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The glial glutamate transporter, GLT-1, is oxidatively modified by 4-hydroxy-2-nonenal in the Alzheimer's disease brain : the role of Aβ1-42

Author
LAUDERBACK, Christopher M1 2 ; HACKETT, Janna M1 ; HUANG, Feng F3 ; KELLER, Jeffrey N3 4 ; SZWEDA, Luke I5 ; MARKESBERY, William R4 6 ; BUTTERFIELD, D. Allan1 2 4
[1] Department of Chemistry, University of Kentucky, Lexington, Kentucky, United States
[2] Center of Membrane Sciences, University of Kentucky, Lexington, Kentucky, United States
[3] Department of Anatomy and Neurobiology, University of Kentucky, Lexington, Kentucky, United States
[4] Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky, United States
[5] Department of Physiology and Biophysics, Case Western Reserve Medical School, Cleveland, Ohio, United States
[6] Department of Neurology and Pathology, University of Kentucky, Lexington, Kentucky, United States
Source

Journal of neurochemistry. 2001, Vol 78, Num 2, pp 413-416 ; ref : 41 ref

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
Keyword (fr)
Démence Alzheimer Excitotoxicité Glutamate Homme Protéine amyloïde β Stress oxydatif Transport biologique Encéphale pathologie Maladie dégénérative Système nerveux central pathologie Système nerveux pathologie Toxicité
Keyword (en)
Alzheimer disease Excitotoxicity Glutamate Human β Amyloid protein Oxidative stress Biological transport Cerebral disorder Degenerative disease Central nervous system disease Nervous system diseases Toxicity
Keyword (es)
Demencia Alzheimer Exitotoxicidad Glutamato Hombre Proteína amiloide β Estrés oxidativo Transporte biológico Encéfalo patología Enfermedad degenerativa Sistema nervosio central patología Sistema nervioso patología Toxicidad
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
14093533

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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