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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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

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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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Maintenance of X- and Y-inactivation of the pseudoautosomal (PAR2) gene SPRY3 is independent from DNA methylation and associated to multiple layers of epigenetic modifications

By De Bonis M.L.   Cerase A.   Strazzullo M.   Hansen R.S.   Chiurazzi P.   Neri G.   D'Esposito M.  

Human Molecular Genetics, Vol. 15, Iss. 7, 2006-04 ,pp. : 1123-1132

Oxford University Press

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Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene

By Chiurazzi Pietro  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2317-2323

Oxford University Press

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