Non-expanded polyglutamine proteins in intranuclear inclusions of hereditary ataxias - triple-labeling immunofluorescence study
- Author
- UCHIHARA, Toshiki1 ; FUJIGASAKI, Hiroto1 2 ; KOYANO, Shigeru1 3 ; NAKAMURA, Ayako1 ; YAGISHITA, Saburo4 ; IWABUCHI, Kiyoshi3
[1] Department of Neuropathology, Tokyo Metropolitan Institute for Neuroscience, 2-6 Musashi-dai, Fuchu, Tokyo, 183-8526, Japan
[2] Department of Neurology, Tokyo Metropolitan Neurological Hospital, 2-6-1, Musashi-dai, Fuchu, Tokyo, 183-8526, Japan
[3] Departments of Neurology and Psychiatry, Kanagawa Rehabilitation Center, Department of Pathology, Kanagawa Rehabilitation Center, 516 Nanasawa, Atsugi, Kanagwa, 243-0121, Japan
[4] Department of Neurology, Yokohama City University, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan - Source
Acta neuropathologica. 2001, Vol 102, Num 2, pp 149-152 ; ref : 20 ref
- Publisher
- Springer, Berlin
- Publication country
- Germany
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aminoacide Atrophie dentatorubropallidoluysienne Distribution Exploration Glutamine Homme Immunohistochimie Inclusion cellulaire Noyau cellulaire Polymère Protubérance annulaire Ataxie spinocérébelleuse Polyglutamine Anatomopathologie Cervelet pathologie Encéphale pathologie Maladie dégénérative Maladie héréditaire Moelle épinière pathologie Système nerveux central pathologie Système nerveux pathologie
- Keyword (en)
- Aminoacid Dentatorubropallidoluysian atrophy Distribution Exploration Glutamine Human Immunohistochemistry Cell inclusion Cell nucleus Polymer Pons varolii Spinocerebellar ataxia Pathology Cerebellar disease Cerebral disorder Degenerative disease Genetic disease Spinal cord disease Central nervous system disease Nervous system diseases
- Keyword (es)
- Aminoácido Atrofia dentatorubropallidoluysiana Distribución Exploración Glutamina Hombre Inmunohistoquímica Inclusión celular Núcleo celular Polímero Protuberancia anular Anatomía patológica Cerebelar enfermedad Encéfalo patología Enfermedad degenerativa Enfermedad hereditaria Médula espinal patología Sistema nervosio central patología Sistema nervioso patología
- Classification
- 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
- 1114198
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
10.1007/s004010100364 
https://dx.doi.org/10.1007/s004010100364
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