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Pleiotropic effects of spastin on neurite growth depending on expression levels

Author
RIANO, Elena1 ; MARTIGNONI, Monica1 ; CAPPELLETTI, Graziella2 ; RUGARLI, Elena I1 6 ; MANCUSO, Giuseppe1 ; CARTELLI, Daniele2 ; CRIPPA, Francesca3 ; TOLDO, Irene4 ; SICILIANO, Gabriele5 ; DI BELLA, Daniela1 ; TARONI, Franco1 ; BASSI, Maria Teresa3
[1] Division of Biochemistry and Genetics, Istituto Neurologico C. Besta, Milan, Italy
[2] Department of Biology, University of Milan, Milan, Italy
[3] E. Medea Scientific Institute, Laboratory of Molecular Biology, Bosisio Parini, Italy
[4] Department of Pediatrics, University of Padua, Padua, Italy
[5] Department of Neuroscience, S. Chiara Hospital, University of Pisa, Pisa, Italy
[6] Department of Neuroscience and Medical Biotechnologies, University of Milano-Bicocca, Milan, Italy
Source

Journal of neurochemistry. 2009, Vol 108, Num 5, pp 1277-1288, 12 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
EB3 hereditary spastic paraplegia microtubule turnover microtubule-severing neurite growth
Keyword (fr)
Croissance Dégénérescence Déplétion Développement Faisceau corticospinal Gène Hippocampe Hypertonie spastique Membre inférieur Microtubule Mutation Neurone Paraplégie spasmodique héréditaire de Strümpell-Lorrain Protéine liaison Cytosquelette Encéphale Maladie dégénérative Maladie héréditaire Pathologie de l'encéphale Pathologie de la moelle épinière Pathologie du muscle strié Pathologie du système nerveux central Pathologie du système nerveux Système nerveux central Trouble du tonus Trouble neurologique Voie motrice pyramidale
Keyword (en)
Growth Degeneration Depletion Development Corticospinal bundle Gene Hippocampus Spasticity Lower limb Microtubule Mutation Neuron Hereditary spastic paraplegia Binding protein Cytoskeleton Encephalon Degenerative disease Genetic disease Cerebral disorder Spinal cord disease Striated muscle disease Central nervous system disease Nervous system diseases Central nervous system Muscle tonus alteration Neurological disorder Pyramidal motor pathway
Keyword (es)
Crecimiento Degeneración Depleción Desarrollo Fascículo corticoespinal Gen Hipocampo Hipertonia espástica Miembro inferior Microtúbulo Mutación Neurona Paraplejía espasmódica hereditaria Strümpell-Lorrain Proteína enlace Citoesqueleto Encéfalo Enfermedad degenerativa Enfermedad hereditaria Encéfalo patología Médula espinal patología Músculo estriado patología Sistema nervosio central patología Sistema nervioso patología Sistema nervioso central Trastorno tono muscular Trastorno neurológico Vía motora piramidal
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
21127613

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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