Search Results - "Bury, Aleksandra E"

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  1. 1

    Reduction in PA28αβ activation in HD mouse brain correlates to increased mHTT aggregation in cell models by Geijtenbeek, Karlijne W, Janzen, Jolien, Bury, Aleksandra E, Sanz-Sanz, Alicia, Hoebe, Ron A, Bondulich, Marie K, Bates, Gillian P, Reits, Eric A J, Schipper-Krom, Sabine

    Published in PloS one (01-12-2022)
    “…Huntington's disease is an autosomal dominant heritable disorder caused by an expanded CAG trinucleotide repeat at the N-terminus of the Huntingtin (HTT) gene…”
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    Journal Article
  2. 2

    Development of a Light-Dependent Protein Histidine Kinase by Bury, Aleksandra E, Hellingwerf, Klaas J

    “…Phosphorylation plays a critical role in facilitating signal transduction in prokaryotic and eukaryotic organisms. Our study introduces a tool for…”
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    Journal Article
  3. 3

    Global Proteome and Ubiquitinome Changes in the Soluble and Insoluble Fractions of Q175 Huntington Mice Brains[S] by Sap, Karen A., Guler, Arzu Tugce, Bezstarosti, Karel, Bury, Aleksandra E., Juenemann, Katrin, Demmers, JeroenA.A., Reits, Eric A.

    Published in Molecular & cellular proteomics (01-09-2019)
    “…Label-free quantitative mass spectrometry techniques were applied to discover proteome and ubiquitinome changes in brain tissue of Huntington's disease mouse…”
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    Journal Article
  4. 4

    Insulin-Degrading Enzyme Efficiently Degrades polyQ Peptides but not Expanded polyQ Huntingtin Fragments by Geijtenbeek, Karlijne W, Aranda, Angela Santiago, Sanz, Alicia Sanz, Janzen, Jolien, Bury, Aleksandra E, Kors, Suzan, Al Amery, Nur, Schmitz, Nina C M, Reits, Eric A J, Schipper-Krom, Sabine

    Published in Journal of Huntington's disease (01-01-2024)
    “…Huntington's disease is an inheritable autosomal dominant disorder caused by an expanded CAG trinucleotide repeat within the Huntingtin gene, leading to a…”
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    Journal Article
  5. 5

    Reduction in PA28[alpha][beta] activation in HD mouse brain correlates to increased mHTT aggregation in cell models by Geijtenbeek, Karlijne W, Janzen, Jolien, Bury, Aleksandra E, Sanz-Sanz, Alicia, Hoebe, Ron A, Bondulich, Marie K, Bates, Gillian P, Reits, Eric A. J, Schipper-Krom, Sabine

    Published in PloS one (27-12-2022)
    “…Huntington's disease is an autosomal dominant heritable disorder caused by an expanded CAG trinucleotide repeat at the N-terminus of the Huntingtin (HTT) gene…”
    Get full text
    Journal Article
  6. 6

    Global Proteome and Ubiquitinome Changes in the Soluble and Insoluble Fractions of Q175 Huntington Mice Brains by Sap, Karen A, Guler, Arzu Tugce, Bezstarosti, Karel, Bury, Aleksandra E, Juenemann, Katrin, Demmers, JeroenA A, Reits, Eric A

    Published in Molecular & cellular proteomics (01-09-2019)
    “…Huntington's disease is caused by a polyglutamine repeat expansion in the huntingtin protein which affects the function and folding of the protein, and results…”
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    Journal Article