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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Haplotype and Interspersion Analysis of the FMR1 CGG Repeat Identifies Two Different Mutational Pathways for the Origin of the Fragile X Syndrome

By Eichler Evan E.   Macpherson James N.   Murray Anna   Jacobs Patricia A.   Chakravarti Aravinda   Nelson David L.  

Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 319-330

Oxford University Press

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In vitro reactivation of the FMR1 gene involved in fragile X syndrome

By Willemsen R.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 109-113

Oxford University Press

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The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndrome

By Kumari Daman   Usdin Karen  

Human Molecular Genetics, Vol. 19, Iss. 23, 2010-12 ,pp. : 4634-4642

Oxford University Press

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Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice

By Iliff Adam J.   Renoux Abigail J.   Krans Amy   Usdin Karen   Sutton Michael A.   Todd Peter K.  

Human Molecular Genetics, Vol. 22, Iss. 6, 2013-03 ,pp. : 1180-1192

Oxford University Press

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