Edg-2 in myelin-forming cells : Isoforms, genomic mapping, and exclusion in Charcot-Marie-Tooth disease
- Author
- ALLARD, J1 ; BARRON, S1 ; TROTTIER, S1 ; CERVERA, P2 ; DAUMAS-DUPORT, C2 ; LEGUERN, E2 ; BRICE, A3 ; SCHWARTZ, J.-C1 ; SOKOLOFF, P1
[1] Unité de Neurobiologie et Pharmacologie Moléculaire, Centre Paul Broca, Paris, France
[2] Service d'Anatomopathologie de l'Hôpital Sainte-Anne, Paris, France
[3] Mécanismes et Conséquences de la Mort Neuronale, INSERM U289, Hôpital de la Pitié-Salpétrière, Paris, France - Source
Glia (New York, NY. Print). 1999, Vol 26, Num 2, pp 176-185 ; ref : 44 ref
- CODEN
- GLIAEJ
- ISSN
- 0894-1491
- Scientific domain
- Cell biology, histology; Physiology, morphology
- Publisher
- Wiley-Liss, New York, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Amyotrophie Charcot Marie Tooth Animal Encéphale Forme moléculaire Génome Liaison génétique Myéline Oligodendrocyte Rat Récepteur biologique Récepteur Edg2 Maladie dégénérative Maladie héréditaire Mammalia Moelle épinière pathologie Neuromusculaire pathologie Névroglie Rodentia Système nerveux central pathologie Système nerveux central Système nerveux pathologie Vertebrata
- Keyword (en)
- Charcot Marie Tooth disease Animal Brain (vertebrata) Molecular form Genome Linkage Myelin Oligodendrocyte Rat Biological receptor Degenerative disease Genetic disease Mammalia Spinal cord disease Neuromuscular diseases Neuroglia Rodentia Central nervous system disease Central nervous system Nervous system diseases Vertebrata
- Keyword (es)
- Amiotrofía Charcot Marie Tooth Animal Encéfalo Forma molecular Genoma Ligamiento genético Mielina Oligodendrocito Rata Receptor biológico Enfermedad degenerativa Enfermedad hereditaria Mammalia Médula espinal patología Neuromuscular patología Neuroglia Rodentia Sistema nervosio central patología Sistema nervioso central Sistema nervioso patología Vertebrata
- 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
- 1764872
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
10.1002/(SICI)1098-1136(199904)26:2<176::AID-GLIA8>3.0.CO;2-K 
https://dx.doi.org/10.1002/(SICI)1098-1136(199904)26:2<176::AID-GLIA8>3.0.CO;2-K
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