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<xml>
<records>
<record>
  <contributors>
    <authors>
      <author>Nilaver, Benjamin</author>
      <author>Thomas, Jeremy</author>
      <author>Appleman, Maria-Luisa</author>
      <author>Kohama, Steven G.</author>
      <author>Urbanski, Henryk F.</author>
    </authors>
  </contributors>
  <titles>
    <title>Macaques exhibit TDP-43 morphology comparable to human aging and dementia</title>
    <translated-title/>
    <tertiary-title/>
  </titles>
  <periodical>
    <full-title/>
  </periodical>
  <alt-periodical>
    <full-title/>
    <abbr-1/>
  </alt-periodical>
  <pages/>
  <section/>
  <volume/>
  <number/>
  <keywords>
    <keyword>Immunohistochemistry</keyword>
    <keyword>Histology</keyword>
    <keyword>Dementia</keyword>
    <keyword>Aging</keyword>
    <keyword>Neuropathology</keyword>
    <keyword>Macaca mulatta</keyword>
    <keyword>Models, Animal</keyword>
    <keyword>TDP-43 Proteinopathies</keyword>
  </keywords>
  <dates>
    <year>2022</year>
    <pub-dates>
      <date>2022-04-14</date>
    </pub-dates>
  </dates>
  <abstract>Transactive response DNA binding protein of 43 kDa (TDP-43) is a ubiquitously expressed nuclear protein involved in RNA metabolism and stress granule formation. Pathological inclusions and mislocalization of this protein in brain cells is pathognomonic or concurrent across a wide range of neurodegenerative diseases, and has been implicated in age-associated cognitive decline. In these pathologies, TDP-43 becomes mislocalized, forming inclusions in the cytoplasm, nucleus, and cell processes. In these inclusions, TDP-43 undergoes aberrant post-translational modifications, often phosphorylation. This investigation assessed the presence of TDP-43 pathology and mislocalization in the amygdala, entorhinal cortex, and prefrontal cortex of aged rhesus macaques. Endogenous TDP-43 pathology in the macaque brain has not been well described. We hypothesized that the macaque exhibits histological TDP-43 phenotypes resembling those found in human neurodegeneration and cognitive decline.</abstract>
  <pub-location/>
  <publisher>Oregon Health and Science University</publisher>
  <issn/>
  <isbn/>
  <custom3/>
  <custom7/>
  <notes/>
  <work-type>Abstract</work-type>
  <electronic-resource-num>10.6083/hm50ts51n</electronic-resource-num>
  <urls>
    <related-urls>
      <url>https://digitalcollections.ohsu.edu/record/9620/files/Nilaver-Benjamin-ResearchWeek2022.pdf</url>
    </related-urls>
  </urls>
  <language/>
</record>

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