Interaction of huntingtin fragments with brain membranes : clues to early dysfunction in Huntington's disease
- Author
- SUOPANKI, Jaana1 ; GOTZ, Claudia2 ; LUTSCH, Gudrun1 ; SCHILLER, Jürgen3 ; HARJES, Phoebe1 ; HERRMANN, Andreas2 ; WANKER, Erich E1
[1] Max Delbrück Center for Molecular Medicine, Berlin, Germany
[2] Institute of Biology/Biophysics, Humboldt University, Berlin, Germany
[3] Institute of Medical Physics and Biophysics, Medical Department, University of Leipzig, Leipzig, Germany - Source
Journal of neurochemistry. 2006, Vol 96, Num 3, pp 870-884, 15 p ; ref : 1 p.3/4
- CODEN
- JONRA9
- ISSN
- 0022-3042
- Scientific domain
- Cell biology, histology; Neurology; Physiology, morphology
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- huntingtin oligomers pathogenesis. fibrillogenesis postsynaptic membranes
- Keyword (fr)
- Age Chorée Huntington Exocytose Interaction Membrane synaptique Phospholipide Postsynaptique Protéine membranaire Récepteur AMPA Récepteur NMDA Souris Sousunité Transport membranaire Trouble fonctionnel Encéphale pathologie Extrapyramidal syndrome Maladie dégénérative Maladie héréditaire Mammalia Rodentia Récepteur glutamate Système nerveux central pathologie Système nerveux central Système nerveux pathologie Vertebrata
- Keyword (en)
- Age Huntington disease Exocytosis Interaction Synaptic membrane Phospholipid Postsynaptic Membrane protein AMPA receptor NMDA receptor Mouse Subunit Membrane transport Dysfunction Cerebral disorder Extrapyramidal syndrome Degenerative disease Genetic disease Mammalia Rodentia Glutamate receptor Central nervous system disease Central nervous system Nervous system diseases Vertebrata
- Keyword (es)
- Edad Corea Huntington Exocitosis Interacción Membrana sináptica Fosfolípido Postsináptico Proteína membranar Receptor AMPA Receptor NMDA Ratón Subunitad Transporte membranal Trastorno funcional Encéfalo patología Extrapiramidal síndrome Enfermedad degenerativa Enfermedad hereditaria Mammalia Rodentia Receptor glutámato Sistema nervosio central patología Sistema nervioso central Sistema nervioso patología Vertebrata
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A01 Nervous system as a whole
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17477394
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1111/j.1471-4159.2005.03620.x 
https://dx.doi.org/10.1111/j.1471-4159.2005.03620.x
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