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Lack of FMRP in the retina: Evidence of a retinal specific transcriptomic profile.

• Authors : Attallah A; Orléans University, University Hospital Center of Orleans, LI(2)RSO, 14, Avenue de l'hôpital, 45100, Orléans, France; Orleans University, CNRS, laboratoire INEM, UMR7355, 3b Rue de la Férollerie, F-45071, Orléans, Cedex 2, France

Subjects: Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/metabolism ; Retina*/Retina*/Retina*/metabolism

• Source: Experimental eye research [Exp Eye Res] 2024 Sep; Vol. 246, pp. 110015. Date of Electronic Publication: 2024 Jul 31.Publisher: Academic Press Country of Publication: England NLM ID: 0370707 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Dietary supplement enriched in antioxidants and omega-3 promotes retinal glutamine synthesis.

• Authors : Attallah A; Université D'Orléans, CHU D'Orléans, LI(2)RSO, 14, Avenue de L'hôpital, 45100, Orléans, France; Université D'Orléans, CNRS, Laboratoire INEM, UMR7355, 3b Rue de La Ferollerie, F-45071, Orléans, Cedex 2, France.

Subjects: Glutamine*/Glutamine*/Glutamine*/metabolism ; Dietary Supplements* ; Antioxidants*/Antioxidants*/Antioxidants*/pharmacology

• Source: Experimental eye research [Exp Eye Res] 2024 Aug; Vol. 245, pp. 109964. Date of Electronic Publication: 2024 Jun 06.Publisher: Academic Press Country of Publication: England NLM ID: 0370707 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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FMR protein: Evidence of an emerging role in retinal aging?

• Authors : 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.

Subjects: Electroretinography* ; Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Retina*/Retina*/Retina*/pathology

• Source: Experimental eye research [Exp Eye Res] 2022 Dec; Vol. 225, pp. 109282. Date of Electronic Publication: 2022 Oct 17.Publisher: Academic Press Country of Publication: England NLM ID: 0370707 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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FMRP-related retinal phenotypes: Evidence of glutamate-glutamine metabolic cycle impairment.

• Authors : 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.

Subjects: Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/Fragile X Mental Retardation Protein*/genetics ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/metabolism

• Source: Experimental eye research [Exp Eye Res] 2022 Nov; Vol. 224, pp. 109238. Date of Electronic Publication: 2022 Sep 05.Publisher: Academic Press Country of Publication: England NLM ID: 0370707 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Agricola

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Il male del Nord : Perché o si fa l'Italia da Sud o si muore

• Authors : Pino Aprile

Subjects: HISTORY / Social History

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Large-conductance calcium-activated potassium channel haploinsufficiency leads to sensory deficits in the visual system: a case report.

• Authors : Perche O; Genetic Department, Centre Hospitalier Régional d'Orléans, Orléans, France.; UMR7355, Immunologie et Neurogénétique Expérimentales et Moléculaires (INEM), Centre National de la Recherche Scientifique (CNRS), Orléans, France.

Subjects: Autism Spectrum Disorder* ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/complications ; Intellectual Disability*/Intellectual Disability*/Intellectual Disability*/genetics

• Source: Journal of medical case reports [J Med Case Rep] 2022 May 05; Vol. 16 (1), pp. 180. Date of Electronic Publication: 2022 May 05.Publisher: BioMed Central Country of Publication: England NLM ID: 101293382 Publication Model: Electronic Cited Medium: Internet ISSN: 1752-1947

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Electroretinography and contrast sensitivity, complementary translational biomarkers of sensory deficits in the visual system of individuals with fragile X syndrome.

• Authors : Perche O; Genetic Department, Centre Hospitalier Régional d'Orléans, Orléans, France.; UMR7355, Centre National de la Recherche Scientifique (CNRS), Orléans, France.

Subjects: Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/complications ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/diagnosis ; Fragile X Syndrome*/Fragile X Syndrome*/Fragile X Syndrome*/genetics

• Source: Journal of neurodevelopmental disorders [J Neurodev Disord] 2021 Oct 08; Vol. 13 (1), pp. 45. Date of Electronic Publication: 2021 Oct 08.Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Internet ISSN: 1866-1955

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Dietary Supplement Enriched in Antioxidants and Omega-3 Promotes Glutamine Synthesis in Müller Cells: A Key Process against Oxidative Stress in Retina.

• Authors : Ardourel M; UMR7355, Experimental and Molecular Immunology and Neurogenetics, CNRS Orléans Campus, 3B rue de la Ferollerie, 45100 Orléans, France.; Experimental and Molecular Immunology and Neurogenetics, University of Orléans, 45100 Orléans, France.

Subjects: Antioxidants/Antioxidants/Antioxidants/*pharmacology ; Ependymoglial Cells/Ependymoglial Cells/Ependymoglial Cells/*drug effects ; Fatty Acids, Omega-3/Fatty Acids, Omega-3/Fatty Acids, Omega-3/*pharmacology

• Source: Nutrients [Nutrients] 2021 Sep 16; Vol. 13 (9). Date of Electronic Publication: 2021 Sep 16.Publisher: MDPI Publishing Country of Publication: Switzerland NLM ID: 101521595 Publication Model: Electronic Cited Medium: Internet ISSN:

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Impaired expression of the COSMOC/MOCOS gene unit in ASD patient stem cells.

• Authors : Rontani P; Aix Marseille University, CNRS, INP, UMR 7051, Marseille, France.; Perche O

Subjects: Asperger Syndrome* ; Autism Spectrum Disorder*/Autism Spectrum Disorder*/Autism Spectrum Disorder*/genetics ; Induced Pluripotent Stem Cells*

• Source: Molecular psychiatry [Mol Psychiatry] 2021 May; Vol. 26 (5), pp. 1606-1618. Date of Electronic Publication: 2020 Apr 23.Publisher: Nature Publishing Group Specialist Journals Country of Publication: England NLM ID: 9607835 Publication Model: Print-Electronic Cited Medium:

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