Search for dissertations about: "HYDROPHOBIC MOLECULES"
Showing result 1 - 5 of 164 swedish dissertations containing the words HYDROPHOBIC MOLECULES.
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1. Hydrophobic interactions of serpins
Abstract : The proteins of the serpin family are primarily but not exclusively proteinase inhibitors, which share a common, similar structure. It is known that this structure undergoes major conformational changes upon cleavage in the serpin reactive site loop, and that these changes include rearrangements within the hydrophobic core of the molecule. READ MORE
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2. Molecular-dynamics simulations of polymeric surfaces for biomolecular applications
Abstract : In-vitro diagnostics plays a very important role in the present healthcare system. It consists of a large variety of medical devices designed to diagnose a medical condition by measuring a target molecule in a sample, such as blood or urine. READ MORE
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3. Amphiphilic Molecules in Aqueous Solution
Abstract : The aim of this thesis was to investigate amphiphilic molecules in aqueous solution. The work was divided into two parts. In the first part the effects of different counterions on phase behavior was investigated, while the second part concerns the 1-monooleoyl-rac-glycerol (MO)/n-octyl-β-D-glucoside (OG)/2H2O-system. READ MORE
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4. Targeting HER2-expressing tumors with potent drug conjugates and fusion toxins based on scaffold proteins
Abstract : Targeted therapy is an emerging treatment for a variety of cancers. Small- sized scaffold proteins are an alternative to conventional antibody-based targeting molecules. READ MORE
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5. Engineering of Affibody molecules for Radionuclide Molecular Imaging and Intracellular Targeting
Abstract : Affibody molecules are small (7 kDa) affinity proteins of non-immunoglobulin origin that have been generated to specifically interact with a large number of clinically important molecular targets.In this thesis, Affibody molecules have been employed as tracers for radionuclide molecular imaging of HER2- and IGF-1R-expressing tumors, paper I-IV, and for surface knock-down of EGFR, paper V. READ MORE