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Helene Bustad Johannessens bilde

Helene Bustad Johannessen

Postdoktor
  • E-postHelene.Bustad.Johannessen@uib.no
  • Telefon+47 913 15 936
  • Besøksadresse
    Institutt for Biomedisin
    Jonas Lies vei 91
    5009 Bergen
    Rom 
    5A113B
  • Postadresse
    Postboks 7804
    5020 Bergen
  1. Myrum, C. et al., Arc is a flexible modular protein capable of reversible self-oligomerization. Biochem J. 2015; 468(1) p.145-158
  2. Bustad, HJ. et al., Conformational stability and activity analysis of two hydroxymethylbilane synthase mutants, K132N and V215E, with different phenotypic association with acute intermittent porphyria. Biosci. Rep. 2013;33(4):e00056
  3. Bustad, HJ, Skjaerven, L. et al., The Peripheral Binding of 14-3-3γ to Membranes Involves Isoform-Specific Histidine Residues. PLoS One. 2012;7(11):e49671
  4. Bustad, HJ. et al., The binding of 14-3-3γ to membranes studied by intrinsic fluorescence spectroscopy. FEBS Lett, 2011. 585(8): p. 1163-1168.
  5. Steinkopf, S. et al., pH-dependent interaction of psychotropic drug with glycerophospholipid monolayers studied by the Langmuir technique. Biophys Chem, 2010. 152(1-3): p. 65-73.
  • 2019. A Pharmacological Chaperone Therapy for Acute Intermittent Porphyria. Molecular Therapy.
  • 2017. In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins. Bioscience Reports. 1-12.
  • 2017. Det er hardt å være forskar! Bioingeniøren. 28-29.
  • 2016. Characterization of Hydroxymethylbilane Synthase and Pharmacological Chaperone Treatment for Acute Intermittent Porphyria.
  • 2015. Arc is a flexible modular protein capable of reversible self-oligomerization. Biochemical Journal. 145-158.
  • 2013. Searching for pharmacological chaperones aiding to stabilize hydroxymethylbilane synthase. The FEBS Journal. 298-298.
  • 2013. Conformational stability and activity analysis of two hydroxymethylbilane synthase mutants, K132N and V215E, with different phenotypic association with acute intermittent porphyria. Bioscience Reports. 617-U203.
  • 2012. The peripheral binding of 14-3-3gamma to membranes involves isoform-specific histidine residues. PLOS ONE.
  • 2011. The binding of 14-3-3 gamma to membranes studied by intrinsic fluorescence spectroscopy. FEBS Letters. 1163-1168.
  • 2010. CHARACTERIZATION OF THE MOLECULAR BASIS OF ACUTE INTERMITTENT PORPHYRIA. Journal of Inherited Metabolic Disease. S177-S177.

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