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  • American Physical Society (APS)  (57)
  • Wiley-Blackwell  (29)
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  • 1
    ISSN: 0886-1544
    Keywords: stress fibers ; fibroblasts ; myosin ; bipolar filaments ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The authors examined the molecular organization of myosin in stress fibers (microfilament bundles) of cultured mouse embryo fibroblasts. To visualize the organization of myosin filaments in these cells, fibroblast cytoskeletons were treated with gelsolin-like protein from bovine brain (hereafter called brain gelsolin), which selectively disrupts actin filaments. As shown earlier [Verkhovsky et al., 1987], this treatment did not remove myosin from the stress fibers. The actin-free cytoskeletons then were lightly sonicated to loosen the packing of the remaining stress fiber components and fixed with glutaraldehyde.Electron microscopy of platinum replicas of these preparations revealed dumbbell-shaped structures of approximately 0.28 μm in length, which were identified as bipolar myosin filaments by using antibodies to fragments of myosin molecule (subfragment I and light meromyosin) and colloidal gold label. Bipolar filaments of myosin in actin-free cytoskeletons were often organized in chains and lattices formed by end-to-end contacts of individual filaments at their head-containing regions. Therefore, after extraction of actin, it was possible for the first time to display bipolar myosin filaments in the stress fibers of cultured cells.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 6 (1993), S. 471-477 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 2-(2-Thienyl)pyrrole and its 3-alkyl-1-vinyl derivatives have been shown (1H NMR) to be protonated by HSO3F, CF3COOH, HCl and HBr at the pyrrole C-5 atom. Reaction with the superacid system HSO3F—SbF5-SO2 results in the equilibrium between pyrrolium and thiophenium ions. The heats of formation (ΔH), charges and HOMO partial electron densities for 2-(2-thienyl)pyrrole and its protonated forms have been calculated by the MNDO method. The calculated ΔH values of thienylpyrrolium and pyrrolythiophenium ions are in agreement with the experimentally observed ratio.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 6 (1983), S. 209-210 
    ISSN: 0935-6304
    Keywords: Liquid Chromatography, HPLC ; Reverse phase mode ; Ion pairing ; Nucleotides ; Fish ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
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  • 4
    ISSN: 1058-8388
    Keywords: Lhx3 ; LIM ; Homeodomain ; Pituitary ; CNS ; Development ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Murine Lhx3 cDNA isolated from the mouse pituitary cDNA library encodes a LIM-type homeodomain protein that contains two tandemly repeated LIM domains and the homeodomain. The identities of predicted amino acid sequences between the mouse Lhx3 and Xenopus Xlim-3 genes are 80, 95, and 97% in the LIM domains 1 and 2, and the homeodomain, respectively, and 84% in the entire protein. 5′-RACE procedures and genomic cloning revealed that two distinct N-terminal sequences arise from two different exons 1a and 1b. Exon 1a encodes a sequence similar to that of Xlim-3, whereas exon 1b encodes a different N-terminus. It is likely that there are two transcription initiation sites in the Lhx3 gene. The Lhx3 transcripts were detected by whole mount in situ hybridization as early as day E9.5 post coitum in Rathke's pouch and the closing neural tube. During subsequent development, Lhx3 expression was observed in the anterior and intermediate but not in the posterior lobes of the pituitary, and in the ventral hindbrain and spinal cord. Northern blot analysis of adult tissues showed that Lhx3 mRNA persists in the pituitary. The expression pattern of Lhx3 is well conserved between Xenopus and mouse, underscoring the functional importance of this gene as a regulator of development. A number of established cell lines of pituitary origin express Lhx3 and therefore constitute a useful tool for further study of Lhx3 gene function. © 1995 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 24 (1982), S. 237-240 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 3 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 951-955 
    ISSN: 1434-1948
    Keywords: Ab initio calculations ; Phosphorus ; Strained molecules ; Substituent effects ; Pericyclic reactions ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: According to quantum chemical calculations at an ab initio level parent 1,2-diphosphete is slightly more stable than its corresponding 1,4-diphosphabutadiene structural isomer. The quantum chemical calculations indicate that substituents at phosphorus and to a much less extent at carbon exert strong influences on the equilibrium geometries of 1,2-diphosphete structures: π donors at phosphorus strongly elongate the P-P bond while electronegative substituents at phosphorus increase the interflap angle of the four-membered ring systems, bringing an envelope conformation to the fore. The lengthening of the P-P bond gives rise to a Möbius-type delocalization within the ring moiety.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 16 (1982), S. 31-38 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The biocompatibility and high gas transfer characteristics of gas-permeable membranes have led to their use for total and supportive cardiopulmonary bypass. The gas transfer rates, particularly of oxygen, have previously been measured with sophisticated apparatus and this has restricted accurate measurements to a few laboratories. A simple chemical technique for measuring the oxygen permeability of synthetic membranes is described, in which sodium hydrosulfite is used to provide the highest possible oxygen gradient and the volume of oxygen crossing the membrane is measured volumetrically. Results agreed with those obtained with orthodox apparatus and replacement of the reducing agent with blood gave much lower oxygen transfer rates demonstrating the rheological influences of the blood upon oxygen transfer.
    Additional Material: 5 Ill.
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Interpolymer reactions between poly(acrylic acid) (PAA) or poly(methacrylic acid) (PMAA) and poly(N-tert-butylaziridine) (PTBA) were studied and compared with the corresponding reactions of these polyacids with linear polyethyleneimine (LPEI). In aqueous alkaline and salt media the presence of the bulky non-polar N-substituent in the main chain of PTBA results in a decrease of stability of polyacid-PTBA polyelectrolyte complexes. LPEI, which forms stronger salt bonds with PAA, substitutes PTBA in the PAA-PTBA polyelectrolyte complexes. Addition of simple salts to aqueous solutions of non-stoichiometric polyelectrolyte complexes (N-PEC) PAA-PTBA and PMAA-PTBA at room temperature causes a phase separation due to macromolecular exchange and disproportionation reactions. At elevated temperatures (T = 40 - 60 °C), however, the macromolecular exchange between different N-PEC particles does not occur and phase separation in aqueous salt solution of the N-PEC's PAA-PTBA, PMAA-PTBA is not observed. This is attributed to hydrophobic interactions in polyacid-PTBA complexes due to the presence of the tert-butyl groups in the latter.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2211-2216 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The interaction between oppositely charged linear and crosslinked polyelectrolytes and the molecular mechanism of the transport of linear polyelectrolytes into oppositely charged gels were studied. The mechanism represents a “relay-race” transfer of polyion segments from one fragment of the polyelectrolyte network to the other via interpolyelectrolyte exchange reaction. Thus, the whole layer of the formed interpolyelectrolyte complex serves as an active zone. The driving force for the transport is produced by interpolyelectrolyte addition reaction on the solution/gel interface.
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 199 (1998), S. 1057-1062 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The competitive binding of fluorescence-tagged poly(methacrylate) polyanions and poly(phosphate) polyanions with different poly(N-alkyl-4-vinylpyridinium) polycation quenchers (alkyl = methyl, ethyl and propyl) was studied in the region 278÷333 K by fluorescence quenching technique. The equilibrium of this interpolyelectrolyte substitution reaction proved to be temperature sensitive except in the case when the poly(N-methyl-4-vinylpyridinium) polycation was used. Thermodynamic parameters of the reaction were determined. The possibility of effective temperature control of the interpolyelectrolyte reaction might be important for understanding, prediction and utilization of transformation processes of complex particles formed by electrostatically complementary (biological) macromolecules.
    Additional Material: 9 Ill.
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