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    <subfield code="a">pmid:32814083</subfield>
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    <subfield code="a">10.1016/j.mad.2020.111327</subfield>
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    <subfield code="a">0047-6374</subfield>
    <subfield code="2">ISSN</subfield>
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    <subfield code="a">1872-6216</subfield>
    <subfield code="2">ISSN</subfield>
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  <datafield tag="037" ind1=" " ind2=" ">
    <subfield code="a">DZNE-2021-00048</subfield>
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    <subfield code="a">English</subfield>
  </datafield>
  <datafield tag="082" ind1=" " ind2=" ">
    <subfield code="a">610</subfield>
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    <subfield code="a">Lountzi, Dimitra</subfield>
    <subfield code="0">P:(DE-2719)2812559</subfield>
    <subfield code="b">0</subfield>
    <subfield code="e">First author</subfield>
    <subfield code="u">dzne</subfield>
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    <subfield code="a">Effects of heterochronic, non-myeloablative bone marrow transplantation on age-related behavioural changes in mice</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="a">Amsterdam [u.a.]</subfield>
    <subfield code="c">2020</subfield>
    <subfield code="b">Elsevier Science</subfield>
  </datafield>
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    <subfield code="a">article</subfield>
    <subfield code="2">DRIVER</subfield>
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    <subfield code="a">Output Types/Journal article</subfield>
    <subfield code="2">DataCite</subfield>
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    <subfield code="a">Journal Article</subfield>
    <subfield code="b">journal</subfield>
    <subfield code="m">journal</subfield>
    <subfield code="0">PUB:(DE-HGF)16</subfield>
    <subfield code="s">1708343226_1852</subfield>
    <subfield code="2">PUB:(DE-HGF)</subfield>
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    <subfield code="a">Journal Article</subfield>
    <subfield code="0">0</subfield>
    <subfield code="2">EndNote</subfield>
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    <subfield code="a">Experiments using heterochronic parabionts, i.e. young and old animals connected surgically and hence developing a shared circulation, have shown that blood-borne factors, transferred from young to old mice and vice versa, play a role in influencing a range of health outcomes associated with advanced age. Previous work has explored the contributory role of plasma-derived factors in mediating such parabiotic effects, including those on aging-associated neural and behavioural impairments. Here, we wanted to identify possible influences that blood-borne cellular factors may have on age-related behavioural phenotypes. Towards this end, we subjected old BALB/c H-2d mice to repetitive non-myeloablative bone marrow transplants (BMT) from young donor animals and assessed effects on behaviour and cognition. We detected expected age-related alterations in our behavioural assays but did not discern any obvious differences between old BMT mice and old control animals. Our study represents the first to look at possible behavioural and cognitive effects of heterochronic, non-myeloablative BMT. Future work should extend this study by including additional behavioural tests in the analysis, addressing whether beneficial effects of BMT may be detectable on other genetic backgrounds and reconciling our findings with those achieved by myeloablative BMT.</subfield>
  </datafield>
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    <subfield code="a">341 - Molecular Signaling (POF3-341)</subfield>
    <subfield code="0">G:(DE-HGF)POF3-341</subfield>
    <subfield code="c">POF3-341</subfield>
    <subfield code="f">POF III</subfield>
    <subfield code="x">0</subfield>
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    <subfield code="a">342 - Disease Mechanisms and Model Systems (POF3-342)</subfield>
    <subfield code="0">G:(DE-HGF)POF3-342</subfield>
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    <subfield code="a">Dataset connected to CrossRef</subfield>
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  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Aging</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Allografts</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Animals</subfield>
    <subfield code="2">MeSH</subfield>
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    <subfield code="a">Behavior, Animal</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Bone Marrow Transplantation</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Mice</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2="2">
    <subfield code="a">Mice, Inbred BALB C</subfield>
    <subfield code="2">MeSH</subfield>
  </datafield>
  <datafield tag="700" ind1="1" ind2=" ">
    <subfield code="a">Henzel, Kristin</subfield>
    <subfield code="0">P:(DE-2719)2810479</subfield>
    <subfield code="b">1</subfield>
    <subfield code="u">dzne</subfield>
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    <subfield code="a">Jazbec, Katerina</subfield>
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    <subfield code="a">Bano, Daniele</subfield>
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    <subfield code="b">3</subfield>
    <subfield code="u">dzne</subfield>
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    <subfield code="a">Krauss, Sybille</subfield>
    <subfield code="0">P:(DE-2719)2421562</subfield>
    <subfield code="b">4</subfield>
    <subfield code="u">dzne</subfield>
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    <subfield code="a">Rožman, Primož</subfield>
    <subfield code="b">5</subfield>
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  <datafield tag="700" ind1="1" ind2=" ">
    <subfield code="a">Ehninger, Dan</subfield>
    <subfield code="0">P:(DE-2719)2289209</subfield>
    <subfield code="b">6</subfield>
    <subfield code="e">Last author</subfield>
    <subfield code="u">dzne</subfield>
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    <subfield code="a">10.1016/j.mad.2020.111327</subfield>
    <subfield code="g">Vol. 191, p. 111327 -</subfield>
    <subfield code="0">PERI:(DE-600)1502520-2</subfield>
    <subfield code="p">111327</subfield>
    <subfield code="t">Mechanisms of ageing and development</subfield>
    <subfield code="v">191</subfield>
    <subfield code="y">2020</subfield>
    <subfield code="x">0047-6374</subfield>
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    <subfield code="a">Deutsches Zentrum für Neurodegenerative Erkrankungen</subfield>
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