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Impaired degradation of mutant α-synuclein by chaperone-mediated autophagy

Author
CUERVO, Ana Maria1 ; STEFANIS, Leonidas2 3 ; FREDENBURG, Ross4 ; LANSBURY, Peter T4 ; SULZER, David5
[1] Department of Anatomy and Structural Biology, Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, NY 10461, United States
[2] Neurobiology Laboratory, Foundation of Biomedical Research of the Academy of Athens, Athens 11527, Greece
[3] Department of Neurology and Pathology, Columbia University, New York, NY 10032, United States
[4] Center for Neurologic Diseases, Brigham and Women's Hospital, Department of Neurology, Harvard Medical School, Cambridge, MA 02139, United States
[5] Departments of Psychiatry and Neurology, Columbia University, Department of Neuroscience, New York State Psychiatric Institute, New York, NY 10032, United States
Source

Science (Washington, D.C.). 2004, Vol 305, Num 5688, pp 1292-1295, 4 p

CODEN
SCIEAS
ISSN
0036-8075
Scientific domain
Multidisciplinary
Publisher
American Association for the Advancement of Science, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Autodestruction Chaperon Dégradation Homme Lysosome Mutation Parkinson maladie Pathogénie Autophagie α-Synucléine Encéphale pathologie Extrapyramidal syndrome Maladie dégénérative Système nerveux central pathologie Système nerveux pathologie
Keyword (en)
Self destruction Chaperone Degradation Human Lysosome Mutation Parkinson disease Pathogenesis Synuclein Cerebral disorder Extrapyramidal syndrome Degenerative disease Central nervous system disease Nervous system diseases
Keyword (es)
Autodestrucción Degradación Hombre Lisosoma Mutación Parkinson enfermedad Patogenia Encéfalo patología Extrapiramidal síndrome Enfermedad degenerativa 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
16090329

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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