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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 1710-1719 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 46 (1990), S. 998-1001 
    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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  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 49 (1993), S. 402-404 
    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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  • 4
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 46 (1990), S. 33-35 
    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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  • 5
    ISSN: 1432-2048
    Keywords: Actin ; Calmodulin ; Ernodesmis ; Microfilament ; Microtubule ; Tubulin ; Wound healing (alga)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The involvement of calmodulin (CaM) in wound-induced cytoplasmic contractions in E. verticillata was investigated. Indirect immunofluorescence of CaM in intact cells showed a faint, reticulate pattern of fluorescence in the cortical cytoplasm. Diffuse fluorescence was evident deeper within the cytoplasm. In contracted cells, CaM co-localizes with actin in the cortical cytoplasm in extensive, longitudinal bundles of microfilaments (MFs), and in an actin-containing reticulum. No association of CaM with tubulin was ever observed in the cortical cytoplasm at any stage of wound-healing. When contraction rates in wounded cells are measured, a lag period of 2 min is followed by a rapid, steady rate of movement over the subsequent 10 min. The delay in the initiation of longitudinal contraction corresponds to the time necessary for the assembly of the longitudinal MF bundles. Cytoplasmic motility was inhibited in a dose-dependent manner by CaM antagonists. In these inhibited cells, MF bundles did not assemble, or were poorly formed. In the latter case, CaM was always found associated with MFs. These results indicate a direct spatial and temporal correlation between CaM and actin, and a potential role for CaM in regulating the formation of functional MF bundles during wound-induced cytoplasmic contraction in Ernodesmis.
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  • 6
    ISSN: 1432-2048
    Keywords: Actin ; Calmodulin ; Ernodesmis ; Membrane skeleton ; Microfilaments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ultrastructural changes in the cortical cytoskeleton during wound-induced cytoplasmic contraction were examined in the coenocytic green alga Ernodesmis verticillata. Both calmodulin (CaM) and actin were localized in intact and contracting cells by immunogold labeling. Within 5 min after wounding, compact microfilament (MF) bundles were observed which increase in diameter as cytoplasmic contraction proceeds. Calmodulin labeling is associated with amorphous material studding the MF bundles, whereas actin labeling occurs along the individual MFs. No MF bundles were ever observed during contraction that were not also labeled with anti-CaM antibodies. In cells treated with the CaM antagonist W-7 (N-[6-aminohexyl]-5-chloro-1-naphtha-lenesulfonamide), MF bundles do not form, and the formation of loosely arranged MFs (similar to nascent bundles in untreated cells) is greatly retarded. We propose that CaM binds indirectly to actin by activating an actin-binding regulatory protein which functions in early stages of the transduction sequence leading to functional MF bundles. Additionally, ultrastructural evidence is presented for a plasma-membrane skeleton or undercoating in this alga.
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  • 7
    ISSN: 1615-6102
    Keywords: Alga ; Actin ; Calmodulin ; Ernodesmis ; Membrane recycling ; Microfilaments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Changes in the plasma membrane surface and in the cortical cytoplasm during wound healing in giant green algal cells ofErnodesmis verticillata (Kützing) Bφrgesen were followed using scanning and transmission electron microscopy. Microvillus-like structures that contain cytoplasmic and cytoskeletal constituents were observed emanating from the surface of the plasma membrane at the retracting/cut end of wounded cells. These delicate structures seem to be remnants of cell wall-plasmalemma connections that draw out the plasma membrane and cortical components from the contracting cytoplasm as it pulls away from the cell wall. Most of these connections break during wound healing and, when contraction stops, the microvillus-like protrusions become progressively shorter. In cells treated with a calmodulin antagonist (W-7), a number of distinctive bodies accumulate that are of unknown composition, are oblong in shape, and have a diameter slightly smaller than the protoplasmic protrusions. Ultrastructural and other data indicate that these bodies result from retrieved constituents of the plasma-membrane protrusions, as they do not accumulate in unwounded drugtreated cells or in cells treated in W-5. These findings suggest that the protoplasmic protrusions accumulate membrane and cytoplasmic components that are retrieved and recycled during wound healing inErnodesmis by a novel mechanism. The combined plasma membrane surfaces of the microvillus-like protrusions may help to account for the drastic decrease in surface area that occurs during wound healing.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 606 (1991), S. 141-155 
    ISSN: 0044-2313
    Keywords: Neopentylruthenium(II) complexes ; H—C bond cleavage ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: H—C Bond Cleavage in Aldehydes by Neopentylruthenium(II) ComplexesNeopentylruthenium complexes of the type (η5-Cp)(L1)(L2)RuCH2CMe3 (1: Cp = C5Me5, L1 = L2 = PMe3; 3, 9, 10 and 11: Cp = C5H5, L2 = PPh3, L1 = PMe3, PMePh2, PMe2Ph and P(OMe)3, respectively) react with benzaldehyde with H—C bond cleavage of the aldehyde function to give the (η5-Cp)(L1)(L2)Ru benzoyl compounds 4, 13-16 and as the result of subsequent decarbonylation the (carbonyl) phenylruthenium complexes 2, 5, 12, 17-19 or mixtures thereof. Para phthaldialdehyde reacts with 1 (ratio 1 : 2) via the carbonyl complex 20 to give the 1,4-bis(ruthenium)benzene compound 21. Aliphatic aldehydes behave similarly: isobutyraldehyde reacts with 3 to give a mixture of the acyl-(22) and alkyl(carbonyl)ruthenium compound 23. 1 reacts with ferrocenealdehyde to give the carbonyl(ferrocenyl)ruthenium complex 25. The molecular structures of 22 and 2 as representatives of acyl- and (carbonyl)organylruthenium complexes, have been determined by X-ray diffraction.
    Notes: Die Neopentylruthenium-Komplexe vom Typ (η5-Cp)(L1)(L2)RuCH2CMe3 (1: Cp = C5Me5, L1 = L2 = PMe3; 3, 9, 10 und 11: Cp = C5H5, L2 = PPh3, L1 = PMe3, PMePh2, PMe2Ph bzw. P(OMe)3) reagieren mit Benzaldehyd unter H—C-Bindungsspaltung an der Aldehydgruppe und anschließender Decarbonylierung zu den entsprechenden Phenylruthenium-Verbindungen (η5-Cp)(CO)(L1)RuPh 2, 5, 12, 17-19 oder zu Mischungen dieser Komplexe mit den Benzoylruthenium-Verbindungen (η5-Cp)(L1)(L2)RuC(O)Ph 4, 13-16, den Vorstufen der Decarbonylierung. Para-Phthaldialdehyd reagiert mit 1 (Verhältnis 1 : 2) über den Carbonylkomplex 20 zum 1,4-Bis(ruthenium)benzol 21. Aliphatische Aldehyde verhalten sich ähnlich wie aromatische, Isobutyraldehyd bildet mit 3 eine Mischung von Acyl- (22) und Alkyl(carbonyl)ruthenium-Verbindung 23. 1 reagiert mit Ferrocenaldehyd zum Carbonyl(ferrocenyl)ruthenium-Komplex 25. Für 22 und 2 als Vertreter der Acyl- und der (Carbonyl)phenylruthenium-Komplexe wurden die Molekülstrukturen röntgenographisch bestimmt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 32 (1994), S. 1557-1571 
    ISSN: 0887-6266
    Keywords: polyurethanes ; cationomers ; morphology ; thermal properties ; tensile properties ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Diphenylmethane-4,4′-diisocyanate based polyether polyurethane cationomers were synthesized using 3-trialkylammonium-(1,2-propanediol)iodide (TAPI) as the chain extender. The ionic content was varied by substituting up to 100% of 3-dialkylamino-1,2-propanediol (DAP) for TAPI. Cationomers with bromine and chlorine ions were prepared from the iodine-based polymer via ion exchange. The morphology and properties of the cationomers were studied as a function of alkyl group, ion content, and anion type using small-angle x-ray scattering, tensile testing, dynamic mechanical thermal analysis, and differential scanning calorimetry. The bulky side groups of DAP and TAPI prevented crystallization in the hard domains, and consequently little or no phase separation was evident in the unionized materials. Polyurethanes with cationic functionality showed dramatic improvements in phase separation and tensile properties. Results suggest tht while ionic interactions are the primary driving force for phase separation, they produce a morphology not typical of ionomers, but rather akin to that of a conventional polyurethane with semicrystalline hard segments. © 1994 John Wiley & Sons, Inc.
    Additional Material: 14 Ill.
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  • 10
    Publication Date: 2002-04-12
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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