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

Author： Willemsen R.  

Publisher： Oxford University Press

ISSN： 1460-2083

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

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

Access to resources Recommend Favorite

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

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

Epigenetic Variation Illustrated by DNA Methylation Patterns of the Fragile-X Gene FMR1

By Stöger Reinhard  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1791-1801

Oxford University Press

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite