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المؤلفون: Martin HGS; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK., Kullmann DM; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK.

المصدر: Cells [Cells] 2023 May 13; Vol. 12 (10). Date of Electronic Publication: 2023 May 13.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409 (Electronic) Linking ISSN: 20734409 NLM ISO Abbreviation: Cells Subsets: MEDLINE

مواضيع طبية MeSH: Purkinje Cells*/metabolism , Purkinje Cells*/pathology , Neural Inhibition* , Kv1.1 Potassium Channel*/genetics , Kv1.1 Potassium Channel*/metabolism , Ataxia*/genetics , Ataxia*/pathology , Ataxia*/physiopathology , Myokymia*/genetics , Myokymia*/pathology , Myokymia*/physiopathology, Animals ; Mice ; Disease Models, Animal ; Synapses/physiology ; Cell Communication ; Synaptic Transmission ; Evoked Potentials ; Mice, Inbred C57BL ; Male ; Female

SCR Disease Name: Episodic Ataxia, Type 1

المؤلفون: Martin HGS; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille 13009, France., Lassalle O; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille 13009, France., Manzoni OJ; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille 13009, France.

المصدر: Cerebral cortex (New York, N.Y. : 1991) [Cereb Cortex] 2017 Dec 01; Vol. 27 (12), pp. 5592-5602.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: United States NLM ID: 9110718 Publication Model: Print Cited Medium: Internet ISSN: 1460-2199 (Electronic) Linking ISSN: 10473211 NLM ISO Abbreviation: Cereb Cortex Subsets: MEDLINE

مواضيع طبية MeSH: Fragile X Syndrome/*metabolism , Long-Term Synaptic Depression/*physiology , Prefrontal Cortex/*growth & development , Prefrontal Cortex/*metabolism , Receptor, Metabotropic Glutamate 5/*metabolism, Aging/metabolism ; Animals ; Endocannabinoids/metabolism ; Endophenotypes ; Excitatory Postsynaptic Potentials/physiology ; Fragile X Mental Retardation Protein/genetics ; Fragile X Mental Retardation Protein/metabolism ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; Patch-Clamp Techniques ; Recovery of Function/physiology ; Signal Transduction ; Tissue Culture Techniques

المؤلفون: Martin HGS; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille, France., Lassalle O; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille, France., Brown JT; Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter, UK., Manzoni OJ; INSERM U901, Marseille 13009, France.; INMED, Marseille 13009, France.; Université de Aix-Marseille, UMR S901, Marseille, France.

المصدر: Cerebral cortex (New York, N.Y. : 1991) [Cereb Cortex] 2016 May; Vol. 26 (5), pp. 2084-2092. Date of Electronic Publication: 2015 Mar 05.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Oxford University Press Country of Publication: United States NLM ID: 9110718 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2199 (Electronic) Linking ISSN: 10473211 NLM ISO Abbreviation: Cereb Cortex Subsets: MEDLINE

مواضيع طبية MeSH: Long-Term Potentiation*, Fragile X Mental Retardation Protein/*physiology , Fragile X Syndrome/*physiopathology , Neurons/*physiology , Prefrontal Cortex/*physiopathology, Action Potentials ; Animals ; Disease Models, Animal ; Electric Stimulation ; Excitatory Postsynaptic Potentials/drug effects ; Fragile X Mental Retardation Protein/genetics ; Fragile X Syndrome/genetics ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Neurons/drug effects ; Prefrontal Cortex/drug effects ; Pyridines/pharmacology ; Receptor, Metabotropic Glutamate 5/antagonists & inhibitors ; Receptor, Metabotropic Glutamate 5/physiology ; Receptors, AMPA/physiology ; Receptors, N-Methyl-D-Aspartate/physiology