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    <title>Schrier, M.</title>
    <link>http://repub.eur.nl/res/aut/2868/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome (Article)</title>
      <link>http://repub.eur.nl/res/pub/10126/</link>
      <pubDate>2003-01-01T00:00:00Z</pubDate>
      <description>Recent studies have reported that alleles in the premutation range in the
      FMR1 gene in males result in increased FMR1 mRNA levels and at the same
      time mildly reduced FMR1 protein levels. Some elderly males with
      premutations exhibit an unique neurodegenerative syndrome characterized by
      progressive intention tremor and ataxia. We describe neurohistological,
      biochemical and molecular studies of the brains of mice with an expanded
      CGG repeat and report elevated Fmr1 mRNA levels and intranuclear
      inclusions with ubiquitin, Hsp40 and the 20S catalytic core complex of the
      proteasome as constituents. An increase was observed of both the number
      and the size of the inclusions during the course of life, which correlates
      with the progressive character of the cerebellar tremor/ataxia syndrome in
      humans. The observations in expanded-repeat mice support a direct role of
      the Fmr1 gene, by either CGG expansion per se or by mRNA level, in the
      formation of the inclusions and suggest a correlation between the presence
      of intranuclear inclusions in distinct regions of the brain and the
      clinical features in symptomatic premutation carriers. This mouse model
      will facilitate the possibilities to perform studies at the molecular
      level from onset of symptoms until the final stage of the disease.</description>
    </item> <item>
      <title>Transport of fragile X mental retardation protein via granules in neurites of PC12 cells (Article)</title>
      <link>http://repub.eur.nl/res/pub/10010/</link>
      <pubDate>2002-12-01T00:00:00Z</pubDate>
      <description>Lack of fragile X mental retardation protein (FMRP) causes fragile X
      syndrome, a common form of inherited mental retardation. FMRP is an RNA
      binding protein thought to be involved in translation efficiency and/or
      trafficking of certain mRNAs. Recently, a subset of mRNAs to which FMRP
      binds with high affinity has been identified. These FMRP-associated mRNAs
      contain an intramolecular G-quartet structure. In neurons, dendritic mRNAs
      are involved in local synthesis of proteins in response to synaptic
      activity, and this represents a mechanism for synaptic plasticity. To
      determine the role of FMRP in dendritic mRNA transport, we have generated
      a stably FMR1-enhanced green fluorescent protein (EGFP)-transfected PC12
      cell line with an inducible expression system (Tet-On) for regulated
      expression of the FMRP-GFP fusion protein. After doxycycline induction,
      FMRP-GFP was localized in granules in the neurites of PC12 cells. By using
      time-lapse microscopy, the trafficking of FMRP-GFP granules into the
      neurites of living PC12 cells was demonstrated. Motile FMRP-GFP granules
      displayed two types of movements: oscillatory (bidirectional) and
      unidirectional anterograde. The average velocity of the granules was 0.19
      micro m/s with a maximum speed of 0.71 micro m/s. In addition, we showed
      that the movement of FMRP-GFP labeled granules into the neurites was
      microtubule dependent. Colocalization studies further showed that the
      FMRP-GFP labeled granules also contained RNA, ribosomal subunits, kinesin
      heavy chain, and FXR1P molecules. This report is the first example of
      trafficking of RNA-containing granules with FMRP as a core constituent in
      living PC12 cells.</description>
    </item>
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