Astroglial FMRP-dependent translational down-regulation of mGluR5 underlies glutamate transporter GLT1 dysregulation in the fragile X mouse

By Higashimori Haruki   Morel Lydie   Huth James   Lindemann Lothar   Dulla Chris   Taylor Amaro   Freeman Mike   Yang Yongjie  

Human Molecular Genetics, Vol. 22, Iss. 10, 2013-05 ,pp. : 2041-2054

Oxford University Press

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82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization

By Bardoni B.  

Human Molecular Genetics, Vol. 12, Iss. 14, 2003-07 ,pp. : 1689-1698

Oxford University Press

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Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegeneration

By Tan Huiping   Qurashi Abrar   Poidevin Mickael   Nelson David L.   Li He   Jin Peng  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 57-65

Oxford University Press

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Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome

By Tucker Ben   Richards Robert I.   Lardelli Michael  

Human Molecular Genetics, Vol. 15, Iss. 23, 2006-12 ,pp. : 3446-3458

Oxford University Press

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Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila

By Qurashi Abrar   Liu Huijie   Ray Laurie   Nelson David L.   Duan Ranhui   Jin Peng  

Human Molecular Genetics, Vol. 21, Iss. 9, 2012-05 ,pp. : 2068-2075

Oxford University Press

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