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Structural Features and Domain Organization of Huntingtin Fibrils

Misfolding and aggregation of huntingtin is one of the hallmarks of Huntington disease, but the overall structure of these aggregates and the mechanisms by which huntingtin misfolds remain poorly understood. Here we used site-directed spin labeling and electron paramagnetic resonance (EPR) spectrosc...

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Détails bibliographiques
Auteurs principaux: Bugg, Charles W., Isas, J. Mario, Fischer, Torsten, Patterson, Paul H., Langen, Ralf
Format: Artigo
Langue:Inglês
Publié: American Society for Biochemistry and Molecular Biology 2012
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3442508/
https://ncbi.nlm.nih.gov/pubmed/22801429
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M112.353839
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