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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

APP-dependent up-regulation of Ptch1 underlies proliferation impairment of neural precursors in Down syndrome

By Trazzi Stefania   Mitrugno Valentina Maria   Valli Emanuele   Fuchs Claudia   Rizzi Simona   Guidi Sandra   Perini Giovanni   Bartesaghi Renata   Ciani Elisabetta  

Human Molecular Genetics, Vol. 20, Iss. 8, 2011-04 ,pp. : 1560-1573

Oxford University Press

Access to resources Recommend Favorite

Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio

By Godler David Eugeny   Tassone Flora   Loesch Danuta Zuzanna   Taylor Annette Kimball   Gehling Freya   Hagerman Randi Jenssen   Burgess Trent   Ganesamoorthy Devika   Hennerich Debbie   Gordon Lavinia   Evans Andrew   Choo K.H.   Slater Howard Robert  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1618-1632

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite