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α-Synuclein promotes clathrin-mediated NMDA receptor endocytosis and attenuates NMDA-induced dopaminergic cell death

Author
FURONG CHENG1 ; XIN LI1 ; YAOHUA LI1 ; CHAODONG WANG1 ; TAO WANG1 ; GUANGWEI LIU1 ; BASKYS, Andrius2 ; UEDA, Kenji1 3 ; CHAN, Piu1 ; SHUN YU1
[1] Department of Neurobiology and the Sino-Japan Joint Laboratory on Neurodegenerative Diseases, Key Laboratory of Neurodegenerative Diseases (Capital Medical University), Ministry of Education, Xuanwu Hospital of China Capital Medical University, Beijing, China
[2] UCLA-Kern Psychiatry Residency Program, Kern Medical Center & Kern County Mental Health, David Geffen School of Medicine at UCLA, Bakersfield, California, United States
[3] Division of Psychobiology, Tokyo Institute of Psychiatry, Tokyo, Japan
Source

Journal of neurochemistry. 2011, Vol 119, Num 3-4, pp 815-825, 11 p ; ref : 1 p.1/4

CODEN
JONRA9
ISSN
0022-3042
Scientific domain
Cell biology, histology; Neurology; Physiology, morphology
Publisher
Wiley-Blackwell, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Author keyword
NMDA RAB5B cytotoxicity endocytosis α-synuclein
Keyword (fr)
Altération Calcium Choc Clathrine Cytoplasme Endocytose Gène Homme Intracellulaire Maladie de Parkinson Mort cellulaire Pathogénie Protéine Récepteur NMDA Suppression Sousunité NR1 Maladie dégénérative Pathologie de l'encéphale Pathologie du système nerveux central Pathologie du système nerveux Récepteur glutamate Syndrome extrapyramidal
Keyword (en)
Alteration Calcium Shock Clathrin Cytoplasm Endocytosis Gene Human Intracellular Parkinson disease Cell death Pathogenesis Protein NMDA receptor Suppression Degenerative disease Cerebral disorder Central nervous system disease Nervous system diseases Glutamate receptor Extrapyramidal syndrome
Keyword (es)
Alteración Calcio Choque Clatrina Citoplasma Endocitosis Gen Hombre Intracelular Parkinson enfermedad Muerte celular Patogenia Proteína Receptor NMDA Supresión Enfermedad degenerativa Encéfalo patología Sistema nervosio central patología Sistema nervioso patología Receptor glutámato Extrapiramidal síndrome
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
24740824

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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