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FMR protein: Evidence of an emerging role in retinal aging?
Ardourel, M; Ranchon-Cole, I; Pâris, A; Felgerolle, C; Acar, N; Lesne, F; Briault, S; Perche, O.
Afiliación
  • Ardourel M; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, 45071, Orléans, Cedex 2, France.
  • Ranchon-Cole I; Université Clermont Auvergne, CHU Clermont-Ferrand, Inserm, Neuro-Dol, F-63000, Clermont-Ferrand, France.
  • Pâris A; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, 45071, Orléans, Cedex 2, France.
  • Felgerolle C; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, 45071, Orléans, Cedex 2, France.
  • Acar N; Eye and Nutrition Research Group, Centre des Sciences du Goût et de l'Alimentation, CNRS, INRAE, Institut Agro, Université Bourgogne Franche-Comté, 21000, Dijon, France.
  • Lesne F; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France.
  • Briault S; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, 45071, Orléans, Cedex 2, France; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France.
  • Perche O; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, 45071, Orléans, Cedex 2, France; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France. Electronic address: olivier.perche@chr-orle
Exp Eye Res ; 225: 109282, 2022 12.
Article en En | MEDLINE | ID: mdl-36265576
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retina / Electrorretinografía / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil Límite: Animals Idioma: En Revista: Exp Eye Res Año: 2022 Tipo del documento: Article País de afiliación: Francia
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Retina / Electrorretinografía / Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil Límite: Animals Idioma: En Revista: Exp Eye Res Año: 2022 Tipo del documento: Article País de afiliación: Francia