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FMRP-related retinal phenotypes: Evidence of glutamate-glutamine metabolic cycle impairment.
Ardourel, Maryvonne; Pâris, Arnaud; Felgerolle, Chloé; Lesne, Fabien; Ranchon-Cole, Isabelle; Briault, Sylvain; Perche, Olivier.
Afiliação
  • Ardourel M; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, F-45071, Orléans Cedex 2, France.
  • Pâris A; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, F-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, F-45071, Orléans Cedex 2, France.
  • Lesne F; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France.
  • Ranchon-Cole I; Université Clermont Auvergne, CHU Clermont-Ferrand, Inserm, Neuro-Dol, F-63000, Clermont-Ferrand, France.
  • Briault S; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, F-45071, Orléans Cedex 2, France.
  • Perche O; Genetic Department, Regional Hospital, 14 Avenue de l'hôpital, 45100, Orléans, France; UMR7355, CNRS, Orléans, France; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 3b rue de la Ferollerie, F-45071, Orléans Cedex 2, France. Electronic address: olivier.perche@chr-orl
Exp Eye Res ; 224: 109238, 2022 11.
Article em En | MEDLINE | ID: mdl-36067823
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Limite: Animals / Humans Idioma: En Revista: Exp Eye Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Limite: Animals / Humans Idioma: En Revista: Exp Eye Res Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França