Caspase activities and tumor necrosis factor receptor R1 (p55) level are elevated in the substantia nigra from Parkinsonian brain
- Author
- MOGI, M1 ; TOGARI, A1 ; KONDO, T2 ; MIZUNO, Y2 ; KOMURE, O3 ; KUNO, S3 ; ICHINOSE, H4 ; NAGATSU, T4
[1] Department of Pharmacology, School of Dentistry, Aichi-Gakuin University, Nagoya, Japan
[2] Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan
[3] Department of Neurology and Clinical Research Center, Utano National Hospital, Kyoto, Japan
[4] Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan - Source
Journal of neural transmission. 2000, Vol 107, Num 3, pp 335-341 ; ref : 1 p.1/4
- CODEN
- JNTMAH
- ISSN
- 0300-9564
- Scientific domain
- Neurology; Physiology, morphology
- Publisher
- Springer, New York, NY
/
Springer, Wien
- Publication country
- Austria
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité enzymatique Cysteine endopeptidases Facteur nécrose tumorale Homme Locus niger Parkinson maladie Récepteur biologique Caspase Encéphale pathologie Encéphale Enzyme Extrapyramidal syndrome Hydrolases Maladie dégénérative Peptidases Système nerveux central pathologie Système nerveux central Système nerveux pathologie
- Keyword (en)
- Enzymatic activity Cysteine endopeptidases Tumor necrosis factor Human Locus niger Parkinson disease Biological receptor Cerebral disorder Brain (vertebrata) Enzyme Extrapyramidal syndrome Hydrolases Degenerative disease Peptidases Central nervous system disease Central nervous system Nervous system diseases
- Keyword (es)
- Actividad enzimática Cysteine endopeptidases Factor necrosis tumoral Hombre Locus níger Parkinson enfermedad Receptor biológico Encéfalo patología Encéfalo Enzima Extrapiramidal síndrome Hydrolases Enfermedad degenerativa Peptidases Sistema nervosio central patología Sistema nervioso central 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
- 1312421
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/s007020050028 
https://dx.doi.org/10.1007/s007020050028
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