Molecular dynamic simulation studies of Q212H, V203G and N173K mutations in prion diseases
The Prion protein (PrP) roots from a collection of diseases identified as transmissible spongiform encephalopathies (TSEs), which are caused by conversion of PrP from its normal cellular form (PrPC) to a misfolded, oligomeric isoform (PrPSc). Prion diseases are considered fatal and until now no know...
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| Format: | Thesis |
| Language: | English |
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2014
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| Online Access: | http://eprints.utm.my/id/eprint/48011/25/SaraAmidianFBME2014.pdf |
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