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  • Book
    Joseph D. Fontes, Darla L. McCarthy.
    Contents:
    Chemical foundations : acid-base chemistry, buffers, and bioenergetics
    Chemistry of carbohydrates, lipids, proteins, and nucleotides
    Biochemical reactions and catalysis
    Protein structure and function
    The TCA cycle and oxidative phosphorylation
    Carbohydrate digestion and metabolism
    Fatty acid metabolism and lipid digestion
    Cholesterol and steroid metabolism
    Protein, amino acid, and one carbon metabolism
    Nucleotide, heme, and iron metabolism
    nutrition and integrated metabolism
    Cellular signaling and posttranslational modifications
    DNA replication and cell cycle
    DNA mutation and repair
    Gene transcription and RNA processing
    Protein translation
    Cell stress and death
    Biochemical and molecular techniques.
    Digital Access Thieme MedOne Education 2019
  • Book
    edited by Ellwyn R. Stoddard, Richard L. Nostrand, and Jonathan P. West.
    Print c1983
  • Article
    Hart DA.
    Infect Immun. 1978 Feb;19(2):457-61.
    ZnCl2 over a very narrow concentration range was found to be mitogenic for hamster lymph node cells but not for thymocytes or splenocytes. Maximal leucine, [3H]uridine, and [3H]thymidine incorporation. Addition of 10 micron ZnCl2 was found to greatly enhance the stimulation observed with the B-lymphocyte mitogen lipopolysaccharide but not with dextran sulfate or the T-lymphocyte mitogen lipopolysaccharide but not with dextran sulfate or the T-lymphocyte mitogen concanavalin A. Although not mitogenic for splenocytes, 10 to 25 micron ZnCl2 slightly enhanced lipopolysaccharide stimulation but not concanavalin A or dextran sulfate stimulation. The effect of ZnCl2 on lipopolysaccharide stimulation was also confirmed with outbred Hartley guinea pig splenocytes and lymph node cells. Zinc chloride (50 micron) was mitogenic for both of these tissues; the response to lipopolysaccharide was enhanced by addition of 50 micron ZnCl2, but the concanavalin A response was unaffected. The possibility that the zinc effect is mediated by proteolytic mechanisms is discussed.
    Digital Access Access Options