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  • 1995-1999  (4)
  • 1997  (4)
  • 1
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: The side-arm domain of neurofilament heavy-chain (NF-H) is heavily phosphorylated in axons. Much of this phosphate is located within a multiphosphorylation repeat (MPR) domain situated toward the carboxy terminus of the molecule. The MPR domain contains the repeat motif KSP of which there are two broad categories, KSPXX and KSPXK. In mouse NF-H, the KSPXK repeats are situated toward the latter part of the MPR domain. We have expressed in mammalian cells fragments of mouse NF-H side-arm containing all of the MPR domain, the latter part of the MPR domain containing the KSPXK repeats, and the complementary amino-terminal part of the MPR domain, which contains the KSPXX repeats. By cotransfecting these fragments with the neurofilament kinases cyclin-dependent kinase-5 (cdk-5)/p35 and glycogen synthase kinase-3α (GSK-3α), we show that cdk-5 induces cellular phosphorylation of the KSPXK-containing fragment of NF-H. Using the transfected fragments, we also map the epitopes for several commonly utilised NF-H monoclonal antibodies and describe the effects that phosphorylation by cdk-5 and GSK-3α have on their reactivities.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Macmillan Magazines Ltd.
    Nature 389 (1997), S. 328-329 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Proteins are intelligent beings. They have evolved to operate in the metabolic maelstrom of a turbulent cellular environment. Transcription factors must know when to switch genes on or off, and the cellular levels of specific ‘signalling’ molecules — lactose, retinoic acid, ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 989-1006 
    ISSN: 0887-624X
    Keywords: emulsion polymerization ; molecular weight distribution ; styrene ; morphology ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Styrene ab initio emulsion polymerizations were conducted at 70°C in an automated reaction calorimeter. Two polymerizations were performed, one above and the other below the critical micelle concentration (CMC) of the surfactant, thus ensuring differing polymerization kinetics between the two: the system below the CMC gave large particles that were expected to follow pseudobulk kinetics, while that above the CMC gave small particles that were expected to follow zero-one kinetics. The evolutions of the molecular weight distributions (MWDs) were characterized by removing samples periodically during the course of the reactions and analyzing with gel permeation chromatography. Interpretation of the data used average molecular weights, the GPC MWDs, and the number MWDs, as functions of conversion. It was found that all of the number MWDs (plotted as ln (number of polymer chains) vs. molecular weight of polymer chains) were concave-up at low molecular weights and become nearly linear at molecular weights (≥3-4 × 106); this linearity is expected from theory. The slope of the high molecular weight region was consistent with theory for the dominant mode for chain stoppage: termination and transfer for the pseudobulk system and (predominantly) chain transfer to monomer for the zero-one system. The most likely explanation for the concavity of the number MWDs is a heterogeneity of radicals: some surface anchored with sulfate end groups and others (with hydrogen end groups arising from transfer to monomer and/or reentry) being more mobile. Thus, two types of termination are proposed: slow reaction-diffusion for the less mobile surface anchored chains, and rapid short-long (center of mass) termination for the more mobile hydrogen-terminated chains. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 989-1006, 1997
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-9368
    Keywords: renin ; renin angiotensin system ; blood pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Renin is an aspartyl protease that is involved in the conversion of angiotensinogen to angitensin II and hence participates in the regulation of blood pressure. Mice are polymorphic for the number of renin genes with some strains harbouring two renin genes, Ren-1d and Ren-2. To study the role of renin Ren-1d in regulating cardiovascular homeostasis, mice with a disrupted Ren-1d gene were created. Analyses of kidney renin mRNA expression in Ren-1d−/−/Ren-2+/+ mice demonstrated that only Ren-2 transcripts were present. Mean arterial blood pressures of Ren-1d+/+/Ren-2+/+, Ren- 1d+/−/Ren-2+/+ and Ren-1d−/−/Ren-2+/+ mice showed no significant differences. These observations demonstrate that the Ren-1d gene product is not essential for normal blood pressure maintenance under normal physiological conditions
    Type of Medium: Electronic Resource
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