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6. Deletion of Fmr1 in parvalbumin-expressing neurons results in dysregulated translation and selective behavioral deficits associated with fragile X syndrome. Kalinowska M; van der Lei MB; Kitiashvili M; Mamcarz M; Oliveira MM; Longo F; Klann E Mol Autism; 2022 Jun; 13(1):29. PubMed ID: 35768828 [TBL] [Abstract][Full Text] [Related]
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8. Astroglial FMRP-dependent translational down-regulation of mGluR5 underlies glutamate transporter GLT1 dysregulation in the fragile X mouse. Higashimori H; Morel L; Huth J; Lindemann L; Dulla C; Taylor A; Freeman M; Yang Y Hum Mol Genet; 2013 May; 22(10):2041-54. PubMed ID: 23396537 [TBL] [Abstract][Full Text] [Related]
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13. Genetic upregulation of BK channel activity normalizes multiple synaptic and circuit defects in a mouse model of fragile X syndrome. Deng PY; Klyachko VA J Physiol; 2016 Jan; 594(1):83-97. PubMed ID: 26427907 [TBL] [Abstract][Full Text] [Related]
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15. Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons. Tabet R; Moutin E; Becker JA; Heintz D; Fouillen L; Flatter E; Krężel W; Alunni V; Koebel P; Dembélé D; Tassone F; Bardoni B; Mandel JL; Vitale N; Muller D; Le Merrer J; Moine H Proc Natl Acad Sci U S A; 2016 Jun; 113(26):E3619-28. PubMed ID: 27233938 [TBL] [Abstract][Full Text] [Related]
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20. Fragile X mental retardation protein replacement restores hippocampal synaptic function in a mouse model of fragile X syndrome. Zeier Z; Kumar A; Bodhinathan K; Feller JA; Foster TC; Bloom DC Gene Ther; 2009 Sep; 16(9):1122-9. PubMed ID: 19571888 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]