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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Instability of a (CGG) 98 repeat in the Fmr1 promoter

By Hirst M.C.   Bontekoe C.J.M.   Bakker C.E.   Nieuwenhuizen I.M.   van der Linde H.   Lans H.   de Lange D.   Oostra B.A.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1693-1699

Oxford University Press

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The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

By Tassone F.  

Human Molecular Genetics, Vol. 12, Iss. 9, 2003-05 ,pp. : 949-959

Oxford University Press

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Analysis of Germline Variation at the FMR1 CGG Repeat Shows Variation in the Normal-Premutated Borderline Range

By Monet Etienne   Chateau Corinne   Hirst Mark C.   Thepot François   Taillandier Agnès   Cibois Olivier   Serre Jean-Louis  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 821-825

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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

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