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    <creators>
      <item>
        <name>
          <family>Zhvania</family>
          <given>Mzia G</given>
        </name>
        <id>mzia_zhvania@iliauni.edu.ge</id>
      </item>
      <item>
        <name>
          <family>Lordkipanidze</family>
          <given>Tamar</given>
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      </item>
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          <given>Vera</given>
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      </item>
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    <title>The Neuronal Porosome Complex
in Mammalian Brain: A Study Using
Electron Microscopic Study</title>
    <ispublished>pub</ispublished>
    <subjects>
      <item>Neuroscience</item>
      <item>Q</item>
    </subjects>
    <divisions>
      <item>ins10</item>
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    <abstract>Porosomes are the universal secretory machinery in cells where
membrane-bound secretory vesicles dock and transiently fuse
(kiss-and-run) to release intravesicular contents to the outside of
the cell during secretion. Earlier it was shown that in rat neurons
12–17 nm cup-shaped lipoprotein porosomes, possessing a central
plug are present at the presynaptic membrane sometimes with
35–50 nm in diameter docked synaptic vesicles. In the current study,
neuronal porosome structures following hypokinetic stress were
evaluated using electron microscopy. Experiments were carried out
to identify and evaluate the porosome structure at the presynaptic
membrane in the rat and cat brain in control and experimentalanimals and to demonstrate the presence of porosomes in the dog
brain. The results reveal for the </abstract>
    <date>2014</date>
    <date_type>published</date_type>
    <publisher>Pan Stanford Publishing </publisher>
    <place_of_pub>Singapour</place_of_pub>
    <pagerange>39-69</pagerange>
    <refereed>TRUE</refereed>
    <book_title>NanoCellBiology: Multimodal Imaging in Biology and Medicine</book_title>
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      <item>
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          <family>Jena</family>
          <given>Bhanu</given>
        </name>
        <id>bjena@med.wayne.edu</id>
      </item>
      <item>
        <name>
          <family>Taatjes </family>
          <given>Douglas</given>
        </name>
      </item>
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