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        <identifier>oai:www.ideals.illinois.edu:2142/19090</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</setSpec>
        <setSpec>col_2142_14797</setSpec>
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        <thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdms11.xsd http://purl.org/dc/elements/1.1/ http://www.ndltd.org/standards/metadata/etdms/1.1/etdmsdc.xsd">
          <dc:contributor>Milner, J.A.</dc:contributor>
          <dc:date>1994</dc:date>
          <dc:creator>Hwang, Kyung Hee</dc:creator>
          <dc:date>2011-05-07T11:56:38Z</dc:date>
          <dc:date>2011-05-07T11:56:38Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:description>Increased cytoplasmic and nuclear selenium retention in CMT-13 cells was correlated with cell growth inhibition caused by selenite supplementation. Greater quantities of cytosolic selenium-containing proteins and a nuclear selenium-containing protein were detected as the quantity of selenium within CMT-13 cells increased. One of the antiproliferation effects of selenite on CMT-13 cells is accompanied by decreased rates of macromolecule synthesis, increased cellular macromolecule contents and increased cell size and multiple nuclei, indicating that enhanced cell fusion occurred. Selenite modulated the S and M phases during the cell cycle. Selenite increased the activity of the 114 KD protein kinase only during the S phase. Selenite treatment during the M phase resulted in a disappearance of a 53 KD kinase and the appearance of a 47 KD kinase. The cellular $\rm\sp{32}P$ incorporation into macromolecules increased when inhibition of cell growth was observed by supplementation of selenite. Selenite generally increased the phosphorylation of nuclear phosphoproteins in the S phase, especially the phosphorylation of a 46 KD protein. Selenite inhibited hyperphosphorylation of the 21, 62 and 108 KD proteins during the M phase. Results of this study suggest that perturbations in protein phosphorylation may explain the ability of selenite to alter cell proliferation.</dc:description>
          <dc:description>Made available in DSpace on 2011-05-07T11:56:38Z (GMT). No. of bitstreams: 2
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  Previous issue date: 1994</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:34:35Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:13:17-05:00
Original Data
Group with Access UIUC Users [automated]
Release Date: none
Reason: ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>ETDs are only available to UIUC Users without author permission</dc:description>
          <dc:description>U of I Only</dc:description>
          <dc:identifier>AAI9503220</dc:identifier>
          <dc:identifier>(UMI)AAI9503220</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/19090</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1994 Hwang, Kyung Hee</dc:rights>
          <dc:subject>Biology, Molecular</dc:subject>
          <dc:subject>Biology, Cell</dc:subject>
          <dc:subject>Agriculture, Animal Culture and Nutrition</dc:subject>
          <dc:title>Effects of selenite on metabolic events during the proliferation of canine mammary tumor cells</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <department>Nutritional Sciences</department>
            <discipline>Nutritional Sciences</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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