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        <identifier>oai:www.ideals.illinois.edu:2142/18927</identifier>
        <datestamp>2023-07-10</datestamp>
        <setSpec>col_2142_5131</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>O'Morchoe, Patricia J.</dc:contributor>
          <dc:creator>Doyle, Michael David</dc:creator>
          <dc:date>2011-05-07T11:51:30Z</dc:date>
          <dc:date>2011-05-07T11:51:30Z</dc:date>
          <dc:date>10000-01-01</dc:date>
          <dc:date>1991</dc:date>
          <dc:description>Intracardiac lymphatic vessels of the rat heart left ventricle were studied quantitatively at the ultrastructural level in order to establish baseline morphometric data and also to assess age-related variability in the accepted visible macromolecular transport pathways. Lymphatic vessels were found in both epicardial and myocardial areas. No endocardial lymphatics were found. Both intercellular and transendothelial visible macromolecular transport pathways were examined in 3, 6, 12, 18, and 28 month old animals. No age-related variations were seen in measurements of intercellular transport pathways, represented by dilatations and channels between adjacent endothelial cells. Transendothelial pathways, represented by cytoplasmic vesicles, showed many significant variations in quantitative measurements among the 5 age groups studied. These changes included an increase with aging in the thickness of myocardial lymphatic endothelial cells, increases and decreases in the mean diameters of lymphatic endothelial vesicles, and a decrease between 6 and 12 month animals in the volume density of lymphatic cytoplasmic vesicles. These age-related variations may have a direct relationship to similar variations in macromolecular transport capacity.</dc:description>
          <dc:description>Made available in DSpace on 2011-05-07T11:51:30Z (GMT). No. of bitstreams: 2
license.txt: 4922 bytes, checksum: 910b249b4beec47e7ab768910c8f966f (MD5)
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  Previous issue date: 1991</dc:description>
          <dc:description>Item marked as restricted to the 'UIUC Users [automated]' Group (id=2) by Howard Ding (hding2@illinois.edu) on 2011-05-07T14:33:29Z
Item is restricted indefinitely.</dc:description>
          <dc:description>Restriction data tranferred 2014-07-01T11:12:21-05:00
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>AAI9210786</dc:identifier>
          <dc:identifier>(UMI)AAI9210786</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2142/18927</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:rights>Copyright 1991 Doyle, Michael David</dc:rights>
          <dc:subject>Biology, Anatomy</dc:subject>
          <dc:subject>Biology, Cell</dc:subject>
          <dc:subject>Computer Science</dc:subject>
          <dc:title>The intraorgan lymphatic system of the rat left ventricle in normalcy and aging</dc:title>
          <dc:type>text</dc:type>
          <degree>
            <discipline>Biology</discipline>
            <grantor>University of Illinois at Urbana-Champaign</grantor>
            <level>Dissertation</level>
            <name>Ph.D.</name>
          </degree>
        </thesis>
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