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Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model
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Insulin-like growth factor-1 and neurotrophin-3 gene therapy prevents motor decline in an X-linked adrenoleukodystrophy mouse model

Roberto Mastroeni, Jean-Charles Bensadoun, Delphine Charvin, Patrick Aebischer, Aurora Pujol et Cédric Raoul
Annals of neurology, Vol.66(1), pp.117-122
07/2009
PMID: 19670442

Résumé

Adrenoleukodystrophy - complications Adrenoleukodystrophy - genetics Analysis of Variance Animals ATP Binding Cassette Transporter, Sub-Family D ATP-Binding Cassette Transporters - genetics Behavior, Animal - physiology Chemokine CCL22 - deficiency Dependovirus - genetics Disease Models, Animal Gene Transfer Techniques Genetic Therapy - methods Green Fluorescent Proteins - genetics Humans Insulin-Like Growth Factor I - cerebrospinal fluid Insulin-Like Growth Factor I - genetics Mice Mice, Knockout Movement Disorders - etiology Movement Disorders - therapy Neurotrophin 3 - cerebrospinal fluid Neurotrophin 3 - genetics

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