 (1995), S. 213-218 
    ISSN: 1045-4861
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The occlusion and stability of five synthetic plugs used to restrict the femoral canal prior to cemented arthroplasty was assessed. A model was employed consisting of a hollow wooden dowel to simulate the canal, with adapters fixed to both ends to accommodate cement insertion and pressurization, and to produce a closed distal cavity. Three different canal diameters within the range accommodated by the plug selected were employed to assess insertion force, distal pressure during both insertion and pressurization of acrylic cement, and plug migration and leakage for each device. There was a wide variation among plugs in the magnitudes of the force and distal pressure upon plug insertion. During cement pressurization, cement leakage and/or plug migration was noted in all trials, and either of these events resulted in pressure rises in the distal cavity. Most notably, differences of only 0.5 mm in the diameter of the canal resulted in marked changes in the occlusion and stability achieved. It is concluded that for the range of canal sizes anticipated intraoperatively, these synthetic plugs appear deficient to varying extents in their ability to occlude or remain stable in the intramedullary canal. © 1995 John Wiley & Sons, Inc.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 7 (1993), S. 569-575 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: Ionic and neutral products of matrix-assisted laser desorption were simultaneously detected in a time-of-flight mass spectrometer. The neutrals were photoionized with coherent vacuum ultraviolet radiation. Mass spectra were obtained for primary and secondary alkyl amines in various absorbing matrices. Based upon relative signal intensities of directly formed analyte ions and photoionized analyte neutrals, the ratio of neutrals-to-ions ejected was found to be of the order of 10000 or greater with desorption irradiances near the threshold for ion formation. The ratio decreased with increasing irradiance of the desorption laser beam. This dependence is consistent with a collisional mechanism tor analyte-ion formation during the desorption event that is initiated by photoionization of the matrix. Matrices which gave large signal intensities of directly formed analyte ions also gave large signal intensities of photoionized analyte neutrals. Conversely, matrices which gave small signal intensities of directly formed arelyte ions also gave small signal intensities of photoionized analyte neutrals. These results suggest that the efficiency of analyte vaporization by matrix-assisted laser desorption is an intrinsic property of the matrix-analyte pair, independent of the ion-formation process.
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  • 10
    ISSN: 1040-7685
    Keywords: Phase behavior ; supercritical fluid chromatography ; supercritical fluid extraction ; modifier ; propylene carbonate ; critical parameters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The phase behavior (P-T-x) of propylene carbonate was studied using a variable volume view cell for the regions applicable to supercritical fluid chromatography (SFC) and extraction (SFE). Type 5 phase behavior was observed. Phase separation was shown to significantly alter retention and selectivity in the analysis of coal extracts by capillary SFC. Propylene carbonate was found to have limited use as a modifier in capillary SFC. With 5.1 mol% propylene carbonate at 60°C, a single phase is maintained only at pressures above 250 atm.Twenty-two methods used to estimate critical pressure (Pc), twenty-seven methods used to estimate critical temperature (Tc), and thirty methods used to estimate critical volume (Vc) were evaluated for various modifiers employed in supercritical fluid chromatography (SFC). None of the methods could predict Pc, Tc, or Vc to within a 5% relative error for all of the modifiers tested. However, several of the methods were successful in predicting Pc, Tc, or Vc to within 5% for select chemical classes of compounds.Four methods used to estimate the vapor-liquid critical loci of binary mixtures not only failed to accurately predict vapor-liquid separation, but failed to predict the type of phase separation occurring. None of the above methods could reliably estimate the critrical parameters of propylene carbonate or the critical parameters of the mixture.
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